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Bevacizumab in metastatic small-bowel adenocarcinoma: A systematic review and meta-analysis
Cancers of the small bowel could account for less than 5% of all gastrointestinal malignancies. Of these tumors, adenocarcinomas were the major histologic subtype and generally carried a poor prognosis. High expression of vascular epithelial growth factor (VEGF) could be seen in small bowel adenocar...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832313/ https://www.ncbi.nlm.nih.gov/pubmed/35154612 http://dx.doi.org/10.1177/2036361318825413 |
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author | Vergara, John Paulo Sacdalan, Danielle Benedict Leoncio Amurao-Amante, Madelaine Sacdalan, Dennis Lee |
author_facet | Vergara, John Paulo Sacdalan, Danielle Benedict Leoncio Amurao-Amante, Madelaine Sacdalan, Dennis Lee |
author_sort | Vergara, John Paulo |
collection | PubMed |
description | Cancers of the small bowel could account for less than 5% of all gastrointestinal malignancies. Of these tumors, adenocarcinomas were the major histologic subtype and generally carried a poor prognosis. High expression of vascular epithelial growth factor (VEGF) could be seen in small bowel adenocarcinomas. A systematic review was conducted here to determine if bevacizumab, a recombinant humanized antibody against VEGF, could offer clinical benefit among patients with metastatic small bowel adenocarcinoma when combined with chemotherapy. A search for relevant published and unpublished studies was performed using PubMed, ScienceDirect, Google Scholar, the American Society of Clinical Oncology meetings library, ClinicalTrials.gov, and ISRCTN registry. Information on study design, methods, intervention, and outcomes were extracted from selected eligible studies. Methodological quality was then assessed using the Newcastle-Ottawa Scale. There was a significant improvement in mean overall survival with the addition of bevacizumab with chemotherapy versus chemotherapy alone. The use of bevacizumab with chemotherapy, likewise improved progression-free survival and objective response rate compared to chemotherapy alone. Continued use of bevacizumab beyond first progression also appeared to show benefit. The conduct of prospective controlled studies by consortia to offset the rarity of small bowel adenocarcinomas could further elucidate the efficacy of bevacizumab in the treatment of this disease. |
format | Online Article Text |
id | pubmed-8832313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-88323132022-02-12 Bevacizumab in metastatic small-bowel adenocarcinoma: A systematic review and meta-analysis Vergara, John Paulo Sacdalan, Danielle Benedict Leoncio Amurao-Amante, Madelaine Sacdalan, Dennis Lee Rare Tumors Review Cancers of the small bowel could account for less than 5% of all gastrointestinal malignancies. Of these tumors, adenocarcinomas were the major histologic subtype and generally carried a poor prognosis. High expression of vascular epithelial growth factor (VEGF) could be seen in small bowel adenocarcinomas. A systematic review was conducted here to determine if bevacizumab, a recombinant humanized antibody against VEGF, could offer clinical benefit among patients with metastatic small bowel adenocarcinoma when combined with chemotherapy. A search for relevant published and unpublished studies was performed using PubMed, ScienceDirect, Google Scholar, the American Society of Clinical Oncology meetings library, ClinicalTrials.gov, and ISRCTN registry. Information on study design, methods, intervention, and outcomes were extracted from selected eligible studies. Methodological quality was then assessed using the Newcastle-Ottawa Scale. There was a significant improvement in mean overall survival with the addition of bevacizumab with chemotherapy versus chemotherapy alone. The use of bevacizumab with chemotherapy, likewise improved progression-free survival and objective response rate compared to chemotherapy alone. Continued use of bevacizumab beyond first progression also appeared to show benefit. The conduct of prospective controlled studies by consortia to offset the rarity of small bowel adenocarcinomas could further elucidate the efficacy of bevacizumab in the treatment of this disease. SAGE Publications 2019-05-14 /pmc/articles/PMC8832313/ /pubmed/35154612 http://dx.doi.org/10.1177/2036361318825413 Text en © The Author(s) 2019 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review Vergara, John Paulo Sacdalan, Danielle Benedict Leoncio Amurao-Amante, Madelaine Sacdalan, Dennis Lee Bevacizumab in metastatic small-bowel adenocarcinoma: A systematic review and meta-analysis |
title | Bevacizumab in metastatic small-bowel adenocarcinoma: A systematic
review and meta-analysis |
title_full | Bevacizumab in metastatic small-bowel adenocarcinoma: A systematic
review and meta-analysis |
title_fullStr | Bevacizumab in metastatic small-bowel adenocarcinoma: A systematic
review and meta-analysis |
title_full_unstemmed | Bevacizumab in metastatic small-bowel adenocarcinoma: A systematic
review and meta-analysis |
title_short | Bevacizumab in metastatic small-bowel adenocarcinoma: A systematic
review and meta-analysis |
title_sort | bevacizumab in metastatic small-bowel adenocarcinoma: a systematic
review and meta-analysis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832313/ https://www.ncbi.nlm.nih.gov/pubmed/35154612 http://dx.doi.org/10.1177/2036361318825413 |
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