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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Oncol.</journal-id>
<journal-title>Frontiers in Oncology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Oncol.</abbrev-journal-title>
<issn pub-type="epub">2234-943X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fonc.2023.1240913</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Oncology</subject>
<subj-group>
<subject>Opinion</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Nutritional counselling for head and neck cancer patients treated with (chemo)radiation therapy: why, how, when, and what?</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Santo</surname>
<given-names>Bianca</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2347811"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Bertini</surname>
<given-names>Niccol&#xf2;</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2336822"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Cattaneo</surname>
<given-names>Carlo Guglielmo</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>De Matteis</surname>
<given-names>Sara</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2612784"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>De Franco</surname>
<given-names>Paola</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2531791"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Grassi</surname>
<given-names>Roberta</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1974391"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Iorio</surname>
<given-names>Giuseppe Carlo</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1089772"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Longo</surname>
<given-names>Silvia</given-names>
</name>
<xref ref-type="aff" rid="aff6">
<sup>6</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/857422"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Boldrini</surname>
<given-names>Luca</given-names>
</name>
<xref ref-type="aff" rid="aff6">
<sup>6</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1259795"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Piras</surname>
<given-names>Antonio</given-names>
</name>
<xref ref-type="aff" rid="aff7">
<sup>7</sup>
</xref>
<xref ref-type="aff" rid="aff8">
<sup>8</sup>
</xref>
<xref ref-type="aff" rid="aff9">
<sup>9</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1492351"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Desideri</surname>
<given-names>Isacco</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1192866"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>De Felice</surname>
<given-names>Francesca</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Salvestrini</surname>
<given-names>Viola</given-names>
</name>
<xref ref-type="aff" rid="aff10">
<sup>10</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1192297"/>
</contrib>
</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Radiation Oncology Unit, Dipartimento di Oncoematologia, Ospedale &#x201c;Vito Fazzi&#x201d;</institution>, <addr-line>Lecce</addr-line>, <country>Italy</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Radiation Oncology Unit, Azienda Ospedaliero-Universitaria Careggi, Department of Experimental and Clinical Biomedical Sciences, University of Florence</institution>, <addr-line>Florence</addr-line>, <country>Italy</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Department of Radiotherapy, Policlinico Umberto I, Department of Radiological, Oncological and Pathological Sciences, &#x201c;Sapienza&#x201d; University of Rome</institution>, <addr-line>Rome</addr-line>, <country>Italy</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>Department of Precision Medicine, University of Campania &#x201c;L. Vanvitelli&#x201d;</institution>, <addr-line>Naples</addr-line>, <country>Italy</country>
</aff>
<aff id="aff5">
<sup>5</sup>
<institution>Department of Oncology, Radiation Oncology, University of Turin</institution>, <addr-line>Turin</addr-line>, <country>Italy</country>
</aff>
<aff id="aff6">
<sup>6</sup>
<institution>Unit&#xe0; Operativa Complessa (UOC) Radioterapia Oncologica, Fondazione Policlinico Universitario Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) &#x201c;A. Gemelli&#x201d;</institution>, <addr-line>Roma</addr-line>, <country>Italy</country>
</aff>
<aff id="aff7">
<sup>7</sup>
