JGH Open (Jun 2021)

Efficacy and safety of modified fluorouracil/leucovorin plus irinotecan and oxaliplatin (mFOLFIRINOX) compared with S‐1 as second‐line chemotherapy in metastatic pancreatic cancer

  • Kenji Ikezawa,
  • Ryosuke Kiyota,
  • Ryoji Takada,
  • Kazuma Daiku,
  • Shingo Maeda,
  • Toshihiro Imai,
  • Yutaro Abe,
  • Yugo Kai,
  • Takuo Yamai,
  • Nobuyasu Fukutake,
  • Tasuku Nakabori,
  • Reiko Ashida,
  • Hiroyuki Uehara,
  • Takahiro Tabuchi,
  • Kazuhiro Katayama,
  • Kazuyoshi Ohkawa

DOI
https://doi.org/10.1002/jgh3.12555
Journal volume & issue
Vol. 5, no. 6
pp. 679 – 685

Abstract

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Abstract Background and Aim The optimal standard second‐line chemotherapy for metastatic pancreatic cancer (MPC) remains unclear. Here, we evaluated the efficacy and safety of modified fluorouracil/leucovorin plus irinotecan and oxaliplatin (mFOLFIRINOX) compared with oral fluoropyrimidine S‐1 as a second‐line chemotherapy in patients with MPC. Methods We retrospectively reviewed 76 consecutive patients with metastatic pancreatic adenocarcinoma who underwent mFOLFIRINOX or S‐1 treatment as a second‐line chemotherapy after gemcitabine plus nab‐paclitaxel (GnP) failure at our department between December 2014 and February 2019. Results Patients who underwent mFOLFIRINOX treatment exhibited significantly better objective response rates (ORRs) and progression‐free survival (PFS) than S‐1 (ORR, 20.0% vs 0%, P = 0.003; PFS, 3.7 vs 2.1 months, P = 0.010). Although baseline patient characteristics of age, performance status, and serum albumin levels differed significantly between the two groups, mFOLFIRINOX was identified as an independent factor of favorable PFS on multivariate analyses. Grade 3–4 neutropenia and peripheral sensory neuropathy occurred more frequently in the mFOLFIRINOX group. The median overall survival from the initiation of second‐line chemotherapy was not significantly longer in the mFOLFIRINOX group than in the S1 group (8.5 vs 5.8 months, respectively; P = 0.213); however, the 8‐month survival rate was significantly higher in the mFOLFIRINOX group (56.0% vs 27.5%, respectively; P = 0.030). Conclusions mFOLFIRINOX as a second‐line regimen contributed to favorable treatment outcomes, but induced more frequent adverse events than S‐1. On multivariate analyses, mFOLFIRINOX was identified as an independent factor with favorable PFS, suggesting that mFOLFIRINOX could be a promising treatment option for patients with GnP failure.

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