The use of ace inhibitors influences the risk of progression of BD-IPMNs under follow-up.


Journal

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]
ISSN: 1424-3911
Titre abrégé: Pancreatology
Pays: Switzerland
ID NLM: 100966936

Informations de publication

Date de publication:
May 2022
Historique:
received: 24 10 2021
revised: 13 03 2022
accepted: 28 03 2022
pubmed: 19 4 2022
medline: 12 5 2022
entrez: 18 4 2022
Statut: ppublish

Résumé

Chemoprevention's ability to slow down or prevent the progression of BD-IPMNs is extremely appealing. Aspirin (ASA), Ace Inhibitors/Angiotensin Receptor Blockers (ACEIs/ARBs) and Statins (STATs) are frequently prescribed drugs with a possible beneficial effect on different cancer types. Their effect on IPMNs is largely unknown. To evaluate the association between the use of ASA, ACEIs/ARBs and STATs and the risk of progression of BD-IPMNs in follow-up. multicenter, retrospective cohort study on patients with presumed BD-IPMNs without relative or absolute indication for surgery. Pharmacological exposures and risk factors were collected. We identified clinically relevant progression (occurrence of radiological absolute or relative indication for surgery) and any progression (occurrence of clinically relevant progression OR any dimension increase OR the occurrence of new cysts). Overall 594 patients were included. ACEIs were associated with a lower occurrence of any progression (HR = 0.70; 95% CI 0.49-0.98, p = 0.04) and clinically relevant progression, HR = 0.42 (95% CI 0.20-0.88; p = 0.02). No significant effect was shown for factors associated with the occurrence of pancreas cancer such as smoking, alcohol consumption and 1st degree family history of pancreas cancer. Among pharmacological exposures, no convincing effect was shown for the chronic use of ASA, ARB and STAT. ACEIs might have an effect in slowing the progression of BD-IPMNs. ASA, STAT and ARBs show no convincing effect on the progression of BD-IPMNs. Further, prospective, and long-term multicenter studies are needed to verify such association and to define the potential underlying mechanisms.

Sections du résumé

BACKGROUND BACKGROUND
Chemoprevention's ability to slow down or prevent the progression of BD-IPMNs is extremely appealing. Aspirin (ASA), Ace Inhibitors/Angiotensin Receptor Blockers (ACEIs/ARBs) and Statins (STATs) are frequently prescribed drugs with a possible beneficial effect on different cancer types. Their effect on IPMNs is largely unknown.
AIM OBJECTIVE
To evaluate the association between the use of ASA, ACEIs/ARBs and STATs and the risk of progression of BD-IPMNs in follow-up.
MATERIALS AND METHODS METHODS
multicenter, retrospective cohort study on patients with presumed BD-IPMNs without relative or absolute indication for surgery. Pharmacological exposures and risk factors were collected. We identified clinically relevant progression (occurrence of radiological absolute or relative indication for surgery) and any progression (occurrence of clinically relevant progression OR any dimension increase OR the occurrence of new cysts).
RESULTS RESULTS
Overall 594 patients were included. ACEIs were associated with a lower occurrence of any progression (HR = 0.70; 95% CI 0.49-0.98, p = 0.04) and clinically relevant progression, HR = 0.42 (95% CI 0.20-0.88; p = 0.02). No significant effect was shown for factors associated with the occurrence of pancreas cancer such as smoking, alcohol consumption and 1st degree family history of pancreas cancer. Among pharmacological exposures, no convincing effect was shown for the chronic use of ASA, ARB and STAT.
CONCLUSIONS CONCLUSIONS
ACEIs might have an effect in slowing the progression of BD-IPMNs. ASA, STAT and ARBs show no convincing effect on the progression of BD-IPMNs. Further, prospective, and long-term multicenter studies are needed to verify such association and to define the potential underlying mechanisms.

