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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Nutr.</journal-id>
<journal-title-group>
<journal-title>Frontiers in Nutrition</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Nutr.</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">2296-861X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fnut.2025.1503294</article-id><article-version article-version-type="Version of Record" vocab="NISO-RP-8-2008"/>
<article-categories>
<subj-group subj-group-type="heading"><subject>Original Research</subject></subj-group>
</article-categories>
<title-group>
<article-title>RETRACTED: The influence of evidence-based nutritional support plans on the nutritional status and adverse effects of radiotherapy in individuals with nasopharyngeal carcinoma</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Fan</surname> <given-names>Xiaomei</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/2639259"/>
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</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Cui</surname> <given-names>Huixia</given-names></name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x002A;</sup></xref>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Funding acquisition" vocab-term-identifier="https://credit.niso.org/contributor-roles/funding-acquisition/">Funding acquisition</role>
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</contrib>
<contrib contrib-type="author">
<name><surname>Peng</surname> <given-names>Haibo</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
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</contrib>
<contrib contrib-type="author">
<name><surname>Liu</surname> <given-names>Shasha</given-names></name>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="methodology" vocab-term-identifier="https://credit.niso.org/contributor-roles/methodology/">Methodology</role>
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</contrib>
<contrib contrib-type="author">
<name><surname>Jiang</surname> <given-names>Li</given-names></name>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
<role vocab="credit" vocab-identifier="https://credit.niso.org/" vocab-term="Data curation" vocab-term-identifier="https://credit.niso.org/contributor-roles/data-curation/">Data curation</role>
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<aff id="aff1"><label>1</label><institution>Clinical Medical College, Chengdu Medical College</institution>, <city>Chengdu</city>, <country country="cn">China</country></aff>
<aff id="aff2"><label>2</label><institution>The First Affiliated Hospital of Chengdu Medical College</institution>, <city>Chengdu</city>, <country country="cn">China</country></aff>
<aff id="aff3"><label>3</label><institution>School of Nursing, Wannan Medical College</institution>, <city>Wuhu</city>, <country country="cn">China</country></aff>
<aff id="aff4"><label>4</label><institution>Chengdu BOE Hospital</institution>, <city>Chengdu</city>, <country country="cn">China</country></aff>
<author-notes><corresp id="c001"><label>&#x002A;</label>Correspondence: Huixia Cui, <email xlink:href="mailto:1319447367@qq.com">1319447367@qq.com</email></corresp></author-notes>
<pub-date publication-format="electronic" date-type="pub" iso-8601-date="2025-04-15">
<day>15</day>
<month>04</month>
<year>2025</year>
</pub-date>
<pub-date publication-format="electronic" date-type="retracted" iso-8601-date="2026-07-13">
<day>13</day>
<month>07</month>
<year>2026</year>
</pub-date>
<pub-date publication-format="electronic" date-type="collection">
<year>2025</year>
</pub-date>
<volume>12</volume>
<elocation-id>1503294</elocation-id>
<history>
<date date-type="received">
<day>28</day>
<month>09</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>28</day>
<month>03</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2025 Fan, Cui, Peng, Liu and Jiang.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Fan, Cui, Peng, Liu and Jiang</copyright-holder>
<license><ali:license_ref start_date="2025-04-15">https://creativecommons.org/licenses/by/4.0/</ali:license_ref>
<license-p>This is an open-access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution License (CC BY)</ext-link>. The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</license-p>
</license>
</permissions>
<abstract>
<sec id="sec1">
<title>Objective</title>
<p>Radiotherapy serves as the primary treatment for patients with nasopharyngeal carcinoma (NPC). However, it frequently results in a progressive decline in nutritional status, which is linked to unfavorable clinical outcomes. This study aims to evaluate the effects of an evidence-based nutritional support program on nutritional status, radiotherapy-related side effects, and quality of life (QoL) in NPC patients undergoing radiotherapy.</p>
</sec>
<sec id="sec2">
<title>Methods</title>
<p>A historical control trial was conducted. Patients with NPC admitted between May 2023 and August 2023 were allocated to the control group and received routine care, whereas those admitted between September 2023 and December 2023 were assigned to the intervention group and provided with a multidisciplinary, professional, individualized, and comprehensive evidence-based nutritional support program. Nutritional status was assessed through anthropometric measurements (e.g., body mass index, BMI), laboratory indicators (hemoglobin and albumin levels), the Nutritional Risk Screening 2002 (NRS2002), and the Patient-Generated Subjective Global Assessment (PG-SGA). Additionally, radiotherapy-related side effects, radiotherapy interruption rates, and QoL were monitored.</p>
</sec>
<sec id="sec3">
<title>Results</title>
<p>Both groups comprised 40 patients each. By the conclusion of radiotherapy, a decline in nutritional status was observed in both groups; however, BMI was higher in the intervention group (23.14&#x202F;&#x00B1;&#x202F;2.62) compared to the control group (21.38&#x202F;&#x00B1;&#x202F;2.73). The NRS2002 score (2.73&#x202F;&#x00B1;&#x202F;1.45) and PG-SGA score (6.13&#x202F;&#x00B1;&#x202F;3.22) in the intervention group were significantly lower than in the control group (3.33&#x202F;&#x00B1;&#x202F;1.16 and 7.73&#x202F;&#x00B1;&#x202F;2.72, respectively; <italic>p</italic>&#x202F;&#x003C;&#x202F;0.05). The incidence of severe malnutrition was significantly lower in the intervention group (52.5%) compared to the control group (75%) (<italic>p</italic>&#x202F;&#x003C;&#x202F;0.05). Albumin and hemoglobin levels were significantly higher in the intervention group (albumin: 120.75&#x202F;&#x00B1;&#x202F;16.52 vs. 113.50&#x202F;&#x00B1;&#x202F;12.08, <italic>p</italic>&#x202F;=&#x202F;0.028; hemoglobin: 41.24&#x202F;&#x00B1;&#x202F;4.54 vs. 37.62&#x202F;&#x00B1;&#x202F;5.04, <italic>p</italic>&#x202F;=&#x202F;0.001). The severity of radiotherapy-related side effects, including radiation-induced oral mucositis, dermatitis, and myelosuppression, was significantly lower in the intervention group (<italic>p</italic>&#x202F;&#x003C;&#x202F;0.05). All patients completed radiotherapy, and no significant difference was observed in radiotherapy interruption rates between groups (control group: 6 interruptions; intervention group: 1 interruption; <italic>p</italic>&#x202F;&#x003E;&#x202F;0.05). Post-radiotherapy QoL scores demonstrated that the intervention group achieved superior outcomes in physical, role, emotional, cognitive, and social functioning (<italic>p</italic>&#x202F;&#x003C;&#x202F;0.05).</p>
</sec>
<sec id="sec4">
<title>Conclusion</title>
<p>Implementing evidence-based nutritional support programs has the potential to prevent the decline in nutritional status among NPC patients receiving radiotherapy, reduce the occurrence of treatment-related side effects, and enhance overall quality of life.</p>
</sec>
</abstract>
<kwd-group>
<kwd>nasopharyngeal carcinoma</kwd>
<kwd>radiotherapy</kwd>
<kwd>nutritional support</kwd>
<kwd>evidence-based nursing</kwd>
<kwd>adverse effects of radiotherapy</kwd>
</kwd-group><funding-group><funding-statement>The author(s) declare that financial support was received for the research and/or publication of this article. This work was supported by Key Clinical Specialty of Sichuan Province (YS00109) and the Wannan Medical College under Grant [number WYRCQD2023043].</funding-statement></funding-group>
<counts>
<fig-count count="1"/>
<table-count count="8"/>
<equation-count count="0"/>
<ref-count count="89"/>
<page-count count="13"/>
<word-count count="9726"/>
</counts>
<custom-meta-group>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Clinical Nutrition</meta-value>
</custom-meta>
</custom-meta-group>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="sec5">
<label>1</label>
<title>Introduction</title>
<p>Nasopharyngeal carcinoma (NPC) is a malignant tumor originating from the epithelial cells of the nasopharyngeal mucosa, posing a significant public health concern (<xref ref-type="bibr" rid="ref1">1</xref>). According to global cancer statistics from 2020, over 130,000 new cases of NPC were reported, with more than 80,000 associated fatalities (<xref ref-type="bibr" rid="ref2">2</xref>).</p>
