Cargando…

Chemotherapy in Pancreatic Cancer: A Systematic Review

Background and Aim: Pancreatic cancer is one of the most fatal cancers. Cytotoxic chemotherapy remains the mainstream treatment for unresectable pancreatic cancer. This systematic review evaluated and compared the overall survival (OS) and progression-free survival (PFS) outcomes obtained from recen...

Descripción completa

Detalles Bibliográficos
Autores principales: Hajatdoost, Leva, Sedaghat, Keyvan, Walker, Erin J., Thomas, Jackson, Kosari, Sam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122094/
https://www.ncbi.nlm.nih.gov/pubmed/30344279
http://dx.doi.org/10.3390/medicina54030048
_version_ 1783352581714608128
author Hajatdoost, Leva
Sedaghat, Keyvan
Walker, Erin J.
Thomas, Jackson
Kosari, Sam
author_facet Hajatdoost, Leva
Sedaghat, Keyvan
Walker, Erin J.
Thomas, Jackson
Kosari, Sam
author_sort Hajatdoost, Leva
collection PubMed
description Background and Aim: Pancreatic cancer is one of the most fatal cancers. Cytotoxic chemotherapy remains the mainstream treatment for unresectable pancreatic cancer. This systematic review evaluated and compared the overall survival (OS) and progression-free survival (PFS) outcomes obtained from recent phase 2 and 3 clinical trials of pancreatic cancer chemotherapy. Materials and methods: Thirty-two studies were included and compared based on chemotherapy agents or combinations used. Additionally, outcomes of first-line versus second-line chemotherapy in pancreatic cancer were compared. Results: In studies that investigated the treatments in adjuvant settings, the highest OS reported was for S-1 in patients, who received prior surgical resection (46.5 months). In neoadjuvant settings, the combination of gemcitabine, docetaxel, and capecitabine prior to the surgical resection had promising outcomes (OS of 32.5 months). In non-adjuvant settings, the highest OS reported was for the combination of temsirolimus plus bevacizumab (34.0 months). Amongst studies that investigated second-line treatment, the highest OS reported was for the combination of gemcitabine plus cisplatin (35.5 months), then temsirolimus plus bevacizumab (34.0 months). Conclusions: There is a need to develop further strategies besides chemotherapy to improve the outcomes in pancreatic cancer treatment. Future studies should consider surgical interventions, combination chemotherapy, and individualized second-line treatment based on the prior chemotherapy.
format Online
Article
Text
id pubmed-6122094
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-61220942018-10-18 Chemotherapy in Pancreatic Cancer: A Systematic Review Hajatdoost, Leva Sedaghat, Keyvan Walker, Erin J. Thomas, Jackson Kosari, Sam Medicina (Kaunas) Review Background and Aim: Pancreatic cancer is one of the most fatal cancers. Cytotoxic chemotherapy remains the mainstream treatment for unresectable pancreatic cancer. This systematic review evaluated and compared the overall survival (OS) and progression-free survival (PFS) outcomes obtained from recent phase 2 and 3 clinical trials of pancreatic cancer chemotherapy. Materials and methods: Thirty-two studies were included and compared based on chemotherapy agents or combinations used. Additionally, outcomes of first-line versus second-line chemotherapy in pancreatic cancer were compared. Results: In studies that investigated the treatments in adjuvant settings, the highest OS reported was for S-1 in patients, who received prior surgical resection (46.5 months). In neoadjuvant settings, the combination of gemcitabine, docetaxel, and capecitabine prior to the surgical resection had promising outcomes (OS of 32.5 months). In non-adjuvant settings, the highest OS reported was for the combination of temsirolimus plus bevacizumab (34.0 months). Amongst studies that investigated second-line treatment, the highest OS reported was for the combination of gemcitabine plus cisplatin (35.5 months), then temsirolimus plus bevacizumab (34.0 months). Conclusions: There is a need to develop further strategies besides chemotherapy to improve the outcomes in pancreatic cancer treatment. Future studies should consider surgical interventions, combination chemotherapy, and individualized second-line treatment based on the prior chemotherapy. MDPI 2018-07-11 /pmc/articles/PMC6122094/ /pubmed/30344279 http://dx.doi.org/10.3390/medicina54030048 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hajatdoost, Leva
Sedaghat, Keyvan
Walker, Erin J.
Thomas, Jackson
Kosari, Sam
Chemotherapy in Pancreatic Cancer: A Systematic Review
title Chemotherapy in Pancreatic Cancer: A Systematic Review
title_full Chemotherapy in Pancreatic Cancer: A Systematic Review
title_fullStr Chemotherapy in Pancreatic Cancer: A Systematic Review
title_full_unstemmed Chemotherapy in Pancreatic Cancer: A Systematic Review
title_short Chemotherapy in Pancreatic Cancer: A Systematic Review
title_sort chemotherapy in pancreatic cancer: a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122094/
https://www.ncbi.nlm.nih.gov/pubmed/30344279
http://dx.doi.org/10.3390/medicina54030048
work_keys_str_mv AT hajatdoostleva chemotherapyinpancreaticcancerasystematicreview
AT sedaghatkeyvan chemotherapyinpancreaticcancerasystematicreview
AT walkererinj chemotherapyinpancreaticcancerasystematicreview
AT thomasjackson chemotherapyinpancreaticcancerasystematicreview
AT kosarisam chemotherapyinpancreaticcancerasystematicreview