Scientists from BMS reported a series of substituted biphenyl derivatives based on their ability in preventing the PD-1:PD-L1 interaction. Extensive characterization and elucidation of the mode of action of these compounds ( Figure 1 ) have been reported in several publications (discussed in detail in the following section). However, further advancement of these interesting but highly hydrophobic small molecules into the clinic has not been reported. The contributions of hotspots for stabilizing PPIs can be either additive or cooperative, and if the targeting of one of the hotspots is not good enough to achieve the desirable activity, design strategies need to be included to cover one or more hotspots. Based on this rationale, the binding mode of Compound 2a (BMS-1001 in Figure 2 ), which contains the 2,3-dihydro-1,4-benzodioxinyl group and polar groups, is more effective in dimerization of PD-L1 ligands with a network of hydrophobic and polar interactions compared to the first-generation BMS-type compounds, which can bind to only hydrophobic cleft (38). Since the last 6 years, several companies including Incyte Corporation, Arising International Inc., Chemocentryx Inc., Polaris Pharmaceuticals, and Guangzhou Maxinovel Pharmaceuticals Co. have discovered a series of small molecule PD-L1 inhibitors based on the biphenyl core (39–41).

Among the new modified biphenyl scaffolds, compounds with C₂ symmetry or pseudosymmetry containing polar groups are gaining a lot of attention than asymmetric structure ( Figure 2 ). The C₂−symmetric small molecule inhibitors of PD-1:PD-L1 interaction containing the lipophilic biphenyl core for binding to PD-L1 at its PD-1 binding site to occupy the hydrophobic cleft have been reported (42). NMR and X-ray co-crystal structural studies indicated that symmetric molecules such as LH1306 and LH1307 induce formation of a more symmetrically arranged PD-L1 dimer than previously reported asymmetric inhibitors. The polar groups 2-(acetamido) ethylamine of BMS-202, incorporated into the C₂ symmetric molecules, LH1306 and LH1307, are reported to extend out the hydrophobic cleft and occupy the solvent-exposed region sandwiched between the AG and C′C β strands of the respective PD-L1 proteins, further enhancing binding to the two PD-L1 monomers via hydrogen bonds and electrostatic interactions. It was also hypothesized that a symmetric compound would induce a flip of sidechain of Tyr56 protein residue to form a new cavity, leading to increased binding affinity to PD-L1, and PD-1/PD-L1 inhibitory activity in physiological conditions as reported for Compound 4 (43). The improved cellular activity of the PD-L1 inhibitor ARB-272572 further demonstrated the importance of C₂-biphenyl skeleton and symmetry with polar (2-hydroxyl ethyl)amino group extended from the hydrophobic cleft (44). Representative structures of compounds disclosed by BMS, Incyte, and C₂ symmetric compounds are presented in Figure 2 .

A number of reports are also emerging recently from the industry and academia using the privileged structure of biphenyl-containing compounds and their various derivatives to improvise the druggability of the molecules. This includes scaffold based on nicotinyl alcohol ether derivative (45–47), resorcinol dibenzyl ether (48), 4-phenylindoline derivatives (49), combining two privileged scaffolds such as biphenyl backbone structure and 2-amino-pyrimidine structure (50), biphenyl-4-carboxamide derivatives (51), incorporating taurine moieties (52), 1-methyl-1H-pyrazolo[4,3-b] pyridine derivatives (53), replacing the linker connecting aryl group and biaryl core with a novel amine linker (54), a series of novel biphenyl pyridines derivatives lacking linker (55), biphenyl methyl nitrophenyl core unit (56), and terphenyl scaffold derived from the rigidified biphenyl inspired structure (57). Representative structures of the compounds disclosed are presented in Figure 3 .

The presence of distinct interface of PPIs involving the loops/strand sequences can be exploited in identifying peptides that mimic the native interaction interface. Checkpoint proteins are membrane proteins with majority of them from the B7 family (58). Most of the members of the B7 family and their ligands belong to the immunoglobulin superfamily (IgSF). All IgSF proteins have a characteristic Ig-fold structure with an IgG domain consisting of anti-parallel β-strands and loops connecting the β-strands with most strands constituting ~10 amino acids. Receptor–ligand interaction of IgSF proteins is mediated either through loops, strands, or loops and strands. Rational design of peptides based on these interacting interfaces is a proven strategy for design of PPI inhibitors (59). However, due to the inherent limitations of peptides in general, the focus has now shifted to peptide mimics by depeptidizing the short stretch of residues with cyclic linkages, un-natural linkages, retro and retro-inverso amides, urea, and non-amide bonds as peptide bond surrogates.

