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Poster session 11

1416P - Associations between metformin and mortality risks in Asian diabetic patients with prostate cancer undergoing androgen deprivation therapy: A retrospective cohort study

Date

10 Sep 2022

Session

Poster session 11

Topics

Tumour Site

Prostate Cancer

Presenters

Yan Hiu Athena Lee

Citation

Annals of Oncology (2022) 33 (suppl_7): S616-S652. 10.1016/annonc/annonc1070

Authors

Y.H.A. Lee1, J.M.H. Hui2, J.S.K. Chan2, K. Liu3, E.C. Dee4, K. Ng5, P. Tang2, G. Tse6, A.C.F. Ng7

Author affiliations

  • 1 Division Of Urology, Department Of Surgery, The Chinese University of Hong Kong - Prince of Wales Hospital, HKSAR - Hong Kong/HK
  • 2 Diabetes Research Unit, Cardiovascular Analytics Group, Hong Kong/HK
  • 3 Division Of Urology, Department Of Surgery, The Chinese University of Hong Kong - Prince of Wales Hospital, Hong Kong/HK
  • 4 Department Of Radiation Oncology, Memorial Sloan Kettering Cancer Center, 10065 - New York/US
  • 5 Department Of Medical Oncology, University College London Hospitals NHS Foundation Trust, NW1 2BU - London/GB
  • 6 Tianjin Key Laboratory Of Ionic-molecular Function Of Cardiovascular Disease, Department Of Cardiology, Tianjin Institute Of Cardiology, The Second Hospital of Tianjin Medical University, 300211 - Tianjin/CN
  • 7 Sh Ho Urology Centre, The Chinese University of Hong Kong, Hong Kong/HK

Resources

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Abstract 1416P

Background

Metformin is associated with lower risks of developing prostate cancer (PCa), but its association with mortality in PCa is unclear. This study examined the associations between metformin use concurrent with androgen deprivation therapy (ADT) and mortality risks in Asian, diabetic patients with PCa.

Methods

Diabetic adults with PCa receiving any ADT attending public hospitals in Hong Kong between December 1999 and March 2021 were retrospectively identified. Patients with <6 months of medical castration without subsequent bilateral orchidectomy, <6 months of concurrent metformin use and ADT, or missing baseline HbA1c were excluded. Metformin users had ≥6 months of concurrent metformin use and ADT, while non-users had no concurrent metformin use and ADT or never used metformin. Included patients were followed up until September 2021. The primary outcome was PCa-related mortality. The secondary outcome was all-cause mortality. Inverse probability treatment weighting was used to balance covariates.

Results

1971 patients (1284 metformin users and 687 non-users; mean age 76.2±7.8 years) were studied. Over a mean follow-up of 4.1±3.2 years, metformin users had significantly lower risks of PCa-related mortality (weighted hazard ratio (wHR) 0.49 [95% confidence interval 0.39-0.61], p<0.001) and all-cause mortality (wHR 0.53 [0.46-0.61], p<0.001), independent of diabetic control or status of chronic kidney disease. Such associations appeared stronger in patients without androgen receptor antagonist or chemotherapy use (Table). Table: 1416P

Weighted comparisons of outcomes by metformin usage with subgroups for androgen receptor antagonist or chemotherapy usage. Weighted hazard ratios (wHR) [95% confidence interval (CI)] were referenced against metformin non-users

All patients Never received androgen receptor antagonist or chemotherapy (N=1096) Received androgen receptor antagonist or chemotherapy (N=875) p value for interaction
wHR [95% CI] p value wHR [95% CI] p value wHR [95% CI] p value
Prostate cancer-related mortality 0.49 [0.39, 0.61] <0.001 0.38 [0.27, 0.52] <0.001 0.59 [0.43, 0.81] 0.001 0.017
All-cause mortality 0.53 [0.46, 0.61] <0.001 0.48 [0.40, 0.57] <0.001 0.60 [0.48, 0.75] <0.001 0.048

Conclusions

Metformin use concurrent with ADT was associated with lower risks of mortality in Asian, diabetic patients with PCa. Its role as adjuvant therapy for PCa warrants further study.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

E.C. Dee: Financial Interests, Institutional, Funding, NIH/NCI Support Grant P30 CA008748: National Institute of Health (NIH)/National Cancer Institute (NCI). All other authors have declared no conflicts of interest.

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