Evidence map›Paper›PMID 41973209›Full record

ArticleUrologie (Heidelberg, Germany)2026

[Update of S3 guideline on metastatic prostate cancer-guideline recommendations and expert consensus].

Marc-Oliver Grimm, Christian Gratzke, Boris Hadaschik, Matthias Eiber, Ken Herrmann, Eva Hellmis, Jörg Klier, Glen Kristiansen, Andreas Wiedemann, Axel Merseburger and 2 more

Abstract readConsensus StatementEnglish Abstract
PubMed Publisher
In one paragraph

Article in Urologie (Heidelberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Marc-Oliver GrimmKlinik und Poliklinik für Urologie, Universitätsklinikum Jena, Friedrich-Schiller Universität, Am Klinikum 1, 07747, Jena, Deutschland. marc-oliver.grimm@med.uni-jena.de.
Christian GratzkeKlinik für Urologie, Universitätsklinikum Freiburg, Freiburg, Deutschland.
Boris HadaschikKlinik für Urologie, Universitätsklinikum Essen, Essen, Deutschland.
Matthias EiberKlinik und Poliklinik für Nuklearmedizin, Klinikum rechts der Isar, Technische Universität München, München, Deutschland.
Ken HerrmannKlinik für Nuklearmedizin, Universitätsklinikum Essen, Essen, Deutschland.
Eva HellmisUrologicum Duisburg, Duisburg, Deutschland.
Jörg KlierStandort Bayenthal, Urologische Partnerschaft Köln, Köln, Deutschland.
Glen KristiansenInstitut für Pathologie, Universitätsklinikum Bonn, Bonn, Deutschland.
Andreas WiedemannKlinik für Urologie, Ev. Krankenhaus Witten gGmbH, Lehrstuhl für Geriatrie, Universität Witten/Herdecke, Witten, Deutschland.
Axel MerseburgerKlinik für Urologie, Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Lübeck, Deutschland.
Margitta RetzUrologische Klinik und Poliklinik, Klinikum rechts der Isar, Technische Universität München, München, Deutschland.
Gunhild von AmsbergMedizinische Klinik und Poliklinik für Hämatologie und Onkologie, Universitäres Cancer Center Hamburg (UCC Hamburg), Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment options for metastatic prostate cancer have evolved and diversified considerably in recent years. In the hormone-sensitive setting (mHSPC), the combination of androgen deprivation therapy (ADT) with androgen receptor pathway inhibitors (ARPI) or abiraterone + prednis(ol)one (Abi), optionally combined with docetaxel, represents the current standard of care. Prior therapy, the principle of switching the mechanism of action, and the patient's individual molecular genetic profile substantially influence treatment selection in the metastatic castration-resistant setting (mCRPC). Testing for genes involved in homologous recombination repair (HRR), particularly BRCA1/2, is essential for the indication of poly(ADP-ribose) polymerase inhibitors (PARPI), which can be used as monotherapy or in combination with an ARPI/Abi, and has prognostic as well as familial implications. Radioligand therapy with lutetium (

Indexed as

Prostatic NeoplasmsProstatic Neoplasms, Castration-ResistantAntineoplastic Combined Chemotherapy ProtocolsHumansMaleNeoplasm MetastasisARPIHomologous recombination repairPARP inhibitorsRadioligand therapySequential therapy

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.