Hallmarks of Resistance to Immune-Checkpoint Inhibitors

Author:

Karasarides Maria1,Cogdill Alexandria P.23ORCID,Robbins Paul B.4,Bowden Michaela5,Burton Elizabeth M.6,Butterfield Lisa H.78ORCID,Cesano Alessandra9,Hammer Christian1011ORCID,Haymaker Cara L.12ORCID,Horak Christine E.13,McGee Heather M.14ORCID,Monette Anne15,Rudqvist Nils-Petter16ORCID,Spencer Christine N.1718,Sweis Randy F.192021ORCID,Vincent Benjamin G.22ORCID,Wennerberg Erik23ORCID,Yuan Jianda24ORCID,Zappasodi Roberta252627ORCID,Lucey Vanessa M. Hubbard1,Wells Daniel K.27,LaVallee Theresa7

Affiliation:

1. 1Worldwide Medical Oncology, Bristol Myers Squibb, Princeton, New Jersey.

2. 2Immunai, New York, New York.

3. 3Department of Immunology, The University of Texas MD Anderson, Houston, Texas.

4. 4Instil Bio, Dallas, Texas.

5. 5Translational Medicine, Bristol Myers Squibb, Cambridge, Massachusetts.

6. 6Department of Surgical Oncology, The University of Texas MD Anderson, Houston, Texas.

7. 7Parker Institute for Cancer Immunotherapy, San Francisco, California.

8. 8Department of Microbiology and Immunology, University of California San Francisco, San Francisco, California.

9. 9ESSA Pharma Inc., South San Francisco, California.

10. 10Department of Cancer Immunology, Genentech, South San Francisco, California.

11. 11Department of Human Genetics, Genentech, South San Francisco, California.

12. 12Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

13. 13Global Drug Development, Bristol Myers Squibb, Lawrenceville, New Jersey.

14. 14Department of Radiation Oncology, City of Hope National Medical Center and Department of Immuno-Oncology, Beckmann Research Institute, City of Hope, Duarte, California.

15. 15Lady Davis Institute for Medical Research, Montréal, Québec, Canada.

16. 16University of Texas MD Anderson Cancer Center, Houston, Texas.

17. 17Department of Informatics, Parker Institute for Cancer Immunotherapy, San Francisco, California.

18. 18University of California San Francisco, San Francisco, California.

19. 19Department of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, Illinois.

20. 20Committee on Immunology, University of Chicago, Chicago, Illinois.

21. 21Comprehensive Cancer Center, University of Chicago, Chicago, Illinois.

22. 22Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina.

23. 23The Institute of Cancer Research, London, UK.

24. 24Translational Oncology, Early Oncology Development Department, Merck Research Laboratories, Rahway, New Jersey.

25. 25Weill Cornell Medicine, New York, New York.

26. 26Ludwig Collaborative and Swim Across America Laboratory, Memorial Sloan Kettering Cancer Center, New York, New York.

27. 27Parker Institute for Cancer Immunotherapy, Memorial Sloan Kettering Cancer Center, New York, New York.

Abstract

Abstract Immune-checkpoint inhibitors (ICI), although revolutionary in improving long-term survival outcomes, are mostly effective in patients with immune-responsive tumors. Most patients with cancer either do not respond to ICIs at all or experience disease progression after an initial period of response. Treatment resistance to ICIs remains a major challenge and defines the biggest unmet medical need in oncology worldwide. In a collaborative workshop, thought leaders from academic, biopharma, and nonprofit sectors convened to outline a resistance framework to support and guide future immune-resistance research. Here, we explore the initial part of our effort by collating seminal discoveries through the lens of known biological processes. We highlight eight biological processes and refer to them as immune resistance nodes. We examine the seminal discoveries that define each immune resistance node and pose critical questions, which, if answered, would greatly expand our notion of immune resistance. Ultimately, the expansion and application of this work calls for the integration of multiomic high-dimensional analyses from patient-level data to produce a map of resistance phenotypes that can be utilized to guide effective drug development and improved patient outcomes.

Funder

CPRIT Research Training Program

NIH NCI

NIH

NCI SPORE

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Immunology

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