Proteins are built from a set of only 20 amino acids, and the side chains, which are unique to each amino acid, exhibit different chemistries. The side chains of amino acids involved in hotspots residues are crucial and participate either in polar contacts or hydrophobic interactions in the interface of PPI contributing to stability and specificity of the interaction. In general, a peptidomimetic is referred as bioactive peptide mimicking molecules with the side chain groups of critical amino acids oriented to enable bioactive conformation to yield desirable pharmacological properties (60). The peptidomimetic structure ranges from molecular scaffolds replacing the peptide backbone, to compounds with modified peptide sequences with improved therapeutic properties (61–64).

Utilization of the design principles described above, several peptidomimetics were identified, but none of the peptidomimetics capable of antagonizing the PD-1 signaling exhibit oral bioavailability (65). Therefore, the native interaction pharmacophore first identified by the reductionist approach comprising of three to five amino acids, as in the case of typical peptidomimetic, was radically redesigned ( Figure 4 ). In this design strategy, compounds with side chain functionalities of the amino acids from the native interaction pharmacophore protrude from a heterocyclic template with no amide bonds, in which the side chains are the critical interacting motifs of PPI hotspots, while the metabolically stable heterocyclic template anchors the amino acid side chains presumably in a required geometry ( Figure 5 ). The novel heterocyclic oxadiazole templates were obtained by fusing two amino acids while presenting the desired amino acid side chains to interact with residues on PD-L1, while bringing in the remaining amino acid(s) from the pharmacophore through the use of linkers such as urea bonds resulting in the compound such as CA-170 (19, 66–68).

Recently, scientists from Guangzhou Medicine Pharmaceutical Biological Co. Ltd. and Nanjing Sanhome Pharmaceutical disclosed in their patent applications the close analogues of the lead PD-L1 inhibitor compound from Aurigene approach: (a) cyclizing oxadiazole head to tail by a short PEG linker (69) and (b) incorporating unnatural amino acids majorly containing cyclobutyl groups for oxadiazole generation instead of α-amino acid reported by Aurigene (70). The detailed profile of these compounds is yet to be published.

As discussed earlier in this article, to improve the clinical response rate, one of the strategies would be to target simultaneously more than one non-redundant checkpoint pathways. It was hypothesized that a substantially reduced native pharmacophore derived from protein–protein interacting interfaces of one of the B7 family protein (such as PD-1) also has the potential to interact with other proteins belonging to IgSF (such as VISTA and TIM3) with structurally similar grooves induced by pockets of sequence similarity (71). A focused library was designed and synthesized using amino acids in the hotspot region including conserved residues in the hotspot regions to identify selective or spectrum-selective inhibitors targeting one or more non-redundant checkpoint signaling pathways such as PD-L1 and VISTA (72), PD-L1 and TIM3 (73, 74), VISTA (75), TIM-3 (76), PD-L1 and T-cell immunoreceptor with immunoglobulin and ITIM domain (TIGIT) (77), TIGIT (78), and cluster of differentiation 47 (CD-47) (79) pathways with desirable physicochemical properties and exposure upon oral administration. It is worth noting that small molecules with dual immune checkpoint inhibition have only been reported from the amino-acids-inspired interface mimic approach.