<institution>Unit&#xe0;&#xa0;Operativa (UO) Radioterapia Oncologica, Villa Santa Teresa</institution>, <addr-line>Palermo</addr-line>, <country>Italy</country>
</aff>
<aff id="aff8">
<sup>8</sup>
<institution>Department of Biomedical Image Processing and Analysis, Ri.Med Foundation</institution>, <addr-line>Palermo</addr-line>, <country>Italy</country>
</aff>
<aff id="aff9">
<sup>9</sup>
<institution>Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, Molecular and Clinical Medicine, University of Palermo</institution>, <addr-line>Palermo</addr-line>, <country>Italy</country>
</aff>
<aff id="aff10">
<sup>10</sup>
<institution>Radiation Oncology Unit, Centro Cyberknife, Istituto Fiorentino di Cura e Assistenza</institution>, <addr-line>Florence</addr-line>, <country>Italy</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by: Dirk Van Gestel, Universit&#xe9; libre de Bruxelles, Belgium</p>
</fn>
<fn fn-type="edited-by">
<p>Reviewed by: Nerina Denaro, IRCCS Ca &#x2018;Granda Foundation Maggiore Policlinico Hospital, Italy</p>
<p>Cathy Lazarus, Icahn School of Medicine at Mount Sinai, United States</p>
</fn>
<fn fn-type="corresp" id="fn001">
<p>*Correspondence: Niccol&#xf2;&#xa0;Bertini, <email xlink:href="mailto:niccolo.bertini@unifi.it">niccolo.bertini@unifi.it</email>
</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>09</day>
<month>01</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="collection">
<year>2023</year>
</pub-date>
<volume>13</volume>
<elocation-id>1240913</elocation-id>
<history>
<date date-type="received">
<day>16</day>
<month>06</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>14</day>
<month>12</month>
<year>2023</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2024 Santo, Bertini, Cattaneo, De Matteis, De Franco, Grassi, Iorio, Longo, Boldrini, Piras, Desideri, De Felice and Salvestrini</copyright-statement>
<copyright-year>2024</copyright-year>
<copyright-holder>Santo, Bertini, Cattaneo, De Matteis, De Franco, Grassi, Iorio, Longo, Boldrini, Piras, Desideri, De Felice and Salvestrini</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). 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.</p>
</license>
</permissions>
<kwd-group>
<kwd>head and neck</kwd>
<kwd>nutrition</kwd>
<kwd>chemotherapy</kwd>
<kwd>radiation therapy</kwd>
<kwd>weight</kwd>
</kwd-group>
<counts>
<fig-count count="0"/>
<table-count count="1"/>
<equation-count count="0"/>
<ref-count count="42"/>
<page-count count="7"/>
<word-count count="2994"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-in-acceptance</meta-name>
<meta-value>Head and Neck Cancer</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1" sec-type="intro">
<title>Introduction</title>
<p>Weight loss is a frequent occurrence among patients with head and neck cancer (HNC) and can be observed before, during, and after cancer treatment, especially radiation therapy (RT) with or without concurrent chemotherapy (CRT). Patients with HNC are at a high risk of malnutrition at the time of diagnosis, and nutritional support or intervention is often needed during and after RT or concurrent CRT. Given the severe consequences of malnutrition and cachexia on treatment outcomes, mortality, morbidity, and quality of life, it is essential to identify patients who are at higher risk of developing this condition. The nutritional status of patients is a crucial factor in terms of adherence to treatment and recovery. Malnutrition may have a significant impact on treatment outcomes and, consequently, tumor progression. However, in clinical practice, identifying and standardizing nutritional interventions can be challenging. In this commentary, we aim to identify the components of screening and assessment that are commonly used in both literature and clinical practice and suggest the appropriate timing for nutritional interventions in patients with HNC undergoing RT or CRT.</p>