<p>The primary treatment for NPC involves radiotherapy, either alone or in combination with other modalities, with radiation serving as the cornerstone of therapy (<xref ref-type="bibr" rid="ref3">3</xref>). Advances in diagnostic and therapeutic approaches, along with improvements in radiotherapy equipment and the widespread adoption of intensity-modulated radiotherapy (IMRT), have contributed to enhanced NPC tumor control and increased survival rates. However, radiotherapy-induced side effects can lead to complications such as taste alterations, oropharyngeal pain, xerostomia, excessive pharyngeal mucus secretion, and dysphagia (<xref ref-type="bibr" rid="ref4">4</xref>) These symptoms tend to worsen as treatment progresses, resulting in a continuous decline in nutritional status, with malnutrition emerging as a prevalent concern among these patients (<xref ref-type="bibr" rid="ref5 ref6 ref7 ref8">5&#x2013;8</xref>). A study conducted by Wan et al. (<xref ref-type="bibr" rid="ref9">9</xref>) reported that the prevalence of malnutrition in NPC patients was 16.8% prior to treatment but escalated to 91.2% by the end of therapy. Research by Tang et al. (<xref ref-type="bibr" rid="ref10">10</xref>) indicated that more than 10% of patients undergoing concurrent chemoradiotherapy experienced significant weight loss by the 10th week of treatment. Similarly, a study by Hong et al. (<xref ref-type="bibr" rid="ref11">11</xref>) found that 20.19% of patients experienced weight loss exceeding 10% by the conclusion of radiotherapy. Furthermore, Kan et al. (<xref ref-type="bibr" rid="ref12">12</xref>) found that 47.1% of patients lost 5&#x2013;10% of their body weight during radiotherapy. A qualitative study identified oral complications, including mucositis, xerostomia, taste alterations, and dysphagia, as among the most challenging issues encountered by NPC patients (<xref ref-type="bibr" rid="ref13">13</xref>). Additionally, research has shown that nearly all NPC patients receiving concurrent chemoradiotherapy develop oral mucositis (<xref ref-type="bibr" rid="ref14">14</xref>). Headaches are also one of the most common symptoms in NPC, and severe headaches can lead to decreased appetite and fatigue. Additionally, the incidence of NPC is highest in individuals aged 40&#x2013;59&#x202F;years (<xref ref-type="bibr" rid="ref1">1</xref>), a group more susceptible to stress and prone to anxiety and depression, which are often associated with gastrointestinal dysfunction and reduced food intake (<xref ref-type="bibr" rid="ref15">15</xref>). Studies indicate that pre-existing malnutrition in NPC patients increases the likelihood of severe taste disturbances, mucositis, dysphagia, and xerostomia following IMRT (<xref ref-type="bibr" rid="ref16">16</xref>). Moreover, malnutrition has been associated with an increased risk of radiotherapy positioning errors and a reduced ability to tolerate and respond to treatment (<xref ref-type="bibr" rid="ref17">17</xref>, <xref ref-type="bibr" rid="ref18">18</xref>). A cohort study (<xref ref-type="bibr" rid="ref19">19</xref>) found that a Nutritional Risk Screening (NRS 2002) score of &#x2265;3 was significantly correlated with survival outcomes in middle-aged NPC patients. Given these findings, improving the nutritional status of NPC patients undergoing radiotherapy, minimizing treatment-related side effects, and enhancing overall quality of life remain critical priorities in both clinical and nursing practice.</p>
<p>Considerable research has been conducted both domestically and internationally on nutritional support for patients with nasopharyngeal carcinoma (NPC). Various intervention models have been identified for their effectiveness in improving the nutritional status of NPC patients undergoing radiotherapy. Personalized Comprehensive Nutritional Management involves selecting the appropriate timing and route of nutritional support based on the patient&#x2019;s condition, developing individualized nutritional plans, and making timely adjustments according to changes in weight and related indicators (<xref ref-type="bibr" rid="ref20 ref21 ref22 ref23 ref24 ref25 ref26">20&#x2013;26</xref>). Systematic Nutritional Management includes a comprehensive assessment of nutritional status by registered dietitians, followed by the formulation of nutritional plans based on energy requirements (<xref ref-type="bibr" rid="ref27">27</xref>). The PDCA Cycle Model consists of four stages&#x2014;Plan (P), Do (D), Check (C), and Act (A)&#x2014;to ensure continuous improvements in care quality (<xref ref-type="bibr" rid="ref28">28</xref>). The Bundle Management Model incorporates nutritional education, nutritional assessment and screening, adequate nutritional intake, prevention and management of treatment-related symptoms, rehabilitation exercise guidance, and psychological support (<xref ref-type="bibr" rid="ref29">29</xref>, <xref ref-type="bibr" rid="ref30">30</xref>). The Multidisciplinary Team (MDT) Collaboration Model involves a team of physicians, dietitians, clinical pharmacists, rehabilitation therapists, psychologists, and clinical nurses working together to optimize patient care (<xref ref-type="bibr" rid="ref31">31</xref>, <xref ref-type="bibr" rid="ref32">32</xref>). Additionally, early nutritional intervention (<xref ref-type="bibr" rid="ref33">33</xref>), oral nutritional supplementation (<xref ref-type="bibr" rid="ref34">34</xref>), and enteral nutrition (<xref ref-type="bibr" rid="ref35">35</xref>) have been demonstrated to enhance the nutritional status of NPC patients. However, these intervention models were primarily designed for other diseases and lack the scientific rigor and specificity required for NPC patients undergoing radiotherapy, making them insufficient in addressing the complex care needs of this population. Evidence-based nursing, which involves identifying clinical questions, integrating theoretical research with nursing experience, and formulating patient care plans based on scientific evidence, has been shown to improve the effectiveness and reliability of patient care (<xref ref-type="bibr" rid="ref36">36</xref>, <xref ref-type="bibr" rid="ref37">37</xref>). This study is the first to apply the evidence-based nutritional support program for NPC patients undergoing radiotherapy in a clinical setting, aiming to evaluate its impact on nutritional status, radiotherapy-related side effects, and quality of life.</p>
</sec>
<sec sec-type="materials|methods" id="sec6">
<label>2</label>
<title>Materials and methods</title>
<sec id="sec7">
<label>2.1</label>
<title>Research subjects</title>
<p>Patients diagnosed with nasopharyngeal carcinoma (NPC) undergoing radiotherapy and admitted to the hospital between May and December 2023 were included in this study. A convenience sampling method was employed, categorizing patients admitted between May and August 2023 into the control group, which received standard nursing care. Patients admitted from September to December 2023 were assigned to the experimental group and received interventions based on an evidence-based nutritional support plan during radiotherapy.</p>
<p>Inclusion criteria were as follows: age&#x202F;&#x2265;&#x202F;18&#x202F;years, confirmed pathological diagnosis of NPC, undergoing radiotherapy, absence of mental disorders, ability to cooperate with treatment, and provision of informed consent with willingness to participate. Exclusion criteria included the presence of severe comorbidities and an estimated survival time of less than 3 months.</p>
<p>A total of 80 patients were enrolled in the study, with 40 patients in each group, all of whom successfully completed the trial. Informed consent was obtained from all participants. Ethical approval for the study was granted by the ethics committee under approval number JZMULL2022075.</p>
</sec>
<sec id="sec8">
<label>2.2</label>
<title>IMRT treatment</title>
<p>All patients underwent intensity-modulated radiation therapy (IMRT) using a 6 MV X-ray linear accelerator. The prescribed radiation dose for the primary tumor and positive cervical lymph nodes ranged from 69.5 to 72.6&#x202F;Gy. High-risk clinical target regions received 60.0&#x202F;Gy, while low-risk subclinical regions were administered 54.0&#x202F;Gy. The cervical lymph node drainage areas were treated with a dose ranging from 50.0 to 56.0&#x202F;Gy. Treatment was delivered in 33 fractions, once daily, five times per week, and was completed within 6&#x2013;7&#x202F;weeks.</p>
</sec>
<sec id="sec9">
<label>2.3</label>
<title>Research methods</title>
<sec id="sec10">
<label>2.3.1</label>
<title>Control group intervention methods</title>
<p>The control group received standard nutritional management. Upon admission, height and weight were measured, and nutritional risk was assessed using the NRS2002 screening tool. During radiotherapy, weight and blood parameters were monitored weekly. Once a patient is diagnosed with malnutrition, the responsible nurse will provide nutritional guidance, the physician will monitor nutritional indicators, and enteral or parenteral nutrition will be initiated based on clinical indications. If necessary, a consultation with the nutrition department will be requested for further assistance. After radiotherapy, regular follow-ups were conducted.</p>
</sec>
<sec id="sec11">
<label>2.3.2</label>
<title>Experimental intervention methods</title>
<p>Building upon the control group protocol, an intervention strategy was developed based on the evidence-based nutritional support plan for NPC patients undergoing radiotherapy (<xref ref-type="bibr" rid="ref38">38</xref>), as detailed below:</p>
<p>A nutritional support team was established, comprising a chief physician responsible for research design and implementation, a head nurse overseeing quality control, two radiation oncologists managing patient conditions and formulating nutritional plans, a nutritionist conducting nutritional training and plan development, two nurses monitoring and recording nutritional intake while providing health education, and two specialized nutrition nurses conducting nutritional screening and assessment, delivering nutritional education, guiding functional exercises, monitoring nutritional status, following up with patients, and collecting data.</p>
<p>Knowledge training: prior to implementation, centralized training sessions were conducted for all medical staff, focusing on the content and execution of the nutritional support plan for NPC patients undergoing radiotherapy. Three training sessions were organized, ensuring that each staff member attended at least two sessions. Various formats, including offline and online training, as well as morning meetings, were utilized to maintain consistency in content delivery.</p>
