TY - JOUR
T1 - 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
AU - Takeda, Masayuki
AU - Shimokawa, Mototsugu
AU - Nakamura, Atsushi
AU - Nosaki, Kaname
AU - Watanabe, Yasutaka
AU - Kato, Terufumi
AU - Hayakawa, Daisuke
AU - Tanaka, Hiroshi
AU - Takahashi, Toshiaki
AU - Oki, Masahide
AU - Tachihara, Motoko
AU - Fujimoto, Daichi
AU - Hayashi, Hidetoshi
AU - Yamaguchi, Kakuhiro
AU - Yamamoto, Shoichiro
AU - Iwama, Eiji
AU - Azuma, Koichi
AU - Hasegawa, Kazuo
AU - Yamamoto, Nobuyuki
AU - Nakagawa, Kazuhiko
N1 - Funding Information:
This study was financially supported by AstraZeneca.
Publisher Copyright:
© 2023 The Author(s)
PY - 2023/3
Y1 - 2023/3
N2 - 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.
AB - 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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U2 - 10.1016/j.lungcan.2023.01.011
DO - 10.1016/j.lungcan.2023.01.011
M3 - Article
C2 - 36731290
AN - SCOPUS:85147111710
SN - 0169-5002
VL - 177
SP - 44
EP - 50
JO - Lung Cancer
JF - Lung Cancer
ER -