Associations between Peripheral Thromboembolic Vascular Disease and Androgen Deprivation Therapy in Asian Prostate Cancer Patients.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
02 10 2019
Historique:
received: 12 05 2019
accepted: 12 09 2019
entrez: 4 10 2019
pubmed: 4 10 2019
medline: 11 11 2020
Statut: epublish

Résumé

This study aimed to investigate the risks of thromboembolic vascular disease following androgen deprivation therapy (ADT) administered to prostate cancer (PCa) patients. A total of 24,464 men with newly diagnosed PCa during 2000-2008 were recruited through a longitudinal health insurance database in Taiwan. All PCa patients were stratified into two: ADT and non-ADT groups. Patients with ADT treatment were grouped into three: surgical castration, chemical castration, and anti-androgen alone. The risks of pulmonary embolism (PE), peripheral arterial occlusion disease (PAOD), and deep vein thrombosis (DVT) were assessed in multiple Cox proportional-hazards regression with time-dependent covariates. During the 12-year follow-up period, incidence rates per 1000 person-years in ADT and non-ADT groups were 2.87 and 1.62 for DVT, 1.00 and 0.52 for PE, and 1.03 and 0.70 for PAOD, respectively. The DVT and PE risks were significantly increased in patients receiving combined androgen blockade (CAB) compared with the counterpart ADT non-recipients. After adjusting for potential risk factors, PCa patients receiving CAB had the highest PE risk (HR = 3.11), followed by DVT risk (HR = 2.53). The DVT risk remained elevated throughout the entire duration of chemical castration. However, high PE risk was observed in patients with ≤720-day treatment duration. No association was found between ADT and PAOD risks. Overall, the risks of PE and DVT were considerably heightened in Asian men subjected to CAB for PCa, whereas PAOD risk was unrelated to such treatments.

Identifiants

pubmed: 31578427
doi: 10.1038/s41598-019-50522-4
pii: 10.1038/s41598-019-50522-4
pmc: PMC6775151
doi:

Substances chimiques

Androgen Antagonists 0
Androgens 0
Antineoplastic Agents, Hormonal 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

14231

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Auteurs

Yu-Chuan Lu (YC)

Institute of Biomedical Engineering, National Taiwan University, Taipei, Taiwan.
Department of Urology, National Taiwan University Hospital, Taipei, Taiwan.

Chao-Yuan Huang (CY)

Department of Urology, National Taiwan University Hospital, Taipei, Taiwan.

Huei-Ming Yeh (HM)

Department of Anesthesiology, National Taiwan University Hospital, Taipei, Taiwan.

Jian-Hua Hong (JH)

Institute of Biomedical Engineering, National Taiwan University, Taipei, Taiwan.
Department of Urology, National Taiwan University Hospital, Taipei, Taiwan.

Chao-Hsiang Chang (CH)

Department of Urology, China Medical University and Hospital, Taichung, Taiwan.
Department of Medicine, College of Medicine, China Medical University and Hospital, Taichung, Taiwan.

Chih-Hsin Muo (CH)

Management Office for Health Data, China Medical University and Hospital, Taichung, Taiwan.

Shiu-Dong Chung (SD)

Division of Urology, Department of Surgery, Far Eastern Memorial Hospital, New Taipei City, Taiwan.
Graduate Program in Biomedical Informatics, College of Informatics, Yuan-Ze University, Chung-Li, Taiwan.

Teng-Kai Yang (TK)

Surgery Department, Yonghe Cardinal Hospital, New Taipei City, Taiwan.

Fu-Shan Jaw (FS)

Institute of Biomedical Engineering, National Taiwan University, Taipei, Taiwan.

Chi-Jung Chung (CJ)

Department of Public Health, China Medical University, Taichung, Taiwan. cjchung1010@gmail.com.
Department of Medical Research, China Medical University Hospital, Taichung, Taiwan. cjchung1010@gmail.com.

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Classifications MeSH