In most of the PD-L1 inhibitor publications, a co-culture assay in which CHO-K1 cells (of Chinese Hamster ovary origin) overexpressing PD-L1 and T-cell receptor activator with the effector Jurkat T cells overexpressing PD-1 and a luciferase gene controlled by the NFAT response element has been used. In such a reporter assay, BMS-1001 and BMS-1166 restored the activation of Jurkat T cells, represented by an increase in luciferase activity (98). However, the potential of the compounds in restoring the activation of effector cells is significantly lower than that observed for the therapeutic antibodies and with lower maximal cell activation levels. Such drastic reduction in the potency of BMS compounds (83) and other derivatives based on the original BMS compounds (49) in the reporter assay has also been confirmed by several other groups (42, 44, 53, 57, 99). In a similar reporter assay system, CA-170, which rescues T cells from the inhibitory activity of PD-L1, did not show activity (93), while a low activity was observed (<1.5 induction of reporter activity at doses ranging from 0.1 to 10 µM) with the most potent small molecule capable (BMS-1166) of potently disrupting the interaction of PD-1:PD-L1 complex (IC₅₀ 7 nM in TR-FRET assay). In comparison, a significant activity was observed for macrocyclic peptide or nivolumab in the same study. Another biphenyl compound, L7, has also been reported to show significantly lower potency compared to its activity in HTRF-based biochemical assay for the disruption of PD-1-PD-L1 interaction (99). Interestingly, the more potent two C₂-symmetric inhibitors LH1306 and LH1307, with IC₅₀ value of 25 and 3 nM, respectively, dose dependently released the PD-1-mediated inhibition of PD-1-expressing Jurkat T cells and induced the activity of luciferase with EC₅₀ values of 4.2 and 0.76 µM, respectively, and the asymmetric version of LH1306 was inactive (42). Similarly, ARB-272572, another symmetric molecule with potent activity (400 pM IC₅₀) in PD-1/PD-L1 HTRF showed significantly lower potency (>40-fold less in the reporter assays, whereas anti-PD-L1 and anti-PD-1 antibodies showed comparable potency in binding and reporter assays (44). Taken together, the available data suggest that the reporter assay system, which is far removed from the physiological context, may not be ideally suited for characterizing all classes of small molecule inhibitors.

Another heterologous functional assay based on the enzyme fragment complementation technology, the commercial PathHunter cell-based PD-1 (SHP-1) signaling assay, has also been used to investigate the potency of PD-L1 inhibitors. This assay utilizes a stable, engineered cell line with enzyme fragment complementation technology for use in studying drug candidates targeting PD-1/PD-L1 pathway. In this assay format, symmetric compounds LH1306 and LH1307 demonstrated 8.2-fold (EC₅₀, 334 nM) and 2.8-fold (EC₅₀, 79 nM) more activity as compared to their asymmetric analogues in commercial PathHunter cell-based PD-1 (SHP-1) signaling assay underscoring the need for C₂-symmetry for optimal functionality (42). However, it is important to note that as in the NFAT reporter assay, the potency of the compounds in the SHP-1 signaling assay was ~10-fold lower compared their potency in PD-1:PD-L1 disruption.

Only a limited number of publications report the characterization of biphenyl compounds in the primary T-cell-based assays. In a peripheral blood mononuclear cell (PBMC)-based assay, BMS-202, one of the early biphenyl compounds with poor cellular activity in the NFAT reporter assay (53), showed significant rescue of interferon gamma (IFN-γ) secretion inhibited by PD-L1 at a lower concentration (100 nM) similar to another biphenyl compound, Compound 58 (54). The biphenyl compound B2 has been shown to induce IFN-γ secretion from the lymph node T cells co-cultured with LLC cells and rescue the inhibition of IFN-γ secretion from PD-L1 of PBMC treated with anti-CD3/anti-CD28, with a potency similar to that observed in biochemical assay for the disruption of PD-1/PD-L1 interaction (56). During the discovery of amino-acid-inspired interface mimic CA-170, a PBMC-based function assay monitoring the rescue of T cells from the inhibitory activity of PD-L1 in inducing proliferation and cytokine secretion was extensively used. In this assay, CA-170 shows the Emax and potency similar to those observed with an anti-PD1 antibody (19). A functional assay in a similar format was recently employed to establish equipotent functional activity as in biochemical assays of modified biphenyl compound, Compound B2, from researchers of Nanjing University and China Pharmaceutical University (56).

