From first line to sequential treatment in the management of metastatic pancreatic cancer Review uri icon

Overview

MeSH Major

  • Carcinoma, Pancreatic Ductal
  • Computational Biology
  • Pancreatic Neoplasms
  • Systems Analysis
  • Systems Biology

abstract

  • The current management of patients with metastatic pancreatic ductal adenocarcinoma (mPDAC) is based on systemic chemotherapy. The results of the MPACT and PRODIGE clinical trials have demonstrated that the combination of nab-paclitaxel and gemcitabine (GEM) as well as FOLFIRINOX regimen result in improvement in overall survival when compared to GEM alone. Treatment guidelines now recommend either one of these two regimens as first line treatment for fit patients with mPDAC. Because no head-to-head comparison between the two regimens exists, the selection of one versus the other is based on clinical criteria. The design and eligibility criteria of these two clinical trials are dissimilar, making the results of the MPACT trial more applicable to the general population of patients with mPDAC. In addition, the combination of nab-paclitaxel and GEM is better tolerated and easier to administer in clinical practice than FOLFIRINOX. Furthermore, when the regimens are studied in comparable patient populations the efficacy results are very similar. Nanoliposomal irinotecan plus 5FU has recently demonstrated a significant increase in efficacy rates after a GEM-based treatment. Importantly, treatment of mPDAC should now be considered as a continuum care for patients who are fit, with second and even third line treatments. Different sequential treatment algorithms are proposed based on available data. In retrospective studies, patients who were managed with GEM-based regimens followed by fluoropyrimidine-based regimens appear to have the most favorable outcome.

publication date

  • January 2018

Research

keywords

  • Review

Identity

Language

  • eng

PubMed Central ID

  • PMC5995948

Digital Object Identifier (DOI)

  • 10.7150/jca.23716

PubMed ID

  • 29896283

Additional Document Info

start page

  • 1978

end page

  • 1988

volume

  • 9

number

  • 11