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Combination of Irinotecan and a Platinum Agent for Poorly Differentiated Neuroendocrine Carcinomas
Extrapulmonary poorly differentiated neuroendocrine carcinoma (PDNEC) is a rare and highly aggressive neoplasm for which the optimal chemotherapy remains unclear. The objective of this study was to evaluate the outcomes of patients with PDNEC treated with cisplatin and irinotecan (IP) and perform a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PAGEPress Publications, Pavia, Italy
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3804814/ https://www.ncbi.nlm.nih.gov/pubmed/24179651 http://dx.doi.org/10.4081/rt.2013.e39 |
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author | Ramella Munhoz, Rodrigo de Mendonça Rego, Juliana Florinda de Celis Ferrari, Anezka Rubim Ignez Braghiroli, Maria Mendonça Bariani, Giovanni Marcelo Hoff, Paulo Perego Costa, Frederico Eduardo Flesch Pfiffer, Túlio Riechelmann, Rachel |
author_facet | Ramella Munhoz, Rodrigo de Mendonça Rego, Juliana Florinda de Celis Ferrari, Anezka Rubim Ignez Braghiroli, Maria Mendonça Bariani, Giovanni Marcelo Hoff, Paulo Perego Costa, Frederico Eduardo Flesch Pfiffer, Túlio Riechelmann, Rachel |
author_sort | Ramella Munhoz, Rodrigo |
collection | PubMed |
description | Extrapulmonary poorly differentiated neuroendocrine carcinoma (PDNEC) is a rare and highly aggressive neoplasm for which the optimal chemotherapy remains unclear. The objective of this study was to evaluate the outcomes of patients with PDNEC treated with cisplatin and irinotecan (IP) and perform a review of the literature. From 2008 to 2012, patients with advanced PDNEC (Ki67≥20%) who received the IP combination were selected for analysis. Radiologic responses were determined through Response Evaluation Criteria In Solid Tumors criteria. Twenty-eight patients were included. The median age at diagnosis was 57 years and the most common presentation was pancreatic PDNEC. Twenty-five patients (89%) received chemotherapy with cisplatin and irinotecan and three received carboplatin and irinotecan. Forty-six percent of the patients achieved objective response and the median time to tumor progression was 3.7 months. The median overall survival was 11.7 months. Thirteen patients (46%) had treatment interruptions or dose reductions due to grade 3/4 toxicity. This retrospective cohort of advanced extrapulmonary PDNEC patients suggests that the IP combination is feasible and resulted in similar response rate and median survival to other treatments previously reported. |
format | Online Article Text |
id | pubmed-3804814 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | PAGEPress Publications, Pavia, Italy |
record_format | MEDLINE/PubMed |
spelling | pubmed-38048142013-10-31 Combination of Irinotecan and a Platinum Agent for Poorly Differentiated Neuroendocrine Carcinomas Ramella Munhoz, Rodrigo de Mendonça Rego, Juliana Florinda de Celis Ferrari, Anezka Rubim Ignez Braghiroli, Maria Mendonça Bariani, Giovanni Marcelo Hoff, Paulo Perego Costa, Frederico Eduardo Flesch Pfiffer, Túlio Riechelmann, Rachel Rare Tumors Article Extrapulmonary poorly differentiated neuroendocrine carcinoma (PDNEC) is a rare and highly aggressive neoplasm for which the optimal chemotherapy remains unclear. The objective of this study was to evaluate the outcomes of patients with PDNEC treated with cisplatin and irinotecan (IP) and perform a review of the literature. From 2008 to 2012, patients with advanced PDNEC (Ki67≥20%) who received the IP combination were selected for analysis. Radiologic responses were determined through Response Evaluation Criteria In Solid Tumors criteria. Twenty-eight patients were included. The median age at diagnosis was 57 years and the most common presentation was pancreatic PDNEC. Twenty-five patients (89%) received chemotherapy with cisplatin and irinotecan and three received carboplatin and irinotecan. Forty-six percent of the patients achieved objective response and the median time to tumor progression was 3.7 months. The median overall survival was 11.7 months. Thirteen patients (46%) had treatment interruptions or dose reductions due to grade 3/4 toxicity. This retrospective cohort of advanced extrapulmonary PDNEC patients suggests that the IP combination is feasible and resulted in similar response rate and median survival to other treatments previously reported. PAGEPress Publications, Pavia, Italy 2013-09-04 /pmc/articles/PMC3804814/ /pubmed/24179651 http://dx.doi.org/10.4081/rt.2013.e39 Text en ©Copyright R. Ramella Munhoz et al. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Ramella Munhoz, Rodrigo de Mendonça Rego, Juliana Florinda de Celis Ferrari, Anezka Rubim Ignez Braghiroli, Maria Mendonça Bariani, Giovanni Marcelo Hoff, Paulo Perego Costa, Frederico Eduardo Flesch Pfiffer, Túlio Riechelmann, Rachel Combination of Irinotecan and a Platinum Agent for Poorly Differentiated Neuroendocrine Carcinomas |
title | Combination of Irinotecan and a Platinum Agent for Poorly Differentiated Neuroendocrine Carcinomas |
title_full | Combination of Irinotecan and a Platinum Agent for Poorly Differentiated Neuroendocrine Carcinomas |
title_fullStr | Combination of Irinotecan and a Platinum Agent for Poorly Differentiated Neuroendocrine Carcinomas |
title_full_unstemmed | Combination of Irinotecan and a Platinum Agent for Poorly Differentiated Neuroendocrine Carcinomas |
title_short | Combination of Irinotecan and a Platinum Agent for Poorly Differentiated Neuroendocrine Carcinomas |
title_sort | combination of irinotecan and a platinum agent for poorly differentiated neuroendocrine carcinomas |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3804814/ https://www.ncbi.nlm.nih.gov/pubmed/24179651 http://dx.doi.org/10.4081/rt.2013.e39 |
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