# Decision regret after reirradiation of the primary site in patients with prostate cancer

**Authors:** Alexander Fabian, Bilgesu Sahin Öztürk, Lars Haack, Severin Rodler, Christof van der Horst, Christian Schulz, Claudia Schmalz, Stefan Huttenlocher, Olaf Wittenstein, Oliver Blanck, Frank-André Siebert, David Krug

PMC · DOI: 10.1016/j.ctro.2025.101019 · Clinical and Translational Radiation Oncology · 2025-07-19

## TL;DR

Most prostate cancer patients who underwent reirradiation for local relapse experienced no or mild decision regret, with factors like symptoms and shared decision-making linked to regret levels.

## Contribution

This study explores decision regret in prostate cancer patients after reirradiation and identifies patient-reported outcomes associated with regret.

## Key findings

- Most patients had no or mild decision regret after reirradiation.
- Decision regret was associated with urinary symptoms, toxicity, shared decision-making, and satisfaction.
- Treatment type (HDR-BT vs. SBRT) was not linked to decision regret.

## Abstract

•The optimal local treatment strategy for radiorecurrent prostate cancer is unknown.•We analyzed decision regret among 31 patients after reirradiation via HDR-BT or SBRT.•Most patients had either no or mild levels of decision regret.•PRO on symptoms, toxicity, SDM and satisfaction were associated with regret.

The optimal local treatment strategy for radiorecurrent prostate cancer is unknown.

We analyzed decision regret among 31 patients after reirradiation via HDR-BT or SBRT.

Most patients had either no or mild levels of decision regret.

PRO on symptoms, toxicity, SDM and satisfaction were associated with regret.

A subset of prostate cancer patients develops local relapse at the primary site after radiotherapy. The optimal local salvage strategy is unknown. Therefore, we aimed to explore prevalence and determinants of decision regret among patients after reirradiation of the primary site.

We surveyed 31 patients in a cross-sectional bi-centre exploratory study. Reirradiation was high dose-rate brachytherapy (HDR-BT) in 21 and stereotactic body radiotherapy (SBRT) in 10 patients. Decision regret (DR) was measured using the Decision Regret Scale (DRS) (range: 0–100; higher values higher regret). Further patient-reported outcomes (PRO) included the EPIC-26, EORTC QLQ-C30, PRO-CTCAE, and PSCC questionnaires. Univariable associations of decision regret and potential determinants were assessed by one-way ANOVA or Pearson’s correlation.

Median age at reirradiation was 75 years. Median time intervals from initial radiotherapy to reirradiation was 8 years and 4 years from reirradiation to survey. The mean DRS score was 10 (SD: 14). No (0 points), mild (1–25 points), or strong regret (>25 points) was reported by 45 % (14/31), 48 % (15/31), and 7 % (2/31) of the patients, respectively. DR was significantly associated with PRO of urinary symptom burden and toxicity as well as levels of shared-decision making and patient satisfaction. HDR-BT vs. SBRT, further local relapse, and progression-free survival were not associated with DR.

DR was mild among prostate cancer patients after reirradiation to the primary site. PRO on symptom burden and shared decision making may be associated with DR. These findings should be validated and may inform treatment decisions on local salvage therapy.

## Linked entities

- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** NPEPPS (aminopeptidase puromycin sensitive) [NCBI Gene 9520] {aka AAP-S, MP100, PSA}, FOLH1 (folate hydrolase 1) [NCBI Gene 2346] {aka FGCP, FOLH, GCP2, GCPII, NAALAD1, PSM}
- **Diseases:** diarrhoea (MESH:D003967), urinary irritative (MESH:D001523), Comorbidity (MESH:D004194), death (MESH:D003643), pain (MESH:D010146), Androgen deprivation (MESH:D014770), abdominal pain (MESH:D015746), genitourinary toxicity (MESH:D000091642), infection (MESH:D007239), Cancer (MESH:D009369), Prostate Cancer (MESH:D011471), urinary symptom (MESH:D059411), Toxicity (MESH:D064420), faecal incontinence (MESH:D014549), DR (MESH:D020195)
- **Chemicals:** Ir-192 (MESH:C000615087), ADT (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12320099/full.md

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Source: https://tomesphere.com/paper/PMC12320099