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Biomarker development for PD-(L)1 axis inhibition: a consensus view from the SITC Biomarkers Committee.
Monette, Anne; Warren, Sarah; Barrett, J Carl; Garnett-Benson, Charlie; Schalper, Kurt A; Taube, Janis M; Topp, Brian; Snyder, Alexandra.
Affiliation
  • Monette A; Lady Davis Institute for Medical Research, Montreal, Québec, Canada.
  • Warren S; Gilead Sciences, Seattle, Washington, USA.
  • Barrett JC; Precede Biosciences, Boston, Massachusetts, USA.
  • Garnett-Benson C; Bristol Myers Squibb, Princeton, New Jersey, USA.
  • Schalper KA; Yale School of Medicine, New Haven, Connecticut, USA.
  • Taube JM; The Mark Foundation Center for Advanced Genomics and Imaging at Johns Hopkins University, Baltimore, Maryland, USA.
  • Topp B; Merck and Co, Rahway, New Jersey, USA.
  • Snyder A; Generate Biomedicines, Somerville, Massachusetts, USA asnyder@generatebiomedicines.com.
J Immunother Cancer ; 12(7)2024 Jul 20.
Article in En | MEDLINE | ID: mdl-39032943
ABSTRACT
Therapies targeting the programmed cell death protein-1/programmed death-ligand 1 (PD-L1) (abbreviated as PD-(L)1) axis are a significant advancement in the treatment of many tumor types. However, many patients receiving these agents fail to respond or have an initial response followed by cancer progression. For these patients, while subsequent immunotherapies that either target a different axis of immune biology or non-immune combination therapies are reasonable treatment options, the lack of predictive biomarkers to follow-on agents is impeding progress in the field. This review summarizes the current knowledge of mechanisms driving resistance to PD-(L)1 therapies, the state of biomarker development along this axis, and inherent challenges in future biomarker development for these immunotherapies. Innovation in the development and application of novel biomarkers and patient selection strategies for PD-(L)1 agents is required to accelerate the delivery of effective treatments to the patients most likely to respond.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers, Tumor Limits: Humans Language: En Journal: J Immunother Cancer Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers, Tumor Limits: Humans Language: En Journal: J Immunother Cancer Year: 2024 Document type: Article Affiliation country: