Evidence map›Paper›PMID 41145121›Full record

GuidelineAktuelle Urologie2025

[Therapy Management of PARP Inhibitor Combinations in mCRPC Clinical Practice].

Margitta Retz, Angelika Borkowetz, Katja Wittenzellner, Heja Aga-Barfknecht, Gunhild von Amsberg

Abstract readEnglish AbstractPractice Guideline
In one paragraph

Guideline in Aktuelle Urologie, 2025. 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

5 authors.

Margitta RetzUrologische Klinik und Poliklinik, TUM Universitätsklinikum Rechts der Isar, München, Deutschland.
Angelika BorkowetzKlinik und Poliklinik für Urologie, Universitätsmedizin Rostock, Rostock, Deutschland.
Katja WittenzellnerMedical Affairs Oncology, Pfizer Pharma GmbH, Berlin, Deutschland.
Heja Aga-BarfknechtMedical Affairs Oncology, Pfizer Pharma GmbH, Berlin, Deutschland.
Gunhild von AmsbergOnkologisches Zentrum/ Martini-Klinik, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Innovative therapeutic approaches, including poly(ADP-ribose)polymerase inhibitors (PARPi), have shown promising results in metastatic castration-resistant prostate cancer (mCRPC), particularly when combined with androgen receptor inhibitors (ARPi). Irrespective of HRR gene mutations, patients benefit from improved radiological progression-free survival and overall survival. The success of PARPi/ARPi combination therapy relies heavily on the effective management of both treatment administration and the associated side-effects. Common haematological side-effects include anaemia, leukopenia, and thrombocytopenia, whereas non-haematological reactions - particularly fatigue, diarrhea, nausea, and constipation - are also clinically relevant. In addition to basic diagnostics and preventive measures, dose adjustments or temporary discontinuation may be required depending on the severity of the side-effects. For anaemia, the most common side-effect, supportive measures such as blood transfusions may be necessary to ensure optimal patient care. This guide provides uro-oncologists with practical recommendations for daily clinical practice.

Indexed as

Androgen Receptor AntagonistsAntineoplastic Combined Chemotherapy ProtocolsPoly(ADP-ribose) Polymerase InhibitorsProstatic Neoplasms, Castration-ResistantHumansMaleAndrogen Receptor AntagonistsPoly(ADP-ribose) Polymerase Inhibitors

Identifiers

PMID41145121
PMCPMC12646740

What OpenQuestion holds

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LicenceCC BY
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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.