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Treatment-related toxicities of apatinib in solid tumors: a meta-analysis
BACKGROUND: Apatinib is a novel small molecular drug targeting vascular endothelial growth factor receptor-2 (VEGFR-2), which is being studied in multiple tumor types. We performed a meta-analysis to quantify the overall incidence and risk of hypertension, proteinuria, and hand-foot-syndrome (HFS) i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114950/ https://www.ncbi.nlm.nih.gov/pubmed/30181815 http://dx.doi.org/10.18632/oncotarget.24215 |
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author | Peng, Ling Ye, Xianghua Hong, Yun Zhang, Junyan Dong, Yongquan Zhao, Qiong |
author_facet | Peng, Ling Ye, Xianghua Hong, Yun Zhang, Junyan Dong, Yongquan Zhao, Qiong |
author_sort | Peng, Ling |
collection | PubMed |
description | BACKGROUND: Apatinib is a novel small molecular drug targeting vascular endothelial growth factor receptor-2 (VEGFR-2), which is being studied in multiple tumor types. We performed a meta-analysis to quantify the overall incidence and risk of hypertension, proteinuria, and hand-foot-syndrome (HFS) in cancer patients receiving apatinib. RESULTS: Altogether, 820 cancer patients from 7 prospective trials were included for the meta-analysis. The incidences of all-grade and high-grade hypertension were 45.4% and 9.7%. The incidences of all-grade and high-grade proteinuria were 45.1% and 3.7%. The incidences of all-grade and high-grade HFS were 35.9% and 8.6%. The RRs of all-grade hypertension, proteinuria and HFS of apatinib compared to placebo were increased (hypertension, RR = 6.53; proteinuria, RR = 2.62, and HFS, RR = 11.45). The RRs of developing high-grade hypertension and HFS were substantially higher than that of placebo (hypertension, RR = 7.73; HFS, RR = 7.23), but not for proteinuria (RR = 2.56, 95% CI: 0.57–11.52). MATERIALS AND METHODS: Prospective phase II and III clinical trials of cancer patients receiving apatinib were searched and included. Summary incidences, relative risk (RR), and 95% confidence intervals (CI) were calculated by using either fixed or random effects models according to the heterogeneity of the studies. CONCLUSIONS: Apatinib is generally well tolerated, and associated with increased risks of all-grade hypertension, proteinuria and HFS, and high-grade hypertension and HFS, but not high-grade proteinuria. |
format | Online Article Text |
id | pubmed-6114950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-61149502018-09-04 Treatment-related toxicities of apatinib in solid tumors: a meta-analysis Peng, Ling Ye, Xianghua Hong, Yun Zhang, Junyan Dong, Yongquan Zhao, Qiong Oncotarget Meta-Analysis BACKGROUND: Apatinib is a novel small molecular drug targeting vascular endothelial growth factor receptor-2 (VEGFR-2), which is being studied in multiple tumor types. We performed a meta-analysis to quantify the overall incidence and risk of hypertension, proteinuria, and hand-foot-syndrome (HFS) in cancer patients receiving apatinib. RESULTS: Altogether, 820 cancer patients from 7 prospective trials were included for the meta-analysis. The incidences of all-grade and high-grade hypertension were 45.4% and 9.7%. The incidences of all-grade and high-grade proteinuria were 45.1% and 3.7%. The incidences of all-grade and high-grade HFS were 35.9% and 8.6%. The RRs of all-grade hypertension, proteinuria and HFS of apatinib compared to placebo were increased (hypertension, RR = 6.53; proteinuria, RR = 2.62, and HFS, RR = 11.45). The RRs of developing high-grade hypertension and HFS were substantially higher than that of placebo (hypertension, RR = 7.73; HFS, RR = 7.23), but not for proteinuria (RR = 2.56, 95% CI: 0.57–11.52). MATERIALS AND METHODS: Prospective phase II and III clinical trials of cancer patients receiving apatinib were searched and included. Summary incidences, relative risk (RR), and 95% confidence intervals (CI) were calculated by using either fixed or random effects models according to the heterogeneity of the studies. CONCLUSIONS: Apatinib is generally well tolerated, and associated with increased risks of all-grade hypertension, proteinuria and HFS, and high-grade hypertension and HFS, but not high-grade proteinuria. Impact Journals LLC 2018-01-13 /pmc/articles/PMC6114950/ /pubmed/30181815 http://dx.doi.org/10.18632/oncotarget.24215 Text en Copyright: © 2018 Peng et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Meta-Analysis Peng, Ling Ye, Xianghua Hong, Yun Zhang, Junyan Dong, Yongquan Zhao, Qiong Treatment-related toxicities of apatinib in solid tumors: a meta-analysis |
title | Treatment-related toxicities of apatinib in solid tumors: a meta-analysis |
title_full | Treatment-related toxicities of apatinib in solid tumors: a meta-analysis |
title_fullStr | Treatment-related toxicities of apatinib in solid tumors: a meta-analysis |
title_full_unstemmed | Treatment-related toxicities of apatinib in solid tumors: a meta-analysis |
title_short | Treatment-related toxicities of apatinib in solid tumors: a meta-analysis |
title_sort | treatment-related toxicities of apatinib in solid tumors: a meta-analysis |
topic | Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114950/ https://www.ncbi.nlm.nih.gov/pubmed/30181815 http://dx.doi.org/10.18632/oncotarget.24215 |
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