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Triplet‐drug chemotherapy combined with anti‐EGFR antibody as an effective therapy for patients with initially unresectable metastatic colorectal cancer: a meta-analysis

The meta-analysis aimed to assess the clinical efficacy of chemotherapeutic triplet‐drug regimen combined with anti‐EGFR antibody in patients with initially unresectable metastatic colorectal cancer (mCRC). A systematic literature search was performed in PubMed Publisher. Studies evaluating FOLFOXIR...

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Autores principales: Tian, Muyou, Li, Huifen, Dong, Wenjing, Li, Yuhong, Jiang, Ting, Lv, Yanhua, Zeng, Jianxiong, Jiang, Xiaomei, Yin, Zhaofeng, Xiao, Jianjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656984/
https://www.ncbi.nlm.nih.gov/pubmed/37978547
http://dx.doi.org/10.1186/s12957-023-03256-7
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author Tian, Muyou
Li, Huifen
Dong, Wenjing
Li, Yuhong
Jiang, Ting
Lv, Yanhua
Zeng, Jianxiong
Jiang, Xiaomei
Yin, Zhaofeng
Xiao, Jianjun
author_facet Tian, Muyou
Li, Huifen
Dong, Wenjing
Li, Yuhong
Jiang, Ting
Lv, Yanhua
Zeng, Jianxiong
Jiang, Xiaomei
Yin, Zhaofeng
Xiao, Jianjun
author_sort Tian, Muyou
collection PubMed
description The meta-analysis aimed to assess the clinical efficacy of chemotherapeutic triplet‐drug regimen combined with anti‐EGFR antibody in patients with initially unresectable metastatic colorectal cancer (mCRC). A systematic literature search was performed in PubMed Publisher. Studies evaluating FOLFOXIRI combine with panitumumab or cetuximab as the therapy for initially unresectable mCRC were included. The primary outcome was objective response rate (ORR) and rate of R0 resections. The secondary outcomes included overall survival (OS), progression-free survival (PFS), and grades 3 or 4 adverse events. R software (version 4.0.2) and RevMan (version 5.3) were used to analyze the extracted data. The studies included were published between 2010 and 2021, involving four single-arm phase II trials and two randomized phase II trials. A total of 6 studies with 282 patients were included. The data showed a significant benefit for the FOLFOXIRI + anti-EGFR antibody arm compared with FOLFOXIRI arm (RR 1.33; 95% CI, 1.13–1.58; I(2) = 0%, P < 0.05). The pooled ORR and pooled rate of R0 resection in patients who receiving FOLFOXIRI + anti-EGFR antibody were 85% (95% CI, 0.78–0.91; I(2) = 58%) and 42% (95% CI, 0.32–0.53; I(2) = 62%), respectively. The range of median PFS between all the six studies was 9.5–15.5 months, with weighted pooled median PFS mean 11.7 months. The range of median OS between all the four studies was 24.7–37 months, with weighted pooled median PFS mean 31.9 months. The common grades 3 and 4 adverse events were diarrhea and neutropenia. Our findings show that triplet-drug chemotherapy (FOLFOXIRI) combined with anti-EGFR antibody (panitumumab or cetuximab) represents a very effective therapeutic combination associated with a significant ORR and R0 rection rate for patients with molecularly unselected and surgically unresectable metastatic CRC.
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spelling pubmed-106569842023-11-18 Triplet‐drug chemotherapy combined with anti‐EGFR antibody as an effective therapy for patients with initially unresectable metastatic colorectal cancer: a meta-analysis Tian, Muyou Li, Huifen Dong, Wenjing Li, Yuhong Jiang, Ting Lv, Yanhua Zeng, Jianxiong Jiang, Xiaomei Yin, Zhaofeng Xiao, Jianjun World J Surg Oncol Research The meta-analysis aimed to assess the clinical efficacy of chemotherapeutic triplet‐drug regimen combined with anti‐EGFR antibody in patients with initially unresectable metastatic colorectal cancer (mCRC). A systematic literature search was performed in PubMed Publisher. Studies evaluating FOLFOXIRI combine with panitumumab or cetuximab as the therapy for initially unresectable mCRC were included. The primary outcome was objective response rate (ORR) and rate of R0 resections. The secondary outcomes included overall survival (OS), progression-free survival (PFS), and grades 3 or 4 adverse events. R software (version 4.0.2) and RevMan (version 5.3) were used to analyze the extracted data. The studies included were published between 2010 and 2021, involving four single-arm phase II trials and two randomized phase II trials. A total of 6 studies with 282 patients were included. The data showed a significant benefit for the FOLFOXIRI + anti-EGFR antibody arm compared with FOLFOXIRI arm (RR 1.33; 95% CI, 1.13–1.58; I(2) = 0%, P < 0.05). The pooled ORR and pooled rate of R0 resection in patients who receiving FOLFOXIRI + anti-EGFR antibody were 85% (95% CI, 0.78–0.91; I(2) = 58%) and 42% (95% CI, 0.32–0.53; I(2) = 62%), respectively. The range of median PFS between all the six studies was 9.5–15.5 months, with weighted pooled median PFS mean 11.7 months. The range of median OS between all the four studies was 24.7–37 months, with weighted pooled median PFS mean 31.9 months. The common grades 3 and 4 adverse events were diarrhea and neutropenia. Our findings show that triplet-drug chemotherapy (FOLFOXIRI) combined with anti-EGFR antibody (panitumumab or cetuximab) represents a very effective therapeutic combination associated with a significant ORR and R0 rection rate for patients with molecularly unselected and surgically unresectable metastatic CRC. BioMed Central 2023-11-18 /pmc/articles/PMC10656984/ /pubmed/37978547 http://dx.doi.org/10.1186/s12957-023-03256-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Tian, Muyou
Li, Huifen
Dong, Wenjing
Li, Yuhong
Jiang, Ting
Lv, Yanhua
Zeng, Jianxiong
Jiang, Xiaomei
Yin, Zhaofeng
Xiao, Jianjun
Triplet‐drug chemotherapy combined with anti‐EGFR antibody as an effective therapy for patients with initially unresectable metastatic colorectal cancer: a meta-analysis
title Triplet‐drug chemotherapy combined with anti‐EGFR antibody as an effective therapy for patients with initially unresectable metastatic colorectal cancer: a meta-analysis
title_full Triplet‐drug chemotherapy combined with anti‐EGFR antibody as an effective therapy for patients with initially unresectable metastatic colorectal cancer: a meta-analysis
title_fullStr Triplet‐drug chemotherapy combined with anti‐EGFR antibody as an effective therapy for patients with initially unresectable metastatic colorectal cancer: a meta-analysis
title_full_unstemmed Triplet‐drug chemotherapy combined with anti‐EGFR antibody as an effective therapy for patients with initially unresectable metastatic colorectal cancer: a meta-analysis
title_short Triplet‐drug chemotherapy combined with anti‐EGFR antibody as an effective therapy for patients with initially unresectable metastatic colorectal cancer: a meta-analysis
title_sort triplet‐drug chemotherapy combined with anti‐egfr antibody as an effective therapy for patients with initially unresectable metastatic colorectal cancer: a meta-analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656984/
https://www.ncbi.nlm.nih.gov/pubmed/37978547
http://dx.doi.org/10.1186/s12957-023-03256-7
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