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Nat Med. 2018 Sep;24(9):1441-1448. doi: 10.1038/s41591-018-0134-3. Epub 2018 Aug 6.

Blood-based tumor mutational burden as a predictor of clinical benefit in non-small-cell lung cancer patients treated with atezolizumab.

Author information

1
UC Davis Comprehensive Cancer Center, Sacramento, CA, USA. drgandara@ucdavis.edu.
2
Genentech, Inc., San Francisco, CA, USA.
3
Lungenfachklinik Immenhausen, Immenhausen, Germany.
4
Kaiser Permanente Medical Center, Vallejo, CA, USA.
5
Foundation Medicine, Inc., Cambridge, MA, USA.
6
State Key Laboratory of Southern China, Department of Clinical Oncology, Chinese University of Hong Kong, Hong Kong, China. tony@clo.cuhk.edu.hk.
7
Genentech, Inc., San Francisco, CA, USA. shames.david@gene.com.

Abstract

Although programmed death-ligand 1-programmed death 1 (PD-L1-PD-1) inhibitors are broadly efficacious, improved outcomes have been observed in patients with high PD-L1 expression or high tumor mutational burden (TMB). PD-L1 testing is required for checkpoint inhibitor monotherapy in front-line non-small-cell lung cancer (NSCLC). However, obtaining adequate tumor tissue for molecular testing in patients with advanced disease can be challenging. Thus, an unmet medical need exists for diagnostic approaches that do not require tissue to identify patients who may benefit from immunotherapy. Here, we describe a novel, technically robust, blood-based assay to measure TMB in plasma (bTMB) that is distinct from tissue-based approaches. Using a retrospective analysis of two large randomized trials as test and validation studies, we show that bTMB reproducibly identifies patients who derive clinically significant improvements in progression-free survival from atezolizumab (an anti-PD-L1) in second-line and higher NSCLC. Collectively, our data show that high bTMB is a clinically actionable biomarker for atezolizumab in NSCLC.

PMID:
30082870
DOI:
10.1038/s41591-018-0134-3
[Indexed for MEDLINE]

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