The use of angiotensin system inhibitors correlates with longer survival in resected pancreatic adenocarcinoma patients.


Journal

HPB : the official journal of the International Hepato Pancreato Biliary Association
ISSN: 1477-2574
Titre abrégé: HPB (Oxford)
Pays: England
ID NLM: 100900921

Informations de publication

Date de publication:
03 2023
Historique:
received: 24 07 2022
revised: 17 10 2022
accepted: 09 12 2022
pubmed: 8 1 2023
medline: 8 3 2023
entrez: 7 1 2023
Statut: ppublish

Résumé

Activities and inhibition of the Renin-Angiotensin-Aldosterone System (RAAS) may affect the survival of resected pancreatic ductal adenocarcinoma (PDAC) patients METHOD: A single-institution retrospective analysis of resected PDAC patients between 2010 and 2019. To estimate the effect of angiotensin system inhibitors (ASIs) on patient survival, we performed Kaplan Meier analysis, Cox Proportional Hazards model, Propensity Score Matching (PSM), and inverse probability weighting (IPW) analysis. 742 patients were included in the analysis. The average age was 67.0 years, with a median follow-up of 24.1 months. The use of ASI was associated with significantly longer overall survival in univariate (p = 0.004) and multivariable (HR = 0.70 [0.56-0.88],p = 0.003) adjusted analysis. In a propensity score-matched cohort of 400 patients, ASI use was again associated with longer overall survival (p = 0.039). Lastly, inverse probability weighting (IPW) analysis suggested that the use of ASI was associated with an average treatment effect on the treated (ATT) of HR = 0.68 [0.53-0.86],p = 0.002) for overall survival. In this single-institution retrospective study focusing on resected PDAC patients, the use of ASI was associated with longer overall survival in multiple statistical models. Prospective clinical trials are needed before routine clinical implementation of ASI as an adjuvant to existing therapy can be recommended.

Sections du résumé

BACKGROUND
Activities and inhibition of the Renin-Angiotensin-Aldosterone System (RAAS) may affect the survival of resected pancreatic ductal adenocarcinoma (PDAC) patients METHOD: A single-institution retrospective analysis of resected PDAC patients between 2010 and 2019. To estimate the effect of angiotensin system inhibitors (ASIs) on patient survival, we performed Kaplan Meier analysis, Cox Proportional Hazards model, Propensity Score Matching (PSM), and inverse probability weighting (IPW) analysis.
RESULTS
742 patients were included in the analysis. The average age was 67.0 years, with a median follow-up of 24.1 months. The use of ASI was associated with significantly longer overall survival in univariate (p = 0.004) and multivariable (HR = 0.70 [0.56-0.88],p = 0.003) adjusted analysis. In a propensity score-matched cohort of 400 patients, ASI use was again associated with longer overall survival (p = 0.039). Lastly, inverse probability weighting (IPW) analysis suggested that the use of ASI was associated with an average treatment effect on the treated (ATT) of HR = 0.68 [0.53-0.86],p = 0.002) for overall survival.
CONCLUSION
In this single-institution retrospective study focusing on resected PDAC patients, the use of ASI was associated with longer overall survival in multiple statistical models. Prospective clinical trials are needed before routine clinical implementation of ASI as an adjuvant to existing therapy can be recommended.

Identifiants

pubmed: 36610939
pii: S1365-182X(22)01677-X
doi: 10.1016/j.hpb.2022.12.002
pii:
doi:

Substances chimiques

Angiotensins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

320-329

Informations de copyright

Copyright © 2022 International Hepato-Pancreato-Biliary Association Inc. Published by Elsevier Ltd. All rights reserved.

Auteurs

Hao Liu (H)

Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.

Ibrahim Nassour (I)

Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.

Steven Lebowitz (S)

School of Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA.

Mark D'Alesio (M)

School of Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA.

Erica Hampton (E)

School of Medicine, University of Pittsburgh, Pittsburgh, PA 15213, USA.

Annissa Desilva (A)

Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.

Abdulrahman Hammad (A)

Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.

Samer AlMasri (S)

Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.

Hussein H Khachfe (HH)

Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.

Aatur Singhi (A)

Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.

Nathan Bahary (N)

Department of Medicine, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.

Kenneth Lee (K)

Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.

Amer Zureikat (A)

Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.

Alessandro Paniccia (A)

Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA. Electronic address: panicciaa2@upmc.edu.

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