<p>At the time of diagnosis, 35%&#x2013;60% of head and neck cancer (HNC) patients are malnourished due to cancer-related impairment such as pain, obstruction, or loss of appetite (<xref ref-type="bibr" rid="B1">1</xref>, <xref ref-type="bibr" rid="B2">2</xref>). Compared to patients with other primary neoplasms, HNC patients are at a higher risk of malnutrition due to the location of the tumor and the impact of the treatment-related side effects on quality of life (<xref ref-type="bibr" rid="B3">3</xref>, <xref ref-type="bibr" rid="B4">4</xref>). Indeed, malnutrition can cause a range of clinical symptoms, including metabolic and electrolytic imbalances, immune system depression, and increased morbidity and mortality (<xref ref-type="bibr" rid="B5">5</xref>). Weight loss can lead to discontinue cancer treatments and to a negative impact on oncological outcomes, with approximately 55% of patients losing an additional 10% or more of their body weight during RT or CRT (<xref ref-type="bibr" rid="B5">5</xref>&#x2013;<xref ref-type="bibr" rid="B7">7</xref>). This note aims to provide an overview on the role of nutritional counseling in HNC patients undergoing CRT, either in an exclusive or adjuvant setting.</p>
</sec>
<sec id="s2">
<title>Screening</title>
<p>Malnutrition screening is an essential component of multimodal care in HNC patients. It involves the systematic identification of patients who are at risk of malnutrition and the provision of appropriate interventions to prevent or treat malnutrition (<xref ref-type="bibr" rid="B8">8</xref>). In this regard, the European Society for Clinical Nutrition and Metabolism (ESPEN) guidelines for screening suggests that the purpose of nutritional screening is to predict the&#xa0;outcome and the impact of nutritional intervention (<xref ref-type="bibr" rid="B9">9</xref>).There are no standardized guidelines regarding nutritional screening. Screening&#xa0;should occur at the time of diagnosis, before treatment begins, and at regular intervals throughout treatment and follow-up. This allows for early identification of malnutrition and&#xa0;timely intervention to prevent or treat it. Despite its acknowledged role, there are no standardized guidelines regarding nutritional screening.</p>
</sec>
<sec id="s3">
<title>Nutritional assessment</title>
<p>The risk of malnutrition is frequent in HNC patients, and for this reason, it is mandatory to primarily identify patients at higher risk. Currently, standardized parameters are adopted, and although there is not a single assessment tool, we suggest that the use of a standardized assessment is essential to identify patients at risk at baseline. The commonly used nutrition assessment tools are the following:</p>
<list list-type="order">
<list-item>
<p>Mini Nutrition Assessment (MNA) includes anthropometric, general, dietary, and autonomy of food self-assessments (self-perception of health and nutrition) (<xref ref-type="bibr" rid="B10">10</xref>&#x2013;<xref ref-type="bibr" rid="B12">12</xref>).</p>
</list-item>
<list-item>
<p>Nutritional Risk Screening 2002 (NRS2002) detects the presence or the risk of undernutrition (<xref ref-type="bibr" rid="B9">9</xref>, <xref ref-type="bibr" rid="B13">13</xref>).</p>
</list-item>
<list-item>
<p>Patient-Generated Subjective Globe Assessment (PG-SGA) is focused on the preeminent interdisciplinary patient assessment and allows for triaging of nutrition interventions (<xref ref-type="bibr" rid="B14">14</xref>).</p>
</list-item>
<list-item>
<p>Malnutrition Universal Screening Tool (MUST) is a five-step screening tool to identify malnourished adults (<xref ref-type="bibr" rid="B15">15</xref>, <xref ref-type="bibr" rid="B16">16</xref>).</p>
</list-item>
</list>
<p>The appropriate nutritional assessment should be performed for all patients before CRT. For defining the severity of malnutrition, we recommend the use of the new GLIM (Global Leadership Initiative on Malnutrition) score, already adopted by ESPEN, ASPEN, FELANPE, and PENSA. In particular, the GLIM&#xa0;includes three phenotypical criteria (weight loss, low BMI, and reduced muscle mass) and two etiological criteria (reduced food&#xa0;intake or absorption and increased disease burden or inflammation) (<xref ref-type="bibr" rid="B17">17</xref>).</p>
</sec>
<sec id="s4">
<title>Nutritional intervention</title>
<p>The aim of the nutritional intervention is to improve the subjective quality of life, enhance anti-tumor treatment effects, reduce the adverse effects of oncological care, prevent the interruption of therapy, and treat RT/CRT-related undernutrition. In this regard, <xref ref-type="table" rid="T1">
<bold>Table&#xa0;1</bold>