<p>Implementation protocol: upon admission, nutritional risk screening and assessment were performed, and relevant nutrition-related indicators were measured. Before radiotherapy, an informational brochure was distributed outlining the radiotherapy process, strategies for preventing and managing side effects, and nutritional guidance. During radiotherapy, a multidisciplinary healthcare team, including physicians, nutritionists, and nurses, developed individualized nutrition plans. Daily nutritional rounds were conducted to monitor nutrition-related symptoms, provide guidance on functional exercises, and perform weekly assessments of nutritional indicators. Following radiotherapy, specialized nutrition nurses carried out follow-up evaluations. The detailed implementation plan is presented in <xref ref-type="table" rid="tab1">Table 1</xref>.</p>
<table-wrap position="float" id="tab1">
<label>Table 1</label>
<caption>
<p>Nutritional support implementation plan for patients with nasopharyngeal carcinoma undergoing radiotherapy.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Time</th>
<th align="left" valign="top">Implementation project</th>
<th align="left" valign="top">Implementation strategy</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">Within 24&#x202F;h of admission</td>
<td align="left" valign="top">Risk Screening</td>
<td align="left" valign="top">1. Nutritional risk assessment will be conducted using the NRS 2002 (Nutritional Risk Screening 2002) scale. This process involves recording height, weight, and body mass index (BMI), documenting dietary intake, and evaluating nutrition-related symptoms along with muscle mass.<break/>2. Routine blood tests and biochemical indicators will be monitored by physicians to ensure comprehensive nutritional and clinical management.</td>
</tr>
<tr>
<td align="left" valign="top">Within 48&#x202F;h of admission</td>
<td align="left" valign="top">Nutritional Assessment</td>
<td align="left" valign="top">1. When the NRS2002 score is &#x2265;3 points, a collaborative assessment of the patient&#x2019;s nutritional status will be conducted by physicians and nurses using the PG-SGA scale.<break/>2. If the PG-SGA score is &#x2265;4 points, an evaluation of the necessity for nutritional therapy.<break/>3. If the PG-SGA score is &#x2265;9 points, radiotherapy should be temporarily suspended, and nutritional support should be administered until improvement is achieved.</td>
</tr>
<tr>
<td align="left" valign="top">Pre-radiotherapy</td>
<td align="left" valign="top">Nutritional Guidance</td>
<td align="left" valign="top">1. The consumption of whole grains and starchy vegetables as the primary source of carbohydrates should be emphasized (<xref ref-type="bibr" rid="ref76">76</xref>).<break/>2. The protein supply should be 1.0&#x2013;1.5&#x202F;g/kg per day, the intake of fish, poultry, eggs, and dairy should be increased to boost protein levels (<xref ref-type="bibr" rid="ref7">7</xref>, <xref ref-type="bibr" rid="ref76 ref77 ref78">76&#x2013;78</xref>).<break/>3. Fat intake should be appropriately increased, focusing on unsaturated fatty acids from sources such as nuts, deep-sea fish, and olive oil. The consumption of saturated fatty acids and trans fats from red meat, full-fat dairy products, and fried foods should be limited, ensuring that total fat intake does not exceed 30% of total energy (<xref ref-type="bibr" rid="ref7">7</xref>, <xref ref-type="bibr" rid="ref76">76</xref>, <xref ref-type="bibr" rid="ref78">78</xref>).<break/>4. Adequate hydration should be maintained, with a recommended intake of 30&#x2013;40&#x202F;mL/kg of body weight per day (<xref ref-type="bibr" rid="ref76">76</xref>).<break/>5. During radiotherapy, oral administration of a triple-strain probiotic combination [Live Combined Bifidobacterium and Lactobacillus Tablets, Per-tablet composition: <italic>Bifidobacterium longum</italic> 0.5&#x202F;&#x00D7;&#x202F;10<sup>7</sup> colony-forming units (CFU); <italic>Lactobacillus bulgaricus</italic> 0.5&#x202F;&#x00D7;&#x202F;10<sup>6</sup> CFU; and <italic>Streptococcus thermophilus</italic> 0.5&#x202F;&#x00D7;&#x202F;10<sup>6</sup> CFU] was implemented to modulate gut microbiota, with the following protocol: 4 tablets per dose, 3 times daily (morning, noon, evening; administered 30&#x202F;min before meals). Daily total intake: <italic>Bifidobacterium longum</italic> 6.0&#x202F;&#x00D7;&#x202F;10<sup>7</sup> CFU/day (0.5&#x202F;&#x00D7;&#x202F;10<sup>7</sup> CFU/tablet&#x202F;&#x00D7;&#x202F;4 tablets&#x202F;&#x00D7;&#x202F;3 doses); <italic>Lactobacillus bulgaricus</italic> and <italic>Streptococcus thermophilus</italic> 6.0&#x202F;&#x00D7;&#x202F;10<sup>6</sup> CFU/day, each (0.5&#x202F;&#x00D7;&#x202F;10<sup>6</sup> CFU/tablet&#x202F;&#x00D7;&#x202F;4 tablets&#x202F;&#x00D7;&#x202F;3 doses) (<xref ref-type="bibr" rid="ref65">65</xref>, <xref ref-type="bibr" rid="ref76">76</xref>). Additionally, the consumption of fresh vegetables and fruits rich in antioxidant nutrients should be increased (<xref ref-type="bibr" rid="ref79">79</xref>, <xref ref-type="bibr" rid="ref80">80</xref>).<break/>6. Healthier cooking methods should be preferred, with smaller, more frequent meals recommended. The intake of pickled and processed foods should be minimized, while the consumption of fresh fruits and vegetables should be increased (<xref ref-type="bibr" rid="ref76">76</xref>, <xref ref-type="bibr" rid="ref80">80</xref>).</td>
</tr>
<tr>
<td align="left" valign="top">During radiotherapy</td>
<td align="left" valign="top">Nutritional Support</td>
<td align="left" valign="top">1. Nutrition nurses perform daily dietary assessments for patients and communicate findings to dietitians and physicians.<break/>2. The dietitian calculates the required energy, protein, and carbohydrate intake based on the patient&#x2019;s weight, activity level, and medical condition, then prescribes an appropriate nutritional plan. Nutrition nurses reinforce adherence to dietary recommendations and provide nutritional education.<break/>3. When enhanced nutritional education and improved oral intake remain insufficient to meet the patient&#x2019;s nutritional requirements, oral nutritional supplements (ONS) with a complete nutritional formula are provided following an assessment by the dietitian (<xref ref-type="bibr" rid="ref81 ref82 ref83">81&#x2013;83</xref>).<break/>4. If oral intake continues to be inadequate despite nutritional education and ONS, or if the patient experiences difficulty in oral feeding, enteral nutrition should be initiated (<xref ref-type="bibr" rid="ref77">77</xref>, <xref ref-type="bibr" rid="ref83">83</xref>). The enteral nutrition regimen is determined by the dietitian.<break/>5. For patients with nasopharyngeal cancer who exhibit gastrointestinal dysfunction, parenteral nutrition or a combination of enteral and parenteral nutrition should be administered (<xref ref-type="bibr" rid="ref4">4</xref>).<break/>6. When oral or enteral nutrition is insufficient, such as in cases of severe oral mucositis or dysphagia, parenteral nutrition is recommended (<xref ref-type="bibr" rid="ref83">83</xref>, <xref ref-type="bibr" rid="ref84">84</xref>). The parenteral nutrition plan is jointly formulated by the physician and dietitian.</td>
</tr>
<tr>
<td align="left" valign="top">During radiotherapy</td>
<td align="left" valign="top">Symptom Management</td>
<td align="left" valign="top">1. Symptoms such as oral ulcers, dry mouth, appetite loss, and taste alterations should be monitored.<break/>2. Oral mucositis: Proper oral hygiene should be maintained, and soft, easy-to-chew foods should be selected. Smoking cessation should be encouraged, while alcohol consumption and irritating foods should be limited. The use of a straw is recommended to reduce direct contact of fluids with affected areas (<xref ref-type="bibr" rid="ref4">4</xref>, <xref ref-type="bibr" rid="ref76">76</xref>, <xref ref-type="bibr" rid="ref85">85</xref>).<break/>3. Xerostomia: The consumption of sweet or acidic foods should be encouraged to stimulate saliva production. Soft or finely chopped foods are recommended, along with cooking methods such as thickening, steaming, or preparing soups (<xref ref-type="bibr" rid="ref85">85</xref>).<break/>4. Dysgeusia: Visually appealing and flavorful foods should be provided, with the use of seasonings to enhance taste (<xref ref-type="bibr" rid="ref76">76</xref>, <xref ref-type="bibr" rid="ref85">85</xref>).<break/>5. Anorexia: Alternatives to pork and beef, such as fish, poultry, eggs, soy products, and milk, should be suggested, ensuring that strong fish odors are avoided. Temporary administration of glucocorticoids or progestins may aid in appetite improvement (<xref ref-type="bibr" rid="ref85">85</xref>).<break/>6. Psychological well-being should be monitored to promptly identify any negative emotions and provide appropriate support (<xref ref-type="bibr" rid="ref85">85</xref>).<break/>7. In cases of severe symptoms, medications should be administered as prescribed by the physician.</td>
</tr>
<tr>
<td align="left" valign="top">During radiotherapy</td>
<td align="left" valign="top">Functional Exercises</td>
<td align="left" valign="top">1. Nurses provide guidance on neck rotation exercises (<xref ref-type="bibr" rid="ref86">86</xref>), recommending sessions of 2&#x2013;3&#x202F;min, three times daily.<break/>2. Mouth opening exercises (<xref ref-type="bibr" rid="ref86">86</xref>) should be performed at least 200 times per day.<break/>3. Teeth clenching exercises (<xref ref-type="bibr" rid="ref86">86</xref>) should be completed in sets of 100 repetitions, three times daily.<break/>4. Muscle exercises should include walking for at least 5&#x202F;min daily or until mild perspiration is observed (<xref ref-type="bibr" rid="ref76">76</xref>, <xref ref-type="bibr" rid="ref77">77</xref>, <xref ref-type="bibr" rid="ref87">87</xref>).</td>
</tr>
<tr>
<td align="left" valign="top">During radiotherapy</td>
