Evidence map›Paper›PMID 39402311›Full record

ArticleEJNMMI research2024

Matched-pair analysis of mCRPC patients receiving

Amir Karimzadeh, Charlotte-Sophie Hecker, Matthias M Heck, Robert Tauber, Calogero D'Alessandria, Wolfgang A Weber, Matthias Eiber, Isabel Rauscher

Abstract read
In one paragraph

Article in EJNMMI research, 2024. 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. Overall Survival with [Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
    Article
  2. Radioligand treatment with [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

8 authors.

Amir Karimzadeh *Department of Nuclear Medicine, School of Medicine, Technical University of Munich, Munich, Germany. amir.karimzadeh@uke.de.
Charlotte-Sophie Hecker *Department of Nuclear Medicine, School of Medicine, Technical University of Munich, Munich, Germany.
Matthias M HeckDepartment of Urology, School of Medicine, Technical University of Munich, Munich, Germany.
Robert TauberDepartment of Urology, School of Medicine, Technical University of Munich, Munich, Germany.
Calogero D'AlessandriaDepartment of Nuclear Medicine, School of Medicine, Technical University of Munich, Munich, Germany.
Wolfgang A WeberDepartment of Nuclear Medicine, School of Medicine, Technical University of Munich, Munich, Germany.
Matthias Eiber *Department of Nuclear Medicine, School of Medicine, Technical University of Munich, Munich, Germany.
Isabel Rauscher *Department of Nuclear Medicine, School of Medicine, Technical University of Munich, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe optimal regimen for

resultsA PSA response (PSA decline ≥ 50%) was achieved in 47.8% and 21.7% of patients in the 4-week and 6-week treatment interval groups, respectively (p = 0.12). There was a trend towards longer PSA-PFS in the 4-week group compared to the 6-week group (median PSA-PFS, 26.0 weeks vs. 18.0 weeks; HR 0.6; p = 0.2). Although not statistically significant, there was a trend towards shorter OS in the 4-week group compared to the 6-week group (median OS, 15.1 months vs. 18.4 months; HR 1.3; p = 0.5). The 4-week group had a significantly greater decrease in leucocyte and platelet counts compared to the 6-week group (38.5% vs. 18.2% and 26.7% vs. 10.7%; p = 0.047 and p = 0.02). Severe adverse events were modest in both groups.

conclusionsIntensifying treatment intervals from 6 weeks to 4 weeks showed some improvements in PSA response and PSA-PFS for mCRPC patients, but did not significantly affect OS. Additionally, bone marrow reserve was significantly reduced with the intensified regimen. Therefore, the overall benefit remains uncertain, and further prospective studies are needed to compare 4-week and 6-week intervals regarding toxicity, treatment response, and outcome.

Indexed as

4-week treatment intervalMetastatic castration-resistant prostate cancer (mCRPC)Prostate-specific membrane antigen (PSMA)Radioligand therapy (RLT)

Identifiers

PMID39402311
PMCPMC11473467

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Registered trials

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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.