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Post Hoc Analysis of Rapid and Deep Prostate-specific Antigen Decline and Patient-reported Health-related Quality of Life in SPARTAN and TITAN Patients with Advanced Prostate Cancer

Authors
 Eric J Small  ;  Kim N Chi  ;  Simon Chowdhury  ;  Katherine B Bevans  ;  Amitabha Bhaumik  ;  Fred Saad  ;  Byung Ha Chung  ;  Lawrence I Karsh  ;  Stéphane Oudard  ;  Peter De Porre  ;  Sabine D Brookman-May  ;  Sharon A McCarthy  ;  Suneel D Mundle  ;  Hirotsugu Uemura  ;  Matthew R Smith  ;  Neeraj Agarwal 
Citation
 EUROPEAN UROLOGY ONCOLOGY, Vol.7(4) : 844-852, 2024-08 
Journal Title
EUROPEAN UROLOGY ONCOLOGY
Issue Date
2024-08
MeSH
Aged ; Androgen Antagonists* / therapeutic use ; Disease Progression ; Humans ; Male ; Middle Aged ; Patient Reported Outcome Measures* ; Prostate-Specific Antigen* / blood ; Prostatic Neoplasms / blood ; Prostatic Neoplasms / drug therapy ; Prostatic Neoplasms / pathology ; Prostatic Neoplasms, Castration-Resistant / drug therapy ; Prostatic Neoplasms, Castration-Resistant / pathology ; Quality of Life* ; Thiohydantoins* / therapeutic use
Keywords
Apalutamide ; Metastatic castration-sensitive prostate cancer ; Nonmetastatic castration-resistant prostate cancer
Abstract
Background: Adding apalutamide to androgen-deprivation therapy (ADT) resulted in a rapid (at 3- and 6-mo treatment) and deep prostate-specific antigen (PSA) decline (to ≤0.2 ng/ml or ≥90% from baseline), improved overall survival, reduced risk of disease progression, and prolonged health-related quality of life (HRQoL) in nonmetastatic castration-resistant prostate cancer (nmCRPC) in SPARTAN and metastatic castration-sensitive PC (mCSPC) in TITAN.

Objective: To evaluate the association of a rapid, deep PSA decline at 3 and 6 mo achieved with the addition of apalutamide to ADT with patient-reported outcomes (PROs) in SPARTAN and TITAN.

Design, setting, and participants: A post hoc analysis of SPARTAN and TITAN PRO data was performed.

Intervention: Apalutamide versus placebo plus concurrent ADT.

Outcome measurements and statistical analysis: PROs were assessed using Functional Assessment of Cancer Therapy-Prostate (FACT-P; SPARTAN and TITAN), Brief Pain Inventory-Short Form (BPI-SF; TITAN), and Brief Fatigue Inventory (BFI; TITAN) at baseline, prespecified cycles during treatment, and after progression for ≤1 yr. The association between a deep PSA decline at landmark 3 or 6 mo of apalutamide and the time to worsening of PROs was assessed using the Kaplan-Meier methodology and Cox proportional-hazard modeling.

Results and limitations: Among 806 SPARTAN and 525 TITAN apalutamide-treated patients, the median treatment duration was 32.9 and 39.3 mo, respectively. Patients achieving a deep PSA decline at 3 mo had longer time to worsening in FACT-P total, FACT-P physical well-being, BPI-SF worst pain intensity, or BFI worst fatigue intensity. The 6-mo PSA decline results were similar. Limitations of patient characteristics in clinical studies should be considered.

Conclusions: Attaining a deep and rapid PSA decline at 3 mo with apalutamide plus ADT was associated with longer preservation of overall HRQoL and physical well-being in nmCRPC and mCSPC.

Patient summary: Quality of life is maintained in individuals with advanced prostate cancer who achieve a deep prostate-specific antigen decline at 3 mo of apalutamide plus drugs that lower male sex hormones.
Full Text
https://www.sciencedirect.com/science/article/pii/S2588931123002808
DOI
10.1016/j.euo.2023.11.015
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Urology (비뇨의학교실) > 1. Journal Papers
Yonsei Authors
Chung, Byung Ha(정병하) ORCID logo https://orcid.org/0000-0001-9817-3660
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/202158
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