Combination of chemotherapy and gefitinib as first-line treatment for patients with advanced lung adenocarcinoma and sensitive EGFR mutations: A randomized controlled trial

被引:113
作者
Han, Baohui [1 ]
Jin, Bo [1 ]
Chu, Tianqing [1 ]
Niu, Yanjie [1 ]
Dong, Yu [1 ]
Xu, Jianlin [1 ]
Gu, Aiqing [1 ]
Zhong, Hua [1 ]
Wang, Huimin [1 ]
Zhang, Xueyan [1 ]
Shi, Chunlei [1 ]
Zhang, Yanwei [1 ]
Zhang, Wei [1 ]
Lou, Yuqing [1 ]
Zhu, Lei [2 ]
Pei, Jun [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Pulm, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Pathol, Shanghai, Peoples R China
关键词
chemotherapy; gefitinib; first-line; lung adenocarcinoma; sensitive EGFR mutations; PHASE-II TRIAL; REVERSES MULTIDRUG-RESISTANCE; CELL-LINES; OPEN-LABEL; SEQUENTIAL ERLOTINIB; 2ND-LINE TREATMENT; CANCER-CELLS; MULTICENTER; GEMCITABINE; THERAPY;
D O I
10.1002/ijc.30806
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To explore the optimal treatment strategy for patients who harbor sensitive EGFR mutations, a head-to-head study was performed to compare chemotherapy and gefitinib in combination or with either agent alone as first-line therapy, in terms of efficacy and safety. A total of 121 untreated patients with advanced lung adenocarcinoma who harbored sensitive EGFR mutations were randomly assigned to receive gefitinib combined with pemetrexed and carboplatin, pemetrexed plus carboplatin or gefitinib alone. The progression-free survival (PFS) of patients in the combination group (17.5 months, 95% CI, 15.3-19.7) was longer than that of patients in the chemotherapy group (5.7 months, 95% CI, 5.2-6.3) or gefitinib (11.9 months, 95% CI, 9.1-14.6) group. The (hazard ratios) HRs of PFS for the combination group vs. chemotherapy and gefitinib groups were 0.16 (95% CI, 0.09-0.29, p < 0.001) and 0.48 (95% CI, 0.29-0.78, p = 0.003), respectively. The overall response rate (ORR) in the combination therapy group, chemotherapy group and the gefitinib group was 82.5%, 32.5% and 65.9%, respectively. The combinational strategy resulted in longer overall survival (OS) than chemotherapy (HR = 0.46, p = 0.016) or gefitinib (HR = 0.36, p = 0.001) alone. Our finding suggested that treatment with pemetrexed plus carboplatin combined with gefitinib could provide better survival benefits for patients with lung adenocarcinoma harboring sensitive EGFR mutations.
引用
收藏
页码:1249 / 1256
页数:8
相关论文
共 37 条
[1]   Korean Ethnicity as Compared with White Ethnicity Is an Independent Favorable Prognostic Factor for Overall Survival in Non-small Cell Lung Cancer before and after the Oral Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor Era [J].
Ahn, Myung-Ju ;
Lee, Jeeyun ;
Park, Yun-Hee ;
Ahn, Jin-Seok ;
Ziogas, Argyrios ;
Zell, Jason A. ;
Park, Keunchil ;
Ou, Sai-Hong Ignatius .
JOURNAL OF THORACIC ONCOLOGY, 2010, 5 (08) :1185-1196
[2]  
[Anonymous], J CLIN ONCOL
[3]   Randomized open-label non-comparative multicenter phase II trial of sequential erlotinib and docetaxel versus docetaxel alone in patients with non-small-cell lung cancer after failure of first-line chemotherapy: GFPC 10.02 study [J].
Auliac, J. B. ;
Chouaid, C. ;
Greiller, L. ;
Monnet, I. ;
Le Caer, H. ;
Falchero, L. ;
Corre, R. ;
Descourt, R. ;
Bota, S. ;
Berard, H. ;
Schott, R. ;
Bizieux, A. ;
Fournel, P. ;
Labrunie, A. ;
Marin, B. ;
Vergnenegre, A. .
