Frontiers in Oncology (Jun 2022)

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

  • Yung-Yeh Su,
  • Yung-Yeh Su,
  • Yung-Yeh Su,
  • Nai-Jung Chiang,
  • Nai-Jung Chiang,
  • Nai-Jung Chiang,
  • Chung-Pin Li,
  • Chung-Pin Li,
  • Chung-Pin Li,
  • Chia-Jui Yen,
  • Shih-Hung Yang,
  • Wen-Chi Chou,
  • Jen-Shi Chen,
  • Tai-Jan Chiu,
  • Yen-Yang Chen,
  • Shih-Chang Chuang,
  • Shih-Chang Chuang,
  • Li-Yuan Bai,
  • Li-Yuan Bai,
  • Chang-Fang Chiu,
  • Chang-Fang Chiu,
  • Chang-Fang Chiu,
  • Cheng-Ming Peng,
  • De-Chuan Chan,
  • Sz-Chi Chiu,
  • Yi-Hsin Yang,
  • Yan-Shen Shan,
  • Yan-Shen Shan,
  • Li‐Tzong Chen,
  • Li‐Tzong Chen,
  • Li‐Tzong Chen,
  • Li‐Tzong Chen

DOI
https://doi.org/10.3389/fonc.2022.800842
Journal volume & issue
Vol. 12

Abstract

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IntroductionThis 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 MethodsThe 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.ResultsOf 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.ConclusionOur 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.

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