Skip to main navigation Skip to search Skip to main content

Dosing Pattern and Early Cumulative Dose of Liposomal Irinotecan in Metastatic Pancreatic Cancer: A Real-World Multicenter Study

  • Yung Yeh Su
  • , Nai Jung Chiang
  • , Chung Pin Li
  • , Chia Jui Yen
  • , Shih Hung Yang
  • , Wen Chi Chou
  • , Jen Shi Chen
  • , Tai Jan Chiu
  • , Yen Yang Chen
  • , Shih Chang Chuang
  • , Li Yuan Bai
  • , Chang Fang Chiu
  • , Cheng Ming Peng
  • , De Chuan Chan
  • , Sz Chi Chiu
  • , Yi Hsin Yang
  • , Yan Shen Shan*
  • , Li‐Tzong Chen
  • *Corresponding author for this work
  • National Cheng Kung University
  • Veterans General Hospital-Taipei
  • National Yang Ming Chiao Tung University
  • National Taiwan University
  • Chang Gung Memorial Hospital
  • Kaohsiung Medical University
  • China Medical University Taichung
  • Chung Shan Medical University
  • Triservice General Hospital Taiwan
  • PharmaEngine, Inc

Research output: Contribution to journalJournal Article peer-review

8 Scopus citations

Abstract

Introduction: This multicenter, real-world cohort study aimed to evaluate the effectiveness of early cumulative dose administration and dosing pattern of liposomal irinotecan plus fluorouracil/leucovorin (nal-IRI+5-FU/LV) in patients with gemcitabine-refractory metastatic pancreatic ductal adenocarcinoma (mPDAC). Material and Methods: The electronic medical records of mPDAC patients treated with nal-IRI+5-FU/LV in nine participating centers were manually reviewed. To accommodate to the NAPOLI-1 study population, only patients with an Eastern Cooperative Oncology Group Performance Score of 0–1 were included. The survival impact of the relative 6-week cumulative dose and dosing pattern (standard vs. reduced starting dose, with and without further dose modification) were investigated. Results: Of the 473 included patients, their median overall survival (mOS) was 6.8 [95% CI, 6.2–7.7] months. The mOS of patients who received a relative 6-week cumulative dose of >80%, 60%–80%, and <60% were 7.9, 8.2, and 4.3 months, respectively (p<0.0001). Their survival impact remained significant after covariate adjustment using Cox regression. The mOS was 8.0–8.2 months in patients with a standard starting dose with and without early dose modification, and 9.3 and 6.7 months in those who had a reduced starting dose with and without escalation in the subsequent treatment, respectively. The incidence of grade 3–4 neutropenia and diarrhea was 23.3% and 2.7%, respectively. Conclusion: Our results support the use of nal-IRI+5-FU/LV in gemcitabine-refractory mPDAC and suggest that a lower starting dose followed by a re-escalation strategy could achieve clinical outcomes comparable to those with standard starting doses in real-world practice.

Original languageEnglish
Article number800842
JournalFrontiers in Oncology
Volume12
DOIs
StatePublished - 22 06 2022

Bibliographical note

Publisher Copyright:
Copyright © 2022 Su, Chiang, Li, Yen, Yang, Chou, Chen, Chiu, Chen, Chuang, Bai, Chiu, Peng, Chan, Chiu, Yang, Shan and Chen.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • dose escalation strategy
  • dose intensity
  • nal-IRI
  • pancreatic cancer
  • real world

Fingerprint

Dive into the research topics of 'Dosing Pattern and Early Cumulative Dose of Liposomal Irinotecan in Metastatic Pancreatic Cancer: A Real-World Multicenter Study'. Together they form a unique fingerprint.

Cite this