Androgen deprivation therapy and acute kidney injury in patients with prostate cancer undergoing definitive radiotherapy.


Journal

Prostate cancer and prostatic diseases
ISSN: 1476-5608
Titre abrégé: Prostate Cancer Prostatic Dis
Pays: England
ID NLM: 9815755

Informations de publication

Date de publication:
06 2023
Historique:
received: 12 02 2021
accepted: 22 06 2021
revised: 12 06 2021
medline: 9 6 2023
pubmed: 24 11 2021
entrez: 23 11 2021
Statut: ppublish

Résumé

Androgen deprivation therapy (ADT) is frequently utilized in conjunction with radiotherapy (RT) in the definitive management of prostate cancer. Prior studies have suggested an association between ADT use and acute kidney injury (AKI), however, these included heterogeneous populations undergoing a variety of treatments and relied on billing codes to ascertain the incidence of AKI. We analyzed a cohort of 27,868 veterans undergoing definitive RT + /- ADT for prostate cancer between 2001 and 2015 using the Veterans Affairs Informatics and Computing Infrastructure (VINCI). Exposure was defined as use of ADT within one year of diagnosis. The primary outcome was AKI, defined by an increase in serum creatinine to at least 1.5 times the baseline value. AKIs were classified as mild, moderate, or severe in accordance with international guidelines. A multivariate competing risks model was used to account for demographic and oncologic factors as well as medications and procedures known to influence the risk of AKI. Most (n = 18,754) men received RT alone; 9,114 men received RT + ADT. The incidence of AKI at two years after diagnosis was 10.5% in the RT + ADT group and 7.9% in the RT group (Gray's test p < 0.01). Multivariate analysis confirmed ADT usage was associated with an increased risk for any AKI (SHR = 1.24, 95% CI = 1.14-1.36, p < 0.01). ADT was also associated with an increased risk of mild AKI (SHR = 1.13, 95% CI = 1.01-1.27, p = 0.04) and moderate AKI (SHR = 1.45, 95% CI = 1.20-1.76, p < 0.01), though not severe AKI (SHR = 1.33, 95% CI = 0.93-1.91, p = 0.11). Our findings confirm that use of ADT is associated with an increased risk of AKI in patients undergoing definitive RT for prostate cancer. Clinicians should be alert to the potential for renal dysfunction in this population.

Sections du résumé

BACKGROUND
Androgen deprivation therapy (ADT) is frequently utilized in conjunction with radiotherapy (RT) in the definitive management of prostate cancer. Prior studies have suggested an association between ADT use and acute kidney injury (AKI), however, these included heterogeneous populations undergoing a variety of treatments and relied on billing codes to ascertain the incidence of AKI.
METHODS
We analyzed a cohort of 27,868 veterans undergoing definitive RT + /- ADT for prostate cancer between 2001 and 2015 using the Veterans Affairs Informatics and Computing Infrastructure (VINCI). Exposure was defined as use of ADT within one year of diagnosis. The primary outcome was AKI, defined by an increase in serum creatinine to at least 1.5 times the baseline value. AKIs were classified as mild, moderate, or severe in accordance with international guidelines. A multivariate competing risks model was used to account for demographic and oncologic factors as well as medications and procedures known to influence the risk of AKI.
RESULTS
Most (n = 18,754) men received RT alone; 9,114 men received RT + ADT. The incidence of AKI at two years after diagnosis was 10.5% in the RT + ADT group and 7.9% in the RT group (Gray's test p < 0.01). Multivariate analysis confirmed ADT usage was associated with an increased risk for any AKI (SHR = 1.24, 95% CI = 1.14-1.36, p < 0.01). ADT was also associated with an increased risk of mild AKI (SHR = 1.13, 95% CI = 1.01-1.27, p = 0.04) and moderate AKI (SHR = 1.45, 95% CI = 1.20-1.76, p < 0.01), though not severe AKI (SHR = 1.33, 95% CI = 0.93-1.91, p = 0.11).
CONCLUSIONS
Our findings confirm that use of ADT is associated with an increased risk of AKI in patients undergoing definitive RT for prostate cancer. Clinicians should be alert to the potential for renal dysfunction in this population.

Identifiants

pubmed: 34811501
doi: 10.1038/s41391-021-00415-3
pii: 10.1038/s41391-021-00415-3
doi:

Substances chimiques

Androgen Antagonists 0
Androgens 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

276-281

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer Nature Limited.

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Auteurs

Michael V Sherer (MV)

Department of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, CA, USA.
VA San Diego Health Care System, La Jolla, CA, USA.

Rishi Deka (R)

Department of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, CA, USA.
VA San Diego Health Care System, La Jolla, CA, USA.

Mia A Salans (MA)

Department of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, CA, USA.
VA San Diego Health Care System, La Jolla, CA, USA.

Tyler J Nelson (TJ)

Department of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, CA, USA.
VA San Diego Health Care System, La Jolla, CA, USA.

Paige Sheridan (P)

Department of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, CA, USA.
VA San Diego Health Care System, La Jolla, CA, USA.

Brent S Rose (BS)

Department of Radiation Medicine and Applied Sciences, University of California San Diego, La Jolla, CA, USA. bsrose@health.ucsd.edu.
VA San Diego Health Care System, La Jolla, CA, USA. bsrose@health.ucsd.edu.

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