Efficacy and safety of abiraterone acetate plus prednisolone in patients with early metastatic castration-resistant prostate cancer who failed first-line androgen-deprivation therapy: a single-arm, phase 4 study.
Abiraterone Acetate
/ adverse effects
Aged
Aged, 80 and over
Androgens
/ deficiency
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Humans
Kaplan-Meier Estimate
Male
Middle Aged
Neoplasm Metastasis
Prednisolone
/ administration & dosage
Progression-Free Survival
Prostatic Neoplasms, Castration-Resistant
/ drug therapy
Treatment Outcome
abiraterone acetate; chemotherapy-naive metastatic castration-resistant prostate cancer
prednisolone
prostate-specific antigen
Journal
Japanese journal of clinical oncology
ISSN: 1465-3621
Titre abrégé: Jpn J Clin Oncol
Pays: England
ID NLM: 0313225
Informations de publication
Date de publication:
01 Apr 2021
01 Apr 2021
Historique:
received:
01
09
2020
accepted:
27
10
2020
pubmed:
17
12
2020
medline:
15
4
2021
entrez:
16
12
2020
Statut:
ppublish
Résumé
The aim was to evaluate the efficacy and safety of abiraterone acetate plus prednisolone in patients with chemotherapy-naïve early metastatic castration-resistant prostate cancer who failed first-line androgen deprivation therapy. Patients with early metastatic castration-resistant prostate cancer with confirmed prostate-specific antigen progression within 1-year or prostate-specific antigen progression without having normal prostate-specific antigen level (<4.0 ng/mL) during first-line androgen deprivation therapy were enrolled and administered abiraterone acetate (1000 mg) plus prednisolone (10 mg). A minimum of 48 patients were required according to Simon's minimax design. The primary endpoint was prostate-specific antigen response rate (≥50% prostate-specific antigen decline by 12 weeks), secondary endpoints included prostate-specific antigen progression-free survival and overall survival. Safety parameters were also assessed. For efficacy, 49/50 patients were evaluable. Median age was 73 (range: 55-86) years. The median duration of initial androgen deprivation therapy was 32.4 (range: 13.4-84.1) weeks and 48 patients experienced prostate-specific antigen progression within 1-year after initiation of androgen deprivation therapy. prostate-specific antigen response rate was 55.1% (95% confidence interval: 40.2%-69.3%), median prostate-specific antigen-progression-free survival was 24.1 weeks, and median overall survival was 102.9 weeks (95% confidence interval: 64.86 not estimable [NE]). Most common adverse event was nasopharyngitis (15/50 patients, 30.0%). The most common ≥grade 3 adverse event was alanine aminotransferase increased (6/50 patients, 12.0%). Abiraterone acetate plus prednisolone demonstrated a high prostate-specific antigen response rate of 55.1%, suggesting tumor growth still depends on androgen synthesis in patients with early metastatic castration-resistant prostate cancer. However, prostate-specific antigen-progression-free survival was shorter than that reported in previous studies. Considering the benefit-risk profile, abiraterone acetate plus prednisolone would be a beneficial treatment option for patients with chemotherapy-naive metastatic prostate cancer who show early castration resistance.
Identifiants
pubmed: 33324967
pii: 6035116
doi: 10.1093/jjco/hyaa225
pmc: PMC8012350
doi:
Substances chimiques
Androgens
0
Prednisolone
9PHQ9Y1OLM
Abiraterone Acetate
EM5OCB9YJ6
Types de publication
Clinical Trial, Phase IV
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
544-551Informations de copyright
© The Author(s) 2020. Published by Oxford University Press.
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