It is important to note that not all studies have reported a good correlation between biochemical and PBMC-based functional assays. For example, Compound 24, a biphenyl asymmetric molecule, showed about 30-fold lower activity in PBMC-based tumor cell line (MDA-MB231) killing assay (Wang 2021). In a co-culture assay using 293T-OS8-hPDL1 cells, and CD3 + T cells, Incyte-011, a symmetric compound, increased IFN-γ production in a dose-dependent manner and reached the peak at the maximum dose of 1 μM, indicating a significant attenuation relative to its biochemical activity (IC₅₀ of 5 nM in HTRF assay), whereas the asymmetric compound Incyte-001 and BMS compounds were not active in this assay. In the same assay, the control PD-L1 antibody atezolizumab was highly active, with IFN-γ production reaching up to 350 pg/ml at 5 nM concentration (84).

Based on the observation that PD-1 antibodies have been shown to upregulate T-cell responses in response to superantigens such as staphylococcal enterotoxin B (SEB) or cytomegalovirus (CMV) antigens, these assays have also been utilized for the characterization of PD-L1 agents. In the SEB-induced PBMC assays, to monitor proliferation and secretion of IL-2 or IFN-γ production, BMS small molecule compounds showed activity only at micromolar concentration, while BMS macrocyclic peptide induced high levels of IL-2 at sub-micromolar concentrations (83). In a separate study, a symmetric compound, ARB-272572, that demonstrated activity in an NAFT reporter assay of 17 nM IC₅₀ displayed a potency of 3 nM in CMV antigen recall assay, still a significant drop-off in the potency relative to that observed in biochemical activity (400 pM IC₅₀ in a cell-free HTRF assay) (44).

Among all the functional assays employed, the best correlation with biochemical potency was observed for selected biphenyl compounds using primary T cells with PBMCs as the source and in the presence of PD-L1. Interestingly, CA-170, which failed to exhibit activity in HTRF based PD-1:PD-L1 disruption and NFAT-reporter-based functional assay, was highly active in the PBMC-based assays, which has now translated into immune activation observed in the clinic (100). Taken together, these findings raise the possibility of PBMC/primary T-cell-based assays, which are used to monitor rescue from the inhibitory activity of PD-L1, in which the addition of PD-L1 brings in the specificity, as the most relevant assay to analyze the immune activation potential of small molecule PD-L1 agents. While this possibility needs to be validated further, it may not be entirely surprising considering that PD-1:PD-L1 interaction is studied in a setup that is a lot closer to the physiological and therapeutic context. It is also important to note that in the PBMC-based assay format, the substitution of human PBMCs with monkey PBMCs or mouse splenocytes along with PD-L1 of monkey or mouse origin allows to evaluate the cross-species functional activity (19).

In the cellular pharmacology studies using human T cells and the rescue of inhibition by PD-L1, both CA-170 and anti-PD-1 antibodies showed a bell-shaped T-cell activation response (101). In these assays, optimal T-cell activation occurs between concentrations of 125–500 nM beyond which there is a substantial reduction in the activity. Such inverse dose response has also been observed in vivo in tumor models with a series of novel benzo[c][1,2,5]oxadiazole derivatives with potent PD-L1 binding and functional activity (99). An inverse dose response was observed with PD-L1-humanized MC38 model, in which compound L24 exhibited significant antitumor efficacy in this model, with 25 mg/kg (TGI 44.2%) exhibiting higher efficacy compared to a higher dose of 50 mg/kg (TGI 30.8%). The likely cause for such a bell-shaped response is the hyperactivation of the immune system leading to activation-induced T-cell death (102), which is detrimental to the effect of the drug.

Among the reported small molecule agents binding and interfering in the function of PD-L1, CA-170 has also been shown to functionally antagonize signalling from PD-L2 (19). In human PBMC or mouse splenocyte-based assays, CA-170 has shown dose-dependent rescue of inhibition of proliferation or cytokine secretion in the presence of either PD-L1 or PD-L2. The potency of CA-170 in these assays for functional antagonisms were similar to that observed with commercially available anti-PD1 antibodies (19), which are known to antagonize signaling originated from either PD-L1 and PD-L2. Unlike PD-L1, the expression of PD-L2 is mainly restricted to professional antigen-presenting cells (APCs) like macrophages and dendritic cells (DCs) and more commonly upregulated in lymphoid malignancies (103). Studies have also indicated that the expression of PD-L2 is independently associated with clinical response in pembrolizumab (anti-PD1)-treated patients, supporting that the presence or absence of PD-L2 expression may also play a role in response to PD-1 axis targeted therapies (104). The consequence of selective inhibition of PD-L1 versus dual inhibition of both PD-L1 and PD-L2 needs to be characterized, specifically in view of greater apparent clinical efficacy of anti-PD1 antibodies capable of blocking signals that originated both from PD-L1 and PD-L relative to the efficacy from anti-PD-L1 antibodies.

