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The efficacy and safety of panitumumab supplementation for colorectal cancer: A meta-analysis of randomized controlled studies
BACKGROUND: The efficacy of panitumumab supplementation for colorectal cancer remains controversial. We conduct a systematic review and meta-analysis to explore the influence of panitumumab supplementation on treatment efficacy of colorectal cancer. METHODS: We search PubMed, EMbase, Web of science,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220441/ https://www.ncbi.nlm.nih.gov/pubmed/32176047 http://dx.doi.org/10.1097/MD.0000000000019210 |
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author | Wang, Chengchen Tan, Chunyan Chen, Xiaopin Chen, Shuangdong |
author_facet | Wang, Chengchen Tan, Chunyan Chen, Xiaopin Chen, Shuangdong |
author_sort | Wang, Chengchen |
collection | PubMed |
description | BACKGROUND: The efficacy of panitumumab supplementation for colorectal cancer remains controversial. We conduct a systematic review and meta-analysis to explore the influence of panitumumab supplementation on treatment efficacy of colorectal cancer. METHODS: We search PubMed, EMbase, Web of science, EBSCO, and Cochrane library databases through June 2019 for randomized controlled trials (RCTs) assessing the efficacy of panitumumab supplementation for colorectal cancer. This meta-analysis is performed using the random-effect model. RESULTS: Five RCTs are included in the meta-analysis. Overall, compared with control group for colorectal cancer, panitumumab supplementation is associated with the increase in objective response for wild-type (WT) KRAS (RR = 1.70; 95% CI = 1.07–2.69; P = .03), but has no remarkable influence on objective response for mutant KRAS (RR = 0.92; 95% CI = 0.79–1.08; P = .32), objective response (RR = 1.35; 95% CI = 1.00–1.83; P = 0.05), progressive disease for WT KRAS (RR = 0.94; 95% CI = 0.85–1.02; P = .15), mortality (RR = 0.86; 95% CI = 0.69–1.08; P = .20), or mortality for WT KRAS (RR = 0.94; 95% CI = 0.84–1.05; P = .28). In addition, grade 3 and 4 adverse events are found to be higher in panitumumab group than those in control group (RR = 1.17; 95% CI = 1.08–1.27; P = .0001; Fig. 8). CONCLUSIONS: Panitumumab supplementation can provide some improvement in objective response for colorectal cancer patients with WT KRAS, but results in the increase in grade 3 and 4 adverse events. |
format | Online Article Text |
id | pubmed-7220441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-72204412020-06-15 The efficacy and safety of panitumumab supplementation for colorectal cancer: A meta-analysis of randomized controlled studies Wang, Chengchen Tan, Chunyan Chen, Xiaopin Chen, Shuangdong Medicine (Baltimore) 4500 BACKGROUND: The efficacy of panitumumab supplementation for colorectal cancer remains controversial. We conduct a systematic review and meta-analysis to explore the influence of panitumumab supplementation on treatment efficacy of colorectal cancer. METHODS: We search PubMed, EMbase, Web of science, EBSCO, and Cochrane library databases through June 2019 for randomized controlled trials (RCTs) assessing the efficacy of panitumumab supplementation for colorectal cancer. This meta-analysis is performed using the random-effect model. RESULTS: Five RCTs are included in the meta-analysis. Overall, compared with control group for colorectal cancer, panitumumab supplementation is associated with the increase in objective response for wild-type (WT) KRAS (RR = 1.70; 95% CI = 1.07–2.69; P = .03), but has no remarkable influence on objective response for mutant KRAS (RR = 0.92; 95% CI = 0.79–1.08; P = .32), objective response (RR = 1.35; 95% CI = 1.00–1.83; P = 0.05), progressive disease for WT KRAS (RR = 0.94; 95% CI = 0.85–1.02; P = .15), mortality (RR = 0.86; 95% CI = 0.69–1.08; P = .20), or mortality for WT KRAS (RR = 0.94; 95% CI = 0.84–1.05; P = .28). In addition, grade 3 and 4 adverse events are found to be higher in panitumumab group than those in control group (RR = 1.17; 95% CI = 1.08–1.27; P = .0001; Fig. 8). CONCLUSIONS: Panitumumab supplementation can provide some improvement in objective response for colorectal cancer patients with WT KRAS, but results in the increase in grade 3 and 4 adverse events. Wolters Kluwer Health 2020-03-13 /pmc/articles/PMC7220441/ /pubmed/32176047 http://dx.doi.org/10.1097/MD.0000000000019210 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 4500 Wang, Chengchen Tan, Chunyan Chen, Xiaopin Chen, Shuangdong The efficacy and safety of panitumumab supplementation for colorectal cancer: A meta-analysis of randomized controlled studies |
title | The efficacy and safety of panitumumab supplementation for colorectal cancer: A meta-analysis of randomized controlled studies |
title_full | The efficacy and safety of panitumumab supplementation for colorectal cancer: A meta-analysis of randomized controlled studies |
title_fullStr | The efficacy and safety of panitumumab supplementation for colorectal cancer: A meta-analysis of randomized controlled studies |
title_full_unstemmed | The efficacy and safety of panitumumab supplementation for colorectal cancer: A meta-analysis of randomized controlled studies |
title_short | The efficacy and safety of panitumumab supplementation for colorectal cancer: A meta-analysis of randomized controlled studies |
title_sort | efficacy and safety of panitumumab supplementation for colorectal cancer: a meta-analysis of randomized controlled studies |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220441/ https://www.ncbi.nlm.nih.gov/pubmed/32176047 http://dx.doi.org/10.1097/MD.0000000000019210 |
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