Apatinib plus Chemotherapy as a Second-Line Treatment in Unresectable Non-Small Cell Lung Carcinoma: A Randomized, Controlled, Multicenter Clinical Trial

Author:

Yu Zongyang1,Cai Xiuyu2,Xu Zhengwu3,He Zhiyong3,Lai Jinhuo4,Wang Wenwu5,Zhang Jing3,Kong Wencui5,Huang Xiaoyan5,Chen Ying5,Shi Yanhong5,Shi Xi6,Zhao Zhongquan5,Ni Min5,Lin Xiangwu5,Chen Siyu5,Wu Xiaolong5,Chen Wujin7,Song Zhengbo8,Huang Cheng3

Affiliation:

1. The 900th Hospital of Joint Logistic Support Force, PLA, Fujian Medical University, Fuzhou, People' Republic of China

2. Sun Yat-sen University Cancer Center, Guangzhou, China

3. Fujian Cancer Hospital and Fujian Medical University Cancer Hospital, Fuzhou, People' Republic of China

4. Affiliated Union Hospital of Fujian Medical University, Fuzhou, People' Republic of China

5. The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, People' Republic of China

6. First Affiliated Hospital of Fujian Medical University, Fuzhou, People' Republic of China

7. Fujian People's Hospital, Fuzhou, People' Republic of China

8. Zhejiang Cancer Hospital, Hangzhou, People' Republic of China

Abstract

Abstract Trial Information Click here to access other published clinical trials. Lessons Learned The efficacy of second-line treatment for advanced non-small cell lung carcinoma (NSCLC) without a sensitizing driver gene mutation is still unsatisfactory. The combination of apatinib and chemotherapy improved progression-free survival in the second-line therapy of advanced NSCLC without a sensitizing mutation. This study offers a new treatment strategy for second-line treatment of such patients but requires confirmation in a larger multi-institutional trial. Background This study explored the efficacy and safety of apatinib combined with single-agent chemotherapy versus single-agent chemotherapy in the second-line treatment of advanced non-small-cell lung carcinoma (NSCLC) without driver mutations. Methods In this double-arm, open label, exploratory clinical study, we enrolled patients with unresectable locally advanced or advanced NSCLC without driver mutations that had progressed following first-line chemotherapy. The subjects were allocated into an experimental group and a control group by 2:1. The experimental group received apatinib combined with four cycles of docetaxel or pemetrexed until disease progression, intolerable toxicity, or discontinuation at the patient' request. The control group only received four cycles of docetaxel or pemetrexed. The primary endpoints were progression-free survival (PFS), and the secondary endpoints were overall survival (OS), disease control rate (DCR), and safety. Results Thirty-seven patients were enrolled. The efficacy of 33 patients was evaluated. The median PFS was 5.47 versus 2.97 months, the DCR was 95% versus 73%, and the objective response rate (ORR) was 27% versus 9% in the experimental versus control group. The OS was still under follow-up. The most common adverse effects included hypertension, hand-foot skin reaction (HFSR), and fatigue. Conclusion Apatinib combined with single-agent chemotherapy may be a novel option for second-line treatment of advanced NSCLC

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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