Evidence map›Paper›PMID 40418331›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2025

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

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

Abstract read
In one paragraph

Article in European journal of nuclear medicine and molecular imaging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Frailty and [Theranostics · 2026
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Moritz B BastianDepartment of Nuclear Medicine, Saarland University, Kirrberger Str., Geb. 50, D-66421, Homburg, Germany. moritz.bastian@uks.eu.ORCID 0009-0008-2106-9548
Benedikt WörlDepartment of Nuclear Medicine, Saarland University, Kirrberger Str., Geb. 50, D-66421, Homburg, Germany.
Arne BlickleDepartment of Nuclear Medicine, Saarland University, Kirrberger Str., Geb. 50, D-66421, Homburg, Germany.
Caroline BurgardDepartment of Nuclear Medicine, Saarland University, Kirrberger Str., Geb. 50, D-66421, Homburg, Germany.
Tilman SpeicherDepartment of Nuclear Medicine, Saarland University, Kirrberger Str., Geb. 50, D-66421, Homburg, Germany.
Mark BartholomäDepartment of Nuclear Medicine, Saarland University, Kirrberger Str., Geb. 50, D-66421, Homburg, Germany.
Andrea Schaefer-SchulerDepartment of Nuclear Medicine, Saarland University, Kirrberger Str., Geb. 50, D-66421, Homburg, Germany.
Stephan MausDepartment of Nuclear Medicine, Saarland University, Kirrberger Str., Geb. 50, D-66421, Homburg, Germany.
Samer EzziddinDepartment of Nuclear Medicine, Saarland University, Kirrberger Str., Geb. 50, D-66421, Homburg, Germany.
Florian RosarDepartment of Nuclear Medicine, Saarland University, Kirrberger Str., Geb. 50, D-66421, Homburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeGiven 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.

methodsIn 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 [

results50% 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.

conclusionThis 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.

Indexed as

Antigens, SurfaceDipeptidesGlutamate Carboxypeptidase IIHeterocyclic Compounds, 1-RingProstatic Neoplasms, Castration-ResistantAgedAged, 80 and overHumansMaleMiddle AgedProstate-Specific AntigenTreatment OutcomeAntigens, SurfaceDipeptidesFOLH1 protein, humanGlutamate Carboxypeptidase IIHeterocyclic Compounds, 1-RingProstate-Specific AntigenPSMA-617ECOG 3EffectiveMCRPCPSMA radioligand therapyRLTSafety

Identifiers

PMID40418331
PMCPMC12589352

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.