</xref> summarizes the main studies analyzing the impact of nutritional counseling and nutritional intervention strategies in HNC patients (<xref ref-type="bibr" rid="B18">18</xref>&#x2013;<xref ref-type="bibr" rid="B32">32</xref>). The onset of oral mucositis in HNC patients during RT or CRT may result in weight loss and intensive dietary counseling, and oral nutrition support is recommended. This is also advised to prevent interruptions to CRT (<xref ref-type="bibr" rid="B33">33</xref>). There are different types of nutritional support that can be adopted to reach the needs of the patient. Main options of nutritional support are oral, enteral, and parenteral. Nutritional interventions include relaxation of previous therapeutic diets, to minimize further nutritional compromise and to positively influence quality of life outcomes (<xref ref-type="bibr" rid="B34">34</xref>). However, this may not necessarily be appropriate, due to the side effects and intensity of treatment regimens. Patients may require more intensive nutritional support methods from the beginning of treatment over and above traditional food fortification methods with the early use of oral nutrition support. The choice of feeding route in HNC patients will depend upon local arrangements; however, clinical considerations should include site of primary tumor, treatment plan and intent, predicted duration of enteral feeding, and patient choice (<xref ref-type="bibr" rid="B35">35</xref>, <xref ref-type="bibr" rid="B36">36</xref>). Tube feeding is recommended if swallowing is impaired or if mucositis is anticipated, which may interfere with oral and/or pharyngeal functionality. If enteral feeding is expected to be required for longer than 4 weeks, then gastrostomy insertion is recommended but not in a prevention way, except for limited cases (<xref ref-type="bibr" rid="B37">37</xref>). The optimal method of tube feeding still remains unclear, and any approach should be discussed with the patient in order to ensure an individualized nutritional care. Moreover, the optimal screening and assessment for suitability and method of gastrostomy insertion by endoscopic, radiological, or surgical approach is essential. Assessment of co-morbidities and contraindications should be taken into account to prevent complications prior to oncological treatment (<xref ref-type="bibr" rid="B35">35</xref>, <xref ref-type="bibr" rid="B36">36</xref>).</p>
<table-wrap id="T1" position="float">
<label>Table&#xa0;1</label>
<caption>
<p>Nutritional counseling and intervention strategies in HNC patients.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="top" align="left">Author/Year</th>
<th valign="top" align="left">Study Type</th>
<th valign="top" align="left">Treatment</th>
<th valign="top" align="left">Population (Number)</th>
<th valign="top" align="left">Time to Intervention</th>
<th valign="top" align="left">Outcomes</th>
<th valign="top" align="left">Conclusions</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="center">Britton et&#xa0;al.<break/>(<xref ref-type="bibr" rid="B18">18</xref>)<break/>2019</td>
<td valign="top" align="left">Randomized controlled trial</td>
<td valign="top" align="left">RT/CRT</td>
<td valign="top" align="left">307</td>
<td valign="top" align="left">Oncology dietitians<break/>delivered EAT (Eating As Treatment) during their usual consultations with a weekly exposure while the patient was receiving RT, and then fortnightly thereafter.</td>
<td valign="top" align="left">NS at end of treatment.</td>
<td valign="top" align="left">NS participants exhibited better nutrition, less weight loss, lower depression scores, fewer RT interruptions, and better QoL scores. The EAT intervention is an effective and achievable intervention.</td>
</tr>
<tr>
<td valign="top" align="center">Orell et&#xa0;al.<break/>(<xref ref-type="bibr" rid="B19">19</xref>)<break/>2019</td>
<td valign="top" align="left">Randomized trial</td>
<td valign="top" align="left">CRT/RT</td>
<td valign="top" align="left">65</td>
<td valign="top" align="left">Prophylactic PEG is inserted to almost all HNC patients either prior to surgery or before the start of (C)RT.</td>
<td valign="top" align="left">NSt (PG-SGA), weight loss, handgrip strength (HGS), body composition, and survival.</td>
<td valign="top" align="left">Individualized on-demand NC is efficacious as intensive counseling in preventing deterioration of NSt and incidence of malnutrition during (C)RT</td>
</tr>
<tr>
<td valign="top" align="center">Sandmael, J.A. et&#xa0;al. (<xref ref-type="bibr" rid="B20">20</xref>)<break/>2017</td>
