How to Increase the Efficacy of Immunotherapy in NSCLC and HNSCC: Role of Radiation Therapy, Chemotherapy, and Other Strategies

In the last years, preclinical and clinical investigations have demonstrated that the immune system maintains a complex functional interaction with cancer cells and its precursors All these findings led to the 3E hypothesis: elimination, equilibrium, escape. Taking into account this scenario, anticancer treatments should aim to reset this complex relationship, driving the tumor-immune system from escape to equilibrium and elimination In this light, different agents can interfere at different phases of the activation of the immune system, that includes processing and presentation of antigens, priming and activation of T cells, recruitment of cytotoxic lymphocytes, engagement of effector T cells. An afferent phase and efferent phase can be identified, , but it is important to recognize the negative regulatory pathways that are commonly engaged within the tumor microenvironment of cancers.Here we discuss the various strategies that can empower the immune response to cancer cells, at various stages of activation and inhibition, discussing the future research needs, especially in the field of non small cell lung cancer (NSCLC) and head and neck squamous cell carcinoma (HNSCC).Main Text An extraordinary large amount of strategies potentially able to elicit and empower an efficient anti-tumor immune-response in cancer patients, has already been described [1]. However, a number of hurdles have delayed the translation of these results in efficacious treatments for many years leaving the immunological treatments confined to malignant melanoma and renal cell carcinoma[2,3]. In the latter few years, the discovery of priming (CTLA-4/B7.1) and effector (PD-1/PDL-1) immune-checkpoints and the availability of highly specific blocking mAbs has lead to a terrific clinical development of the immune-oncology approaches Some of these mAbs, especially those directed to PD-1 (Nivolumab and Pembrolizumab) expressed on activated CTLs, or PDL-1 (Atezolizumab, Durvalumab, and Avelumab) expressed on inflammatory and cancer cells, have in fact, gained a stable role in the treatment of very common malignancies such as non small cell lung cancer (NSCLC), head and neck squamous cell carcinoma (HNSCC), and urological malignancies, where they are capable ofproducprovideing significant benefit to many patients and prolonging their survival in about a quarter of the cases[4].Even though this kind of strategy is considered quite successful, it is however, hampered by the fact that its efficacy is unpredictable and is associated to immune-related adverse events (irAEs) and unsustainable costs. At the present, the identification of reliable biomarkers of response to immune-oncology treatments as well as the design of combined strategies to enhance their efficacy and field of action represent one of the mainstream t immune-oncology research lines. PD-1/PDL-1is a peripheral immune-checkpointaimed to attenuate the cytotoxic response of tumor-specific infiltrating lymphocytes. Thus its blockade by anti PD-1 (Nivolumab and Pembrolizumab) or anti PDL-1 mAbs (Atezolizumab,Durvalumab, and Avelumab) rescues these CTLs and triggers a fast cytolytic effect in the tumor tissue [5]. This effect may triggera rapid antitumor effect;neverthelessthis renewed CTL reaction is not sufficient alone to prolong patients’ survival. In fact the antitumor activity of these reactivated cells, is more or less rapidly extinguished if a continuous and self-sustained supply of fresh tumor-specific immune-effectors does not occur (immunopriming) [6]. Experimental evidence suggests in fact, the achievement of a prolonged patient survival requires a continuous immune-priming, in order to avoid CTL exhaustion in the tumor and to prevent an adaptive response by the tumor cells[7-8].In this context, CTLA-4/B7.1 immune-check point, acts by attenuating the proliferative activity of antigen specific CTL clones, expressing CTLA-4 and by stimulating the immune-suppressive activity of immune-regulatory T cells (Tregs). Its blockade by Ipilimumab and Tremelimumab, two mAbs to CTLA-4, represents a valid therapeutic option for both metastatic malignant melanoma and renal cell carcinoma and is under clinical investigation in combination with effector PD1/PDL-1immunocheckpoint blockade [9-12]. An efficient Immune-priming however, requires the expression of multiple tumor associate (TAAs) and tumor specific antigens (TSAs) by cancer cells, released as consequence of cancer-associated inflammation, necrosis, previous use of cytotoxic drugs or radiation therapy [13].A number of studies have shown that the efficacy of both immune-effectors and antigen cross-priming may be hardened by cancer vaccines, specific anticancer treatments (radiotherapy, chemotherapy, steroid hormones, and immune-adjuvant agents), hypoxic response and/or tumor associated inflammation[14-15]. (Figure 1) Radiation therapy in particular, together with its direct cyto-reductive activity on tumor burden is also capable of eliciting radio-induced DNA damage on target cells and triggering specific immunological effects [16] which are believed to be responsible for the “abscopal effects” observed in those rare cases, where tumor irradiation is paralleled by regression of non irradiated tumor sites [17-18].This hypothesis is in line with the results of a large number of studies showing that tumor irradiation may really influence all the phases of the immune-response. Tumor irradiation may in fact, trigger immunogenic cell death and significant release of TAAs and TSAs in a context of immunological danger signal. The latter is consequent to DNA damage by radiation which is able to activate of Damage-Associated-Molecularbiochemical Patterns (DAMP) which in turn are able of enhancing tumor antigens presentation to CTL precursors and their proliferation in the draining lymph-nodes [19]. Furthermore, the irradiated-tumor cells release inflammatory cytokines, chemokines (such as CXCL16) and tumor vessel associated adhesion molecules (VCAM-I and ICAM-I) able to reinforce the presence of activated CTLs in the tumor site [19-20-21]. Finally, strong evidence does exists concerning the ability of radiation therapy to induce up-regulation of class I MHC, multiple death receptors (eg. FAS, NKG2DL) in the target cells thus enhancing their susceptibility to recognition and killing by tumor specific CTLs [19]. Clinical evidences in line with these preclinical results have also been reported. IAn abscopal response to radiation was recorded in metastatic NSCLC patients who were receiving immunological treatment with ipilimumab[22].We recently carried out a retrospective analysis in advanced NSCLC patients enrolled in the BEVA2017, who had received an immune-modulating treatment with metronomic chemotherapy (mPE) +/- bevacizumab (mPEBev) reporting that that the use of radiotherapy given on palliative setting, was associated to a prolonged survival and that this effect was indeed correlated to a significant treatment-related increase in activated DCs and effector memory CTLs [23]. Similarly, in a retrospective analysis of the KEYNOTE-001 phase I study aimed to investigate Pembrolizumab in a cohort of 495 patients advanced NSCLC patients, it has been detected a much longer PFS and OS in a group of 97 patients who had received radiation therapy prior immunotherapy [24]. Finally, a perspective randomized phase III study in un-resectable lung stage III cancer patients aimed to receive chemoradiation followed by Durvalumab or placebo for 12 months (PACIFIC) reported a significant advantage in PFS in the experimental arm, which was unrelated to PDL-1 expression in the tumor [25]. In HNSCC, the immune system is known to have a pivotal role, as high density of tumour-infiltrating lymphocytes (TILs) is associated with improved outcome of patients [26-27 ] while tumor tissues and draining lymph-nodes respectively, present a high density of CTLs expressing PD-1 and regulatory Tregs over-expressing CTLA-4; a finding that clearly suggests a high suppressive activity of either peripheral and central immune-checkpoints in these patients [28].Based on this solid rationale, PD-1 blockade with Nivolumab, Pembrolizumab and Durvalumab represented a concrete option for the treatment of recurrent or metastatic HNSCC to be investigated. At the present, the results of three large trials in HNSCC patients on or after frontline platinum-based chemotherapy, concur to show an median overall response rate of 11.3-18%, with a median time to progression of 9.7 months and a 32%reduced risk of death at one year of [29-33]. These encouraging results led to the design of a number of clinical trials which are currently ongoing with the specific aim of combining tumor irradiation with immunological agents and/or immune-check point blockade in patients with advanced HNSCC (see Table 1).On these premises, a rationale use of radiation therapy may be included among the various strategies that could potentially increase the efficacy of of immunotherapy at different disease settings. We believe that more successful immune-oncological trials should take in consideration this knowledge to improve their benefit NSCLC and HNSCC patients. Figure 1 The figure describes the critical mechanisms involved in three phases of the immune-response against cancer and available drugs and strategies which may improve its efficacy Upper row : Specific cell lineages, molecular structures and immune-checkpoints involved in immunopriming process (A), T cell Homing (B), and modulation of CTL mediated Tumor cell killing (C ). Bottom row : Strategies (AKA radiation therapy), cytotoxic Drugs, cytokines and Immunocheckpoint inhibitors interfering with the immunopriming (A), T cell Homing (B), and T cell mediated killing (C ). APCs= antigen presenting cells; CTL-TCR = cytotoxic T lymphocites – T cell Receptor; HLA = Human Leucocyte Antigen; MDSCs = myeloid derived suppressor cells; TAA, Tumor Associated Antigen; TSA, Tumor Specific Antigen; ICD = Immunogenic Cell Death inducers; GM-CSF =Granulocyte-macrophage colony-stimulating factor; IFNs = interferons; ASI= active specific immunotherapy; TKI = tyrosine kinase inhibitor; CTLA-4= Cytotoxic T cell antigen -4; PD-1= Programmed cell death receptor-1; PDL= Programmed cell death ligand