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Gemcitabine plus nab-paclitaxel for locally advanced or borderline resectable pancreatic cancer
Overall survival in a phase III study for metastatic pancreatic cancer has significantly improved with gemcitabine (GEM) plus nab-paclitaxel. However, to date, there is limited data on the efficacy and safety of its use for patients with locally advanced (LA) or borderline resectable pancreatic canc...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838159/ https://www.ncbi.nlm.nih.gov/pubmed/31700023 http://dx.doi.org/10.1038/s41598-019-52486-x |
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author | Tsujimoto, Akiko Sudo, Kentaro Nakamura, Kazuyoshi Kita, Emiri Hara, Ryusuke Takayama, Wataru Ishii, Hiroshi Yamaguchi, Taketo |
author_facet | Tsujimoto, Akiko Sudo, Kentaro Nakamura, Kazuyoshi Kita, Emiri Hara, Ryusuke Takayama, Wataru Ishii, Hiroshi Yamaguchi, Taketo |
author_sort | Tsujimoto, Akiko |
collection | PubMed |
description | Overall survival in a phase III study for metastatic pancreatic cancer has significantly improved with gemcitabine (GEM) plus nab-paclitaxel. However, to date, there is limited data on the efficacy and safety of its use for patients with locally advanced (LA) or borderline resectable pancreatic cancer (BRPC). Here, we investigated the efficacy and safety of first-line GEM plus nab-paclitaxel for LA or BRPC. We retrospectively analysed consecutive patients with pathologically confirmed, untreated LA or BRPC who started receiving first-line GEM plus nab-paclitaxel. A total of 30 patients (LA, n = 22; BRPC, n = 8) were analysed. Twelve patients (40%) without distant metastasis received additional chemoradiotherapy using S-1. Laparotomy was performed on 8 patients and 6 (20%; LA, n = 3; BR, n = 3) achieved R0 resection. Objective response rate was 44.8%. For all patients, median progression-free survival and overall survival were 14.8 and 29.9 months, respectively. Median overall survival for LA was 24.1 months with a 2-year survival rate of 50.8%. The most frequently observed grade 3 or 4 toxicities were neutropenia (73%) and biliary infection (13%). First-line GEM plus nab-paclitaxel was well-tolerated and feasible with an encouraging survival for LA or BRPC. |
format | Online Article Text |
id | pubmed-6838159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68381592019-11-14 Gemcitabine plus nab-paclitaxel for locally advanced or borderline resectable pancreatic cancer Tsujimoto, Akiko Sudo, Kentaro Nakamura, Kazuyoshi Kita, Emiri Hara, Ryusuke Takayama, Wataru Ishii, Hiroshi Yamaguchi, Taketo Sci Rep Article Overall survival in a phase III study for metastatic pancreatic cancer has significantly improved with gemcitabine (GEM) plus nab-paclitaxel. However, to date, there is limited data on the efficacy and safety of its use for patients with locally advanced (LA) or borderline resectable pancreatic cancer (BRPC). Here, we investigated the efficacy and safety of first-line GEM plus nab-paclitaxel for LA or BRPC. We retrospectively analysed consecutive patients with pathologically confirmed, untreated LA or BRPC who started receiving first-line GEM plus nab-paclitaxel. A total of 30 patients (LA, n = 22; BRPC, n = 8) were analysed. Twelve patients (40%) without distant metastasis received additional chemoradiotherapy using S-1. Laparotomy was performed on 8 patients and 6 (20%; LA, n = 3; BR, n = 3) achieved R0 resection. Objective response rate was 44.8%. For all patients, median progression-free survival and overall survival were 14.8 and 29.9 months, respectively. Median overall survival for LA was 24.1 months with a 2-year survival rate of 50.8%. The most frequently observed grade 3 or 4 toxicities were neutropenia (73%) and biliary infection (13%). First-line GEM plus nab-paclitaxel was well-tolerated and feasible with an encouraging survival for LA or BRPC. Nature Publishing Group UK 2019-11-07 /pmc/articles/PMC6838159/ /pubmed/31700023 http://dx.doi.org/10.1038/s41598-019-52486-x Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tsujimoto, Akiko Sudo, Kentaro Nakamura, Kazuyoshi Kita, Emiri Hara, Ryusuke Takayama, Wataru Ishii, Hiroshi Yamaguchi, Taketo Gemcitabine plus nab-paclitaxel for locally advanced or borderline resectable pancreatic cancer |
title | Gemcitabine plus nab-paclitaxel for locally advanced or borderline resectable pancreatic cancer |
title_full | Gemcitabine plus nab-paclitaxel for locally advanced or borderline resectable pancreatic cancer |
title_fullStr | Gemcitabine plus nab-paclitaxel for locally advanced or borderline resectable pancreatic cancer |
title_full_unstemmed | Gemcitabine plus nab-paclitaxel for locally advanced or borderline resectable pancreatic cancer |
title_short | Gemcitabine plus nab-paclitaxel for locally advanced or borderline resectable pancreatic cancer |
title_sort | gemcitabine plus nab-paclitaxel for locally advanced or borderline resectable pancreatic cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838159/ https://www.ncbi.nlm.nih.gov/pubmed/31700023 http://dx.doi.org/10.1038/s41598-019-52486-x |
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