<td valign="top" align="left">Randomized controlled pilot trial</td>
<td valign="top" align="left">RT</td>
<td valign="top" align="left">41</td>
<td valign="top" align="left">Exercise and NI during RT or after RT.</td>
<td valign="top" align="left">Feasibility, efficacy.</td>
<td valign="top" align="left">Exercise and NI is feasible for patients with HNC during RT, and the intervention is potentially effective in mitigating loss of muscle mass both during and after RT.</td>
</tr>
<tr>
<td valign="top" align="center">Capozzi et&#xa0;al. (<xref ref-type="bibr" rid="B21">21</xref>)<break/>2016</td>
<td valign="top" align="left">Randomized trial</td>
<td valign="top" align="left">RT/CRT</td>
<td valign="top" align="left">60</td>
<td valign="top" align="left">Patients were randomly assigned to either the 12-week immediate lifestyle intervention group or the 12-week delayed lifestyle intervention group.</td>
<td valign="top" align="left">PO: body composition<break/>SO: fitness, quality of life, depression, and NSt.</td>
<td valign="top" align="left">Common interventions to manage side effects focus on NC, although NC alone does not significantly mitigate muscle and functional loss. Physical activity has been recognized as an important intervention for general cancer populations, helping patients to manage side effects throughout treatment.</td>
</tr>
<tr>
<td valign="top" align="center">L&#xf8;nbro, S. et&#xa0;al. (<xref ref-type="bibr" rid="B22">22</xref>)<break/>2013</td>
<td valign="top" align="left">Randomized, stratified and parallel-grouped feasibility trial</td>
<td valign="top" align="left">RT/CRT</td>
<td valign="top" align="left">30</td>
<td valign="top" align="left">12-week immediate lifestyle intervention vs. 12-week delayed intervention.</td>
<td valign="top" align="left">Whole body lean body mass and fat mass.</td>
<td valign="top" align="left">Progressive resistance training increase body mass, muscle strength, and functional performance in both groups.</td>
</tr>
<tr>
<td valign="top" align="center">Cereda et&#xa0;al. (<xref ref-type="bibr" rid="B23">23</xref>)<break/>2018</td>
<td valign="top" align="left">Randomized, pragmatic, parallel-group controlled trial</td>
<td valign="top" align="left">RT/CRT</td>
<td valign="top" align="left">159</td>
<td valign="top" align="left">NC in combination with ONS or without ONS from the start of RT and continuing for up to 3 months after its end.</td>
<td valign="top" align="left">PO: change in body weight at the end of RT<break/>SO: changes in protein&#x2013;calorie intake, muscle strength, phase angle, and QoL and anticancer treatment tolerance.</td>
<td valign="top" align="left">ONS results in better weight maintenance, increased protein&#x2013;calorie intake, improved QoL, and was associated with better anti-cancer treatment tolerance.</td>
</tr>
<tr>
<td valign="top" align="center">Jiang et&#xa0;al.<break/>(<xref ref-type="bibr" rid="B24">24</xref>)<break/>2018</td>
<td valign="top" align="left">Randomized trial</td>
<td valign="top" align="left">CRT</td>
<td valign="top" align="left">100</td>
<td valign="top" align="left">Each measurement were assessed within 1 week before CRT (baseline), within 3 days before the end of CRT and 3 months after the end of CRT. Patients were examined once a week to assess the severity of mucositis.</td>
<td valign="top" align="left">To determine the effect of ONS on the outcomes of weight, fat-free mass, fat-free mass index, and laboratory parameters, the dependent continuous variable, analysis of covariate variance was used to compare the ONS group.with the control group.</td>
<td valign="top" align="left">ONS had beneficial outcomes in terms of reducing weight loss, minimizing BMI decrease and increasing protein intake in loco-regionally advanced nasopharyngeal cancer patients during<break/>CRT.</td>
</tr>
<tr>
<td valign="top" align="center">Machon et&#xa0;al.<break/>(<xref ref-type="bibr" rid="B25">25</xref>)<break/>2012</td>
<td valign="top" align="left">Prospective non-controlled phase II pilot study</td>
<td valign="top" align="left">CRT</td>
<td valign="top" align="left">46</td>
<td valign="top" align="left">Patients were followed up by a dietician and a radiotherapist once a week during RCT and for the following 2 months post-CRT.</td>
