# Expanding the scope of PSMA-RLT: evaluating treatment in challenging mCRPC patients with poor performance status (ECOG 3)

**Authors:** Moritz B. Bastian, Benedikt Wörl, Arne Blickle, Caroline Burgard, Tilman Speicher, Mark Bartholomä, Andrea Schaefer-Schuler, Stephan Maus, Samer Ezziddin, Florian Rosar

PMC · DOI: 10.1007/s00259-025-07346-4 · European Journal of Nuclear Medicine and Molecular Imaging · 2025-05-26

## TL;DR

This study shows that PSMA-targeted radioligand therapy is a feasible and well-tolerated treatment for advanced prostate cancer patients with poor performance status.

## Contribution

The study provides first insights into the safety and efficacy of PSMA-RLT in mCRPC patients with ECOG 3 status.

## Key findings

- Half of the patients achieved stable disease or partial biochemical response.
- Median overall survival was 2.8 months with manageable toxicity.
- Severe adverse events were rare and no major renal toxicity was observed.

## Abstract

Given the increasing inclusion of ECOG 3 patients in oncology practice, data on this subgroup in the context of prostate-specific membrane antigen (PSMA)-targeted radioligand therapy (RLT) remain limited. This study evaluates the safety and outcome of PSMA-RLT in metastatic castration-resistant prostate cancer (mCRPC) patients with ECOG performance status 3.

In this analysis, a cohort of 18 mCRPC patients with ECOG performance status 3 who received PSMA-RLT was examined. The median number of treatment cycles was 2 (range: 1–10), with a mean cumulative administered activity of 21.5 ± 15.0 GBq (range: 2.7–62.6 GBq) of [177Lu]Lu-PSMA-617. Outcome and adverse events including hematologic and renal toxicities, fatigue, and xerostomia were analyzed.

50% of patients achieved either stable disease or a partial biochemical response. Median progression-free survival and overall survival were 1.3 months and 2.8 months, respectively. Severe adverse events were uncommon, occurring in three patients: one developed grade 3 leukopenia, another experienced grade 3 thrombocytopenia, and one patient had pancytopenia of grade 3/4. No higher RLT-induced grade of renal toxicity and xerostomia were observed, whilst symptoms of fatigue improved in the cohort.

This study indicates that PSMA-RLT is a feasible and overall well-tolerated treatment for mCRPC ECOG 3 patients with manageable toxicity profile. Despite limited survival outcomes, ECOG 3 status may be considered not to be a categorical exclusion criterion for RLT. Future prospective studies should further investigate the role of PSMA-RLT in this challenging subgroup.

The online version contains supplementary material available at 10.1007/s00259-025-07346-4.

## Linked entities

- **Proteins:** FOLH1 (folate hydrolase 1)
- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** FOLH1 (folate hydrolase 1) [NCBI Gene 2346] {aka FGCP, FOLH, GCP2, GCPII, NAALAD1, PSM}
- **Diseases:** castration-resistant prostate cancer (MESH:D064129), toxicity (MESH:D064420), renal toxicity (MESH:D007674), leukopenia (MESH:D007970), fatigue (MESH:D005221), thrombocytopenia (MESH:D013921), pancytopenia (MESH:D010198), hematologic and renal toxicities (MESH:D006402), xerostomia (MESH:D014987)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12589352/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12589352/full.md

---
Source: https://tomesphere.com/paper/PMC12589352