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.


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
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

544-551

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press.

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Auteurs

K Kobayashi (K)

Department of Urology, Federation of National Public Service Personnel Mutual Aid Associations Yokosuka Kyosai Hospital, Kanagawa, Japan.

N Okuno (N)

Department of Urology, Independent Administrative Institution National Hospital Organization Sagamihara Hospital, Kanagawa, Japan.

G Arai (G)

Department of Urology, Dokkyo Medical University Saitama Medical Center, Saitama, Japan.

H Nakatsu (H)

Department of Urology, Asahi General Hospital, Chiba, Japan.

A Maniwa (A)

Department of Urology, Independent Administrative Institution National Hospital Organization Shizuoka Medical Center, Shizuoka, Japan.

N Kamiya (N)

Department of Urology, Toho University Sakura Medical Center, Chiba, Japan.

T Satoh (T)

Department of Urology, Kitasato University School of Medicine, Kanagawa, Japan.

H Kikukawa (H)

Department of Urology, Independent Administrative Institution National Hospital Organization Kumamoto Medical Center, Kumamoto, Japan.

Y Nasu (Y)

Department of Urology, Japan Organization of Occupational Health and Safety Okayama Rosai Hospital, Okayama, Japan.

H Uemura (H)

Department of Urology and Renal Transplantation, Yokohama City University Medical Center, Kanagawa, Japan.

T Nakashima (T)

Department of Urology, Ishikawa Prefectural Central Hospital, Ishikawa, Japan.

K Mikami (K)

Department of Urology, Chibaken Saiseikai Narashino Hospital, Chiba, Japan.

M Iinuma (M)

Department of Urology, Independent Administrative Institution National Hospital Organization Mito Medical Center, Ibaraki, Japan.

K Tanabe (K)

Department of Urology, Tokyo Women's Medical University Hospital, Tokyo, Japan.

J Furukawa (J)

Department of Urology, National University Corporation Kobe University Hospital, Hyogo, Japan.

H Kobayashi (H)

Janssen Pharmaceutical K.K., Tokyo, Japan.

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