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

Author:

Hosomi Yukio1,Morita Satoshi2,Sugawara Shunichi3,Kato Terufumi4,Fukuhara Tatsuro5,Gemma Akihiko6,Takahashi Kazuhisa7,Fujita Yuka8,Harada Toshiyuki9,Minato Koichi10,Takamura Kei11,Hagiwara Koichi12,Kobayashi Kunihiko13,Nukiwa Toshihiro14,Inoue Akira15,

Affiliation:

1. Tokyo Metropolitan Komagome Hospital, Tokyo, Japan

2. Kyoto University Graduate School of Medicine, Kyoto, Japan

3. Sendai Kousei Hospital, Sendai, Japan

4. Kanagawa Cardiovascular and Respiratory Center, Yokohama, Japan

5. Miyagi Cancer Center, Natori, Japan

6. Nippon Medical School, Tokyo, Japan

7. Juntendo University Graduate School of Medicine, Tokyo, Japan

8. Asahikawa Medical Center, Asahikawa, Japan

9. Japan Community Health Care Organization Hokkaido Hospital, Sapporo, Japan

10. Gunma Prefectural Cancer Center, Ota, Japan

11. Obihiro Kosei General Hospital, Obihiro, Japan

12. Jichi Medical University, Shimotsuke, Japan

13. Saitama Medical University, Hidaka, Japan

14. Tohoku University, Sendai, Japan

15. Tohoku University School of Medicine, Sendai, Japan

Abstract

PURPOSE Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor combined with cytotoxic chemotherapy is highly effective for the treatment of advanced non–small-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.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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