The detailed characterization of PD-L1 targeting compounds originally described by the BMS group was carried out by Prof. Holak and colleagues, and they have extensively published on the mechanism of action, binding mode based on X-ray structure determination, confirmation of binding, and functionality by various methods (35). One of their major contributions to the field is in identifying the molecular details of the human PD-1/PD-L1 interaction using X-ray structure of hPD-1:PD-L1 complex, which led to the identification of three hotspot pockets in PD-L1, the binding of which can lead to inhibition of PD-1:PD-L1 interaction (35). Among these pockets, two are rich in hydrophobic amino acids with considerable hydrophobicity and one in hydrophilic amino acids. The direct binding of BMS compounds to PD-L1 via NMR assays and the structural basis for these compounds (BMS-8 and BMS-202) in targeting PD-L1 were delineated (85). Using crystal structure studies, it was demonstrated that these compounds inhibit the PD-1:PD-L1 interaction by inducing PD-L1 dimerization through PD-1 interacting surface. The BMS compounds reported in these studies were targeted to the reported hydrophobic hotspots 1 and 2. In a subsequent publication, the same group also reported that BMS compounds, specifically BMS-200, based on 2,3-dihydro-1,4-benzdioxinyl group induced an enlarged interaction interface that results in the open “face-back” tunnel through the PD-L1 dimer (38). This result indicates that BMS-200 induces conformational changes in PD-L1, and the ligand binding site of PD-L1 to be more flexible than it was previously seen. The crystal structure of the less cytotoxic compounds (BMS-1001 and 1166) from the BMS compounds series indicated that the deep hydrophobic pocket harboring BMS-202 is transformed into a tunnel in the PD-L1/BMS-1166 structure by rotation of the Tyr56 sidechain, which may be responsible for increased potency of the compounds compared to their predecessors (98). Using multiple molecular modeling methods, computational insights into the small molecule induced PD-L1 dimerization, suggesting the tendency of BMS small-molecule inhibitors to interact with one PD-L1 monomer first followed by dimer formation for an advantage of stability has been provided (105).

The more active (in both binding and functional assays) C₂-symmetic inhibitor Compound LH1307 was found to extend across the AFGCC’ faces of the PD-L1 proteins, forming an extended hydrophobic tunnel through the PD-L1 homodimer (42). In this molecule, the biphenyl moiety helped in anchoring the compound in the hydrophobic core of the homodimer, while the polar groups in the solvent exposed helped in bringing the two PD-L1 monomers through a network of hydrogen bonds and electrostatic interactions with the polar residues on the AB and CC’ strands of the PD-L1. Greater potency of such symmetrical compound was due to the binding two equivalent sites in the PD-L1 homodimer by virtue of its C₂-symmetric nature (42). Incyte and Arbutus have also utilized the inherent C2-symmetry in the PD-L1 dimer by symmetrizing their molecules to achieve greater potency ( Figure 6 ).

A recent review (106) summarizes the phenomenon of drug-induced protein dimerization, as the mechanism to modulate the target activity is not unique to PD-L1. Other examples of drug-induced protein homodimer stabilization include compounds that stabilize Max and TLR2 homodimers. In these examples, the same dimer sequestration principle occurs with the compounds, which shape an interfacial binding tunnel between two monomeric protein units. Interestingly, compounds used to promote homo-dimerization of matrix metalloproteinases for crystallographic studies also include a biphenyl unit (107).

A cellular mechanism for the functional antagonism of the biphenyl compound BMS-1166 based on the role of glycosylation on the critical residues of PD-L1 protein has also been proposed (108). The four N-glycosylation sites (Asn35, Asn192, Asn 200, and Asn 219) present in the extracellular domain of PD-L1 is necessary for the stability of ligand protein, and except Asn 35, all other glycosylation sites are critical for its interaction with receptor (90, 109). BMS-1166 partially and specifically inhibits PD-L1 glycosylation and functionally inactivates PD-L1 by blocking its export from the endoplasmic reticulum to Golgi (108). It is not known if the newer C₂ symmetric compounds also have an impact on PD-L1 by this mechanism.

