Afatinib in patients with advanced non-small cell lung cancer harboring HER2 mutations, previously treated with chemotherapy: A phase II trial

被引:25
|
作者
Fan, Yun [1 ]
Chen, Jianhua [2 ]
Zhou, Chengzhi [3 ]
Wang, Huijuan [4 ]
Shu, Yongqian [5 ]
Zhang, Jacky [6 ]
Hua, Hairui [6 ]
Huang, Dennis Chin-Lun [7 ]
Zhou, Caicun [8 ]
机构
[1] Zhejiang Canc Hosp, Hangzhou, Peoples R China
[2] Hunan Canc Hosp, Changsha, Peoples R China
[3] Guangzhou Med Univ, Affiliated Hosp 1, Guangzhou, Guangdong, Peoples R China
[4] Zhengzhou Univ, Henan Canc Hosp, Affiliated Canc Hosp, Zhengzhou, Peoples R China
[5] Nanjing Med Univ, Affiliated Hosp 1, Nanjing, Jiangsu, Peoples R China
[6] Boehringer Ingelheim China Investment Co Ltd, Shanghai, Peoples R China
[7] Boehringer Ingelheim Taiwan Ltd, Taipei, Taiwan
[8] Shanghai Pulm Hosp, Med Oncol, Shanghai, Peoples R China
关键词
Afatinib; HER2; NSCLC; TARGETED THERAPY; EGFR; ERLOTINIB; MUTANT;
D O I
10.1016/j.lungcan.2020.07.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Despite 1-4 % of NSCLC tumors harboring mutations in the HER2 gene, there are no approved HER2-pathway-targeted treatments available. We report an open-label, single-arm, multicenter phase II study investigating the efficacy and safety of afatinib in Asian patients with HER2-mutation positive (HER2m+) NSCLC. Methods: Eligible patients for Part A had confirmed stage IIIb/IV HER2m + NSCLC, had failed one or two prior lines of chemotherapy, and were EGFR/HER2-inhibitor naive. Patients received oral afatinib 40 mg/day in continuous 28-day cycles, until disease progression or intolerable adverse events (AEs). Patients qualified for Part B if they had > 12 weeks' clinical benefit and Eastern Cooperative Oncology Group performance status <= 2. In Part B, patients were to receive afatinib at the last received dose, plus paclitaxel 80 mg/m(2) weekly, until disease progression or intolerable AEs. The primary endpoint in Part A was objective response (OR); secondary endpoints included disease control (DC), progression-free survival (PFS), and overall survival (OS). Further exploratory endpoints were OR, DC, and PFS in Part B. Results: Eighteen patients received afatinib in Part A. No patient achieved an OR; 11 patients (61.1 %) achieved stable disease, and six patients (33.3 %) had progressive disease. DC rate was therefore 61.1 % (95 % confidence interval [CI]: 35.7, 82.7). A decrease in tumor size from baseline of > 0 to < 30 % was observed in eight patients. At the time of analysis, 16 patients (88.9 %) had progressed or died. Median PFS was 2.76 months (95 % CI: 1.87, 4.60) and median OS was 10.02 months (95 % CI: 8.47, 10.08). All patients experienced >= 1 AE, most commonly diarrhea (66.7 %) and rash (33.3 %). No patients met the inclusion criteria for Part B, and recruitment was slow; therefore, the study was terminated. Conclusions: This study found no clinical benefit of afatinib for EGFR TKI-naive patients with HER2m + NSCLC.
引用
收藏
页码:209 / 213
页数:5
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