Abstract 1634P
Background
The EAU guidelines and the latest recommendations from the US Prostate Cancer Conference suggest a castration threshold of 20 ng/dl. However, the current NCCN and AUA guidelines still recommend a castration standard of 50 ng/dl. It remains unknown whether there is a relationship between maintaining lower testosterone levels and the prognosis of non-metastatic CRPC patients.
Methods
We conducted a retrospective analysis based on two phase III clinical trials (SPARTAN, ARAMIS). Patients received the currently recommended first-line treatment regimens (ADT+apalutamide or ADT+darolutamide) were classified into two groups according to their maintenance levels of serum testosterone during treatment: below 20 ng/dl and above 20 ng/dl. The study endpoint was MFS. IPTW method was employed to balance patients’ baseline characteristics. Kaplan-Meier analysis, multivariable Cox regression models, and Cox models that included testosterone levels as a time-dependent covariate were utilized to investigate the influence of maintenance levels of serum testosterone on disease progression.
Results
Baseline characteristics were well balanced between the low testosterone group and the high testosterone group after applying IPTW weights. Kaplan-Meier analysis revealed that serum testosterone maintenance levels were not associated with disease progression in either trial. In both multivariable Cox regression models and time-dependent Cox regression models, serum testosterone maintenance levels remained unrelated to disease progression, using below 20 ng/dl as the reference group (multivariable Cox: SPARTAN HR, 0.67 [95% CI, 0.44-0.99; P < 0.05], ARAMIS HR, 0.83 [95% CI, 0.57-1.23; P = 0.362]; time-dependent Cox: SPARTAN HR, 0.85 [95% CI, 0.60-1.21; P = 0.365], ARAMIS HR, 0.77 [95% CI, 0.58-1.17; P = 0.222]). The results obtained by setting testosterone levels as a continuous variable were similar.
Conclusions
Among men all with testosterone <50 ng/ml, maintenance serum testosterone levels were not associated with disease progression in the first-line management of nmCRPC with NHTs. The prognostic value of maintaining testosterone levels in patients with nmCRPC is limited.
Clinical trial identification
NCT01946204, NCT02200614.
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1687P - Perceptions of genetic testing and lived experiences in women with locally advanced or metastatic ovarian cancer: A focus on BRCAm and BRCAwt patients
Presenter: María Jesús Rubio Pérez
Session: Poster session 11
1688P - Psychosocial distress and spirituality among elderly patients with cancer in Nigeria
Presenter: Zainab Ogunjimi
Session: Poster session 11
1689TiP - The social stigma of smokers and patients with lung cancer: Detection of phoenomenon and testing of EMDR (eye movement desensitization and reprocessing) intervention
Presenter: Domenico Galetta
Session: Poster session 11
1692P - A phase Ib/IIa trial to evaluate the safety and efficacy of PM8002/ BNT327, a bispecific antibody targeting PD-L1 and VEGF-A, as a monotherapy in patients with advanced renal cell carcinoma
Presenter: Xinan Sheng
Session: Poster session 11
1693P - CaboPoint: Final results from a phase II study of cabozantinib after checkpoint inhibitor (CPI) combinations in patients with advanced renal cell carcinoma (aRCC)
Presenter: Laurence Albiges
Session: Poster session 11
1695P - Phase I LITESPARK-018: Dose escalation study of belzutifan in advanced pretreated clear cell renal cell carcinoma (ccRCC)
Presenter: Ulka Vaishampayan
Session: Poster session 11
1696P - A phase I/ II trial of pazopanib (Paz) alternating (alt) with bevacizumab (Bev) in treatment-naïve metastatic clear cell renal cell carcinoma (mccRCC) patients (pts): Phase II results
Presenter: Saby George
Session: Poster session 11
1697P - Phase II randomized double-blind trial of axitinib (Axi) +/- PF 04518600, an OX40 antibody (PFOX) after PD1/PDL1 antibody (IO) therapy (Tx) in metastatic renal cell carcinoma (mRCC): Final analysis
Presenter: Sarmad Sadeghi
Session: Poster session 11
1698P - Avelumab + axitinib (Ave + Axi) vs sunitinib (Sun) in advanced renal cell carcinoma (aRCC): Final analysis of patient (pt)-reported outcomes (PROs) and quality-adjusted time without symptoms or toxicity (Q-TWiST)
Presenter: Balaji Venugopal
Session: Poster session 11