Immune Checkpoint Blockade in Lower Gastrointestinal Cancers: A Systematic Review

K C Wilson1,2,3, M P Flood4,5,6, D Oh6

  • 1Department of Surgical Oncology, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia. Kasmira.wilson@petermac.org.

Abstract

Insights

Immune checkpoint blockade shows promise for advanced colorectal and anal cancers, with some patients achieving complete responses. Further research is needed to personalize this immunotherapy for lower gastrointestinal tumors.

Area of Science:

  • Oncology
  • Immunotherapy
  • Gastrointestinal Cancers

Background:

  • Limited treatment options for refractory metastatic colorectal and anal cancers necessitate novel therapies.
  • Immune checkpoint blockade (ICB) demonstrates potential in various cancer types.
  • This review evaluates ICB's role in lower gastrointestinal malignancies.

Purpose of the Study:

  • To assess the current application and efficacy of immune checkpoint blockade in patients with lower gastrointestinal tumors.
  • To review clinical trial data on ICB for colorectal and anal cancers.

Main Methods:

  • Systematic literature search of Embase, Medline, and Cochrane databases.
  • Inclusion of English-language clinical trials of ICB for primary lower gastrointestinal tumors.
  • Focus on studies reporting overall survival, progression-free survival, or response to therapy.

Main Results:

  • Ten studies (972 abstracts screened) were included, evaluating ICB in 833 patients with colorectal cancer and 62 with anal cancer.
  • Common ICB agents included pembrolizumab, nivolumab, durvalumab, atezolizumab, tremelimumab, and ipilimumab.
  • Complete responses were observed in 20 colorectal cancer patients and 2 anal cancer patients; partial responses in 111 colorectal and 11 anal cancer patients.

Conclusions:

  • A subset of patients with advanced lower gastrointestinal tumors achieved complete responses to ICB.
  • Data suggest potential benefit from first-line or combination immunotherapy for specific patient populations.
  • Further investigation is warranted to individualize immunotherapy treatment strategies for these cancers.

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