<td align="left" valign="top">Nutritional Monitoring</td>
<td align="left" valign="top">1. Weekly NRS2002 nutritional risk screenings are conducted by nurses, along with monitoring of weight and BMI. PG-SGA assessments are performed for patients identified as nutritionally at risk (<xref ref-type="bibr" rid="ref76">76</xref>, <xref ref-type="bibr" rid="ref88">88</xref>).<break/>2. Daily rounds are conducted by specialized nutrition nurses, physicians, and nutritionists to monitor nutritional intake and assess symptoms that may affect nutrition (<xref ref-type="bibr" rid="ref88">88</xref>).<break/>3. Physicians perform weekly evaluations of routine blood tests and biochemical markers, including serum albumin, prealbumin, electrolytes, and C-reactive protein (<xref ref-type="bibr" rid="ref76">76</xref>, <xref ref-type="bibr" rid="ref88">88</xref>).</td>
</tr>
<tr>
<td align="left" valign="top">Post-radiotherapy (to 3&#x202F;months)</td>
<td align="left" valign="top">Follow-up</td>
<td align="left" valign="top">1. Following discharge, specialized nutrition nurses conduct follow-ups, establish a WeChat group to share nutritional information for nasopharyngeal carcinoma patients undergoing radiotherapy, and provide biweekly phone follow-ups until symptoms affecting nutritional intake are resolved (<xref ref-type="bibr" rid="ref88">88</xref>, <xref ref-type="bibr" rid="ref89">89</xref>).<break/>2. Outpatient follow-up care will be provided for patients with severe nutritional symptoms.</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
</sec>
<sec id="sec12">
<label>2.4</label>
<title>Observation indicators</title>
<sec id="sec13">
<label>2.4.1</label>
<title>Physical measurement indicators: including height, weight, and body mass index (BMI)</title>
</sec>
<sec id="sec14">
<label>2.4.2</label>
<title>Laboratory tests: hemoglobin and albumin levels were compared between groups</title>
</sec>
<sec id="sec15">
<label>2.4.3</label>
<title>Nutritional status</title>
<p>Nutritional risk screening was conducted using the NRS2002 scoring system (<xref ref-type="bibr" rid="ref39">39</xref>), which comprises three components: &#x2460; Nutritional status impairment score (0&#x2013;3 points); &#x2461; Disease severity score (0&#x2013;3 points); &#x2462; Age score: 0 points for patients under 70&#x202F;years, and 1 point for those aged &#x2265;70&#x202F;years. The total score ranges from 0 to 7, with scores below 3 indicating no nutritional risk and scores of 3 or higher suggesting nutritional risk.</p>
<p>Nutritional assessment was performed using the PG-SGA scoring system (<xref ref-type="bibr" rid="ref40">40</xref>), which consists of two components: patient self-assessment (A score) and healthcare professional assessment (B score). The self-assessment component includes weight changes, dietary intake, symptoms, and physical activity. The professional assessment component evaluates disease severity (B score), stress level (C score), and findings from physical examinations (D score). The total score is obtained by summing the A&#x2013;D scores. A total score of 0&#x2013;1 indicates adequate nutrition, 2&#x2013;8 suggests potential or moderate malnutrition, and scores of 9 or above indicate severe malnutrition.</p>
</sec>
<sec id="sec16">
<label>2.4.4</label>
<title>Adverse reaction incidence during radiotherapy</title>
<p>Adverse reactions were assessed using the Radiation Therapy Oncology Group (RTOG) criteria for acute radiation injury (<xref ref-type="bibr" rid="ref41">41</xref>), including oral mucositis, radiation dermatitis, and bone marrow suppression.</p>
<p>Radiation-induced Oral Mucosal Inflammation: Grade 0: No changes observed; Grade 1: Mucosal congestion with mild pain, able to tolerate a regular or soft diet; Grade 2: Patchy mucositis or moderate pain, able to tolerate a soft liquid diet; Grade 3: Confluent fibrous mucositis with severe pain, restricted to a liquid diet, requiring intravenous nutritional supplementation; Grade 4: Mucosal ulceration, bleeding, or necrosis, unable to consume any food.</p>
<p>Radiation Dermatitis: Grade 0: No visible changes; Grade 1: Follicular dark red spots, dry desquamation, and reduced sweating; Grade 2: Tender or bright red spots, patchy wet desquamation, moderate edema; Grade 3: Confluent wet desquamation with deep edema; Grade 4: Ulceration, bleeding, or necrosis.</p>
<p>Bone marrow suppression: (classified by white blood cell count): Grade 0: &#x2265;4.0&#x202F;&#x00D7;&#x202F;10<sup>9</sup>/L; Grade 1: 3.0&#x2013;4.0&#x202F;&#x00D7;&#x202F;10<sup>9</sup>/L; Grade 2: 2.0&#x2013;3.0&#x202F;&#x00D7;&#x202F;10<sup>9</sup>/L; Grade 3: 1.0&#x2013;2.0&#x202F;&#x00D7;&#x202F;10<sup>9</sup>/L; Grade 4: &#x003C;1.0&#x202F;&#x00D7;&#x202F;10<sup>9</sup>/L.</p>
</sec>
<sec id="sec17">
<label>2.4.5</label>
<title>Interruptions in radiotherapy: any unplanned treatment discontinuation during radiotherapy was recorded as an interruption</title>
</sec>
<sec id="sec18">
<label>2.4.6</label>
<title>Quality of life assessment in both cohorts</title>
<p>Quality of life was evaluated using the EORTC QLQ-C30 questionnaire, 3rd edition, developed by the European Organization for Research and Treatment of Cancer (<xref ref-type="bibr" rid="ref42">42</xref>). This assessment included five functional domains: physical functioning, role functioning, cognitive functioning, emotional functioning, and social functioning. Each domain was scored from 0 to 100, with higher scores indicating better functional outcomes.</p>
</sec>
</sec>
<sec id="sec19">
<label>2.5</label>
<title>Data collection techniques</title>
<p>General patient data were collected through inquiries conducted at the time of admission. Nutritional status was assessed and documented both before and after radiotherapy, while laboratory test results were obtained from the case management system. The severity of oral mucositis and radiation dermatitis was evaluated and recorded individually by specialized nutrition nurses. Data on bone marrow suppression were extracted from the case management system, documenting the most severe adverse reactions observed during radiotherapy. Quality of life assessments were conducted by specialized nutrition nurses through one-on-one interviews with patients before and after radiotherapy.</p>
</sec>
<sec id="sec20">
<label>2.6</label>
<title>Statistical analysis procedures</title>
<p>Data analysis was conducted using SPSS 23.0 statistical software. Categorical variables were presented as frequencies and percentages, and comparisons between groups were performed using the Chi-square test or Fisher&#x2019;s exact test when expected frequencies were less than five. Normally distributed continuous variables were expressed as mean&#x202F;&#x00B1;&#x202F;standard deviation (Mean&#x202F;&#x00B1;&#x202F;SD), with group comparisons conducted using the independent samples <italic>t</italic>-test. For non-normally distributed continuous variables or ordinal data, results were reported as median and interquartile range (Median [IQR]), and comparisons between groups were performed using the Mann&#x2013;Whitney <italic>U</italic> test, a non-parametric rank-sum test. A significance threshold of <italic>p</italic>&#x202F;&#x003C;&#x202F;0.05 was considered statistically significant.</p>
</sec>
</sec>
<sec sec-type="results" id="sec21">
<label>3</label>
<title>Results</title>
<sec id="sec22">
<label>3.1</label>
<title>Baseline information</title>
<p>A comparison of general characteristics between the control and experimental groups showed no statistically significant differences (<italic>p</italic>&#x202F;&#x003E;&#x202F;0.05), as presented in <xref ref-type="table" rid="tab2">Table 2</xref>.</p>
<table-wrap position="float" id="tab2">
<label>Table 2</label>
<caption>
<p>Comparison of the baseline information between the two groups [(<inline-formula>
<mml:math id="M1">
<mml:mover accent="true">
<mml:mi>x</mml:mi>
<mml:mo stretchy="true">&#x00AF;</mml:mo>
</mml:mover>
</mml:math>
</inline-formula>&#x202F;&#x00B1;&#x202F;s)/<italic>n</italic>(%)].</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Items</th>
<th align="center" valign="top">Control group (<italic>n</italic> =&#x202F;40)</th>
<th align="center" valign="top">Experimental group (<italic>n</italic> =&#x202F;40)</th>
<th align="center" valign="top"><inline-formula>
<mml:math id="M2">
<mml:msup>
<mml:mi>x</mml:mi>
<mml:mn>2</mml:mn>
</mml:msup>
</mml:math>
</inline-formula>/t</th>
<th align="center" valign="top"><italic>p</italic>-value</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">Age</td>
<td align="center" valign="top">56.78&#x202F;&#x00B1;&#x202F;12.61</td>
<td align="center" valign="top">54.08&#x202F;&#x00B1;&#x202F;11.62</td>
<td align="center" valign="top">1.018</td>
<td align="center" valign="top">0.312</td>
</tr>
<tr>
<td align="left" valign="top">Sex</td>
<td/>
<td/>
<td align="center" valign="top">2.851</td>
<td align="center" valign="top">0.091</td>
</tr>
<tr>
<td align="left" valign="top">Male</td>
<td align="center" valign="top">24(60)</td>
<td align="center" valign="top">31(77.7)</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Female</td>
<td align="center" valign="top">16(40)</td>
<td align="center" valign="top">9(22.5)</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Education status</td>
<td/>
<td/>
<td align="center" valign="top">6.139</td>
<td align="center" valign="top">0.189</td>
</tr>
<tr>
<td align="left" valign="top">Primary school</td>
<td align="center" valign="top">19(47.5)</td>
<td align="center" valign="top">22(55)</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Junior high school</td>
<td align="center" valign="top">15(37.5)</td>
<td align="center" valign="top">7(17.5)</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Senior high school</td>
<td align="center" valign="top">2(5)</td>
<td align="center" valign="top">7(17.5)</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="middle">College and above polytechnic school</td>
