Hypofractionated radiation therapy combined with androgen deprivation therapy for high‐risk localized prostate cancer

Introduction This study aimed to analyse the treatment outcomes of moderately hypofractionated radiation therapy (RT) combined with androgen deprivation therapy (ADT) and the prognostic implications of prostate‐specific antigen (PSA) kinetics in high‐risk localized prostate cancer. Methods The medic...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of medical imaging and radiation oncology 2024-04, Vol.68 (3), p.333-341
Hauptverfasser: Lee, Tae Hoon, Pyo, Hongryull, Yoo, Gyu Sang, Jeon, Seong Soo, Seo, Seong Il, Jeong, Byong Chang, Jeon, Hwang Gyun, Sung, Hyun Hwan, Kang, Minyong, Song, Wan, Chung, Jae Hoon, Bae, Bong Kyung, Park, Won
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Introduction This study aimed to analyse the treatment outcomes of moderately hypofractionated radiation therapy (RT) combined with androgen deprivation therapy (ADT) and the prognostic implications of prostate‐specific antigen (PSA) kinetics in high‐risk localized prostate cancer. Methods The medical records of 140 patients who underwent definitive RT (70 Gy in 28 fractions) combined with ADT were retrospectively reviewed. ADT consists of a gonadotropin‐releasing hormone agonist and an anti‐androgen. Clinical outcomes included the biochemical failure rate (BFR), clinical failure rate (CFR), overall survival (OS) and prostate cancer–specific survival (PCSS). The BFR and CFR were stratified by the PSA nadir and the time to the PSA nadir, respectively. Acute and late genitourinary and gastrointestinal adverse events were also recorded. Results The 5‐year BFR, CFR, OS and PCSS rates were 9.8%, 4.5%, 90.2% and 98.7%, respectively. Ninety‐five (67.9%) patients achieved a PSA nadir of 0.01 ng/mL. Patients with a PSA nadir >0.01 ng/mL had a significantly higher BFR and CFR (BFR, P = 0.001; CFR, P = 0.027), even after adjusting for other prognostic factors [per 0.1 ng/mL; BFR, hazard ratio (HR) 4.440, P 
ISSN:1754-9477
1754-9485
DOI:10.1111/1754-9485.13639