A Blueprint to Advance Colorectal Cancer Immunotherapies.

Published

Journal Article

Immunotherapy is rapidly becoming a standard of care for many cancers. However, colorectal cancer had been generally resistant to immunotherapy, despite features in common with sensitive tumors. Observations of substantial clinical activity for checkpoint blockade in colorectal cancers with defective mismatch repair (microsatellite instability-high tumors) have reignited interest in the search for immunotherapies that could be extended to the larger microsatellite stable (MSS) population. The Cancer Research Institute and Fight Colorectal Cancer convened a group of scientists, clinicians, advocates, and industry experts in colorectal cancer and immunotherapy to compile ongoing research efforts, identify gaps in translational and clinical research, and provide a blueprint to advance immunotherapy. We identified lack of a T-cell inflamed phenotype (due to inadequate T-cell infiltration, inadequate T-cell activation, or T-cell suppression) as a broad potential explanation for failure of checkpoint blockade in MSS. The specific cellular and molecular underpinnings for these various mechanisms are unclear. Whether biomarkers with prognostic value, such as the immunoscores and IFN signatures, would also predict benefit for immunotherapies in MSS colon cancer is unknown, but if so, these and other biomarkers for measuring the potential for an immune response in patients with colorectal cancer will need to be incorporated into clinical guidelines. We have proposed a framework for research to identify immunologic factors that may be modulated to improve immunotherapy for colorectal cancer patients, with the goal that the biomarkers and treatment strategies identified will become part of the routine management of colorectal cancer. Cancer Immunol Res; 5(11); 942-9. ©2017 AACR.

Full Text

Duke Authors

Cited Authors

  • Le, DT; Hubbard-Lucey, VM; Morse, MA; Heery, CR; Dwyer, A; Marsilje, TH; Brodsky, AN; Chan, E; Deming, DA; Diaz, LA; Fridman, WH; Goldberg, RM; Hamilton, SR; Housseau, F; Jaffee, EM; Kang, SP; Krishnamurthi, SS; Lieu, CH; Messersmith, W; Sears, CL; Segal, NH; Yang, A; Moss, RA; Cha, E; O'Donnell-Tormey, J; Roach, N; Davis, AQ; McAbee, K; Worrall, S; Benson, AB

Published Date

  • November 2017

Published In

Volume / Issue

  • 5 / 11

Start / End Page

  • 942 - 949

PubMed ID

  • 29038296

Pubmed Central ID

  • 29038296

Electronic International Standard Serial Number (EISSN)

  • 2326-6074

Digital Object Identifier (DOI)

  • 10.1158/2326-6066.CIR-17-0375

Language

  • eng

Conference Location

  • United States