Comparison of infection risk between enzalutamide and abiraterone in patients with prostate cancer

Author:

Lee Yan Hiu Athena12ORCID,Chan Jeffrey Shi Kai2ORCID,Leung Chi Ho1,Liu Alex Qinyang1,Dee Edward Christopher3ORCID,Ng Kenrick4,Shamash Johnathan4,Tse Gary2567,Wai Leung David Ka1,Ng Chi Fai18ORCID

Affiliation:

1. Division of Urology Department of Surgery Faculty of Medicine The Chinese University of Hong Kong Hong Kong China

2. Cardio‐Oncology Research Unit Cardiovascular Analytics Group PowerHealth Research Institute Hong Kong China

3. Department of Radiation Oncology Memorial Sloan Kettering Cancer Center New York New York USA

4. Department of Medical Oncology Barts Cancer Centre London UK

5. Tianjin Key Laboratory of Ionic‐Molecular Function of Cardiovascular Disease Department of Cardiology Tianjin Institute of Cardiology Second Hospital of Tianjin Medical University Tianjin China

6. Kent and Medway Medical School Canterbury Kent UK

7. School of Nursing and Health Studies Hong Kong Metropolitan University Hong Kong China

8. SH Ho Urology Centre The Chinese University of Hong Kong Hong Kong China

Abstract

AbstractBackgroundEnzalutamide and abiraterone may differ in their immunomodulatory effects, and the prednisone coadministered with abiraterone can be immunosuppressive. This study aimed to compare the risk of different types of infection in patients with prostate cancer receiving enzalutamide or abiraterone in combination with androgen deprivation therapy.MethodsPatients with prostate cancer receiving enzalutamide or abiraterone in addition to androgen deprivation therapy in Hong Kong between December 1999 to March 2021 were identified in this retrospective cohort study and followed up until September 2021, death, or crossover. Outcomes, including any sepsis, pneumonia, urinary tract infection, cellulitis or skin abscess, central nervous system infections, and tuberculosis, were analyzed as both time‐to‐event outcomes (multivariable Fine‐Gray regression, with mortality considered a competing event) and recurrent‐event outcomes (multivariable negative binomial regression).ResultsAltogether, 1582 patients were analyzed (923 abiraterone users; 659 enzalutamide users) with a median follow‐up of 10.6 months (interquartile range: 5.3–19.9 months). Compared to abiraterone users, enzalutamide users had lower cumulative incidences of sepsis (adjusted subhazard ratio [SHR] 0.70 [0.53–0.93], p = .014), pneumonia (adjusted SHR 0.76 [0.59–0.99], p = .040), and cellulitis or skin abscess (adjusted SHR 0.55 [0.39–0.79], p = .001), but not urinary tract infection (adjusted SHR 0.91 [0.62–1.35], p = .643). Associations between exposure and central nervous system infections and tuberculosis were not assessed because of low event rates. Analyzing the outcomes as recurrent events gave similar results. Enzalutamide use may be associated with a lower risk of urinary tract infection in patients with diabetes mellitus.ConclusionsCompared to abiraterone users, enzalutamide users have significantly lower risks of sepsis, pneumonia, cellulitis, or skin abscess.

Publisher

Wiley

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