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Meta-analyses of treatment standards for pancreatic cancer
Pancreatic cancer is the most lethal common cancer with an estimated 5-year survival rate of 6–7% (across all stages). The only potential curative therapy is surgical resection in those with localized disease. Adjuvant (postoperative) therapy confers a survival advantage over postoperative observati...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4774516/ https://www.ncbi.nlm.nih.gov/pubmed/26998283 http://dx.doi.org/10.3892/mco.2015.716 |
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author | GONG, JUN TULI, RICHARD SHINDE, ARVIND HENDIFAR, ANDREW E. |
author_facet | GONG, JUN TULI, RICHARD SHINDE, ARVIND HENDIFAR, ANDREW E. |
author_sort | GONG, JUN |
collection | PubMed |
description | Pancreatic cancer is the most lethal common cancer with an estimated 5-year survival rate of 6–7% (across all stages). The only potential curative therapy is surgical resection in those with localized disease. Adjuvant (postoperative) therapy confers a survival advantage over postoperative observation alone. Neoadjuvant (preoperative) therapy offers the potential to downstage initially unresectable tumors for resection, sterilize resection margins and decrease locoregional recurrence, and identify a subset of patients with aggressive disease for whom surgery will not be beneficial. Induction chemotherapy followed by consolidation chemoradiation is another recommended approach in those with locally advanced disease. For those who cannot be downstaged, cannot tolerate surgery, or were diagnosed with metastatic disease, treatment remains palliative with chemotherapy being a critical component of this approach. Recently, intensive combination chemotherapy has been shown to improve survival rates in comparison to gemcitabine alone in advanced disease. The past few decades have afforded an accumulation of high-level evidence regarding neoadjuvant, adjuvant and palliative therapies in pancreatic cancer. There are numerous reviews discussing recent retrospective studies, prospective studies and randomized controlled trials in each of these areas. However, reviews of optimal and recommended treatment strategies across all stages of pancreatic cancer that focus on the highest levels of hierarchical evidence, such as meta-analyses, are limited. The discussion of novel therapeutics is beyond the scope of this review. However, an extensive and the most current collection of meta-analyses of first-line systemic and locoregional treatment options for all stages of pancreatic cancer to date has been accumulated. |
format | Online Article Text |
id | pubmed-4774516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-47745162016-03-18 Meta-analyses of treatment standards for pancreatic cancer GONG, JUN TULI, RICHARD SHINDE, ARVIND HENDIFAR, ANDREW E. Mol Clin Oncol Review Pancreatic cancer is the most lethal common cancer with an estimated 5-year survival rate of 6–7% (across all stages). The only potential curative therapy is surgical resection in those with localized disease. Adjuvant (postoperative) therapy confers a survival advantage over postoperative observation alone. Neoadjuvant (preoperative) therapy offers the potential to downstage initially unresectable tumors for resection, sterilize resection margins and decrease locoregional recurrence, and identify a subset of patients with aggressive disease for whom surgery will not be beneficial. Induction chemotherapy followed by consolidation chemoradiation is another recommended approach in those with locally advanced disease. For those who cannot be downstaged, cannot tolerate surgery, or were diagnosed with metastatic disease, treatment remains palliative with chemotherapy being a critical component of this approach. Recently, intensive combination chemotherapy has been shown to improve survival rates in comparison to gemcitabine alone in advanced disease. The past few decades have afforded an accumulation of high-level evidence regarding neoadjuvant, adjuvant and palliative therapies in pancreatic cancer. There are numerous reviews discussing recent retrospective studies, prospective studies and randomized controlled trials in each of these areas. However, reviews of optimal and recommended treatment strategies across all stages of pancreatic cancer that focus on the highest levels of hierarchical evidence, such as meta-analyses, are limited. The discussion of novel therapeutics is beyond the scope of this review. However, an extensive and the most current collection of meta-analyses of first-line systemic and locoregional treatment options for all stages of pancreatic cancer to date has been accumulated. D.A. Spandidos 2016-03 2015-12-18 /pmc/articles/PMC4774516/ /pubmed/26998283 http://dx.doi.org/10.3892/mco.2015.716 Text en Copyright: © Gong et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Review GONG, JUN TULI, RICHARD SHINDE, ARVIND HENDIFAR, ANDREW E. Meta-analyses of treatment standards for pancreatic cancer |
title | Meta-analyses of treatment standards for pancreatic cancer |
title_full | Meta-analyses of treatment standards for pancreatic cancer |
title_fullStr | Meta-analyses of treatment standards for pancreatic cancer |
title_full_unstemmed | Meta-analyses of treatment standards for pancreatic cancer |
title_short | Meta-analyses of treatment standards for pancreatic cancer |
title_sort | meta-analyses of treatment standards for pancreatic cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4774516/ https://www.ncbi.nlm.nih.gov/pubmed/26998283 http://dx.doi.org/10.3892/mco.2015.716 |
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