<td align="center" valign="top">1(2.5)</td>
<td align="center" valign="top">1(2.5)</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Medical insurance type</td>
<td/>
<td/>
<td align="center" valign="top">0.524</td>
<td align="center" valign="top">0.469</td>
</tr>
<tr>
<td align="left" valign="top">Social insurance</td>
<td align="center" valign="top">26(65)</td>
<td align="center" valign="top">29(72.5)</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Agricultural Cooperative</td>
<td align="center" valign="top">14(35)</td>
<td align="center" valign="top">11(27.5)</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Marital status</td>
<td/>
<td/>
<td align="center" valign="top">1.013</td>
<td align="center" valign="top">0.314</td>
</tr>
<tr>
<td align="left" valign="top">Married</td>
<td align="center" valign="top">39(97.5)</td>
<td align="center" valign="top">40(100)</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Single/divorced</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">0</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Widowed</td>
<td align="center" valign="top">1(2.5)</td>
<td align="center" valign="top">0</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Disease stage</td>
<td/>
<td/>
<td align="center" valign="top">1.468</td>
<td align="center" valign="top">0.69</td>
</tr>
<tr>
<td align="left" valign="top">I</td>
<td align="center" valign="top">1(2.5)</td>
<td align="center" valign="top">2(5)</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">II</td>
<td align="center" valign="top">5(12.5)</td>
<td align="center" valign="top">6(15)</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">III</td>
<td align="center" valign="top">28(70)</td>
<td align="center" valign="top">29(72.5)</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">IV</td>
<td align="center" valign="top">6(15)</td>
<td align="center" valign="top">3(7.5)</td>
<td/>
<td/>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="sec23">
<label>3.2</label>
<title>Nutritional status comparison pre- and post-radiotherapy</title>
<p>Before the initiation of radiotherapy, no significant differences were observed between the groups in terms of nutritional scores (NRS2002 and PG-SGA), BMI, or laboratory indicators (hemoglobin, and albumin) (<italic>p</italic>&#x202F;&#x003E;&#x202F;0.05). Following radiotherapy, both groups exhibited an increase in NRS2002 and PG-SGA scores, resulting in a higher prevalence of malnutrition. However, the increase in scores for the experimental group was significantly lower than that of the control group (<italic>p</italic>&#x202F;&#x003C;&#x202F;0.05). Post-treatment, the experimental group demonstrated higher BMI, hemoglobin, and albumin levels compared to the control group, with significant differences identified (<italic>p</italic>&#x202F;&#x003C;&#x202F;0.05), as shown in <xref ref-type="table" rid="tab3">Table 3</xref>.</p>
<table-wrap position="float" id="tab3">
<label>Table 3</label>
<caption>
<p>Comparison of nutritional indicators between two groups of patients.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Items</th>
<th align="left" valign="top">Groups</th>
<th align="center" valign="top">Before radiotherapy</th>
<th align="center" valign="top">End of radiotherapy</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top" rowspan="4">BMI</td>
<td align="left" valign="top">Control group (<italic>n</italic> =&#x202F;40)</td>
<td align="center" valign="top">22.55&#x202F;&#x00B1;&#x202F;2.84</td>
<td align="center" valign="top">21.38&#x202F;&#x00B1;&#x202F;2.73</td>
</tr>
<tr>
<td align="left" valign="top">Experimental group (<italic>n</italic> =&#x202F;40)</td>
<td align="center" valign="top">22.72&#x202F;&#x00B1;&#x202F;2.03</td>
<td align="center" valign="top">23.14&#x202F;&#x00B1;&#x202F;2.62</td>
</tr>
<tr>
<td align="left" valign="top"><italic>t</italic></td>
<td align="center" valign="top">0.313</td>
<td align="center" valign="top">2.951</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic>-value</td>
<td align="center" valign="top">0.755</td>
<td align="center" valign="top">0.004</td>
</tr>
<tr>
<td align="left" valign="top" rowspan="4">NRS2002</td>
<td align="left" valign="top">Control group (<italic>n</italic> =&#x202F;40)</td>
<td align="center" valign="top">1.50&#x202F;&#x00B1;&#x202F;1.04</td>
<td align="center" valign="top">3.33&#x202F;&#x00B1;&#x202F;1.16</td>
</tr>
<tr>
<td align="left" valign="top">Experimental group (<italic>n</italic> =&#x202F;40)</td>
<td align="center" valign="top">1.55&#x202F;&#x00B1;&#x202F;1.11</td>
<td align="center" valign="top">2.73&#x202F;&#x00B1;&#x202F;1.45</td>
</tr>
<tr>
<td align="left" valign="top"><italic>t</italic></td>
<td align="center" valign="top">0.467</td>
<td align="center" valign="top">2.041</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic>-value</td>
<td align="center" valign="top">0.642</td>
<td align="center" valign="top">0.045</td>
</tr>
<tr>
<td align="left" valign="top" rowspan="4">PG-SGA</td>
<td align="left" valign="top">Control group (<italic>n</italic> =&#x202F;40)</td>
<td align="center" valign="top">3.08&#x202F;&#x00B1;&#x202F;1.72</td>
<td align="center" valign="top">7.73&#x202F;&#x00B1;&#x202F;2.72</td>
</tr>
<tr>
<td align="left" valign="top">Experimental group (<italic>n</italic> =&#x202F;40)</td>
<td align="center" valign="top">3.10&#x202F;&#x00B1;&#x202F;1.96</td>
<td align="center" valign="top">6.13&#x202F;&#x00B1;&#x202F;3.22</td>
</tr>
<tr>
<td align="left" valign="top"><italic>t</italic></td>
<td align="center" valign="top">1.736</td>
<td align="center" valign="top">2.402</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic>-value</td>
<td align="center" valign="top">0.087</td>
<td align="center" valign="top">0.019</td>
</tr>
<tr>
<td align="left" valign="top" rowspan="4">Hemoglobin</td>
<td align="left" valign="top">Control group (<italic>n</italic> =&#x202F;40)</td>
<td align="center" valign="top">119.00&#x202F;&#x00B1;&#x202F;15.56</td>
<td align="center" valign="top">113.50&#x202F;&#x00B1;&#x202F;12.08</td>
</tr>
<tr>
<td align="left" valign="top">Experimental group (<italic>n</italic> =&#x202F;40)</td>
<td align="center" valign="top">120.35&#x202F;&#x00B1;&#x202F;9.60</td>
<td align="center" valign="top">120.75&#x202F;&#x00B1;&#x202F;16.52</td>
</tr>
<tr>
<td align="left" valign="top"><italic>t</italic></td>
<td align="center" valign="top">0.208</td>
<td align="center" valign="top">2.24</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic>-value</td>
<td align="center" valign="top">0.836</td>
<td align="center" valign="top">0.028</td>
</tr>
<tr>
<td align="left" valign="top" rowspan="4">Seralbumin</td>
<td align="left" valign="top">Control group (<italic>n</italic> =&#x202F;40)</td>
<td align="center" valign="top">41.04&#x202F;&#x00B1;&#x202F;4.84</td>
<td align="center" valign="top">37.62&#x202F;&#x00B1;&#x202F;5.04</td>
</tr>
<tr>
<td align="left" valign="top">Experimental group (<italic>n</italic> =&#x202F;40)</td>
<td align="center" valign="top">42.74&#x202F;&#x00B1;&#x202F;3.83</td>
<td align="center" valign="top">41.24&#x202F;&#x00B1;&#x202F;4.54</td>
</tr>
<tr>
<td align="left" valign="top"><italic>t</italic></td>
<td align="center" valign="top">0.061</td>
<td align="center" valign="top">3.377</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic>-value</td>
<td align="center" valign="top">0.952</td>
<td align="center" valign="top">0.001</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>During radiotherapy, most patients experienced a decrease in body weight. By the end of treatment, both groups exhibited varying degrees of weight loss. The median weight reduction in the control group was significantly greater at 5.08 (1.67, 7.39) compared to 2.05 (1.89, 4.45) in the experimental group. Additionally, the percentage of weight loss was more pronounced in the control group, with a statistically significant difference observed (<italic>p</italic>&#x202F;&#x003C;&#x202F;0.05). Notably, 20% of patients in the control group experienced a weight loss exceeding 10% by the end of treatment, as detailed in <xref ref-type="table" rid="tab4">Table 4</xref>.</p>
<table-wrap position="float" id="tab4">
<label>Table 4</label>
<caption>
<p>Comparison of weight loss between two groups [kg/<italic>n</italic>(%)].</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top" rowspan="2">Groups</th>
<th align="center" valign="top" rowspan="2"><italic>M</italic> (P25, P75)</th>
<th align="center" valign="top" colspan="3">Weight loss percentage</th>
</tr>
<tr>
<th align="center" valign="top">&#x003C;5%</th>
<th align="center" valign="top">5%&#x202F;~&#x202F;10%</th>
<th align="center" valign="top">&#x003E;10%</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">Control group (<italic>n</italic>&#x202F;=&#x202F;40)</td>
<td align="center" valign="middle">5.08 (1.67, 7.39)</td>
<td align="center" valign="middle">17 (42.5%)</td>
<td align="center" valign="middle">15 (37.5%)</td>
<td align="center" valign="middle">8 (20%)</td>
</tr>
<tr>
<td align="left" valign="middle">Experimental group (<italic>n</italic>&#x202F;=&#x202F;40)</td>
<td align="center" valign="middle">2.05 (1.89, 4.45)</td>
<td align="center" valign="middle">28 (50.9%)</td>
<td align="center" valign="middle">8 (20%)</td>
<td align="center" valign="middle">4 (10%)</td>
</tr>
<tr>
<td align="left" valign="middle"><italic>Z</italic></td>
<td/>
<td align="center" valign="middle" colspan="3">&#x2212;2.396</td>
</tr>
<tr>
<td align="left" valign="middle"><italic>P</italic>-value</td>
<td/>
<td align="center" valign="middle" colspan="3">0.017</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>At the conclusion of radiotherapy, PG-SGA scores in both groups were elevated compared to pre-treatment levels, indicating a decline in nutritional status. The proportion of patients classified with severe malnutrition increased, with the control group exhibiting a significantly higher incidence (75%) compared to the experimental group (52.5%), demonstrating a statistically significant difference (<italic>p</italic>&#x202F;&#x003C;&#x202F;0.05), as illustrated in <xref ref-type="fig" rid="fig1">Figure 1</xref>.</p>
