Phase II open-label study investigating apalutamide in patients with biochemical progression after radical prostatectomy

Apalutamide, a competent inhibitor of the androgen receptor, has shown promising clinical efficacy results for patients with advanced prostate cancer. Here, we describe the rationale and design for the SAVE trial, a multi-center, Phase II study, wherein 202 men with biochemical progression after radical prostatectomy are randomly assigned 1:1 to apalutamide plus salvage radiotherapy (SRT) or androgen-deprivation therapy with an luteinizing hormone-releasing hormone agonist or antagonist plus SRT. The primary objective is to compare sexual function between the two treatment arms based on the expanded prostate cancer index-26 sexual domain score at nine months after start of hormonal treatment. The key secondary objectives are to assess quality of life, to evaluate the safety profile and the short-term efficacy of apalutamide in combination with SRT. <b>ClinicalTrials.gov identifier:</b> NCT03899077.

Publication Details

Journal
Figshare
Published
2025-03-06
DOI
https://doi.org/10.6084/m9.figshare.28548350.v1
Primary Topic
Prostate Cancer Treatment and Research
Type
article
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0.00
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article

Phase II open-label study investigating apalutamide in patients with biochemical progression after radical prostatectomy

Figshare
Prostate Cancer Treatment and Research
article

Phase II open-label study investigating apalutamide in patients with biochemical progression after radical prostatectomy

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Abstract

Apalutamide, a competent inhibitor of the androgen receptor, has shown promising clinical efficacy results for patients with advanced prostate cancer. Here, we describe the rationale and design for the SAVE trial, a multi-center, Phase II study, wherein 202 men with biochemical progression after radical prostatectomy are randomly assigned 1:1 to apalutamide plus salvage radiotherapy (SRT) or androgen-deprivation therapy with an luteinizing hormone-releasing hormone agonist or antagonist plus SRT. The primary objective is to compare sexual function between the two treatment arms based on the expanded prostate cancer index-26 sexual domain score at nine months after start of hormonal treatment. The key secondary objectives are to assess quality of life, to evaluate the safety profile and the short-term efficacy of apalutamide in combination with SRT. <b>ClinicalTrials.gov identifier:</b> NCT03899077.

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Prostate Cancer Treatment and Research
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