Pan-tumor genomic biomarkers for PD-1 checkpoint blockade–based immunotherapy

Author:

Cristescu Razvan1ORCID,Mogg Robin1,Ayers Mark1,Albright Andrew1,Murphy Erin1,Yearley Jennifer1,Sher Xinwei1ORCID,Liu Xiao Qiao1ORCID,Lu Hongchao1,Nebozhyn Michael1,Zhang Chunsheng1,Lunceford Jared K.1ORCID,Joe Andrew1,Cheng Jonathan1,Webber Andrea L.1ORCID,Ibrahim Nageatte1ORCID,Plimack Elizabeth R.2ORCID,Ott Patrick A.3,Seiwert Tanguy Y.4ORCID,Ribas Antoni5ORCID,McClanahan Terrill K.1,Tomassini Joanne E.1ORCID,Loboda Andrey1,Kaufman David1

Affiliation:

1. Merck & Co., Kenilworth, NJ 07033, USA.

2. Fox Chase Cancer Center, Philadelphia, PA 19111, USA.

3. Dana-Farber Cancer Institute, Boston, MA 02215, USA.

4. University of Chicago, Chicago, IL 60637, USA.

5. University of California, Los Angeles, Los Angeles, CA 90095, USA.

Abstract

Mining immunotherapy clinical trials Clinical trial data can provide a wealth of information about how drugs work. Yet such information often belongs to pharmaceutical companies and is rarely accessible to the scientific community at large. Cristescu et al. provide exploratory analysis of a cancer genomics dataset, collected from four separate clinical trials of Merck's PD-1 immunotherapy drug, pembrolizumab. This informative public resource examines more than 300 patient samples representing 22 different tumor types. Two widely used signatures that currently predict immunotherapy response are tumor mutational burden and a “hot” T cell–inflamed microenvironment. The study analyzed these two proposed biomarkers in combination to see what predictive clinical utility they may hold. Science , this issue p. eaar3593

Funder

Merck and Co., Inc.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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