Evidence map›Paper›PMID 41309998›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2026

Comparison of mCRPC [

Florian Rosar, Fadi Khreish, Caroline Burgard, Artyom Fursov, Arne Blickle, Mark Bartholomä, Stephan Maus, Moritz B Bastian, Tilman Speicher, Andrea Schaefer-Schuler and 1 more

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in European journal of nuclear medicine and molecular imaging, 2026. 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. Efficacy and outcomes of [European journal of nuclear medicine and molecular imaging · 2026
    Article
  2. Outcomes of [European journal of nuclear medicine and molecular imaging · 2026
    Article
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

11 authors.

Florian RosarDepartment of Nuclear Medicine, Saarland University - Medical Center, Homburg, Germany.
Fadi KhreishDepartment of Nuclear Medicine, Saarland University - Medical Center, Homburg, Germany.
Caroline BurgardDepartment of Nuclear Medicine, Saarland University - Medical Center, Homburg, Germany.
Artyom FursovDepartment of Nuclear Medicine, Saarland University - Medical Center, Homburg, Germany.
Arne BlickleDepartment of Nuclear Medicine, Saarland University - Medical Center, Homburg, Germany.
Mark BartholomäDepartment of Nuclear Medicine, Saarland University - Medical Center, Homburg, Germany.
Stephan MausDepartment of Nuclear Medicine, Saarland University - Medical Center, Homburg, Germany.
Moritz B BastianDepartment of Nuclear Medicine, Saarland University - Medical Center, Homburg, Germany.
Tilman SpeicherDepartment of Nuclear Medicine, Saarland University - Medical Center, Homburg, Germany.
Andrea Schaefer-SchulerDepartment of Nuclear Medicine, Saarland University - Medical Center, Homburg, Germany.
Samer EzziddinDepartment of Nuclear Medicine, Saarland University - Medical Center, Homburg, Germany. samer.ezziddin@uks.eu.ORCID 0000-0003-4110-3375

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeSeveral clinical and preclinical studies showed that ARPI medication such as enzalutamide increases the expression of PSMA in mCRPC patients and may potentially act as a sensitizer for PSMA RLT. In this study we aim to provide insight into the efficacy and safety profile of concurrent treatment with [

methodsIn total n = 63 mCRPC patients received [

resultsPatients treated with PSMA RLT in combination with enzalutamide achieved a significantly higher response rate (61.9% vs. 43.5%) and experienced a significantly longer PFS (6.1 months vs. 3.5 months). Statistically significant difference in OS between the groups was not reached (p = 0.097). The adverse event profiles between the treatment groups did not differ for renal toxicity, hematoxicities and xerostomia but a more frequent rate of low-grade fatigue in the enzalutamide group was observed. The combination of PSMA RLT and enzalutamide was both safe and overall well tolerated.

conclusionThe results suggest that concurrent medication of enzalutamide during PSMA RLT may enhance response and clinical outcomes, underscoring the potential of this specific combination as a promising approach in mCRPC. Future studies, ideally in prospective setting with larger patient cohorts are warranted.

Indexed as

DipeptidesHeterocyclic Compounds, 1-RingLutetiumPhenylthiohydantoinProstatic Neoplasms, Castration-ResistantAgedAged, 80 and overBenzamidesHumansMaleMiddle AgedNitrilesProstate-Specific AntigenRadioisotopesTreatment OutcomeBenzamidesDipeptidesenzalutamideHeterocyclic Compounds, 1-RingLutetiumLutetium-177NitrilesPhenylthiohydantoinProstate-Specific AntigenPSMA-617RadioisotopesEnzalutamidemCRPCProstate cancerPSMARadioligand therapyRadiosensitizerRLT

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.