| Literature DB >> 32211792 |
Eriko Miyawaki1, Haruyasu Murakami1, Keita Mori2, Nobuaki Mamesaya1, Takahisa Kawamura1, Haruki Kobayashi1, Shota Omori1, Kazushige Wakuda1, Akira Ono1, Hirotsugu Kenmotsu1, Tateaki Naito1, Toshiaki Takahashi1.
Abstract
Epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer is less likely to express programmed death-ligand 1 (PD-L1) than tumors with wild-type EGFR and is associated with poor response to pembrolizumab. To understand the relationship between EGFR mutation and PD-L1 expression in pembrolizumab response, we retrospectively evaluated the factors contributing to the high tumor proportion score in 155 EGFR-mutant non-small cell lung cancer cases and their associated response to pembrolizumab. Uncommon EGFR mutations were significantly associated with a PD-L1 tumor proportion score ≥ 50% compared to common EGFR mutations. The objective response rate to pembrolizumab of 14 patients was 36%, including 22% in patients with common EGFR mutations, 60% in patients with uncommon EGFR mutations and 75% in patients with both uncommon mutations and a PD-L1 tumor proportion score ≥ 50%. A PD-L1 tumor proportion score ≥ 50% was more frequent in non-small cell lung cancer patients harboring uncommon EGFR mutations and was associated with pembrolizumab efficacy.Entities:
Keywords: EGFR mutation; non-small cell lung cancer; pembrolizumab; programmed death-ligand 1
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Year: 2020 PMID: 32211792 DOI: 10.1093/jjco/hyaa033
Source DB: PubMed Journal: Jpn J Clin Oncol ISSN: 0368-2811 Impact factor: 3.019