<td valign="top" align="left">Effects of an NS containing amino acids, &#x3c9;-3 fatty acids, and ribonucleic acids on inflammatory and oxidative markers status before and during CRT.</td>
<td valign="top" align="left">NS could improve inflammatory state and could prevent severe acute mucositis in HNC patients.</td>
</tr>
<tr>
<td valign="top" align="center">Sykes et&#xa0;al. (<xref ref-type="bibr" rid="B26">26</xref>)<break/>2022</td>
<td valign="top" align="left">Prospective, randomized controlled<break/>trial</td>
<td valign="top" align="left">Surgery</td>
<td valign="top" align="left">49</td>
<td valign="top" align="left">Optimization of NSt was attempted via a multimodal intervention: (1) Preoperative Dietitian Consultation<break/>(2) ONS</td>
<td valign="top" align="left">The scored PG-SGA was validated to triage NI in oncology patients. Participants completed the MD Anderson Dysphagia Inventory to assess swallowing-related factors. Data were collected during the inpatient hospital course and up to 30 days following discharge from the hospital.</td>
<td valign="top" align="left">Preoperative nutrition optimization shows potential to reduce weight loss normally experienced by patients with HNC prior to surgical extirpation, especially among those with subjective dysphagia.</td>
</tr>
<tr>
<td valign="top" align="center">Blake et&#xa0;al. (<xref ref-type="bibr" rid="B27">27</xref>) 2021</td>
<td valign="top" align="left">Prospective cohort study</td>
<td valign="top" align="left">RT/CRT</td>
<td valign="top" align="left">111</td>
<td valign="top" align="left">All high risk patients were referred to an oncology dietitian for an &#x201c;early&#x201d; 1-h pre-treatment counseling session, which was aimed to be delivered at least 2 weeks prior to treatment commencement. Patients who proceeded with prophylactic gastrostomy placement were recommended to commence the proactive EN protocol as soon as safe to do so post gastrostomy insertion, ideally prior to treatment commencement.</td>
<td valign="top" align="left">PO: percentage weight change. SO: changes in percentage fat mass and percentage fat-free mass and change in SGA category.</td>
<td valign="top" align="left">A new pre-treatment model of nutrition care that combined early dietary counselling with a proactive EN protocol was effective in generating a clinically important reduction in weight loss and reduced decline in NSt.</td>
</tr>
<tr>
<td valign="top" align="center">Ho et&#xa0;al. (<xref ref-type="bibr" rid="B28">28</xref>)<break/>2021</td>
<td valign="top" align="left">Prospective cohort study</td>
<td valign="top" align="left">CRT</td>
<td valign="top" align="left">243</td>
<td valign="top" align="left">Questionnaire including lifestyle habits (smoking, alcohol drinking, and use of betel quid), comorbidity, and NSt assessment within 7 days of CRT initiation. NC was provided by a registered dietician to each patient using face-to-face interviews at least every 2 weeks during CRT.</td>
<td valign="top" align="left">OS, Comparison of body weight change during concurrent CRT, treatment completeness and CRT related death according to the different nutritional counseling groups.</td>
<td valign="top" align="left">HNC patients, regardless of pretreatment NSt, should immediately receive NC prior to CRT.</td>
</tr>
<tr>
<td valign="top" align="center">Jantharapattana and Orapipatpong (<xref ref-type="bibr" rid="B29">29</xref>)<break/>2019</td>
<td valign="top" align="left">Randomized controlled trial</td>
<td valign="top" align="left">Surgery</td>
<td valign="top" align="left">62</td>
<td valign="top" align="left">All patients were scheduled for surgery within 7&#x2013;14 days after receiving a preoperative evaluation to prevent the treatment delay. During the perioperative period, the patients were assigned to receive their NSu at least 7 days before surgery and then 14 days postoperatively. At 14 days, 2 months, and 4 months postoperatively, the weight, BMI, lean body mass, and body compositions of all participants were measured or calculated, and blood tests was analyzed.</td>
<td valign="top" align="left">Effect on body weight changes, on lean body mass and body composition, on hematology and biochemistry, and complications related to surgery and hospitalization</td>
