Abstract

Radiotherapy remains one of the contemporary cornerstones of cancer treatment in the neoadjuvant, curative, adjuvant and palliative settings, either in isolation or as a multimodal approach. Moreover, recent advances in targeted immune checkpoint therapy have firmly established immunotherapy as the fourth pillar in cancer therapy alongside surgery, chemotherapy and notably radiotherapy. There is emerging evidence to suggest both radioresistance and reduced efficacy of immune checkpoint blockade (ICB) are potentiated by the tumour microenvironment (TME) and in fact modulating aspects of this immunosuppressive milieu is instrumental to unlocking anti-tumour immunity. The response rates of Upper Gastrointestinal (UGI) malignancies to ICB remains modest at 10–15%, compared to melanoma at 20–40%. Harnessing the effects of radiotherapy through remodelling of the TME using ICB as a radiosensitisor is an avenue showing promise. Here we explore the rationale behind combining radiotherapy with ICB, as a symbiotic relationship in shifting the balance in favour of anti-tumour immunity. We discuss the effects of radiotherapy on immunogenic cell death, the concept of the abscopal effect, the importance of the cGAS STING pathway, and their relevance in the context of the tumour microenvironment. Furthermore, dosing and timing of radiotherapy and ICB is now being evaluated for its synergistic effects on host tumour immunity, and we review the ongoing efforts and current available literature for single agent and dual agent ICB in combination multimodal therapy for both locally advanced operable and metastatic disease of the upper gastrointestinal tract.

Highlights

  • After years of effort to harness the immune system for the treatment of cancer, the advent of antibodies which target ‘immune checkpoints’, including programmed cell death protein 1 (PD-1) and cytotoxic lymphocyte antigen 4 (CTLA-4), has increased interest in immunological aspects of conventional therapies

  • The response rates for clinically approved immune checkpoint inhibitors (ICIs) in melanoma and non-small cell lung cancer are approximately 20–40% [2]; in upper gastrointestinal tract (UGI) cancers, this decreases to 10–15% and ICIs are largely confined to salvage treatment of advanced disease, with its use in the neoadjuvant and curative setting confined to select cases [3]

  • Oesophageal squamous cell carcinoma (OSCC), Tri-modality treatment of surgery, chemotherapy and radiotherapy is the standard of care while in gastric cancer (GC) adjuvant chemotherapy depends oncarcinoma surgical margins in oesophageal adenocarcinoma (OAC) and oesophageal use squamous cell (OSCC),and theinextent of cancer lymph(GC)

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Summary

Introduction

After years of effort to harness the immune system for the treatment of cancer, the advent of antibodies which target ‘immune checkpoints’, including programmed cell death protein 1 (PD-1) and cytotoxic lymphocyte antigen 4 (CTLA-4), has increased interest in immunological aspects of conventional therapies. Oesophageal squamous cell carcinoma (OSCC), Tri-modality treatment of surgery, chemotherapy and radiotherapy is the standard of care while in gastric cancer (GC) adjuvant chemotherapy depends oncarcinoma surgical margins in oesophageal adenocarcinoma (OAC) and oesophageal use squamous cell (OSCC),and theinextent of cancer lymph(GC). Anddeath the extent of lymph node triggers damage-induced cellThis death in activating cancer cells but canDNA sensors, modify the antigenicity and thecell adjuvanticity of is by cytosolic inducing immunogenic death, enhancing tumours. This is by activating immunogenic cell[6].

The Abscopal Effect
Neoantigen Generation and Expression
Remodelling of the Tumour Microenvironment
Immunotherapy as a Radiosensitiser
Single Agent Immunotherapy
Locally Advanced Disease
Definitive Chemoradiotherapy
Systemic Treatment of Advanced Disease
50 Gy in 28 fractions
Radiation Dose
Radiation Timing
Radiation Adverse Effects
Future Directions
Findings
Conclusions
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