Induction of a two-step internalization process as the mechanism of action for a C₂-skeleton biphenyl compounds has recently been published by the Arbutus group (44). In this process, Compound ARB-272572 inhibits the PD-1/PD-L1 axis by inducing cell surface PD-L1 dimerization via cis-interacting homodimers triggering a rapid loss of cell surface PD-L1 by rapid internalization into the cytosol, thereby preventing any further interaction with PD-1-expressing cell types. The formation of homodimer as illustrated by a crystal structure where ARB 272542 (44) bound within a hydrophobic pocket created between two PD-L1 proteins followed by rapid internalization into the cytosol is reported to be the primary mechanism contributing to cellular potency. Similar to the publication by Arbutus, Incyte had previously described inhibitor-induced internalization, but the structure of the specific compound was not revealed (110). Apart from the clinical candidate, Incyte also reported INCB-090244, which binds and internalizes surface PD-L1 in vivo in a dose-dependent manner, and orally dosed INCB-090244 exhibits single agent activity and increases infiltrating T cells in two distinct humanized mouse models (110). Although the induction of PD-L1 internalization has been reported only with C₂-symmetric molecules., it is not clear if the C₂ symmetry and the resulting interaction are prerequisites for inducing internalization.

In the mechanism of action of PD-L1 inhibitor that induces internalization, PD-L1 is no longer available on the cell surface not only to interact with its cognate receptor PD-1 but also for its other reported binding partner Cluster of Differentiation 24 (CD80) (111). This may have unwanted consequences based on the reported finding indicating that PD-L1 also exerts an immunostimulatory effect by repressing the CTLA-4 pathway (112). The reduced cell surface PD-L1 levels could lead to greater availability of CD80 to its cognate receptor CTLA-4 leading to immune suppression. Hence, the disappearance of PD-L1 on the cell surface because of the internalization and its functional consequence may need to be studied further, as the checkpoint biology is still emerging (113).

Lack of binding of amino-acids-inspired interface mimic CA-170 to either PD-1 or PD-L1 or disruption of PD-1:PD-L1 complex in various biophysical and biochemical assays has been discussed in the literature along with postulating alternative unknown mechanism of action for these compounds (82, 83, 93). In view of the use of proteins expressed in heterologous expression systems lacking appropriate post-translational modifications, recently, the binding of CA-170 to PD-L1 has been established by cellular NMR spectroscopy using full-length PD-L1 expressed in mammalian cells (19). Compared to the biphenyl-based small molecule inhibitors (38, 98), CA-170 is highly polar and thus likely interacts with PD-L1 at a solvent exposed region. Observed functional antagonism in PD-L1 signaling and direct binding to PD-L1 in the cellular context without the disruption of the PD1:PD-L1 complex support the formation of a defective ternary complex as the mechanism of action of CA-170 (19) ( Figure 6 ). This mode of action of CA-170 is analogous to that of two reported anti-PD1 antibodies that antagonize PD-1 signaling without interfering in PD-1:PD-L1 complex formation (114, 115).

Several unique features of small molecule agents targeting PD-L1 compared to antibodies against PD-1 and PD-L1 emphasize the potential need to adapt strategies that are different than those that have worked well for approved PD-1 and PD-L1 antibodies. Target engagement analysis in circulation that is widely used for antibody-based therapeutics may not work for small molecule reversible agents because of their distinct binding kinetics including faster off-rate. In the absence of the direct target engagement, dose selection for expansion studies my need to be decided based on the exposure and its correlation with pharmacodynamic effects observed in both preclinical and clinical setting.

Because of the substantially smaller size of small molecule PD-L1 agents, a significantly higher number of molecules (300´ or more) are delivered compared an antibody-based agents at the same dosage level. If the potency of a small molecule PD-L1 agent is similar to anti-PD-1/PD-L1 antibody in primary T-cell-based functional assays, specifically in the rescue of inhibition by PD-L1 (as has been shown for amino-acids-inspired interface mimic CA-170 and several biphenyl derivatives), it is important to think through the consequence of achieving very high molar exposure in the clinic relative to antibodies. As discussed earlier in this article, because of the observed bell-shaped T-cell activation response in preclinical studies, the conventional approach in oncology such as first determining the maximum tolerated dose (MTD), followed by dose expansion at the MTD, may not be ideal and in fact may be highly counterproductive for an immune-activating agent.

