Sequential Use of Anaplastic Lymphoma Kinase Inhibitors in Japanese Patients With ALK-Rearranged NoneSmall-Cell Lung Cancer: A Retrospective Analysis

被引:9
作者
Asao, Tetsuhiko [1 ,3 ]
Fujiwara, Yutaka [1 ,2 ]
Itahashi, Kota [1 ]
Kitahara, Shinsuke [1 ]
Goto, Yasushi [1 ]
Horinouchi, Hidehito [1 ]
Kanda, Shintaro [1 ]
Nokihara, Hiroshi [1 ]
Yamamoto, Noboru [1 ,2 ]
Takahashi, Kazuhisa [3 ]
Ohe, Yuichiro [1 ]
机构
[1] Natl Canc Ctr, Dept Thorac Oncol, Tokyo, Japan
[2] Natl Canc Ctr, Dept Expt Therapeut, Tokyo, Japan
[3] Juntendo Univ, Grad Sch Med, Dept Resp Med, Tokyo, Japan
关键词
Alectinib; Combined PFS; Crizotinib; OPEN-LABEL; CHEMOTHERAPY; CRIZOTINIB; CERITINIB; SURVIVAL;
D O I
10.1016/j.cllc.2016.11.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sequential anaplastic lymphoma kinase (ALK) inhibitors for ALK-rearranged nonesmall-cell lung cancer (NSCLC) in Japanese patients were retrospectively reviewed. Thirteen patients received crizotinib followed by alectinib. The combined median progression-free survival and 5-year survival rates of patients who received sequential ALK inhibitors were 35.2 months and 77.8%. Making full use of multiple ALK inhibitors might be important to prolonging survival in patients with ALK-rearranged NSCLC. Background: Second-generation anaplastic lymphoma kinase (ALK) inhibitors, such as alectinib and ceritinib, have recently been approved for treatment of ALK-rearranged nonesmall-cell lung cancer (NSCLC). An optimal strategy for using 2 or more ALK inhibitors has not been established. We sought to investigate the clinical impact of sequential use of ALK inhibitors on these tumors in clinical practice. Patients and Methods: Patients with ALK-rearranged NSCLC treated from May 2010 to January 2016 at the National Cancer Center Hospital were identified, and their outcomes were evaluated retrospectively. Results: Fifty-nine patients with ALK-rearranged NSCLC had been treated and 37 cases were assessable. Twenty-six received crizotinib, 21 received alectinib, and 13 (35.1%) received crizotinib followed by alectinib. Response rates and median progression-free survival (PFS) on crizotinib and alectinib (after crizotinib failure) were 53.8% (95% confidence interval [CI], 26.7%-80.9%) and 38.4% (95% CI, 12.0%-64.9%), and 10.7 (95% CI, 5.3-14.7) months and 16.6 (95% CI, 2.9-not calculable), respectively. The median PFS of patients on sequential therapy was 35.2 months (95% CI, 12.7 months-not calculable). The 5-year survival rate of ALK-rearranged patients who received 2 sequential ALK inhibitors from diagnosis was 77.8% (95% CI, 36.5%-94.0%). Conclusion: The combined PFS and 5-year survival rates in patients who received sequential ALK inhibitors were encouraging. Making full use of multiple ALK inhibitors might be important to prolonging survival in patients with ALK-rearranged NSCLC.
引用
收藏
页码:E251 / E258
页数:8
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