<fig position="float" id="fig1">
<label>Figure 1</label>
<caption>
<p>Distribution of PG-SGA scores of two groups.</p>
</caption>
<graphic xlink:href="fnut-12-1503294-g001.tif" mimetype="image" mime-subtype="tiff"/>
</fig>
</sec>
<sec id="sec24">
<label>3.3</label>
<title>Adverse reactions to radiotherapy comparison</title>
<p>Both groups exhibited varying degrees of adverse reactions to radiotherapy. However, the incidence of radiation mucositis, radiation dermatitis, and bone marrow suppression was significantly lower in the experimental group compared to the control group (<italic>p</italic>&#x202F;&#x003C;&#x202F;0.05), as presented in <xref ref-type="table" rid="tab5">Table 5</xref>. No statistically significant differences were observed in white blood cell, neutrophil, and lymphocyte counts between the two groups, as shown in <xref ref-type="table" rid="tab6">Table 6</xref>.</p>
<table-wrap position="float" id="tab5">
<label>Table 5</label>
<caption>
<p>Comparison of incidence and severity of adverse reactions to radiotherapy <italic>n</italic>(%).</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Items</th>
<th align="left" valign="top">Group</th>
<th align="center" valign="top">Grade 0</th>
<th align="center" valign="top">Grade 1</th>
<th align="center" valign="top">Grade 2</th>
<th align="center" valign="top">Grade 3</th>
<th align="center" valign="top">Grade 4</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top" rowspan="4">Oral mucositis</td>
<td align="left" valign="top">Control group (<italic>n</italic>&#x202F;=&#x202F;40)</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">6(15%)</td>
<td align="center" valign="top">22(55%)</td>
<td align="center" valign="top">12(30%)</td>
<td align="center" valign="top">1(2.5%)</td>
</tr>
<tr>
<td align="left" valign="top">Experimental group (<italic>n</italic>&#x202F;=&#x202F;40)</td>
<td align="center" valign="top">0</td>
<td align="center" valign="top">20(50%)</td>
<td align="center" valign="top">14(35%)</td>
<td align="center" valign="top">6(15%)</td>
<td align="center" valign="top">0(0%)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>Z</italic></td>
<td/>
<td align="center" valign="top">&#x2212;3.114</td>
<td/>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic>-value</td>
<td/>
<td align="center" valign="top">0.002</td>
<td/>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top" rowspan="4">Radiodermatitis</td>
<td align="left" valign="top">Control group (<italic>n</italic>&#x202F;=&#x202F;40)</td>
<td align="center" valign="top">1(2.5%)</td>
<td align="center" valign="top">19(47.5%)</td>
<td align="center" valign="top">16(40%)</td>
<td align="center" valign="top">4(10%)</td>
<td align="center" valign="top">0(0%)</td>
</tr>
<tr>
<td align="left" valign="top">Experimental group (<italic>n</italic>&#x202F;=&#x202F;40)</td>
<td align="center" valign="top">14(35%)</td>
<td align="center" valign="top">19(47.5%)</td>
<td align="center" valign="top">5(12.5%)</td>
<td align="center" valign="top">2 (5%)</td>
<td align="center" valign="top">0 (0%)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>Z</italic></td>
<td align="center" valign="top" colspan="5">&#x2212;3.899</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic>-value</td>
<td align="center" valign="top" colspan="5">&#x003C;0.001</td>
</tr>
<tr>
<td align="left" valign="top" rowspan="4">Myelosuppression</td>
<td align="left" valign="top">Control group (<italic>n</italic>&#x202F;=&#x202F;40)</td>
<td align="center" valign="top">25(62.5%)</td>
<td align="center" valign="top">8(20%)</td>
<td align="center" valign="top">4(10%)</td>
<td align="center" valign="top">3(7.5%)</td>
<td align="center" valign="top">0(0%)</td>
</tr>
<tr>
<td align="left" valign="top">Experimental group (<italic>n</italic>&#x202F;=&#x202F;40)</td>
<td align="center" valign="top">33(82.5%)</td>
<td align="center" valign="top">6(15%)</td>
<td align="center" valign="top">2(5%)</td>
<td align="center" valign="top">1(2.5%)</td>
<td align="center" valign="top">0(0%)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>Z</italic></td>
<td align="center" valign="top" colspan="5">&#x2212;2.075</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic>-value</td>
<td align="center" valign="top" colspan="5">0.038</td>
</tr>
</tbody>
</table>
</table-wrap>
<table-wrap position="float" id="tab6">
<label>Table 6</label>
<caption>
<p>Comparison of laboratory indicators between two groups (<inline-formula>
<mml:math id="M3">
<mml:mover accent="true">
<mml:mi>x</mml:mi>
<mml:mo stretchy="true">&#x00AF;</mml:mo>
</mml:mover>
</mml:math>
</inline-formula>&#x202F;&#x00B1;&#x202F;s).</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Items</th>
<th align="left" valign="top">Groups</th>
<th align="center" valign="top">Before radiotherapy</th>
<th align="center" valign="top">End of radiotherapy</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top" rowspan="4">Leukocyte</td>
<td align="left" valign="top">Control group (<italic>n</italic> =&#x202F;40)</td>
<td align="center" valign="top">5.42&#x202F;&#x00B1;&#x202F;1.57</td>
<td align="center" valign="top">5.05&#x202F;&#x00B1;&#x202F;2.28</td>
</tr>
<tr>
<td align="left" valign="top">Experimental group (<italic>n</italic> =&#x202F;40)</td>
<td align="center" valign="top">5.26&#x202F;&#x00B1;&#x202F;1.62</td>
<td align="center" valign="top">5.77&#x202F;&#x00B1;&#x202F;1.07</td>
</tr>
<tr>
<td align="left" valign="top"><italic>t</italic></td>
<td align="center" valign="top">0.444</td>
<td align="center" valign="top">3.56</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic></td>
<td align="center" valign="top">0.815</td>
<td align="center" valign="top">0.167</td>
</tr>
<tr>
<td align="left" valign="top" rowspan="4">Neutrophil granulocyte</td>
<td align="left" valign="top">Control group (<italic>n</italic> =&#x202F;40)</td>
<td align="center" valign="middle">3.46&#x202F;&#x00B1;&#x202F;1.45</td>
<td align="center" valign="middle">3.63&#x202F;&#x00B1;&#x202F;1.90</td>
</tr>
<tr>
<td align="left" valign="top">Experimental group (<italic>n</italic> =&#x202F;40)</td>
<td align="center" valign="top">3.18&#x202F;&#x00B1;&#x202F;1.38</td>
<td align="center" valign="top">3.52&#x202F;&#x00B1;&#x202F;1.46</td>
</tr>
<tr>
<td align="left" valign="top"><italic>t</italic></td>
<td align="center" valign="top">0.914</td>
<td align="center" valign="top">0.274</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic></td>
<td align="center" valign="top">0.858</td>
<td align="center" valign="top">0.264</td>
</tr>
<tr>
<td align="left" valign="top" rowspan="4">Leukomonocyte</td>
<td align="left" valign="top">Control group (<italic>n</italic> =&#x202F;40)</td>
<td align="center" valign="top">1.27&#x202F;&#x00B1;&#x202F;0.51</td>
<td align="center" valign="top">0.52&#x202F;&#x00B1;&#x202F;0.25</td>
</tr>
<tr>
<td align="left" valign="top">Experimental group (<italic>n</italic> =&#x202F;40)</td>
<td align="center" valign="top">1.31&#x202F;&#x00B1;&#x202F;0.53</td>
<td align="center" valign="top">0.55&#x202F;&#x00B1;&#x202F;0.23</td>
</tr>
<tr>
<td align="left" valign="top"><italic>t</italic></td>
<td align="center" valign="top">0.289</td>
<td align="center" valign="top">3.56</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic></td>
<td align="center" valign="top">0.974</td>
<td align="center" valign="top">0.167</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="sec25">
<label>3.4</label>
<title>Treatment interruptions between cohorts</title>
<p>All patients in both cohorts successfully completed radiotherapy, with no statistically significant difference in interruption rates (<italic>p</italic>&#x202F;&#x003E;&#x202F;0.05). However, the proportion of patients experiencing treatment interruptions was lower in the experimental group compared to the control group, as shown in <xref ref-type="table" rid="tab7">Table 7</xref>. Among those who interrupted radiotherapy, three patients in the control group were unable to resume treatment due to a combination of severe malnutrition and radiation-induced oral mucositis. Additionally, three other patients in the control group suspended radiotherapy due to grade III bone marrow suppression. In contrast, only one patient in the experimental group temporarily discontinued radiotherapy, solely due to grade III bone marrow suppression.</p>
<table-wrap position="float" id="tab7">
<label>Table 7</label>
<caption>
<p>Interruption of radiotherapy <italic>n</italic>(%).</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Groups</th>
<th align="center" valign="top">Radiation therapy not interrupted <italic>n</italic>(%)</th>
<th align="center" valign="top">Interruption of radiotherapy <italic>n</italic>(%)</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">Control group (<italic>n</italic>&#x202F;=&#x202F;40)</td>
<td align="center" valign="middle">34(85%)</td>
<td align="center" valign="middle">6(15%)</td>
</tr>
<tr>
<td align="left" valign="middle">Experimental group (<italic>n</italic>&#x202F;=&#x202F;40)</td>
<td align="center" valign="middle">39(97.5%)</td>
<td align="center" valign="middle">1(2.5%)</td>
</tr>
<tr>
<td align="left" valign="middle">
<inline-formula>
<mml:math id="M4">
<mml:msup>
<mml:mi>x</mml:mi>
<mml:mn>2</mml:mn>
</mml:msup>
</mml:math>
</inline-formula>
</td>
<td align="center" valign="middle" colspan="2">2.505</td>
</tr>
<tr>
<td align="left" valign="middle"><italic>P-value</italic></td>
<td align="center" valign="middle" colspan="2">0.113</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="sec26">
<label>3.5</label>
<title>Comparison of quality of life between the two groups</title>
