Gefitinib Alone Versus Gefitinib Plus Chemotherapy for Non-Small-Cell Lung Cancer With Mutated Epidermal Growth Factor Receptor: NEJ009 Study

被引:381
作者
Hosomi, Yukio [1 ]
Morita, Satoshi [2 ]
Sugawara, Shunichi [3 ]
Kato, Terufumi [4 ]
Fukuhara, Tatsuro [5 ]
Gemma, Akihiko [6 ]
Takahashi, Kazuhisa [7 ]
Fujita, Yuka [8 ]
Harada, Toshiyuki [9 ]
Minato, Koichi [10 ]
Takamura, Kei [11 ]
Hagiwara, Koichi [12 ]
Kobayashi, Kunihiko [13 ]
Nukiwa, Toshihiro [14 ]
Inoue, Akira [15 ]
Kudoh, S.
Nagao, K.
Nakai, Y.
Yoshioka, T.
Harada, M.
Isobe, T.
Kasai, T.
Oizumi, S.
Kamimura, M.
Watanabe, S.
Okamoto, H.
Shingyoji, M.
Osaki, Y.
Hasegawa, Y.
Koyama, S.
Isobe, H.
Morikawa, N.
Ishida, T.
Ishii, Y.
Takiguchi, Y.
Watanabe, H.
Kurokawa, H.
Sunaga, N.
Mori, Y.
Tabata, T.
Nakagawa, T.
Kuyama, S.
Kiura, K.
Usui, K.
Soejima, K.
Nishitsuji, M.
Kinoshita, I
Taima, K.
Nishimura, N.
Kishi, K.
机构
[1] Tokyo Metropolitan Komagome Hosp, Tokyo, Japan
[2] Kyoto Univ, Grad Sch Med, Kyoto, Japan
[3] Sendai Kousei Hosp, Sendai, Miyagi, Japan
[4] Kanagawa Cardiovasc & Resp Ctr, Yokohama, Kanagawa, Japan
[5] Miyagi Canc Ctr, Natori, Miyagi, Japan
[6] Nippon Med Sch, Tokyo, Japan
[7] Juntendo Univ, Grad Sch Med, Tokyo, Japan
[8] Asahikawa Med Ctr, Asahikawa, Hokkaido, Japan
[9] Hokkaido Hosp, Japan Community Hlth Care Org, Sapporo, Hokkaido, Japan
[10] Gunma Prefectural Canc Ctr, Ota, Japan
[11] Obihiro Kosei Gen Hosp, Obihiro, Hokkaido, Japan
[12] Jichi Med Univ, Shimotsuke, Tochigi, Japan
[13] Saitama Med Univ, Hidaka, Japan
[14] Tohoku Univ, Sendai, Miyagi, Japan
[15] Tohoku Univ, Sch Med, Sendai, Miyagi, Japan
关键词
OPEN-LABEL; 1ST-LINE TREATMENT; EUROPEAN-ORGANIZATION; PHASE-III; ERLOTINIB; OSIMERTINIB; MULTICENTER; AFATINIB; QLQ-C30;
D O I
10.1200/JCO.19.01488
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor combined with cytotoxic chemotherapy is highly effective for the treatment of advanced nonsmall-cell lung cancer (NSCLC) with EGFR mutations; however, little is known about the efficacy and safety of this combination compared with that of standard therapy with EGFR- tyrosine kinase inhibitors alone. METHODS We randomly assigned 345 patients with newly diagnosed metastatic NSCLC with EGFR mutations to gefitinib combined with carboplatin plus pemetrexed or gefitinib alone. Progression-free survival (PFS), PFS2, and overall survival (OS) were sequentially analyzed as primary end points according to a hierarchical sequential testing method. Secondary end points were objective response rate (ORR), safety, and quality of life. RESULTS The combination group demonstrated a better ORR and PFS than the gefitinib group (ORR, 84% v 67% [P < .001]; PFS, 20.9 v 11.9 months; hazard ratio for death or disease progression, 0.490 [P < .001]), although PFS2 was not significantly different (20.9 v 18.0 months; P = .092). Median OS in the combination group was also significantly longer than in the gefitinib group (50.9 v 38.8 months; hazard ratio for death, 0.722; P = .021). The rate of grade >= 3 treatment-related adverse events, such as hematologic toxicities, in the combination group was higher than in the gefitinib group (65.3% v 31.0%); there were no differences in quality of life. One treatment-related death was observed in the combination group. CONCLUSION Compared with gefitinib alone, gefitinib combined with carboplatin plus pemetrexed improved PFS in patients with untreated advanced NSCLC with EGFR mutations with an acceptable toxicity profile, although its OS benefit requires further validation. (C) 2019 by American Society of Clinical Oncology
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页码:115 / +
页数:18
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