<td valign="top" align="left">Body weight changes in malnourished patients with HNC following surgery were not influenced by Eicosapentaenoic acid additives to perioperative NSu. The NSt and postoperative morbidities of the malnourished patients primarily depended on the adequacy of caloric intake.</td>
</tr>
<tr>
<td valign="top" align="center">Boisselier et&#xa0;al. (<xref ref-type="bibr" rid="B30">30</xref>)<break/>2020</td>
<td valign="top" align="left">Phase III double-blind multicenter study</td>
<td valign="top" align="left">CRT</td>
<td valign="top" align="left">172</td>
<td valign="top" align="left">ONS of either a formula enriched with l-arginine and omega-3 fatty and ribonucleic acids (experimental arm), or an isocaloric isonitrogenous control (control arm), for 5 days before each of three cycles of cisplatin. Intention-to-treat and per-protocol analyses were undertaken, along with subgroup analyses of &#x2265;75% compliant patients, to compare the incidence of acute mucositis and 36-month survival.</td>
<td valign="top" align="left">PO: efficacy of the same immunonutrient supplement on severe mucositis. SO: tolerance, compliance to oral supplementation, chemotherapy interruptions and delays, quality of life, and progression-free survival and overall survival at 1, 2, and 3 years</td>
<td valign="top" align="left">Immunomodulating formula failed to reduce severe mucositis during CRT, but the long-term survival of compliant HNC patients was improved.</td>
</tr>
<tr>
<td valign="top" align="center">Carvalho et&#xa0;al. (<xref ref-type="bibr" rid="B31">31</xref>)<break/>2017</td>
<td valign="top" align="left">Randomized controlled trial</td>
<td valign="top" align="left">CT</td>
<td valign="top" align="left">53</td>
<td valign="top" align="left">The control group received powdered HH supplement during 4 weeks. The experimental group received liquid HH supplement, ready for consumption, enriched with EPA from fish oil (2 g/440 ml) for the same period.<break/>The adherence to the supplementation was evaluated weekly through phone calls and in the return visits after 4 weeks of NI.</td>
<td valign="top" align="left">Inflammatory profile</td>
<td valign="top" align="left">Effect of NS with HH formula enriched with EPA on the inflammatory profile of patients with oral cavity cancer in antineoplastic pretreatment. However, the supplementation during 4 weeks was not able to promote significant changes in the inflammatory profile of the patients.</td>
</tr>
<tr>
<td valign="top" align="center">Brown et&#xa0;al. (<xref ref-type="bibr" rid="B32">32</xref>)<break/>2017</td>
<td valign="top" align="left">Randomized controlled trial</td>
<td valign="top" align="left">Surgery/RT/CRT</td>
<td valign="top" align="left">131</td>
<td valign="top" align="left">All patients received education on the care of their feeding tube during their overnight elective admission for gastrostomy placement.<break/>In the standard care arm, patients were commenced on EN via their prophylactic gastrostomy by the dietitian when indicated.<break/>For patients in the intervention group, this meant initiation of enteral nutrition via their prophylactic gastrostomy immediately following tube placement prior to commencement of treatment, until completion of treatment. Patients were asked to maintain a self-reporting diary of their daily prescribed enteral nutrition intake, and any barriers to this prescription.</td>
<td valign="top" align="left">PO: percentage weight change with additional nutrition outcomes, including body composition (fat mass and fat-free mass) and nutritional status.<break/>SO: quality of life, tertiary endpoints: tolerance to (C)RT, rate of unplanned hospital admissions and gastrostomy complications.</td>
<td valign="top" align="left">The early NI did not improve outcomes, but poor adherence to nutrition recommendations impacted on potential outcomes.</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>PO, primary outcome; S, second outcome; OR, oral nutrition; NS, nutritional support; QoL, quality of life; BMI, Body Mass Index; NI, nutrition intervention; NSt, nutritional status; NC, nutrition counseling; ONS, oral nutritional supplements; HH, hypercaloric and hyperproteic; NSu, nutritional supplement; EN, enteral nutrition; EN, enteral nutrition.