Abiraterone acetate plus prednisolone for metastatic patients starting hormone therapy: 5-year follow-up results from the STAMPEDE randomised trial (NCT00268476).
Abiraterone Acetate
/ therapeutic use
Aged
Androgen Antagonists
/ therapeutic use
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Follow-Up Studies
Hormones
Humans
Male
Prednisolone
/ therapeutic use
Prednisone
/ therapeutic use
Prostatic Neoplasms
/ pathology
Prostatic Neoplasms, Castration-Resistant
/ drug therapy
Retrospective Studies
Treatment Outcome
abiraterone
clinical trial
hormone therapy
phase III
prostate cancer
randomised controlled trial
survival
Journal
International journal of cancer
ISSN: 1097-0215
Titre abrégé: Int J Cancer
Pays: United States
ID NLM: 0042124
Informations de publication
Date de publication:
01 08 2022
01 08 2022
Historique:
revised:
15
02
2022
received:
10
12
2021
accepted:
22
02
2022
pubmed:
13
4
2022
medline:
9
6
2022
entrez:
12
4
2022
Statut:
ppublish
Résumé
Abiraterone acetate plus prednisolone (AAP) previously demonstrated improved survival in STAMPEDE, a multiarm, multistage platform trial in men starting long-term hormone therapy for prostate cancer. This long-term analysis in metastatic patients was planned for 3 years after the first results. Standard-of-care (SOC) was androgen deprivation therapy. The comparison randomised patients 1:1 to SOC-alone with or without daily abiraterone acetate 1000 mg + prednisolone 5 mg (SOC + AAP), continued until disease progression. The primary outcome measure was overall survival. Metastatic disease risk group was classified retrospectively using baseline CT and bone scans by central radiological review and pathology reports. Analyses used Cox proportional hazards and flexible parametric models, accounting for baseline stratification factors. One thousand and three patients were contemporaneously randomised (November 2011 to January 2014): median age 67 years; 94% newly-diagnosed; metastatic disease risk group: 48% high, 44% low, 8% unassessable; median PSA 97 ng/mL. At 6.1 years median follow-up, 329 SOC-alone deaths (118 low-risk, 178 high-risk) and 244 SOC + AAP deaths (75 low-risk, 145 high-risk) were reported. Adjusted HR = 0.60 (95% CI: 0.50-0.71; P = 0.31 × 10
Identifiants
pubmed: 35411939
doi: 10.1002/ijc.34018
pmc: PMC9321995
doi:
Substances chimiques
Androgen Antagonists
0
Hormones
0
Prednisolone
9PHQ9Y1OLM
Abiraterone Acetate
EM5OCB9YJ6
Prednisone
VB0R961HZT
Types de publication
Journal Article
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
422-434Subventions
Organisme : Cancer Research UK
ID : 12518
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12023/25
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_00004/01
Pays : United Kingdom
Organisme : Cancer Research UK
ID : CRUK_A12459
Pays : United Kingdom
Commentaires et corrections
Type : CommentIn
Informations de copyright
© 2022 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC.
Références
Int J Cancer. 2022 Aug 1;151(3):422-434
pubmed: 35411939
Eur Urol. 2019 Dec;76(6):719-728
pubmed: 31447077
N Engl J Med. 2019 Jul 4;381(1):13-24
pubmed: 31150574
Ann Oncol. 2018 May 1;29(5):1235-1248
pubmed: 29529169
Lancet Oncol. 2019 May;20(5):686-700
pubmed: 30987939
Ann Oncol. 2019 Dec 1;30(12):1992-2003
pubmed: 31560068
Lancet. 2018 Dec 1;392(10162):2353-2366
pubmed: 30355464
N Engl J Med. 2015 Aug 20;373(8):737-46
pubmed: 26244877
Lancet. 2016 Mar 19;387(10024):1163-77
pubmed: 26719232
N Engl J Med. 2017 Jul 27;377(4):352-360
pubmed: 28578607
BMJ Open. 2019 Sep 30;9(9):e030215
pubmed: 31575572
N Engl J Med. 2019 Jul 11;381(2):121-131
pubmed: 31157964
J Clin Oncol. 2021 Jul 10;39(20):2294-2303
pubmed: 33914595
Lancet. 2022 Jan 29;399(10323):447-460
pubmed: 34953525
J Clin Oncol. 2019 Nov 10;37(32):2974-2986
pubmed: 31329516
J Clin Oncol. 2022 Mar 10;40(8):825-836
pubmed: 34757812
N Engl J Med. 2017 Jul 27;377(4):338-351
pubmed: 28578639