A phase II study (WJOG12819L) to assess the efficacy of osimertinib in patients with EGFR mutation-positive NSCLC in whom systemic disease (T790M-negative) progressed after treatment with first- or second-generation EGFR TKIs and platinum-based chemotherapy

奥西默替尼 医学 T790米 内科学 肺癌 肿瘤科 进行性疾病 临床终点 突变 疾病 非小细胞肺癌 化疗 临床研究阶段 临床试验 表皮生长因子受体 癌症 吉非替尼 遗传学 基因 埃罗替尼 生物 A549电池
作者
Masayuki Takeda,Mototsugu Shimokawa,Atsushi Nakamura,Kaname Nosaki,Yasutaka Watanabe,Terufumi Kato,Daisuke Hayakawa,Hiroshi Tanaka,Toshiaki Takahashi,Masahide Oki,Motoko Tachihara,Daichi Fujimoto,Hidetoshi Hayashi,Kakuhiro Yamaguchi,Shoichiro Yamamoto,Eiji Iwama,Koichi Azuma,Kazuo Hasegawa,Nobuyuki Yamamoto,Kazuhiko Nakagawa
出处
期刊:Lung Cancer [Elsevier BV]
卷期号:177: 44-50 被引量:9
标识
DOI:10.1016/j.lungcan.2023.01.011
摘要

BACKGROUND: Osimertinib is a third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) that is an established standard treatment option for chemotherapy-naive patients with EGFR mutation-positive non-small cell lung cancer (NSCLC). However, of such patients who have received prior treatment with a first- or second-generation EGFR TKI, only approximately half are eligible for osimertinib therapy because its indication as second-line treatment and beyond is limited to metastatic NSCLC that is positive for the T790M resistance mutation of the EGFR gene. This study was initiated at the request of a dedicated network for patients with lung cancer in Japan. METHODS: We conducted a phase II study to assess the efficacy of osimertinib in patients with EGFR mutation-positive NSCLC in whom systemic disease (T790M-negative) progressed after treatment with first- or second-generation EGFR TKIs and platinum-based chemotherapy. The primary end point was response rate (assessed by a central imaging reviewer). RESULTS: From August 2020 to February 2021, 55 patients from 15 institutions were enrolled in the study. The overall response for primary analysis was achieved in 16 patients (29.1 %; 95 % CI, 17.6-42.9), which exceeded the threshold response rate necessary for analysis. Stable disease was found in 16 patients (29.1 %), and progressive disease, in 18 (32.7 %). The median length of progression-free survival (PFS) was 4.07 months (95 % CI 2.10-4.30), and the rate of 12-month PFS was 17.3 %. CONCLUSIONS: Osimertinib demonstrated modest antitumor activity against progressive EGFR T790M-negative disease.

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