<p>Before radiotherapy, the EORTC QLQ-C30 questionnaire revealed no statistically significant differences in functional domains between the two groups (<italic>p</italic>&#x202F;&#x003E;&#x202F;0.05). By the end of radiotherapy, scores for physical, role, emotional, cognitive, and social functioning had improved in both groups. However, the experimental group demonstrated a significantly greater improvement, with statistically significant differences (<italic>p</italic>&#x202F;&#x003C;&#x202F;0.05), as detailed in <xref ref-type="table" rid="tab8">Table 8</xref>.</p>
<table-wrap position="float" id="tab8">
<label>Table 8</label>
<caption>
<p>Comparison of EORTC QLQ-C30 scores between two groups of patients.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th>Time</th>
<th align="left" valign="top">Group</th>
<th align="center" valign="top">Physical function</th>
<th align="center" valign="top">Role function</th>
<th align="center" valign="top">Emotional function</th>
<th align="center" valign="top">Cognitive function</th>
<th align="center" valign="top">Social function</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top" rowspan="2">Before radiotherapy</td>
<td align="left" valign="top">Control group</td>
<td align="center" valign="top">66.32&#x202F;&#x00B1;&#x202F;7.07</td>
<td align="center" valign="top">65.24&#x202F;&#x00B1;&#x202F;9.05</td>
<td align="center" valign="top">65.41&#x202F;&#x00B1;&#x202F;9.23</td>
<td align="center" valign="top">64.41&#x202F;&#x00B1;&#x202F;9.46</td>
<td align="center" valign="top">62.50&#x202F;&#x00B1;&#x202F;7.93</td>
</tr>
<tr>
<td align="left" valign="top">Experimental group</td>
<td align="center" valign="top">65.99&#x202F;&#x00B1;&#x202F;6.71</td>
<td align="center" valign="top">64.74&#x202F;&#x00B1;&#x202F;10.48</td>
<td align="center" valign="top">67.74&#x202F;&#x00B1;&#x202F;7.39</td>
<td align="center" valign="top">64.74&#x202F;&#x00B1;&#x202F;9.80</td>
<td align="center" valign="top">63.41&#x202F;&#x00B1;&#x202F;10.81</td>
</tr>
<tr>
<td align="left" valign="top"><italic>t</italic></td>
<td/>
<td align="center" valign="top">0.216</td>
<td align="center" valign="top">0.228</td>
<td align="center" valign="top">&#x2212;1.247</td>
<td align="center" valign="top">&#x2212;0.155</td>
<td align="center" valign="top">&#x2212;0.433</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic>-value</td>
<td/>
<td align="center" valign="top">0.829</td>
<td align="center" valign="top">0.82</td>
<td align="center" valign="top">0.216</td>
<td align="center" valign="top">0.877</td>
<td align="center" valign="top">0.666</td>
</tr>
<tr>
<td align="left" valign="top" rowspan="2">End of radiotherapy</td>
<td align="left" valign="top">Control group</td>
<td align="center" valign="top">70.66&#x202F;&#x00B1;&#x202F;7.95</td>
<td align="center" valign="top">71.67&#x202F;&#x00B1;&#x202F;10.98</td>
<td align="center" valign="top">77.20&#x202F;&#x00B1;&#x202F;9.37</td>
<td align="center" valign="top">73.87&#x202F;&#x00B1;&#x202F;9.37</td>
<td align="center" valign="top">66.99&#x202F;&#x00B1;&#x202F;9.92</td>
</tr>
<tr>
<td align="left" valign="top">Experimental group</td>
<td align="center" valign="top">77.00&#x202F;&#x00B1;&#x202F;7.98</td>
<td align="center" valign="top">79.58&#x202F;&#x00B1;&#x202F;11.79</td>
<td align="center" valign="top">83.49&#x202F;&#x00B1;&#x202F;9.63</td>
<td align="center" valign="top">80.16&#x202F;&#x00B1;&#x202F;9.63</td>
<td align="center" valign="top">71.50&#x202F;&#x00B1;&#x202F;10.26</td>
</tr>
<tr>
<td align="left" valign="top"><italic>t</italic></td>
<td/>
<td align="center" valign="top">&#x2212;3.556</td>
<td align="center" valign="top">&#x2212;3.105</td>
<td align="center" valign="top">&#x2212;2.961</td>
<td align="center" valign="top">&#x2212;2.961</td>
<td align="center" valign="top">&#x2212;1.996</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic>-value</td>
<td/>
<td align="center" valign="top">0.001</td>
<td align="center" valign="top">0.003</td>
<td align="center" valign="top">0.004</td>
<td align="center" valign="top">0.004</td>
<td align="center" valign="top">0.049</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
</sec>
<sec sec-type="discussion" id="sec27">
<label>4</label>
<title>Discussion</title>
<p>Nasopharyngeal carcinoma (NPC), a common malignant tumor, has been associated with the Epstein&#x2013;Barr virus (EBV) (<xref ref-type="bibr" rid="ref43">43</xref>). In recent years, NPC has increasingly been regarded as a chronic disease. However, a global burden study examining NPC in children and adolescents, along with projections for 2040 (<xref ref-type="bibr" rid="ref44">44</xref>), indicates a rising age-standardized incidence rate (ASIR), highlighting a substantial disease burden. Malnutrition in NPC patients arises from multiple factors, primarily malignant cachexia caused by tumor metabolism, leading to anorexia. Additionally, radiotherapy-related adverse effects further exacerbate the condition. NPC predominantly affects younger and middle-aged males, with peak incidence occurring between the ages of 40 and 59 (<xref ref-type="bibr" rid="ref1">1</xref>). This demographic is more susceptible to psychological stress, which can contribute to gastrointestinal dysfunction and reduced food intake (<xref ref-type="bibr" rid="ref15">15</xref>). Furthermore, misunderstandings about nutrition among patients and their families may negatively impact nutritional health. Therefore, the implementation of a scientifically based nutritional support plan is essential. The application of evidence-based approaches in clinical nursing allows for the integration of nursing challenges with evidence-based nursing practice (<xref ref-type="bibr" rid="ref45">45</xref>). This approach not only enhances the quality of care but also facilitates the continuous advancement of professional knowledge, improving the scientific rigor and overall effectiveness of nursing interventions (<xref ref-type="bibr" rid="ref46">46</xref>). However, the gap between evidence-based findings and clinical practice remains the most significant challenge in evidence-based nursing. Consequently, the primary task facing nursing professionals today is to scientifically and systematically integrate evidence-based findings into clinical nursing practice. Additionally, they must explore and develop evidence-based nursing protocols that align with actual clinical realities.</p>
<sec id="sec28">
<label>4.1</label>
<title>Evidence-based nutritional support plans for NPC patients undergoing radiotherapy can improve nutritional status</title>
<p>Malnutrition is commonly observed in patients with NPC at an early stage and progressively worsens during radiotherapy. This condition not only negatively affects treatment outcomes (<xref ref-type="bibr" rid="ref47">47</xref>) but also decreases quality of life, increases hospitalization costs, and has a substantial impact on prognosis (<xref ref-type="bibr" rid="ref48">48</xref>). Research conducted by He et al. (<xref ref-type="bibr" rid="ref49">49</xref>) has demonstrated that a high nutritional risk is a predictor of poor clinical prognosis in elderly NPC patients. Several studies (<xref ref-type="bibr" rid="ref50 ref51 ref52 ref53">50&#x2013;53</xref>) have consistently validated the association between prognostic nutritional indices and survival outcomes in NPC patients, emphasizing their predictive significance. Nutritional challenges are increasingly recognized, and various intervention strategies have been incorporated into clinical practice. These interventions include nutritional counseling (<xref ref-type="bibr" rid="ref54">54</xref>), oral nutritional supplementation (<xref ref-type="bibr" rid="ref34">34</xref>, <xref ref-type="bibr" rid="ref55">55</xref>, <xref ref-type="bibr" rid="ref56">56</xref>), and enteral nutritional support (<xref ref-type="bibr" rid="ref57">57</xref>), all of which aim to improve nutritional status. Additionally, poor nutritional status has been linked to an increased severity of side effects (<xref ref-type="bibr" rid="ref16">16</xref>). Therapies involving thalidomide (<xref ref-type="bibr" rid="ref58">58</xref>), honey (<xref ref-type="bibr" rid="ref59">59</xref>), glutamine (<xref ref-type="bibr" rid="ref60">60</xref>), and probiotics (<xref ref-type="bibr" rid="ref61">61</xref>) have been suggested as potential approaches for alleviating oral mucositis and improving nutritional status.</p>
<p>Weight loss is one of the primary manifestations of malnutrition in patients. Previous studies (<xref ref-type="bibr" rid="ref6">6</xref>, <xref ref-type="bibr" rid="ref62">62</xref>) have indicated that about 90&#x2013;96% of NPC patients experience weight loss during radiotherapy. In this study, weight loss was observed in both groups following radiotherapy, but the reduction was more pronounced in the control group, with 20% of patients experiencing a body weight loss exceeding 10%. These findings align with the results reported by Hong et al. (<xref ref-type="bibr" rid="ref11">11</xref>), who documented a weight loss rate of 20.4%. The Patient-Generated Subjective Global Assessment (PG-SGA), a specialized tool for evaluating the nutritional status of cancer patients (<xref ref-type="bibr" rid="ref17">17</xref>, <xref ref-type="bibr" rid="ref63">63</xref>), was used in this study. The results showed an increase in PG-SGA scores in both groups after radiotherapy, with severe malnutrition identified in 80% of patients in the control group and 55% in the intervention group. The nutritional outcomes observed in this study were slightly better than those reported by Wei et al. (<xref ref-type="bibr" rid="ref26">26</xref>), which may be attributed to advancements in medical technology, improvements in radiotherapy equipment, increased awareness of nutritional management, and the relatively small sample size of the study. These findings suggest that standardized nutritional support can improve nutritional status, minimize weight loss, and reduce the severity of malnutrition. Albumin and hemoglobin levels are commonly used laboratory indicators for assessing nutritional status. A cohort study (<xref ref-type="bibr" rid="ref33">33</xref>) demonstrated that early nutritional intervention could improve albumin and hemoglobin levels. Consistently, the findings of this study indicated that although both groups experienced a decline in these indicators following radiotherapy, the intervention group exhibited better outcomes than the control group. This suggests that nutritional support can slow the deterioration of hematological parameters.</p>
