The impact of angiogenesis inhibitors on survival of patients with small cell lung cancer

被引:12
作者
Shi, Xiaoshun [1 ,2 ]
Dong, Xiaoying [1 ]
Young, Sylvia [2 ]
Chen, Allen Menglin [3 ,4 ]
Liu, Xiguang [1 ]
Zheng, Zhouxia [3 ,4 ]
Huang, Kailing [3 ,4 ]
Lu, Di [1 ]
Feng, Siyang [1 ]
Morahan, Grant [2 ]
Cai, Kaican [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Thorac Surg, 1838 North Guangzhou Ave, Guangzhou 510515, Guangdong, Peoples R China
[2] Univ Western Australia, Ctr Med Res, Harry Perkins Inst Med Res, Nedlands, WA, Australia
[3] Mendel Genes Inc, Guangzhou, Guangdong, Peoples R China
[4] Mendel Genes Inc, Manhattan Beach, CA USA
来源
CANCER MEDICINE | 2019年 / 8卷 / 13期
关键词
angiogenesis inhibitors; network meta-analysis; randomized controlled trial; small cell lung cancer; target drugs; ENDOTHELIAL GROWTH-FACTOR; RANDOMIZED PHASE-II; DOUBLE-BLIND; MAINTENANCE SUNITINIB; 1ST-LINE TREATMENT; PLUS ETOPOSIDE; CHEMOTHERAPY; THERAPY; BEVACIZUMAB; COMBINATION;
D O I
10.1002/cam4.2462
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Small cell lung cancer (SCLC) is a highly invasive and lethal neuroendocrine tumor. Antiangiogenic drugs have been reported in the treatment of SCLC. We aimed to provide a comprehensive evaluation of the impact of angiogenic inhibitors on SCLC survival using network meta-analysis. Methods The impact of five angiogenesis inhibitors, that is, vandetanib (Van), bevacizumab (Bev), Rh-endostatin (End), sunitinib (Sun), and thalidomide (Tha), on progression-free survival (PFS) and overall survival (OS) was evaluated by conducting a network meta-analysis. RNA sequencing data were downloaded from publicly available databases. Results Nine phase II and III randomized controlled trials (RCTs), that involved 1599 participants, that investigated angiogenesis inhibitors in the treatment of SCLC were included in this meta-analysis. Sun and Bev achieved better PFS than Tha (Bev VS. Tha, HR = 0.88, 95% CI: 0.79-0.98, Sun VS. Tha, HR = 0.80, 95% CI: 0.65-1.00). Moreover, Sun and Bev were superior to placebo in terms of PFS (Bev VS. Placebo, HR = 0.89, 95%CI: 0.81-0.97, Sun VS. Placebo, HR = 0.81, 95% CI: 0.66-1.00). Based on this study, we found no significant difference of OS of SCLC. The angiogenesis pathway and expression of target genes were globally deactivated in SCLC tissue. Conclusion Results of this network meta-analysis indicate that the PFS outcome of SCLC with Sun or Bev drugs is superior to that of Tha. The improved therapeutic impact of angiogenesis inhibitors on SCLC needs more evidence, such as long-term observation in clinical trials, to be validated.
引用
收藏
页码:5930 / 5938
页数:9
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