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A Meta-Analysis to Assess the Efficacy of HER2-Targeted Treatment Regimens in HER2-Positive Metastatic Colorectal Cancer (mCRC)

Recent trials provide evidence that HER2 is a potential new target for patients with colorectal cancer. While HER2-positive tumors do not show a very encouraging response to anti-HER2-positive agents like trastuzumab alone, promising results have been observed when combined with other synergisticall...

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Autores principales: Chitkara, Akshit, Bakhtiar, Muhammad, Sahin, Ibrahim Halil, Hsu, Dennis, Zhang, Janie, Anamika, FNU, Mahnoor, Mahnoor, Ahmed, Rabeea, Gholami, Sepideh, Saeed, Anwaar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10528053/
https://www.ncbi.nlm.nih.gov/pubmed/37754515
http://dx.doi.org/10.3390/curroncol30090600
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author Chitkara, Akshit
Bakhtiar, Muhammad
Sahin, Ibrahim Halil
Hsu, Dennis
Zhang, Janie
Anamika, FNU
Mahnoor, Mahnoor
Ahmed, Rabeea
Gholami, Sepideh
Saeed, Anwaar
author_facet Chitkara, Akshit
Bakhtiar, Muhammad
Sahin, Ibrahim Halil
Hsu, Dennis
Zhang, Janie
Anamika, FNU
Mahnoor, Mahnoor
Ahmed, Rabeea
Gholami, Sepideh
Saeed, Anwaar
author_sort Chitkara, Akshit
collection PubMed
description Recent trials provide evidence that HER2 is a potential new target for patients with colorectal cancer. While HER2-positive tumors do not show a very encouraging response to anti-HER2-positive agents like trastuzumab alone, promising results have been observed when combined with other synergistically acting tyrosine kinase inhibitors (TKIs). Our meta-analysis was conducted following the Cochrane Handbook and written following the PRISMA guidelines. The protocol was registered on PROSPERO with the registration number CRD42022338935. After a comprehensive search for relevant articles, 14 CTs were identified and uploaded to Rayyan, and six trials were ultimately selected for inclusion. The meta-analysis revealed that a median of three prior lines of therapy was used before enrolling in the six trials comprising 238 patients with HER2-positive metastatic colorectal cancer (mCRC). The pooled objective response rate (ORR) and disease control rate (DCR) were 31.33% (95% confidence interval [CI] 24.27–38.39) and 74.37% (95% CI 64.57–84.17), respectively. The pooled weighted progression-free survival (PFS) was 6.2 months. The pooled ORR and DCR meta-analysis indicate a significant response to HER2-targeted therapy in this patient in HER2-positive mCRC. Additionally, a pooled PFS of 6.2 months suggests that HER2-targeted treatment regimens are associated with a meaningful improvement in survival outcomes in this population.
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spelling pubmed-105280532023-09-28 A Meta-Analysis to Assess the Efficacy of HER2-Targeted Treatment Regimens in HER2-Positive Metastatic Colorectal Cancer (mCRC) Chitkara, Akshit Bakhtiar, Muhammad Sahin, Ibrahim Halil Hsu, Dennis Zhang, Janie Anamika, FNU Mahnoor, Mahnoor Ahmed, Rabeea Gholami, Sepideh Saeed, Anwaar Curr Oncol Systematic Review Recent trials provide evidence that HER2 is a potential new target for patients with colorectal cancer. While HER2-positive tumors do not show a very encouraging response to anti-HER2-positive agents like trastuzumab alone, promising results have been observed when combined with other synergistically acting tyrosine kinase inhibitors (TKIs). Our meta-analysis was conducted following the Cochrane Handbook and written following the PRISMA guidelines. The protocol was registered on PROSPERO with the registration number CRD42022338935. After a comprehensive search for relevant articles, 14 CTs were identified and uploaded to Rayyan, and six trials were ultimately selected for inclusion. The meta-analysis revealed that a median of three prior lines of therapy was used before enrolling in the six trials comprising 238 patients with HER2-positive metastatic colorectal cancer (mCRC). The pooled objective response rate (ORR) and disease control rate (DCR) were 31.33% (95% confidence interval [CI] 24.27–38.39) and 74.37% (95% CI 64.57–84.17), respectively. The pooled weighted progression-free survival (PFS) was 6.2 months. The pooled ORR and DCR meta-analysis indicate a significant response to HER2-targeted therapy in this patient in HER2-positive mCRC. Additionally, a pooled PFS of 6.2 months suggests that HER2-targeted treatment regimens are associated with a meaningful improvement in survival outcomes in this population. MDPI 2023-09-07 /pmc/articles/PMC10528053/ /pubmed/37754515 http://dx.doi.org/10.3390/curroncol30090600 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Systematic Review
Chitkara, Akshit
Bakhtiar, Muhammad
Sahin, Ibrahim Halil
Hsu, Dennis
Zhang, Janie
Anamika, FNU
Mahnoor, Mahnoor
Ahmed, Rabeea
Gholami, Sepideh
Saeed, Anwaar
A Meta-Analysis to Assess the Efficacy of HER2-Targeted Treatment Regimens in HER2-Positive Metastatic Colorectal Cancer (mCRC)
title A Meta-Analysis to Assess the Efficacy of HER2-Targeted Treatment Regimens in HER2-Positive Metastatic Colorectal Cancer (mCRC)
title_full A Meta-Analysis to Assess the Efficacy of HER2-Targeted Treatment Regimens in HER2-Positive Metastatic Colorectal Cancer (mCRC)
title_fullStr A Meta-Analysis to Assess the Efficacy of HER2-Targeted Treatment Regimens in HER2-Positive Metastatic Colorectal Cancer (mCRC)
title_full_unstemmed A Meta-Analysis to Assess the Efficacy of HER2-Targeted Treatment Regimens in HER2-Positive Metastatic Colorectal Cancer (mCRC)
title_short A Meta-Analysis to Assess the Efficacy of HER2-Targeted Treatment Regimens in HER2-Positive Metastatic Colorectal Cancer (mCRC)
title_sort meta-analysis to assess the efficacy of her2-targeted treatment regimens in her2-positive metastatic colorectal cancer (mcrc)
topic Systematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10528053/
https://www.ncbi.nlm.nih.gov/pubmed/37754515
http://dx.doi.org/10.3390/curroncol30090600
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