</sec>
<sec id="sec29">
<label>4.2</label>
<title>Evidence-based nutritional support plans for NPC patients undergoing radiotherapy can reduce the incidence of side effects and decrease treatment interruptions</title>
<p>Radiation-induced oral mucositis, dermatitis, and bone marrow suppression are common adverse effects observed in patients with NPC undergoing radiotherapy (<xref ref-type="bibr" rid="ref4">4</xref>). A meta-analysis on the incidence of oral mucositis associated with NPC radiotherapy (<xref ref-type="bibr" rid="ref64">64</xref>) indicated that nearly all NPC patients develop radiation-induced oral mucositis, with more than half experiencing severe mucosal inflammation. While mild cases can be managed symptomatically, severe manifestations may require treatment delays or discontinuation, potentially compromising patient prognosis. Bifidobacterium is one of the most common probiotics, and its antitumor and immunomodulatory effects have been demonstrated in recent years (<xref ref-type="bibr" rid="ref65">65</xref>, <xref ref-type="bibr" rid="ref66">66</xref>).Emerging evidence highlights the dual role of Bifidobacterium in potentiating radiotherapy efficacy through tumor microenvironment (TME) modulation (<xref ref-type="bibr" rid="ref67">67</xref>). Clinically, a systematic review of 15 randomized controlled trials (RCTs) demonstrated that Bifidobacterium-based interventions significantly reduce the incidence of grade&#x202F;&#x2265;&#x202F;3 oral mucositis and ameliorate treatment-related symptoms (e.g., diarrhea, fatigue) in patients undergoing radiochemotherapy (<xref ref-type="bibr" rid="ref68">68</xref>). Ji et al. (<xref ref-type="bibr" rid="ref69">69</xref>) reported that continuous improvements in nutritional care can mitigate the severity of radiation-induced oral mucositis. Similarly, a retrospective study (<xref ref-type="bibr" rid="ref20">20</xref>) confirmed that personalized and continuous nutritional management can reduce the incidence of treatment-related side effects during radiotherapy. These findings align with the results of this study. Research conducted in western China (<xref ref-type="bibr" rid="ref35">35</xref>) has also shown that home-based enteral nutrition can improve bone marrow suppression in patients. Consistently, the present study found that nutritional interventions alleviated the severity of bone marrow suppression, the severity of myelosuppression was significantly lower in the intervention group. Although no statistically significant differences were observed in white blood cell, lymphocyte, and neutrophil counts between the two groups, this may be attributed to increased clinical awareness of bone marrow suppression, the timely administration of leukopoietic agents and the short duration of nutritional support. In future research, the impact of nutritional support should be continuously observed to obtain further data.</p>
<p>Although both groups completed radiotherapy without a statistically significant difference in treatment interruption rates, the data indicate that treatment interruptions were less frequent in the experimental group compared to the control group. This difference may be influenced by the relatively small sample size.</p>
</sec>
<sec id="sec30">
<label>4.3</label>
<title>Evidence-based nutritional support plans for NPC patients undergoing radiotherapy can improve quality of life</title>
<p>With advancements in medical care, cancer patients increasingly focus not only on survival duration but also on quality of life. Qualitative studies (<xref ref-type="bibr" rid="ref70">70</xref>), meta-analyses (<xref ref-type="bibr" rid="ref71">71</xref>), and longitudinal studies (<xref ref-type="bibr" rid="ref72">72</xref>) have demonstrated that NPC patients undergoing radiotherapy often experience a decline in quality of life due to the burden of nutritional symptoms, leading to depression and psychological distress.</p>
<p>The intervention plan implemented in this study prioritized the management of nutritional symptoms, encouraged functional exercises, and addressed negative emotions in a timely manner. The results indicated that patients in the experimental group achieved higher scores in physical, role, emotional, cognitive, and social functioning on the EORTC QLQ-C30 scale at the end of radiotherapy compared to the control group. This evidence suggests that the nutritional support plan effectively enhances quality of life for NPC patients during radiotherapy. These findings align with the research conducted by Meng et al. (<xref ref-type="bibr" rid="ref33">33</xref>) and Huang et al. (<xref ref-type="bibr" rid="ref27">27</xref>). Additionally, previous studies (<xref ref-type="bibr" rid="ref73">73</xref>) have identified a low Comprehensive Nutritional Index (CNI) as being associated with poorer quality of life and unfavorable survival outcomes, underscoring the necessity for further interventions aimed at improving nutritional status to enhance both quality of life and survival rates in NPC patients.</p>
<p>Previous studies have shown that evidence-based nursing programs can reduce postoperative wound pain and complications in patients following finger tendon surgery (<xref ref-type="bibr" rid="ref74">74</xref>), as well as alleviate postpartum anxiety (<xref ref-type="bibr" rid="ref75">75</xref>). The intervention strategy applied in this study was developed based on evidence and adapted to clinical practice, ensuring its effectiveness and feasibility in clinical settings. Standardized protocols were implemented for nutritional risk screening and assessment, along with defined timing and principles for nutritional support. A multidisciplinary team designed individualized nutrition plans, with a strong focus on symptom management, functional exercise, and follow-up care. This comprehensive, continuous, and dynamic approach to nutrition management throughout treatment significantly reduced weight loss, mitigated the decline in hematological parameters, and alleviated the severity of malnutrition.</p>
</sec>
</sec>
<sec sec-type="conclusions" id="sec31">
<label>5</label>
<title>Conclusion</title>
<p>The evidence-based nutritional support plan for NPC patients undergoing radiotherapy has been shown to effectively improve nutritional status, reduce treatment-related side effects, and enhance quality of life. These findings highlight its significant clinical applicability and provide a reference for the implementation of nutritional support in NPC patients receiving radiotherapy. This study aims to contribute to the establishment of a theoretical framework for integrating evidence-based nursing into nutritional care for NPC patients undergoing radiotherapy.</p>
</sec>
<sec id="sec32">
<label>6</label>
<title>Limitations of the study</title>
<p>This study was conducted on NPC patients undergoing radiotherapy at a single hospital, resulting in a limited sample size and restricted geographic representation. Additionally, continuous monitoring was not performed to evaluate the long-term effects of the intervention. Various factors may influence the implementation of nutritional support plans, including hospital staff availability, patient compliance, financial constraints, insurance coverage, and religious beliefs. Future research should focus on multi-center studies with larger sample sizes and extended follow-up periods. Furthermore, fostering collaboration among families, healthcare institutions, and community support networks is essential to improving patients&#x2019; nutritional status and overall quality of life.</p>
</sec>
</body>
<back>
<sec sec-type="data-availability" id="sec33">
<title>Data availability statement</title>
<p>The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.</p>
</sec>
<sec sec-type="ethics-statement" id="sec34">
<title>Ethics statement</title>
<p>The studies involving humans were approved by Ethics Committee of Jinzhou Medical University. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation was not required from the participants or the participants&#x2019; legal guardians/next of kin in accordance with the national legislation and institutional requirements.</p>
</sec>
<sec sec-type="author-contributions" id="sec35">
<title>Author contributions</title>
<p>XF: Conceptualization, Funding acquisition, Investigation, Methodology, Resources, Writing &#x2013; original draft. HC: Funding acquisition, Supervision, Writing &#x2013; original draft, Writing &#x2013; review &#x0026; editing. HP: Data curation, Formal analysis, Writing &#x2013; review &#x0026; editing. SL: Methodology, Writing &#x2013; original draft. LJ: Data curation, Writing &#x2013; original draft.</p>
</sec>

<sec sec-type="COI-statement" id="sec37">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="ai-statement" id="sec38">
<title>Generative AI statement</title>
<p>The authors declare that no Gen AI was used in the creation of this manuscript.</p>
</sec>
<sec sec-type="disclaimer" id="sec39">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
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</ref-list><fn-group><fn id="fn0001" fn-type="custom" custom-type="edited-by"><p>Edited by: Bin Wang, Sichuan University, China</p></fn>
<fn id="fn0002" fn-type="custom" custom-type="reviewed-by"><p>Reviewed by: Luz-Ma.-Adriana Balderas-Pe&#x00F1;a, Instituto Mexicano del Seguro Social, Mexico</p><p>Denisse Castro-Eguiluz, National Council of Science and Technology (CONACYT), Mexico</p></fn></fn-group></back>
</article>