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

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. METHOD...

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Autores principales: Shi, Xiaoshun, Dong, Xiaoying, Young, Sylvia, Chen, Allen Menglin, Liu, Xiguang, Zheng, Zhouxia, Huang, Kailing, Lu, Di, Feng, Siyang, Morahan, Grant, Cai, Kaican
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6792507/
https://www.ncbi.nlm.nih.gov/pubmed/31433125
http://dx.doi.org/10.1002/cam4.2462
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author Shi, Xiaoshun
Dong, Xiaoying
Young, Sylvia
Chen, Allen Menglin
Liu, Xiguang
Zheng, Zhouxia
Huang, Kailing
Lu, Di
Feng, Siyang
Morahan, Grant
Cai, Kaican
author_facet Shi, Xiaoshun
Dong, Xiaoying
Young, Sylvia
Chen, Allen Menglin
Liu, Xiguang
Zheng, Zhouxia
Huang, Kailing
Lu, Di
Feng, Siyang
Morahan, Grant
Cai, Kaican
author_sort Shi, Xiaoshun
collection PubMed
description 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.
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spelling pubmed-67925072019-10-21 The impact of angiogenesis inhibitors on survival of patients with small cell lung cancer Shi, Xiaoshun Dong, Xiaoying Young, Sylvia Chen, Allen Menglin Liu, Xiguang Zheng, Zhouxia Huang, Kailing Lu, Di Feng, Siyang Morahan, Grant Cai, Kaican Cancer Med Clinical Cancer Research 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. John Wiley and Sons Inc. 2019-08-21 /pmc/articles/PMC6792507/ /pubmed/31433125 http://dx.doi.org/10.1002/cam4.2462 Text en © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Shi, Xiaoshun
Dong, Xiaoying
Young, Sylvia
Chen, Allen Menglin
Liu, Xiguang
Zheng, Zhouxia
Huang, Kailing
Lu, Di
Feng, Siyang
Morahan, Grant
Cai, Kaican
The impact of angiogenesis inhibitors on survival of patients with small cell lung cancer
title The impact of angiogenesis inhibitors on survival of patients with small cell lung cancer
title_full The impact of angiogenesis inhibitors on survival of patients with small cell lung cancer
title_fullStr The impact of angiogenesis inhibitors on survival of patients with small cell lung cancer
title_full_unstemmed The impact of angiogenesis inhibitors on survival of patients with small cell lung cancer
title_short The impact of angiogenesis inhibitors on survival of patients with small cell lung cancer
title_sort impact of angiogenesis inhibitors on survival of patients with small cell lung cancer
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6792507/
https://www.ncbi.nlm.nih.gov/pubmed/31433125
http://dx.doi.org/10.1002/cam4.2462
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