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Prior irinotecan exposure does not preclude benefit to liposomal irinotecan in patients with metastatic pancreatic ductal adenocarcinoma

BACKGROUND: Subgroup analyses of the NAPOLI‐1 study identified that among patients who were irinotecan naïve prior to entering the clinical trial, a survival benefit was observed between the study arm and control arm. This treatment benefit was not observed among those previously exposed to irinotec...

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Autores principales: Yu, Kenneth H., Cockrum, Paul, Surinach, Andy, Lamarre, Neil, Wang, Shu, O'Reilly, Eileen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166959/
https://www.ncbi.nlm.nih.gov/pubmed/36934451
http://dx.doi.org/10.1002/cam4.5714
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author Yu, Kenneth H.
Cockrum, Paul
Surinach, Andy
Lamarre, Neil
Wang, Shu
O'Reilly, Eileen M.
author_facet Yu, Kenneth H.
Cockrum, Paul
Surinach, Andy
Lamarre, Neil
Wang, Shu
O'Reilly, Eileen M.
author_sort Yu, Kenneth H.
collection PubMed
description BACKGROUND: Subgroup analyses of the NAPOLI‐1 study identified that among patients who were irinotecan naïve prior to entering the clinical trial, a survival benefit was observed between the study arm and control arm. This treatment benefit was not observed among those previously exposed to irinotecan. This study sought to understand the impact of prior exposure to irinotecan on clinical outcomes among patients treated with liposomal irinotecan in the real‐world setting. METHODS: This retrospective observational study utilized a nationwide electronic health record (EHR)‐derived deidentified database. Data for adult patients with mPDAC treated with liposomal irinotecan‐based regimens between January 2016 and October 2020 were analyzed. Patient characteristics, overall survival (OS), and progression‐free survival (PFS) were assessed. Cox proportional hazard methods were used to calculate hazard ratios (HRs). HRs were adjusted for demographics and relevant clinical covariates. RESULTS: Six hundred and seventy‐five patients with mPDAC treated with a liposomal irinotecan‐based regimen were included. The unadjusted OS HR was 1.3 (95% CI: 1.1–1.6, p < 0.001) and unadjusted PFS was HR 1.4 (95% CI: 1.2–1.7, p < 0.001). After adjustment for baseline characteristics, the adjusted OS HR was 1.0 (95% CI: 0.8–1.3, p = 0.8836) and the adjusted PFS HR was 1.1 (95% CI: 0.8–1.4, p = 0.5626). CONCLUSIONS: Prior irinotecan was not found to be a significant predictor of patient outcomes in those later treated with liposomal irinotecan. Thus, the results may inform the rationale for utilizing liposomal irinotecan combination therapy following prior irinotecan exposure in mPDAC, in particular where the prior irinotecan exposure was more distant in time.
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spelling pubmed-101669592023-05-10 Prior irinotecan exposure does not preclude benefit to liposomal irinotecan in patients with metastatic pancreatic ductal adenocarcinoma Yu, Kenneth H. Cockrum, Paul Surinach, Andy Lamarre, Neil Wang, Shu O'Reilly, Eileen M. Cancer Med RESEARCH ARTICLES BACKGROUND: Subgroup analyses of the NAPOLI‐1 study identified that among patients who were irinotecan naïve prior to entering the clinical trial, a survival benefit was observed between the study arm and control arm. This treatment benefit was not observed among those previously exposed to irinotecan. This study sought to understand the impact of prior exposure to irinotecan on clinical outcomes among patients treated with liposomal irinotecan in the real‐world setting. METHODS: This retrospective observational study utilized a nationwide electronic health record (EHR)‐derived deidentified database. Data for adult patients with mPDAC treated with liposomal irinotecan‐based regimens between January 2016 and October 2020 were analyzed. Patient characteristics, overall survival (OS), and progression‐free survival (PFS) were assessed. Cox proportional hazard methods were used to calculate hazard ratios (HRs). HRs were adjusted for demographics and relevant clinical covariates. RESULTS: Six hundred and seventy‐five patients with mPDAC treated with a liposomal irinotecan‐based regimen were included. The unadjusted OS HR was 1.3 (95% CI: 1.1–1.6, p < 0.001) and unadjusted PFS was HR 1.4 (95% CI: 1.2–1.7, p < 0.001). After adjustment for baseline characteristics, the adjusted OS HR was 1.0 (95% CI: 0.8–1.3, p = 0.8836) and the adjusted PFS HR was 1.1 (95% CI: 0.8–1.4, p = 0.5626). CONCLUSIONS: Prior irinotecan was not found to be a significant predictor of patient outcomes in those later treated with liposomal irinotecan. Thus, the results may inform the rationale for utilizing liposomal irinotecan combination therapy following prior irinotecan exposure in mPDAC, in particular where the prior irinotecan exposure was more distant in time. John Wiley and Sons Inc. 2023-03-19 /pmc/articles/PMC10166959/ /pubmed/36934451 http://dx.doi.org/10.1002/cam4.5714 Text en © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle RESEARCH ARTICLES
Yu, Kenneth H.
Cockrum, Paul
Surinach, Andy
Lamarre, Neil
Wang, Shu
O'Reilly, Eileen M.
Prior irinotecan exposure does not preclude benefit to liposomal irinotecan in patients with metastatic pancreatic ductal adenocarcinoma
title Prior irinotecan exposure does not preclude benefit to liposomal irinotecan in patients with metastatic pancreatic ductal adenocarcinoma
title_full Prior irinotecan exposure does not preclude benefit to liposomal irinotecan in patients with metastatic pancreatic ductal adenocarcinoma
title_fullStr Prior irinotecan exposure does not preclude benefit to liposomal irinotecan in patients with metastatic pancreatic ductal adenocarcinoma
title_full_unstemmed Prior irinotecan exposure does not preclude benefit to liposomal irinotecan in patients with metastatic pancreatic ductal adenocarcinoma
title_short Prior irinotecan exposure does not preclude benefit to liposomal irinotecan in patients with metastatic pancreatic ductal adenocarcinoma
title_sort prior irinotecan exposure does not preclude benefit to liposomal irinotecan in patients with metastatic pancreatic ductal adenocarcinoma
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166959/
https://www.ncbi.nlm.nih.gov/pubmed/36934451
http://dx.doi.org/10.1002/cam4.5714
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