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Younger Age Is Associated With Slower PSA Decline After Low-Dose-Rate Brachytherapy for Localized Prostate Cancer.

Created on 08 Oct 2026

Authors

Yasushi Nakai, Kenta Onishi, Makito Miyake, Kaori Yamaki, Fumiaki Isohashi, Isao Asakawa, Nobumichi Tanaka

Published in

International journal of urology : official journal of the Japanese Urological Association. Volume 33. Issue 10. Pages e70653.

Abstract

To evaluate the association of age with PSA kinetics and biochemical control after low-dose-rate brachytherapy (LDR-BT).
We retrospectively analyzed 347 patients treated with LDR-BT alone without androgen deprivation therapy between 2004 and 2015. Longitudinal PSA changes were evaluated using linear mixed-effects models with natural cubic splines for time. Age was modeled as a continuous fixed effect, including interactions with the spline terms for time. Time to PSA nadir < 0.2 ng/mL was evaluated using Cox proportional hazards models, whereas biochemical recurrence was evaluated using Fine-Gray competing-risk regression with death treated as a competing event.
Younger age was significantly associated with slower PSA decline over 5 years (p < 0.001). Each 1-year increase in age was associated with model-estimated PSA levels relative to baseline that were 4.6%, 6.4%, and 4.3% lower at 1, 3, and 5 years, respectively. This association remained significant after adjustment for Gleason grade group and treatment era and after excluding patients with PSA bounce (both p < 0.001). Median time to PSA nadir < 0.2 ng/mL was 54 months in patients aged < 65 years and 36 months in those aged ≥ 75 years. Increasing age was associated with earlier achievement of PSA nadir < 0.2 ng/mL (HR 1.04 per year, 95% CI 1.02-1.06) but was not significantly associated with biochemical recurrence.
Age was significantly associated with PSA kinetics following LDR-BT, with younger patients showing slower PSA decline and a delayed achievement of PSA nadir < 0.2 ng/mL. However, these age-related differences were not associated with biochemical recurrence.

PMID:
42844157
Bibliographic data and abstract were imported from PubMed on 08 Oct 2026.

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