Abstract

Simple SummaryIn 2018, colorectal cancer (CRC) was declared the fourth most deadly cancer worldwide. Unfortunately, a quarter of all patients are diagnosed at late stages, when curative surgery is not possible, rendering systemic therapy and/or best supportive care as the only options. To our knowledge, this is the first systematic review assessing response and survival rates in patients with mCRC treated with immune-checkpoint inhibitors (ICIs). Our study established that ICIs show potentially superior response rates in mCRC patients, though only in those with high microsatellite instability (MSI). Nivolumab + regorafenib was reported to provide encouraging response in low-MSI (MSI-L) patients; however, additional studies using cohort randomization are required. Further studies are required, particularly regarding the mechanism of resistance to ICIs in MSI-L patients.Background. Colorectal cancer (CRC) is the fourth most deadly cancer worldwide. Unfortunately, a quarter of the patients are diagnosed at late stages, when surgical options are limited. Targeted therapies, particularly immune-checkpoint inhibitors (ICIs), are the latest addition and have been studied herein regarding their efficacy outcomes. Methods. Clinical studies were identified through the PubMed, Scopus and Cochrane databases. Any trial that evaluated ICIs in patients with metastatic CRC (mCRC) and reported the objective response rate was deemed eligible. Data analysis was performed by employing the random-effects model in STATA v.17. Results. A total of 461 articles were identified; 13 clinical trials were included, encompassing a total cohort of 1209 patients. Our study determined that a single PD-1/PD-L1 checkpoint blockade provides durable clinical response in mCRC patients with high microsatellite instability (MSI-H). The combinatorial therapy of CTLA-4 + PD-1 inhibitors also showed high response rates in pre-treated MSI-H patients. The single-arm REGONIVO trial reported durable clinical response in patients with microsatellite stable (MSS) status. Conclusions. Our study surmises that PD-1/PD-L1 inhibitors as well as combination therapy with CTLA-4 and PD-1 inhibitors show encouraging response rates in mCRC patients, albeit exclusively in patients with cancer that are of MSI-H status. A single study suggests that nivolumab + regorafenib can reach a durable response rate in MSS patients; however, further studies in larger randomized settings are required.

Highlights

  • Colorectal cancer (CRC) is the fourth most common cause of cancer-related mortality, 1

  • This study aims to comprehensively summarize existing knowledge regarding response or low microsatellite instability (MSI-L) [20], where the efficacy of immune-checkpoint inhibitors (ICIs) is yet to be defined

  • For the purpose of this study, we utilized the following eligibility criteria: (1) patients agent or in combination with chemotherapeutic/biological agents; (3) ORR was reported; with metastatic CRC (mCRC); (2) programmed cell death-1 (PD-1), programmed cell death ligand 1 (PD-L1), cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) inhibitors used for treatment either as a single agent

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Summary

Introduction

Colorectal cancer (CRC) is the fourth most common cause of cancer-related mortality, 1. Introduction accounting for 10% of all annually diagnosed worldwide [1]. (CRC) ismalignancies the fourth most common cause ofis cancer-related most common cancer in women andofthe third most common in men [2], with the[1]. Despite the availability of screening programs, most common cancer in women and the third most common in men [2], with the yearly incidence to surpass. 25% of all new CRC cases are still diagnosed advanced stages the [4,5] (Figure 1). Any trial that evaluated ICIs in patients with metastatic CRC (mCRC) and reported the objective response rate was deemed eligible. A total of 461 articles were identified; 13 clinical trials were included, encompassing a total cohort of 1209 patients

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