Adverse metabolic consequences of androgen deprivation therapy (ADT) on Asian patients with prostate cancer: Primary results from the real-life experience of ADT in Asia (READT) study.


Journal

The Prostate
ISSN: 1097-0045
Titre abrégé: Prostate
Pays: United States
ID NLM: 8101368

Informations de publication

Date de publication:
06 2023
Historique:
revised: 10 02 2023
received: 25 10 2022
accepted: 02 03 2023
medline: 24 4 2023
pubmed: 21 3 2023
entrez: 20 3 2023
Statut: ppublish

Résumé

Androgen deprivation therapy (ADT) use in prostate cancer (PCa) has seen a rising trend. We investigated the relationship between ADT and adverse changes in metabolic parameters in an Asian population. This is an international prospective multicenter single-arm cohort yielded from the real-life experience of ADT in Asia (READT) registry. Consecutive ADT-naïve patients diagnosed of PCa and started on ADT were prospectively recruited from 2016 and analyzed. Baseline patient characteristics, PCa disease status, and metabolic parameters were documented. Patients were followed up at 6-month interval for up to 5 years. Metabolic parameters including body weight, lipid profiles, and glycemic profiles were recorded and analyzed. 589 patients were eligible for analysis. ADT was associated with adverse glycemic profiles, being notable at 6 months upon ADT initiation and persisted beyond 1 year. Comparing to baseline, fasting glucose level and hemoglobin A1c level increased by 4.8% (p < 0.001) and 2.7% (p < 0.001), respectively. Triglycerides level was also elevated by 16.1% at 6th month and by 20.6% at 12th month compared to baseline (p < 0.001). Mean body weight was 1.09 kg above baseline at 18th month (p < 0.001). ADT was associated with adverse metabolic parameters in terms of glycemic profiles, lipid profiles, and body weight in the Asian population. These changes developed early in the treatment and can persist beyond the first year. Regular monitoring of the biochemical profiles during treatment is paramount in safeguarding the patients' metabolic health.

Sections du résumé

BACKGROUND
Androgen deprivation therapy (ADT) use in prostate cancer (PCa) has seen a rising trend. We investigated the relationship between ADT and adverse changes in metabolic parameters in an Asian population.
METHODS
This is an international prospective multicenter single-arm cohort yielded from the real-life experience of ADT in Asia (READT) registry. Consecutive ADT-naïve patients diagnosed of PCa and started on ADT were prospectively recruited from 2016 and analyzed. Baseline patient characteristics, PCa disease status, and metabolic parameters were documented. Patients were followed up at 6-month interval for up to 5 years. Metabolic parameters including body weight, lipid profiles, and glycemic profiles were recorded and analyzed.
RESULTS
589 patients were eligible for analysis. ADT was associated with adverse glycemic profiles, being notable at 6 months upon ADT initiation and persisted beyond 1 year. Comparing to baseline, fasting glucose level and hemoglobin A1c level increased by 4.8% (p < 0.001) and 2.7% (p < 0.001), respectively. Triglycerides level was also elevated by 16.1% at 6th month and by 20.6% at 12th month compared to baseline (p < 0.001). Mean body weight was 1.09 kg above baseline at 18th month (p < 0.001).
CONCLUSION
ADT was associated with adverse metabolic parameters in terms of glycemic profiles, lipid profiles, and body weight in the Asian population. These changes developed early in the treatment and can persist beyond the first year. Regular monitoring of the biochemical profiles during treatment is paramount in safeguarding the patients' metabolic health.

Identifiants

pubmed: 36938957
doi: 10.1002/pros.24519
doi:

Substances chimiques

Androgens 0
Androgen Antagonists 0
Lipids 0

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

801-808

Informations de copyright

© 2023 The Authors. The Prostate published by Wiley Periodicals LLC.

Références

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Auteurs

Chris H M Wong (CHM)

Department of Surgery, SH Ho Urology Centre, The Chinese University of Hong Kong, Hong Kong, Hong Kong.
Department of Surgery, Division of Urology, Prince of Wales Hospital, Shatin, Hong Kong.

Ning Xu (N)

Department of Surgery, The First Affiliated Hospital, Fujian Medical University, Fuzhou, China.

Jasmine Lim (J)

Department of Surgery, Urology Unit, University of Malaya, Kuala Lumpur, Malaysia.

Kuo-Kang Feng (KK)

Department of Urology, Hsin-Chu BioMedical Park Hospital, National Taiwan University Hospital, Taipei, Taiwan.

Wayne K W Chan (WKW)

Department of Surgery, Division of Urology, Kwong Wah Hospital, Mongkok, Kowloon, Hong Kong.

Marco T Y Chan (MTY)

Department of Surgery, Division of Urology, Tuen Mun Hospital, Hong Kong, Hong Kong.

Steven Ch Leung (SC)

Department of Surgery, SH Ho Urology Centre, The Chinese University of Hong Kong, Hong Kong, Hong Kong.
Department of Surgery, Division of Urology, Prince of Wales Hospital, Shatin, Hong Kong.

Dong-Ning Chen (DN)

Department of Surgery, The First Affiliated Hospital, Fujian Medical University, Fuzhou, China.

Yun-Zhi Lin (YZ)

Department of Surgery, The First Affiliated Hospital, Fujian Medical University, Fuzhou, China.

Peter K F Chiu (PKF)

Department of Surgery, SH Ho Urology Centre, The Chinese University of Hong Kong, Hong Kong, Hong Kong.
Department of Surgery, Division of Urology, Prince of Wales Hospital, Shatin, Hong Kong.

Chi Hang Yee (CH)

Department of Surgery, SH Ho Urology Centre, The Chinese University of Hong Kong, Hong Kong, Hong Kong.
Department of Surgery, Division of Urology, Prince of Wales Hospital, Shatin, Hong Kong.

Jeremy Y C Teoh (JYC)

Department of Surgery, SH Ho Urology Centre, The Chinese University of Hong Kong, Hong Kong, Hong Kong.
Department of Surgery, Division of Urology, Prince of Wales Hospital, Shatin, Hong Kong.

Chiu-Yuen Huang (CY)

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

Wei-Sien Yeoh (WS)

Department of Surgery, Urology Unit, University of Malaya, Kuala Lumpur, Malaysia.

Teng-Aik Ong (TA)

Department of Surgery, Urology Unit, University of Malaya, Kuala Lumpur, Malaysia.

Yong Wei (Y)

Department of Surgery, The First Affiliated Hospital, Fujian Medical University, Fuzhou, China.

Chi-Fai Ng (CF)

Department of Surgery, SH Ho Urology Centre, The Chinese University of Hong Kong, Hong Kong, Hong Kong.
Department of Surgery, Division of Urology, Prince of Wales Hospital, Shatin, Hong Kong.

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