Crizotinib versus Chemotherapy in Asian Patients with ALK-Positive Advanced Non-small Cell Lung Cancer

被引:44
作者
Nishio, Makoto [1 ]
Kim, Dong-Wan [2 ]
Wu, Yi-Long [3 ]
Nakagawa, Kazuhiko [4 ]
Solomon, Benjamin J. [5 ]
Shaw, Alice T. [6 ]
Hashigaki, Satoshi [7 ]
Ohki, Emiko [7 ]
Usari, Tiziana [8 ]
Paolini, Jolanda [8 ]
Polli, Anna [8 ]
Wilner, Keith D. [9 ]
Mok, Tony [10 ,11 ]
机构
[1] Canc Inst Hosp JFCR, Thorac Oncol Ctr, Tokyo, Japan
[2] Seoul Natl Univ Hosp, Seoul, South Korea
[3] Guangdong Lung Canc Inst, Guangzhou, Guangdong, Peoples R China
[4] Kindai Univ, Osaka, Japan
[5] Peter MacCallum Canc Ctr, Melbourne, Vic, Australia
[6] Massachusetts Gen Hosp, Boston, MA 02114 USA
[7] Pfizer Oncol, Tokyo, Japan
[8] Pfizer Oncol, Milan, Italy
[9] Pfizer Oncol, La Jolla, CA USA
[10] Hong Kong Canc Inst, State Key Lab South China, Shatin, Hong Kong, Peoples R China
[11] Chinese Univ Hong Kong, Shatin, Hong Kong, Peoples R China
来源
CANCER RESEARCH AND TREATMENT | 2018年 / 50卷 / 03期
关键词
Asia; Carboplatin; Cisplatin; Crizotinib; Non-small cell lung carcinoma; Pemetrexed; NSCLC;
D O I
10.4143/crt.2017.280
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Crizotinib has demonstrated superior progression-free survival (PFS) and objective response rates (ORRs) versus chemotherapy in previously treated and untreated patients with anaplastic lymphoma kinase (ALK)-positive advanced non-small cell lung cancer (NSCLC). We report the safety and efficacy of crizotinib in Asian subpopulations of two global phase III trials. Materials and Methods This analysis evaluated previously treated and untreated patients in two randomized, open-label phase III trials of crizotinib versus chemotherapy in ALK-positive advanced NSCLC in second-line (PROFILE 1007) and first-line settings (PROFILE 1014). Efficacy and safety were analyzed by race in the intention-to-treat and "as-treated" populations for efficacy and safety endpoints, respectively. Results In previously treated (n=157) and untreated (n=157) Asian patients, PFS was statistically significantly longer with crizotinib versus chemotherapy (hazard ratio for PFS, 0.526; 95% confidence interval, 0.363 to 0.762; p < 0.001 and hazard ratio, 0.442; 95% confidence interval, 0.302 to 0.648; p < 0.001, respectively). Similar antitumor activity was seen in the non-Asian and overall populations. ORRs were statistically significantly higher with crizotinib versus chemotherapy in both Asian and non-Asian previously treated and untreated patients (p < 0.05). The most common treatment-emergent adverse events (any grade) with crizotinib were vision disorder, diarrhea, and nausea, which were observed at a comparable incidence across Asian and non-Asian populations, irrespective of previous treatment status. Most adverse events were mild to moderate in severity. Conclusion These data, currently the only analysis showing Asian and non-Asian populations in the same study, support the efficacy and safety of crizotinib in Asian patients with previously treated or untreated ALK-positive advanced NSCLC.
引用
收藏
页码:691 / 700
页数:10
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