Abstract

There are a wide range of therapies for metastatic colorectal cancer (CRC) available, but outcomes remain suboptimal. Learning the role of the immune system in cancer development and progression led to advances in the treatment over the last decade. While the field is rapidly evolving, PD-1, and PD-L1 inhibitors have a leading role amongst immunomodulatory agents. They act against pathways involved in adaptive immune suppression resulting in immune checkpoint blockade. Immunotherapy has been slow to impact the management of this patient population due to disappointing results, mainly when used broadly. Nevertheless, some patients with microsatellite-instability-high (MSI-H) or mismatch repair-deficient (dMMR) CRC appear to be susceptible to checkpoint inhibitors with objective and sustained clinical responses, providing a new therapeutic option for patients with advanced disease. This article provides a comprehensive review of the early and late phase trials with the updated data of PD-1/PD-L1 inhibitors alone or in combination with other therapies (immunotherapy, targeted therapy and chemotherapy). While data is still limited, many ongoing trials are underway, testing the efficacy of these agents in CRC. Current and future challenges of PD-1 and PD-L1 inhibitors are also discussed.

Highlights

  • Colorectal cancer (CRC) is the third most common cancer in men and the second in women worldwide

  • The first study to show the clinical efficacy of PD-1 blockade in the microsatellite instability subset of colorectal cancer patients was with Pembrolizumab, an Anti-PD1 inhibitor

  • Clinical activity of pembrolizumab 10 mg/kg was evaluated in 3 patient groups: those with deficient MMR (dMMR) metastatic colorectal cancer (mCRC), proficient mismatch repair (pMMR) and a third group that included patients with dMMR in other malignancies [13]

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Summary

Introduction

Colorectal cancer (CRC) is the third most common cancer in men and the second in women worldwide. The incidence across the globe is different in various countries, but about 55% of the cases occur in more developed regions. Despite this fact, geographic patterns are very similar in men and women [1]. Estimates indicate that nearly half of patients with CRC are found with hepatic metastasis during the follow-up of their disease [2]. Patients with metastatic colorectal cancer (mCRC) have a median overall survival (OS) of 26 months for RAS-mutated and 30 months for those with RAS wild-type status [3, 4]

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