Progression-Free and Overall Survival of Patients With ALK Rearrangement-Positive Non-Small Cell Lung Cancer Treated Sequentially With Crizotinib and Alectinib

被引:33
|
作者
Watanabe, Satomi [1 ]
Hayashi, Hidetoshi [1 ]
Okamoto, Kunio [2 ]
Fujiwara, Kimiko [3 ]
Hasegawa, Yoshikazu [4 ]
Kaneda, Hiroyasu [2 ]
Tanaka, Kaoru [1 ]
Takeda, Masayuki [1 ]
Nakagawa, Kazuhiko [1 ]
机构
[1] Kinki Univ, Dept Med Oncol, Fac Med, 377-2 Ohno Higashi, Osaka, Osaka 5898511, Japan
[2] Kishiwada Municipal Hosp, Dept Med Oncol, Osaka, Japan
[3] Kinki Univ Hosp, Dept Pharm, Fac Med, Osaka, Japan
[4] Izumi Municipal Hosp, Dept Med Oncol, Osaka, Japan
关键词
ALK-TKI; Anaplastic lymphoma kinase; NSCLC; OS; PFS; EML4-ALK FUSION GENE; ANTITUMOR-ACTIVITY; PHASE; 1/2; INHIBITOR; CHEMOTHERAPY; RESISTANCE; CH5424802; AF-001JP; MODELS; KINASE;
D O I
10.1016/j.cllc.2016.05.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We identified 11 patients with ALK-rearranged non-small cell lung cancer treated with sequential crizotinib and alectinib. The median combined progression-free survival and overall survival in the present study was 18.2 and 48.6 months, respectively. These findings suggest that this regimen produces durable survival and therefore warrants further investigation. Introduction: Anaplastic lymphoma kinase (ALK) tyrosine kinase inhibitors (TKIs) show marked therapeutic efficacy in patients with non-small cell lung cancer (NSCLC) harboring the echinoderm microtubule-associated protein-like 4-ALK fusion gene. The effect on overall survival (OS) of sequential treatment with the first-and second-generation ALK-TKIs crizotinib and alectinib, respectively, has remained unknown. We have examined the clinical outcome of such sequential treatment in a retrospective analysis of patients with ALK-rearranged NSCLC. Materials and Methods: Eleven patients with ALK-rearranged NSCLC treated with crizotinib followed by alectinib were identified. The progression-free survival (PFS) and OS for these patients were determined from a retrospective review of their medical records. Results: The median PFS on crizotinib or alectinib was 6.1 months (range, 1.0-15.4 months) and 15.2 months (range, 1.0-28.3 months), respectively. The median combined PFS for both crizotinib and alectinib was 18.2 months (range, 10.4-43.7 months). Crizotinib was continued beyond radiographic evidence of progressive disease in 6 of the 11 patients, with a median duration of postprogression crizotinib treatment of 9.4 months (range, 020.5 months). The OS period from the diagnosis of metastatic disease or the initiation of crizotinib treatment was 51.1 months (range, 20.9-69.5 months) and 48.6 months (range, 19.8-50.1 months), respectively. Conclusion: Our retrospective study has revealed durable survival for alectinib treatment after crizotinib failure in patients with ALK-rearranged NSCLC.
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收藏
页码:528 / 534
页数:7
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