Evidence map›Paper›PMID 41402631›Full record

ReviewUrologie (Heidelberg, Germany)2026

[Poly (ADP-ribose) polymerase inhibitor combination therapy in metastatic castration-resistant prostate cancer].

Carsten Ohlmann, Christian Gratzke, Laura-Maria Krabbe

Abstract readEnglish AbstractReview
PubMed Publisher
In one paragraph

Review 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

3 authors.

Carsten OhlmannKlinik für Urologie, Johanniter-Kliniken Bonn, Johanniterstr. 3-5, 53113, Bonn, Deutschland. Carsten.Ohlmann@bn.johanniter-kliniken.de.
Christian GratzkeKlinik für Urologie, Universitätsklinikum Freiburg, Breisacher Straße 153, 79110, Freiburg, Deutschland.
Laura-Maria KrabbeKliniken für Urologie der Standorte Humboldt-Klinikum, Klinikum am Urban und Klinikum im Friedrichshain, Vivantes Netzwerk für Gesundheit, Am Nordgraben 2, 13509, Berlin, Deutschland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetastatic castration-resistant prostate cancer (mCRPC) remains a therapeutic challenge. Poly(adenosine diphosphate-ribose) polymerase inhibitors (PARPi) combined with new hormonal agents (NHA) offer novel treatment options.

objectiveThis review summarizes the current status of PARPi + NHA combination therapy in mCRPC. MATERIALS AND

methodsSummary of relevant phase II and III trials on PARPi + NHA and the G‑BA (Gemeinsame Bundesausschuss) decision as well as the current S3 guideline recommendations.

resultsPARPi + NHA demonstrated improved efficacy compared to NHA alone in an all-comers population that received prior androgen deprivation therapy (ADT) or docetaxel therapy. In particular the subgroup of patients with homologous recombination repair (HRR) and breast cancer (BRCA) 1/2 mutations had the best outcomes. Olaparib + abiraterone, talazoparib + enzalutamide, and niraparib + abiraterone are approved combinations, expanding treatment options in mCRPC.

conclusionPARPi + NHA represent a significant advance in mCRPC therapy. Molecular genetic testing for HRR mutations, especially BRCA 1/2, is crucial for treatment planning.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsPoly(ADP-ribose) Polymerase InhibitorsProstatic Neoplasms, Castration-ResistantHumansMalePoly(ADP-ribose) Polymerase InhibitorsCombination therapyMonotherapyMutationsPARP inhibitorsRecombination repair

Identifiers

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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.