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Original Articles: Clinical Oncology

Use of 5α-reductase inhibitors and survival of oesophageal and gastric cancer in a nationwide Swedish cohort study

, , &
Pages 438-443 | Received 27 Feb 2023, Accepted 11 May 2023, Published online: 22 May 2023
 

Abstract

Background

We hypothesised that the use of the anti-androgenic drug 5α-reductase inhibitors (5-ARIs) improves survival in patients with oesophago-gastric cancer.

Methods

This nationwide Swedish population-based cohort study included men who underwent surgery for oesophageal or gastric cancer between 2006-2015, with follow-up until the end of 2020. Multivariable Cox regression estimated hazard ratios (HR) for associations between 5-ARIs use and 5-year all-cause mortality (main outcome) and 5-year disease-specific mortality (secondary outcome). The HR was adjusted for age, comorbidity, education, calendar year, neoadjuvant chemo(radio)therapy, tumour stage, and resection margin status.

Results

Among 1769 patients with oesophago-gastric cancer, 64 (3.6%) were users of 5-ARIs. Compared to non-users, users of 5-ARIs were not at any decreased risk of 5-year all-cause mortality (adjusted HR 1.13, 95% CI 0.79-1.63) or 5-year disease-specific mortality (adjusted HR 1.10, 95% CI 0.79-1.52). Use of 5-ARIs was not associated with any decreased risk of 5-year all-cause mortality in subgroup analyses stratified by categories of age, comorbidity, tumour stage, or tumour subtype (oesophageal or cardia adenocarcinoma, non-cardia gastric adenocarcinoma, or oesophageal squamous cell carcinoma).

Conclusion

This study did not support the hypothesis of improved survival among users of 5-ARIs after curatively intended treatment for oesophago-gastric cancer.

Author contributions

All authors designed the study. The data was retrieved by F.M. from a previously established cohort (SWEGASS). The data was analysed by S.R. and validated by F.M. S.R. interpreted the results and drafted the paper. All listed authors revised the paper and approved the final version of the article, including the authorship list. S.X. is the guarantor of this work and, as such, had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

Ethics approval

This study was approved by the Regional Ethical Review Board in Stockholm (reference number (2017/141-31/2). The study was performed in accordance with the Declaration of Helsinki.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Data availability statement

Data supporting the results are available upon request.

Additional information

Funding

This study was funded partly by Swedish Cancer Society (grant number 19 0043 and 22 2038) and Swedish Research Council (grant number 2019-00209).