Immunotherapy in Gastrointestinal Malignancies.

Adv Exp Med Biol

Investigational Cancer Therapeutics, The University of Texas MD Anderson Center, Houston, TX, USA.

Published: July 2020

AI Article Synopsis

  • GI cancers have diverse types and their interaction with the immune system is complex, which affects the success of immunotherapies.
  • While some immunotherapies like anti-PD-1 have been FDA approved for specific GI cancer cases, overall results have been underwhelming compared to other solid tumors.
  • To improve outcomes, new treatment strategies and combinations, along with better biomarkers, are necessary to make immunotherapy effective for more patients with GI cancers.

Article Abstract

Gastrointestinal (GI) cancers represent a variety of malignancies, each with a unique interplay between the tumor and local immune microenvironment. The successes that immunotherapy, particularly immune checkpoint inhibition, has brought to various other solid tumors have largely not yielded the same benefits to patients with GI cancers. There are subsets of patients for whom immunotherapy has been FDA approved in recent years. For example, anti-PD-1 therapy is approved for patients with pretreated hepatocellular carcinoma. Additionally, patients with PD-L1-positive gastric cancer are eligible to receive anti-PD-1 therapy in the third line setting. Outside of the rare subset of patients who harbor MSI-H/dMMR tumors, the vast majority of patients with colorectal, anal, biliary tract, and pancreatic cancers have not responded to single-agent immune checkpoint inhibitors. Innovative techniques with thoughtful treatment combinations, adoptive cell therapy, CAR-T cells, as well as novel predictive biomarkers are needed to bring the benefits of immunotherapy to the majority of patients with GI malignancies.

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Source
http://dx.doi.org/10.1007/978-3-030-41008-7_5DOI Listing

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