# Association Between Time to PSA Nadir, Radiologic Progression, and PSA Progression in mHSPC Patients Treated with Abiraterone or Enzalutamide

**Authors:** Ugur Ozkerim, Oguzcan Kinikoglu, Deniz Isik, Yunus Emre Altintas, Seval Ay Ersoy, Heves Surmeli, Hatice Odabas, Tugba Basoglu, Nedim Turan

PMC · DOI: 10.3390/jcm15010386 · Journal of Clinical Medicine · 2026-01-05

## TL;DR

This study finds that a shorter time to lowest PSA levels in prostate cancer patients may predict better radiologic outcomes, but not biochemical ones.

## Contribution

The study evaluates TTN as a potential biomarker for early risk stratification in mHSPC patients treated with ARPIs.

## Key findings

- Shorter TTN was linked to longer radiologic progression-free survival.
- TTN was not independently predictive of PSA progression-free survival.
- Enzalutamide was associated with reduced risk of radiologic progression compared to abiraterone.

## Abstract

Background: Time to prostate-specific antigen (PSA) nadir (TTN) has been proposed as an early indicator of treatment responsiveness in metastatic hormone-sensitive prostate cancer (mHSPC). However, its prognostic relevance in patients treated with next-generation androgen receptor pathway inhibitors (ARPIs), such as abiraterone or enzalutamide, remains incompletely defined. Methods: This retrospective cohort study included 147 patients with mHSPC treated with abiraterone or enzalutamide between 2019 and 2024. TTN, PSA kinetics, radiologic progression-free survival (rPFS), and PSA progression-free survival (PSA-PFS) were analyzed using Kaplan–Meier methods and multivariable Cox regression. TTN was evaluated both as a continuous variable and dichotomized at the cohort median (≤9 vs. >9 months). Results: TTN distributions were comparable between treatment groups (median 9.0 vs. 6.0 months, p = 0.197). Patients with a shorter TTN (≤9 months) experienced significantly longer median rPFS compared with those with longer TTN (>9 months) (10.7 vs. 7.95 months; p = 0.036). No significant association was observed between TTN and PSA-PFS (9.3 vs. 10.75 months; p = 0.34). In multivariable analysis, enzalutamide was independently associated with a reduced risk of radiologic progression compared with abiraterone (HR 0.622; 95% CI 0.441–0.877), whereas TTN was not an independent predictor. Conclusions: A shorter TTN was associated with improved radiologic outcomes, suggesting that rapid PSA suppression may reflect more favorable disease biology in patients receiving ARPI therapy. Although TTN showed limited value in predicting biochemical progression, it may serve as a simple and accessible biomarker for early risk stratification and tailoring follow-up intensity in mHSPC. Validation in larger, multicenter cohorts is warranted.

## Linked entities

- **Chemicals:** abiraterone (PubChem CID 132971), enzalutamide (PubChem CID 15951529)
- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** AR (androgen receptor) [NCBI Gene 367] {aka AIS, AR8, DHTR, HPCX3, HUMARA, HYSP1}, KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}
- **Diseases:** metastatic (MESH:D000092182), hormone-sensitive prostate cancer (MESH:D011471)
- **Chemicals:** Enzalutamide (MESH:C540278), ARPI (-), Abiraterone (MESH:C089740)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12786526/full.md

## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12786526/full.md

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Source: https://tomesphere.com/paper/PMC12786526