LUNG CANCER, 2014, 85 (03) :415-419
[4]   Thymidylate synthase and dihydrofolate reductase expression in non-small cell lung carcinoma: The association with treatment efficacy of pemetrexed [J].
Chen, Chung-Yu ;
Chang, Yih-Leong ;
Shih, Jin-Yuan ;
Lin, Jou-Wei ;
Chen, Kuan-Yu ;
Yang, Chih-Hsin ;
Yu, Chong-Jen ;
Yang, Pan-Chyr .
LUNG CANCER, 2011, 74 (01) :132-138
[5]   Annual report on status of cancer in China, 2011 [J].
Chen, Wanqing ;
Zheng, Rongshou ;
Zeng, Hongmei ;
Zhang, Siwei ;
He, Jie .
CHINESE JOURNAL OF CANCER RESEARCH, 2015, 27 (01) :2-12
[6]   Randomized Phase II Trial of Gefitinib With and Without Pemetrexed as First-Line Therapy in Patients With Advanced Nonsquamous Non-Small-Cell Lung Cancer With Activating Epidermal Growth Factor Receptor Mutations [J].
Cheng, Ying ;
Murakami, Haruyasu ;
Yang, Pan-Chyr ;
He, Jianxing ;
Nakagawa, Kazuhiko ;
Kang, Jin Hyoung ;
Kim, Joo-Hang ;
Wang, Xin ;
Enatsu, Sotaro ;
Puri, Tarun ;
Orlando, Mauro ;
Yang, James Chih-Hsin .
JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (27) :3258-+
[7]   Putative cancer stem cells in malignant pleural mesothelioma show resistance to cisplatin and pemetrexed [J].
Cortes-Dericks, Lourdes ;
Carboni, Giovanni L. ;
Schmid, Ralph A. ;
Karoubi, Golnaz .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2010, 37 (02) :437-444
[8]   Lapatinib (Tykerb, GW572016) reverses multidrug resistance in cancer cells by inhibiting the activity of ATP-binding cassette subfamily B member 1 and G member 2 [J].
Dai, Chun-ling ;
Tiwari, Amit K. ;
Wu, Chung-Pu ;
Su, Xiao-dong ;
Wang, Si-Rong ;
Liu, Dong-geng ;
Ashby, Charles R., Jr. ;
Huang, Yan ;
Robey, Robert W. ;
Liang, Yong-ju ;
Chen, Li-ming ;
Shi, Cheng-Jun ;
Ambudkar, Suresh V. ;
Chen, Zhe-Sheng ;
Fu, Li-wu .
CANCER RESEARCH, 2008, 68 (19) :7905-7914
[9]   Sequential use of vinorelbine followed by gefitinib enhances the antitumor effect in NSCLC cell lines poorly responsive to reversible EGFR tyrosine kinase inhibitors [J].
Dal Bello, M. G. ;
Alama, A. ;
Barletta, G. ;
Coco, S. ;
Truini, A. ;
Vanni, I. ;
Boccardo, S. ;
Genova, C. ;
Rijavec, E. ;
Biello, F. ;
Bottoni, G. ;
Sambuceti, G. ;
Grossi, F. .
INTERNATIONAL JOURNAL OF CANCER, 2015, 137 (12) :2947-2958
[10]   A randomised phase II study of pemetrexed versus pemetrexed plus erlotinib as second-line treatment for locally advanced or metastatic non-squamous non-small cell lung cancer [J].
Dittrich, Christian ;
Papai-Szekely, Zsolt ;
Vinolas, Nuria ;
Sederholm, Christer ;
Hartmann, Joerg T. ;
Behringer, Dirk ;
Kazeem, Gbenga ;
Desaiah, Durisala ;
Leschinger, Monika I. ;
von Pawel, Joachim .
EUROPEAN JOURNAL OF CANCER, 2014, 50 (09) :1571-1580