Absolute Prostate Specific Antigen after 6 Months of Androgen Deprivation Therapy Is a Predictor of Overall and Cancer-Specific Mortality in Men with Hormone-Sensitive Prostate Cancer.


Journal

The Journal of urology
ISSN: 1527-3792
Titre abrégé: J Urol
Pays: United States
ID NLM: 0376374

Informations de publication

Date de publication:
08 2022
Historique:
pubmed: 29 3 2022
medline: 16 7 2022
entrez: 28 3 2022
Statut: ppublish

Résumé

We sought to determine if absolute prostate specific antigen (PSA) value after 6 months of androgen deprivation therapy (ADT) is predictive of subsequent survival in patients with prostate adenocarcinoma. We performed a retrospective review of men receiving care within the Veterans Health Administration who initiated ADT for prostate adenocarcinoma. We used low- (≤0.2 ng/ml), intermediate- (>0.2 to 4 ng/ml) and high-risk (>4 ng/ml) absolute PSA values after 6-9 months of ADT, previously described in Southwest Oncology Group trial 9346. The primary endpoints were all-cause mortality and prostate cancer-specific mortality (PCSM). Kaplan-Meier survival curves for each PSA category were estimated and log-rank test was conducted. We employed Cox regression analysis adjusted for covariates and inverse propensity score weights associated with PSA categories to estimate the PSA category association with PCSM and all-cause mortality. We identified 9,170 patients in our cohort. Following ADT induction, 3,508 patients had low, 3,419 had intermediate and 2,243 had high PSA values. Two- and 5-year survival rates for low, intermediate and high PSA groups were 93.9% and 85.2% vs 88.6% and 71.2% vs 63.6% and 38.6%, respectively (p <0.0001). Patients in the high and intermediate PSA categories had a 15-fold and 3-fold higher risk of PCSM compared to those with PSA <0.2 ng/ml (p <0.0001). Absolute PSA in hormone-sensitive prostate cancer after 6-9 months of ADT is a predictor of overall mortality and PCSM. This measure can rapidly assess the efficacy of new interventions in phase 2 clinical trials.

Identifiants

pubmed: 35343252
doi: 10.1097/JU.0000000000002676
doi:

Substances chimiques

Androgen Antagonists 0
Androgens 0
Prostate-Specific Antigen EC 3.4.21.77

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

317-324

Commentaires et corrections

Type : CommentIn

Auteurs

Furkan Dursun (F)

Department of Urology, University of Texas Health San Antonio, San Antonio, Texas.
UT Health San Antonio/MD Anderson Mays Cancer Center, San Antonio, Texas.

Chen-Pin Wang (CP)

South Texas Veterans Health Care System, San Antonio, Texas.

Daniel MacCarthy (D)

South Texas Veterans Health Care System, San Antonio, Texas.

Ahmed M Mansour (AM)

Department of Urology, University of Texas Health San Antonio, San Antonio, Texas.
UT Health San Antonio/MD Anderson Mays Cancer Center, San Antonio, Texas.

Deepak K Pruthi (DK)

Department of Urology, University of Texas Health San Antonio, San Antonio, Texas.
UT Health San Antonio/MD Anderson Mays Cancer Center, San Antonio, Texas.

Dharam Kaushik (D)

Department of Urology, University of Texas Health San Antonio, San Antonio, Texas.
UT Health San Antonio/MD Anderson Mays Cancer Center, San Antonio, Texas.

Ian M Thompson (IM)

CHRISTUS Santa Rosa Health System, San Antonio, Texas.

Michael A Liss (MA)

Department of Urology, University of Texas Health San Antonio, San Antonio, Texas.
UT Health San Antonio/MD Anderson Mays Cancer Center, San Antonio, Texas.

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Classifications MeSH