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Clinical outcomes of FOLFIRINOX in locally advanced pancreatic cancer: A single center experience

Systemic chemotherapy or chemoradiotherapy is the initial primary option for patients with locally advanced pancreatic cancer (LAPC). This study analyzed the effect of FOLFIRINOX and assessed the factors influencing conversion to surgical resectability for LAPC. Sixty-four patients with LAPC who rec...

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Autores principales: Lee, Jongchan, Lee, Jong-chan, Gromski, Mark A., Kim, Hyoung Woo, Kim, Jinwon, Kim, Jaihwan, Hwang, Jin-Hyeok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320053/
https://www.ncbi.nlm.nih.gov/pubmed/30558029
http://dx.doi.org/10.1097/MD.0000000000013592
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author Lee, Jongchan
Lee, Jong-chan
Gromski, Mark A.
Kim, Hyoung Woo
Kim, Jinwon
Kim, Jaihwan
Hwang, Jin-Hyeok
author_facet Lee, Jongchan
Lee, Jong-chan
Gromski, Mark A.
Kim, Hyoung Woo
Kim, Jinwon
Kim, Jaihwan
Hwang, Jin-Hyeok
author_sort Lee, Jongchan
collection PubMed
description Systemic chemotherapy or chemoradiotherapy is the initial primary option for patients with locally advanced pancreatic cancer (LAPC). This study analyzed the effect of FOLFIRINOX and assessed the factors influencing conversion to surgical resectability for LAPC. Sixty-four patients with LAPC who received FOLFIRINOX as initial chemotherapy were enrolled retrospectively. Demographic characteristics, tumor status, interval/dosage/cumulative relative dose intensity (cRDI) of FOLFIRINOX, conversion to resection, and clinical outcomes were reviewed and factors associated with conversion to resectability after FOLFIRINOX were analyzed. After administration of FOLFIRINOX (median 9 cycles, 70% of cRDI), the median patient overall survival (OS) was 17.0 months. Fifteen of 64 patients underwent surgery and R0 resection was achieved in 11 patients. During a median follow-up time of 9.4 months after resection, cumulative recurrence rate was 28.5% at 18 months after resection. The estimated median OS was significantly longer for the resected group (>40 months vs 13 months). There were no statistical differences between the resected and non-resected groups in terms of baseline characteristics, tumor status and hematologic adverse effects. The patients who received standard dose of FOLFIRINOX had higher probability of subsequent resection compared with patients who received reduced dose, although cRDIs did not differ between groups. FOLFIRINOX is an active regimen in patients with LAPC, given acceptable resection rates and promising R0 resection rates. Additionally, our data demonstrate it is advantageous for obtaining resectability to administer FOLFIRINOX without dose reduction.
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spelling pubmed-63200532019-01-14 Clinical outcomes of FOLFIRINOX in locally advanced pancreatic cancer: A single center experience Lee, Jongchan Lee, Jong-chan Gromski, Mark A. Kim, Hyoung Woo Kim, Jinwon Kim, Jaihwan Hwang, Jin-Hyeok Medicine (Baltimore) Research Article Systemic chemotherapy or chemoradiotherapy is the initial primary option for patients with locally advanced pancreatic cancer (LAPC). This study analyzed the effect of FOLFIRINOX and assessed the factors influencing conversion to surgical resectability for LAPC. Sixty-four patients with LAPC who received FOLFIRINOX as initial chemotherapy were enrolled retrospectively. Demographic characteristics, tumor status, interval/dosage/cumulative relative dose intensity (cRDI) of FOLFIRINOX, conversion to resection, and clinical outcomes were reviewed and factors associated with conversion to resectability after FOLFIRINOX were analyzed. After administration of FOLFIRINOX (median 9 cycles, 70% of cRDI), the median patient overall survival (OS) was 17.0 months. Fifteen of 64 patients underwent surgery and R0 resection was achieved in 11 patients. During a median follow-up time of 9.4 months after resection, cumulative recurrence rate was 28.5% at 18 months after resection. The estimated median OS was significantly longer for the resected group (>40 months vs 13 months). There were no statistical differences between the resected and non-resected groups in terms of baseline characteristics, tumor status and hematologic adverse effects. The patients who received standard dose of FOLFIRINOX had higher probability of subsequent resection compared with patients who received reduced dose, although cRDIs did not differ between groups. FOLFIRINOX is an active regimen in patients with LAPC, given acceptable resection rates and promising R0 resection rates. Additionally, our data demonstrate it is advantageous for obtaining resectability to administer FOLFIRINOX without dose reduction. Wolters Kluwer Health 2018-12-14 /pmc/articles/PMC6320053/ /pubmed/30558029 http://dx.doi.org/10.1097/MD.0000000000013592 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle Research Article
Lee, Jongchan
Lee, Jong-chan
Gromski, Mark A.
Kim, Hyoung Woo
Kim, Jinwon
Kim, Jaihwan
Hwang, Jin-Hyeok
Clinical outcomes of FOLFIRINOX in locally advanced pancreatic cancer: A single center experience
title Clinical outcomes of FOLFIRINOX in locally advanced pancreatic cancer: A single center experience
title_full Clinical outcomes of FOLFIRINOX in locally advanced pancreatic cancer: A single center experience
title_fullStr Clinical outcomes of FOLFIRINOX in locally advanced pancreatic cancer: A single center experience
title_full_unstemmed Clinical outcomes of FOLFIRINOX in locally advanced pancreatic cancer: A single center experience
title_short Clinical outcomes of FOLFIRINOX in locally advanced pancreatic cancer: A single center experience
title_sort clinical outcomes of folfirinox in locally advanced pancreatic cancer: a single center experience
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320053/
https://www.ncbi.nlm.nih.gov/pubmed/30558029
http://dx.doi.org/10.1097/MD.0000000000013592
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