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Usefulness of bevacizumab-induced hypertension in patients with metastatic colorectal cancer: an updated meta-analysis
We tested the hypothesis that bevacizumab-induced hypertension may be a useful predictor for objective response rate, progression-free and overall survival in patients with metastatic colorectal cancer via a comprehensive meta-analysis. Search process, article selection and data extraction were inde...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6046235/ https://www.ncbi.nlm.nih.gov/pubmed/29969436 http://dx.doi.org/10.18632/aging.101478 |
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author | Zhang, Chun-Jing Zhang, Shu-Ying Zhang, Chun-Di Lin, Chun-Rong Li, Xue-Yan Li, Qiu-Yan Yu, Hai-Tao |
author_facet | Zhang, Chun-Jing Zhang, Shu-Ying Zhang, Chun-Di Lin, Chun-Rong Li, Xue-Yan Li, Qiu-Yan Yu, Hai-Tao |
author_sort | Zhang, Chun-Jing |
collection | PubMed |
description | We tested the hypothesis that bevacizumab-induced hypertension may be a useful predictor for objective response rate, progression-free and overall survival in patients with metastatic colorectal cancer via a comprehensive meta-analysis. Search process, article selection and data extraction were independently performed by two investigators. Statistical analyses were conducted using the STATA/SE software. Fourteen independent studies and 2292 study subjects were synthesized. Overall relative risk of objective response rate for bevacizumab-induced hypertension was 2.03 (95% confidence interval [CI]: 1.18-3.48, p=0.01), with significant heterogeneity and publication bias, whereas unbiased estimate was nonsignificant after considering potentially missing studies. Overall hazard ratio for progression-free survival was 0.58 (95% CI: 0.43-0.77, p<0.001), with significant heterogeneity and publication bias, and unbiased estimate was significant (hazard ratio: 0.52, 95% CI: 0.41-0.66, p<0.001). Overall hazard ratio for overall survival was 0.51 (95% CI: 0.39-0.65, p<0.001), and this estimate was not likely confounded by heterogeneity or publication bias. Subgroup and meta-regression analyses suggested that hypertension grade of controls, sample size, age and gender were possible causes of heterogeneity. Taken together, our findings indicate that bevacizumab-induced hypertension can predict progress-free survival and overall survival in patients with metastatic colorectal cancer, whereas its prediction for objective response rate was nonsignificant. |
format | Online Article Text |
id | pubmed-6046235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-60462352018-07-17 Usefulness of bevacizumab-induced hypertension in patients with metastatic colorectal cancer: an updated meta-analysis Zhang, Chun-Jing Zhang, Shu-Ying Zhang, Chun-Di Lin, Chun-Rong Li, Xue-Yan Li, Qiu-Yan Yu, Hai-Tao Aging (Albany NY) Research Paper We tested the hypothesis that bevacizumab-induced hypertension may be a useful predictor for objective response rate, progression-free and overall survival in patients with metastatic colorectal cancer via a comprehensive meta-analysis. Search process, article selection and data extraction were independently performed by two investigators. Statistical analyses were conducted using the STATA/SE software. Fourteen independent studies and 2292 study subjects were synthesized. Overall relative risk of objective response rate for bevacizumab-induced hypertension was 2.03 (95% confidence interval [CI]: 1.18-3.48, p=0.01), with significant heterogeneity and publication bias, whereas unbiased estimate was nonsignificant after considering potentially missing studies. Overall hazard ratio for progression-free survival was 0.58 (95% CI: 0.43-0.77, p<0.001), with significant heterogeneity and publication bias, and unbiased estimate was significant (hazard ratio: 0.52, 95% CI: 0.41-0.66, p<0.001). Overall hazard ratio for overall survival was 0.51 (95% CI: 0.39-0.65, p<0.001), and this estimate was not likely confounded by heterogeneity or publication bias. Subgroup and meta-regression analyses suggested that hypertension grade of controls, sample size, age and gender were possible causes of heterogeneity. Taken together, our findings indicate that bevacizumab-induced hypertension can predict progress-free survival and overall survival in patients with metastatic colorectal cancer, whereas its prediction for objective response rate was nonsignificant. Impact Journals 2018-06-21 /pmc/articles/PMC6046235/ /pubmed/29969436 http://dx.doi.org/10.18632/aging.101478 Text en Copyright © 2018 Zhang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY) 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Zhang, Chun-Jing Zhang, Shu-Ying Zhang, Chun-Di Lin, Chun-Rong Li, Xue-Yan Li, Qiu-Yan Yu, Hai-Tao Usefulness of bevacizumab-induced hypertension in patients with metastatic colorectal cancer: an updated meta-analysis |
title | Usefulness of bevacizumab-induced hypertension in patients with metastatic colorectal cancer: an updated meta-analysis |
title_full | Usefulness of bevacizumab-induced hypertension in patients with metastatic colorectal cancer: an updated meta-analysis |
title_fullStr | Usefulness of bevacizumab-induced hypertension in patients with metastatic colorectal cancer: an updated meta-analysis |
title_full_unstemmed | Usefulness of bevacizumab-induced hypertension in patients with metastatic colorectal cancer: an updated meta-analysis |
title_short | Usefulness of bevacizumab-induced hypertension in patients with metastatic colorectal cancer: an updated meta-analysis |
title_sort | usefulness of bevacizumab-induced hypertension in patients with metastatic colorectal cancer: an updated meta-analysis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6046235/ https://www.ncbi.nlm.nih.gov/pubmed/29969436 http://dx.doi.org/10.18632/aging.101478 |
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