AI Article Synopsis

  • A multicenter study was conducted to assess how the cumulative dose and dosing patterns of liposomal irinotecan plus fluorouracil/leucovorin (nal-IRI+5-FU/LV) affect survival in patients with gemcitabine-refractory metastatic pancreatic ductal adenocarcinoma (mPDAC).
  • The study reviewed medical records of 473 patients, finding that higher cumulative doses of the treatment led to significantly longer median overall survival (mOS), with those receiving >80% of the dose surviving the longest.
  • The findings indicate that starting treatment with a lower dose followed by potential dose increases can achieve survival rates similar to a standard dose approach, highlighting the effectiveness of nal-IRI+5-F

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9256928PMC
http://dx.doi.org/10.3389/fonc.2022.800842DOI Listing

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