Classically, dose–response to drugs is generally considered to be sigmoidal in nature where the biological effect increases linearly with dose until the threshold concentrations whereby inhibition proceeds in a linear fashion until saturation is achieved. However, there are examples in various classes of drugs where the dose–response curve deviates from the sigmoidal curve and exhibits a hormetic (bell-, U-, or J-shaped) dose–response. A classic example of bell-shaped clinical response for an immunomodulating agent was reported for IFN-γ several decades ago with efforts that resulted in identifying optimal immunomodulatory dose (OID) (117). Preclinical and clinical studies have suggested that the OID of may not be the clinical MTD (118–120). Hence, the clinical trials carried out with IFN-γ at MTD resulting in low response rate was attributed to failure in treating the patients at an optimal OID. Such bell-shared clinical response has also been noted with small molecule immunotherapeutic agents such as STING agonists (121) or TLR agonists (122). It is also worth noting that a bell-shaped clinical response has also been reported for anti-PD1 antibody nivolumab (123, 124), a finding that is not widely highlighted.

Clinical exposure-efficacy data of small molecule PD-L1 agents are slowly unfolding, and they indicate an inverse dose relationship in efficacy. Radhakrishnan et al. reported the clinical benefit for CA-170 at a dosage of 400 mg QD compared to 800 mg QD dose (101). Analysis of safety profile of the drug also indicated higher incidence of irAEs at the lower dosage of 400 mg. Additionally, there was a strong overall trend of improved CBR and PFS with 400 mg when compared to the higher dose (800 mg) in both lung cancer and Hodgkin lymphoma. These agree with preclinical findings showing a bell-shaped curve of immune activation likely due to activation-induced cell death with CA-170 (discussed earlier in this article). Observed clinical activity of CA-170 at lower dose is also consistent with the exposure achieved at optimal dose of 10 mg/kg in preclinical models (19). A recent preclinical study also reported potent anticancer efficacy of CA-170 at a dose of 10 mg/kg in carcinogen-induced mouse lung tumorigenesis model (20). Clinical efficacy data are not yet reported for INCB-086550, but peripheral pharmacodynamic activity in Phase 1 studies is reported for a low dose (100, 200 mg QD dosing or 200, 400 mg BID dosing), and Phase 2 dosing is currently ongoing (dosage not disclosed) orally twice a day.

The clinical and preclinical data of CA-170 discussed here highlight the need to adjust the optimal immunomodulatory dose for attaining clinical efficacy. In the absence of any tolerability issues, the recommended Phase 2 dose (RP2D) for a small molecule PD-L1 agent is likely the dose that achieves a reliable immune response/pharmacodynamics (assessed by monitoring T cells or other immune cells in the tumor microenvironment) and hints of clinical efficacy or exposure that shows anti-tumor efficacy in preclinical models. Further studies on the dose−efficacy relationship and the underlying mechanisms need to be understood further to achieve complete benefit of these agents in clinic.

Since most of the reported small molecule inhibitors target PD-L1 as opposed to PD-1, with the exception of limited reports (125), clinical indications in which anti-PD-L1 antibodies have shown good efficacy could be more appropriate for PD-L1 small molecule agents. Unlike PD-1 antibodies that block signaling from both PD-L1 and PD-L2, PD-L1 antibodies do not impact PD-L2 signaling. On the other hand, PD-L1 antibodies also block the interaction of PD-L1 with CD80. Even though there is a significant overlap in the approved clinical indications for PD-1 antibodies versus PD-L1 antibodies, there are specific indications including Hodgkin lymphoma, head and neck cancer, and colorectal cancers in which only PD-1 antibodies are approved. In the absence of head-to-head comparison and the dependence on cross-study comparisons, it is not clear if these differences are due to differential biology expected from PD-1-targeted agents versus those targeting PD-L1. However, these points may need to be taken into consideration during the development of PD-L1-targeted agents.