Updated 5-year results for short course abiraterone acetate and LHRH agonist for unfavorable intermediate and favorable high-risk prostate cancer.


Journal

Prostate cancer and prostatic diseases
ISSN: 1476-5608
Titre abrégé: Prostate Cancer Prostatic Dis
Pays: England
ID NLM: 9815755

Informations de publication

Date de publication:
22 Feb 2024
Historique:
received: 01 02 2024
accepted: 13 02 2024
revised: 06 02 2024
medline: 23 2 2024
pubmed: 23 2 2024
entrez: 22 2 2024
Statut: aheadofprint

Résumé

Combined androgen deprivation therapy (ADT) and radiotherapy (RT) improves outcomes for intermediate and high-risk prostate cancer. Treatment intensification with abiraterone acetate/prednisone (AAP) provides additional benefit for high-risk disease. We previously reported 3-year outcomes of a single-arm prospective multicenter trial (AbiRT trial) of 33 patients with unfavorable intermediate risk (UIR) and favorable high risk (FHR) prostate cancer undergoing short course, combination therapy with ADT, AAP, and RT. Here we report the final analysis demonstrating a high rate of testosterone recovery (97%) and excellent biochemical progression-free survival (97%) at 5 years. These data support comparative prospective studies of shorter, more potent ADT courses in favorable high-risk prostate cancer.

Identifiants

pubmed: 38388778
doi: 10.1038/s41391-024-00811-5
pii: 10.1038/s41391-024-00811-5
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : U.S. Department of Defense (United States Department of Defense)
ID : W81XWH-09-1-0152
Organisme : U.S. Department of Defense (United States Department of Defense)
ID : W81XWH-14-2-0198

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer Nature Limited.

Références

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Auteurs

Ryan E Fecteau (RE)

Department of Radiation Oncology, Duke University, Durham, NC, USA.
Duke Cancer Institute, Duke University School of Medicine, Durham, NC, USA.

Bridget F Koontz (BF)

East Carolina University Brody School of Medicine, Greenville, NC, USA.

Karen E Hoffman (KE)

Department of Genitourinary Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Susan Halabi (S)

Duke Cancer Institute, Duke University School of Medicine, Durham, NC, USA.

Lauren E Howard (LE)

Duke Cancer Institute, Duke University School of Medicine, Durham, NC, USA.

Monika Anand (M)

Duke Cancer Institute, Duke University School of Medicine, Durham, NC, USA.

Daniel J George (DJ)

Duke Cancer Institute, Duke University School of Medicine, Durham, NC, USA.
Department of Medicine, Division of Medical Oncology, Duke University, Durham, NC, USA.

Tian Zhang (T)

Department of Internal Medicine, Division of Hematology/Oncology, UT Southwestern Medical Center, Dallas, TX, USA.

William R Berry (WR)

Duke Cancer Institute, Duke University School of Medicine, Durham, NC, USA.
Department of Medicine, Division of Medical Oncology, Duke University, Durham, NC, USA.

W Robert Lee (WR)

Department of Radiation Oncology, Duke University, Durham, NC, USA.

Michael R Harrison (MR)

Duke Cancer Institute, Duke University School of Medicine, Durham, NC, USA.
Department of Medicine, Division of Medical Oncology, Duke University, Durham, NC, USA.

Paul G Corn (PG)

Department of Genitourinary Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Andrew J Armstrong (AJ)

Duke Cancer Institute, Duke University School of Medicine, Durham, NC, USA. andrew.armstrong@duke.edu.
Department of Medicine, Division of Medical Oncology, Duke University, Durham, NC, USA. andrew.armstrong@duke.edu.

Classifications MeSH