Identifiants

pubmed: 35431111
pii: S1424-3903(22)00109-0
doi: 10.1016/j.pan.2022.03.020
pii:
doi:

Substances chimiques

Angiotensin Receptor Antagonists 0
Angiotensin-Converting Enzyme Inhibitors 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

516-524

Informations de copyright

Copyright © 2022 IAP and EPC. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest Prof Del Chiaro received a research grant from Haemonetics, Inc and is co-PI of a Boston Scientific sponsored study on the use of intra-operative pancreatoscopy in IPMN's patients. Prof Arnelo is co-PI of a Boston Scientific sponsored study on the use of intra-operative pancreatoscopy in IPMN's patients. Dr. Valente has been a consultant for Boston Scientific for lectures unrelated to the topic of the article. The other authors declare no possible conflicts of interest. Writing assistance: The current paper has undergone language editing from Alison M Dieden translations. The language editing was paid by Dr Roberto Valente's research grant from Cancerforskningsfonden Norrland/Lions CancerforskningsfondAMP 21-1058. Specific author contributions: Roberto Valente, Marco Del Chiaro and Gabriele Capurso planned the study. Roberto Valente, Giulia Zerboni, Laura Zarantonello, Giuseppe Vanella and Alessandro Fogliati collected the data. Roberto Valente performed the statistical analysis. Roberto Valente, Marco del Chiaro, Gabriele Capurso and Stefano Crippa interpreted data. Roberto Valente, Marco Del Chiaro and Gabriele Capurso drafted the manuscript. Stefano Crippa, Urban Arnelo, Giuseppe Vanella, Giulia Zerboni, Laura Zarantonello, Alessandro Fogliati, Paolo Giorgio Arcidiacono, Miroslav Vujasinovic, Johannes Matthias Lohr, Massimo Falconi, Gabriele Capurso and Marco Del Chiaro reviewed and approved the final draft.

Auteurs

Roberto Valente (R)

Division of Surgery, CLINTEC, Karolinska Institutet, Stockholm, Sweden; Department of Surgery and Perioperative Sciences, Surgery, Umeå University Hospital, Umeå, Sweden; Digestive and Liver Disease Unit, Sant'Andrea Hospital, Sapienza University of Rome, Rome, Italy; Department of Surgical Oncology, Anschutz Medical Campus, University of Colorado, Denver, USA.

Stefano Crippa (S)

Pancreatic Surgery Unit, Pancreas Translational and Clinical Research Centre, San Raffaele Scientific Institute, IRCCS, Milan, Italy.

Urban Arnelo (U)

Division of Surgery, CLINTEC, Karolinska Institutet, Stockholm, Sweden; Department of Surgery and Perioperative Sciences, Surgery, Umeå University Hospital, Umeå, Sweden.

Giuseppe Vanella (G)

Pancreatobiliary Endoscopy and EUS Division, Pancreas Translational and Clinical Research Centre, San Raffaele Scientific Institute, IRCCS, Milan, Italy; Digestive and Liver Disease Unit, Sant'Andrea Hospital, Sapienza University of Rome, Rome, Italy.

Giulia Zerboni (G)

Digestive and Liver Disease Unit, Sant'Andrea Hospital, Sapienza University of Rome, Rome, Italy.

Laura Zarantonello (L)

Division of Surgery, Uppsala University Hospital, Uppsala, Sweden.

Alessandro Fogliati (A)

Pancreatic Surgery Unit, Pancreas Translational and Clinical Research Centre, San Raffaele Scientific Institute, IRCCS, Milan, Italy.

Paolo Giorgio Arcidiacono (PG)

Pancreatobiliary Endoscopy and EUS Division, Pancreas Translational and Clinical Research Centre, San Raffaele Scientific Institute, IRCCS, Milan, Italy.

Miroslav Vujasinovic (M)

Department for Upper Abdominal Diseases, Karolinska University Hospital and Department of Medicine Huddinge, Karolinska Institute, Sweden.

Johannes Matthias Lohr (JM)

Division of Surgery, CLINTEC, Karolinska Institutet, Stockholm, Sweden.

Massimo Falconi (M)

Pancreatic Surgery Unit, Pancreas Translational and Clinical Research Centre, San Raffaele Scientific Institute, IRCCS, Milan, Italy.

Gabriele Capurso (G)

Pancreatobiliary Endoscopy and EUS Division, Pancreas Translational and Clinical Research Centre, San Raffaele Scientific Institute, IRCCS, Milan, Italy; Digestive and Liver Disease Unit, Sant'Andrea Hospital, Sapienza University of Rome, Rome, Italy. Electronic address: capurso.gabriele@hsr.it.

Marco Del Chiaro (M)

Department of Surgical Oncology, Anschutz Medical Campus, University of Colorado, Denver, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH