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Hallmarks of Resistance to Immune-Checkpoint Inhibitors.
Karasarides, Maria; Cogdill, Alexandria P; Robbins, Paul B; Bowden, Michaela; Burton, Elizabeth M; Butterfield, Lisa H; Cesano, Alessandra; Hammer, Christian; Haymaker, Cara L; Horak, Christine E; McGee, Heather M; Monette, Anne; Rudqvist, Nils-Petter; Spencer, Christine N; Sweis, Randy F; Vincent, Benjamin G; Wennerberg, Erik; Yuan, Jianda; Zappasodi, Roberta; Lucey, Vanessa M Hubbard; Wells, Daniel K; LaVallee, Theresa.
Afiliación
  • Karasarides M; Worldwide Medical Oncology, Bristol Myers Squibb, Princeton, New Jersey.
  • Cogdill AP; Immunai, New York, New York.
  • Robbins PB; Department of Immunology, The University of Texas MD Anderson, Houston, Texas.
  • Bowden M; Instil Bio, Dallas, Texas.
  • Burton EM; Translational Medicine, Bristol Myers Squibb, Cambridge, Massachusetts.
  • Butterfield LH; Department of Surgical Oncology, The University of Texas MD Anderson, Houston, Texas.
  • Cesano A; Parker Institute for Cancer Immunotherapy, San Francisco, California.
  • Hammer C; Department of Microbiology and Immunology, University of California San Francisco, San Francisco, California.
  • Haymaker CL; ESSA Pharma Inc., South San Francisco, California.
  • Horak CE; Department of Cancer Immunology, Genentech, South San Francisco, California.
  • McGee HM; Department of Human Genetics, Genentech, South San Francisco, California.
  • Monette A; Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Rudqvist NP; Global Drug Development, Bristol Myers Squibb, Lawrenceville, New Jersey.
  • Spencer CN; Department of Radiation Oncology, City of Hope National Medical Center and Department of Immuno-Oncology, Beckmann Research Institute, City of Hope, Duarte, California.
  • Sweis RF; Lady Davis Institute for Medical Research, Montréal, Québec, Canada.
  • Vincent BG; University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Wennerberg E; Department of Informatics, Parker Institute for Cancer Immunotherapy, San Francisco, California.
  • Yuan J; University of California San Francisco, San Francisco, California.
  • Zappasodi R; Department of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, Illinois.
  • Lucey VMH; Committee on Immunology, University of Chicago, Chicago, Illinois.
  • Wells DK; Comprehensive Cancer Center, University of Chicago, Chicago, Illinois.
  • LaVallee T; Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina.
Cancer Immunol Res ; 10(4): 372-383, 2022 04 01.
Article en En | MEDLINE | ID: mdl-35362046
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.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Antineoplásicos Inmunológicos / Neoplasias Límite: Humans Idioma: En Revista: Cancer Immunol Res Año: 2022 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Antineoplásicos Inmunológicos / Neoplasias Límite: Humans Idioma: En Revista: Cancer Immunol Res Año: 2022 Tipo del documento: Article