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<p>The type and volume of enteral nutrition will depend upon patients&#x2019; symptoms and current intake and is likely to change throughout and after treatment. There are no data to suggest a role for cancer-specific enteral formulae. Monitoring nutritional intervention is essential, as compliance with recommendations can be a problem and should be organized weekly during CRT. Supplementation with immunonutrient-enriched formulas such as arginine, nucleotides (RNA), and omega-3 fatty acids up to the end of (C)RT or until withdrawal in HNC patients during RT and CRT may improve or maintain nutrition status (<xref ref-type="bibr" rid="B37">37</xref>&#x2013;<xref ref-type="bibr" rid="B39">39</xref>). Moreover, it can delay the onset of oral mucositis and reduce the incidence of severe oral mucositis (<xref ref-type="bibr" rid="B38">38</xref>&#x2013;<xref ref-type="bibr" rid="B40">40</xref>). Much evidence is showing a possible beneficial effect of immunonutrition on the control of the onset of local recurrences of the disease after esophagectomy, an improvement in immunosurveillance mechanisms, and a reduction in inflammatory status. Finally, by modulating gene expression, the immunonutrition may make it easier for the body to adapt to systemic inflammation and oxidative stress induced by RCTs and may improve 3-year survival (<xref ref-type="bibr" rid="B25">25</xref>, <xref ref-type="bibr" rid="B30">30</xref>, <xref ref-type="bibr" rid="B41">41</xref>, <xref ref-type="bibr" rid="B42">42</xref>). However, further studies focusing on the timing, dosage, and duration of immunonutrition in HNC patients are awaited.</p>
</sec>
<sec id="s5" sec-type="conclusions">
<title>Conclusion</title>
<p>In conclusion, HNC patients undergoing cancer treatment are at high risk of malnutrition before, during, and after oncological care. The nutritional screening, assessment, and support play a crucial role on the maintenance of nutritional status providing specific interventions such as oral nutritional supplements increasing dietary intake and preventing therapy-associated weight loss. It is well-reported in the literature that the interruption of CRT may contribute to worse oncological outcomes. In this regard, the present overview highlighted that an adequate nutritional screening, assessment, and interventions might increase the adherence of HNC patients to oncological treatments and encourages radiation oncologists to set up multidisciplinary care paths.</p>
</sec>
<sec id="s6" sec-type="author-contributions">
<title>Author contributions</title>
<p>BS: Conceptualization, Methodology, Validation, Formal analysis, Data curation, Writing - original draft, Writing - review and editing, Supervision. NB: Methodology, Data curation, Writing &#x2013; original draft, Writing &#x2013; review and editing, Visualization. CC: Methodology, Data curation, Writing &#x2013; original draft, Writing &#x2013; review and editing, Visualization. SM: Methodology, Data curation, Writing &#x2013; original draft, Writing &#x2013; review and editing, Visualization. PF: Conceptualization, Validation, Formal analysis, Writing &#x2013; review and editing, Visualization, Supervision. RG: Conceptualization, Validation, Formal analysis, Writing &#x2013; review and editing, Visualization, Supervision. GCI: Conceptualization, Validation, Formal analysis, Writing &#x2013; review and editing, Visualization, Supervision. SL: Data curation, Writing &#x2013; original draft, Writing &#x2013; review and editing. LB: Conceptualization, Validation, Formal analysis, Writing &#x2013; review and editing, Visualization, Supervision. AP: Conceptualization, Validation, Formal analysis, Writing &#x2013; review and editing, Visualization, Supervision. ID: Conceptualization, Validation, Formal analysis, Writing &#x2013; review and editing, Visualization, Supervision. FF: Conceptualization, Validation, Formal analysis, Writing &#x2013; review and editing, Visualization, Supervision. VS: Conceptualization, Methodology, Data curation, Writing &#x2013; original draft, Writing &#x2013; review and editing. All authors contributed to the article and approved the submitted version.</p>
</sec>
</body>
<back>
<sec id="s7" sec-type="COI-statement">
<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>
<p>The reviewer ND is currently organizing a Research Topic with the authors GCI, ID.</p>
</sec>
<sec id="s8" sec-type="disclaimer">
<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>
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