Association of SGLT2 Inhibitor Initiation and PSA Response in Prostate Cancer

被引:0
作者
Aber, Etan R. [1 ]
Carducci, Michael A. [2 ]
Paller, Channing J. [2 ]
Denmeade, Sam R. [2 ]
Rourke, Kelli [2 ]
Marshall, Catherine H. [2 ]
Markowski, Mark C. [2 ]
机构
[1] NCI, Genitourinary Malignancies Branch, NIH, Bethesda, MD USA
[2] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr, Dept Oncol, Baltimore, MD 21218 USA
关键词
biochemical recurrence; prostate cancer; SGLT2; inhibitor; GROWTH;
D O I
10.1002/pros.24841
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionNon-castrating therapies are an unmet clinical need for patients with advanced prostate cancer. To maximize quality of life and prioritize cardiovascular health, we investigated SGLT2 inhibitors as a non-castrating therapy in patients with prostate cancer.Materials and MethodsWe conducted a retrospective analysis of patients with either local or biochemically recurrent prostate cancer who initiated therapy with an SGLT2 inhibitor without concurrent androgen deprivation therapy. The primary endpoint was an estimated PSA50 response rate. A secondary endpoint was PSA any response rate.ResultsA total of nine patients (median age 63 years old; 44.4% Black; median PSA 3.7; 33.3% localized, 66.7% biochemically recurrent) were included. The PSA50 and PSAany response rate were 22.2% (N = 2/9) and 44.4% (N = 4/9), respectively.ConclusionsPatients with localized or biochemically recurrent prostate cancer achieved PSA responses to SGLT2 inhibitors. These findings justify prospective studies in patients with prostate cancer.
引用
收藏
页码:391 / 394
页数:4
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