Statin therapy and its association with long-term survival after colon cancer surgery.


Journal

Surgery
ISSN: 1532-7361
Titre abrégé: Surgery
Pays: United States
ID NLM: 0417347

Informations de publication

Date de publication:
04 2022
Historique:
received: 03 05 2021
revised: 23 07 2021
accepted: 01 08 2021
pubmed: 12 9 2021
medline: 20 4 2022
entrez: 11 9 2021
Statut: ppublish

Résumé

The current study aimed to address the clinical equipoise regarding the association of ongoing statin therapy at time of surgery with long-term postoperative mortality rates after elective, curative, surgical resections of colon cancer by analyzing data from a large validated national register. All adults with stage I to III colon cancer who underwent elective surgery with curative intent between January 2007 and October 2016 were retrieved from the Swedish Colorectal Cancer Register, a prospectively collected national register. Patients were identified as having ongoing statin therapy if they filled a prescription within 12 months pre- and postoperatively. Study outcomes included 5-year all-cause and cancer-specific postoperative mortality. To reduce the impact of confounding from covariates owing to nonrandomization, the inverse probability of treatment weighting method was used. Subsequently, Cox proportional hazards models were fitted to the weighted cohorts. In total, 19,118 patients underwent elective surgery for colon cancer in the specified period, of whom 31% (5,896) had ongoing statin therapy. Despite being older, having a higher preoperative risk, and having more comorbidities, patients with statin therapy had a higher postoperative survival. After inverse probability of treatment weighting, patients with statin therapy displayed a significantly lower mortality risk up to 5 years after surgery for both all-cause (hazard ratio 0.68, 95% confidence interval 0.63-0.74, P < .001) and cancer-specific mortality (hazard ratio 0.76, 95% confidence interval 0.66-0.89, P < .001). The results of this study indicate that statin therapy is associated with a sustained reduction in all-cause and cancer-specific mortality up to 5 years after elective colon cancer surgery. The findings warrant validation in future prospective clinical trials.

Sections du résumé

BACKGROUND
The current study aimed to address the clinical equipoise regarding the association of ongoing statin therapy at time of surgery with long-term postoperative mortality rates after elective, curative, surgical resections of colon cancer by analyzing data from a large validated national register.
METHODS
All adults with stage I to III colon cancer who underwent elective surgery with curative intent between January 2007 and October 2016 were retrieved from the Swedish Colorectal Cancer Register, a prospectively collected national register. Patients were identified as having ongoing statin therapy if they filled a prescription within 12 months pre- and postoperatively. Study outcomes included 5-year all-cause and cancer-specific postoperative mortality. To reduce the impact of confounding from covariates owing to nonrandomization, the inverse probability of treatment weighting method was used. Subsequently, Cox proportional hazards models were fitted to the weighted cohorts.
RESULTS
In total, 19,118 patients underwent elective surgery for colon cancer in the specified period, of whom 31% (5,896) had ongoing statin therapy. Despite being older, having a higher preoperative risk, and having more comorbidities, patients with statin therapy had a higher postoperative survival. After inverse probability of treatment weighting, patients with statin therapy displayed a significantly lower mortality risk up to 5 years after surgery for both all-cause (hazard ratio 0.68, 95% confidence interval 0.63-0.74, P < .001) and cancer-specific mortality (hazard ratio 0.76, 95% confidence interval 0.66-0.89, P < .001).
CONCLUSION
The results of this study indicate that statin therapy is associated with a sustained reduction in all-cause and cancer-specific mortality up to 5 years after elective colon cancer surgery. The findings warrant validation in future prospective clinical trials.

Identifiants

pubmed: 34507829
pii: S0039-6060(21)00769-8
doi: 10.1016/j.surg.2021.08.002
pii:
doi:

Substances chimiques

Hydroxymethylglutaryl-CoA Reductase Inhibitors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

890-896

Informations de copyright

Copyright © 2021 The Author(s). Published by Elsevier Inc. All rights reserved.

Auteurs

Arvid Pourlotfi (A)

Department of Surgery, Orebro University Hospital, Orebro, Sweden; School of Medical Sciences, Orebro University, Orebro, Sweden.

Rebecka Ahl Hulme (R)

School of Medical Sciences, Orebro University, Orebro, Sweden; Division of Trauma and Emergency Surgery, Department of Surgery, Karolinska University Hospital, Stockholm, Sweden; Division of Surgery, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.

Maximilian Peter Forssten (MP)

Department of Surgery, Orebro University Hospital, Orebro, Sweden; School of Medical Sciences, Orebro University, Orebro, Sweden.

Gabriel Sjolin (G)

Department of Surgery, Orebro University Hospital, Orebro, Sweden; School of Medical Sciences, Orebro University, Orebro, Sweden.

Gary A Bass (GA)

School of Medical Sciences, Orebro University, Orebro, Sweden; Division of Traumatology, Emergency Surgery and Surgical Critical Care, University of Pennsylvania, Philadelphia, PA.

Yang Cao (Y)

Clinical Epidemiology and Biostatistics, School of Medical Sciences, Orebro University, Orebro, Sweden.

Peter Matthiessen (P)

Department of Surgery, Orebro University Hospital, Orebro, Sweden; School of Medical Sciences, Orebro University, Orebro, Sweden.

Shahin Mohseni (S)

Department of Surgery, Orebro University Hospital, Orebro, Sweden; School of Medical Sciences, Orebro University, Orebro, Sweden; Division of Trauma and Emergency Surgery, Department of Surgery, Orebro University Hospital, Orebro, Sweden. Electronic address: mohsenishahin@yahoo.com.

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