Evidence map›Paper›PMID 42661511›Full record

ArticleInternational journal of urology : official journal of the Japanese Urological Association2026

Real-World Outcomes of Olaparib in Japanese Patients With BRCA-Mutated Metastatic Castration-Resistant Prostate Cancer: Exploratory Analysis of BRCA2 Loss and Microsatellite Instability Status.

Takuhisa Nukaya, Taku Naiki, Hiromitsu Watanabe, Keita Nakane, Teruo Inamoto, Takahiro Yasui, Takuya Koie, Kiyoshi Takahara

Abstract readMulticenter Study
In one paragraph

Article in International journal of urology : official journal of the Japanese Urological Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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.

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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.

Takuhisa NukayaDepartment of Urology, Fujita Health University School of Medicine, Toyoake, Japan.ORCID https://orcid.org/0009-0007-9902-1694
Taku NaikiDepartment of Nephro-Urology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.ORCID https://orcid.org/0000-0002-7638-6048
Hiromitsu WatanabeDepartment of Urology, Hamamatsu University School of Medicine, Hamamatsu, Japan.ORCID https://orcid.org/0000-0001-5186-7139
Keita NakaneDepartment of Urology, Gifu University Graduate School of Medicine, Gifu, Japan.ORCID https://orcid.org/0000-0002-2589-1722
Teruo InamotoDepartment of Urology, Hamamatsu University School of Medicine, Hamamatsu, Japan.ORCID https://orcid.org/0000-0002-1351-1315
Takahiro YasuiDepartment of Nephro-Urology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.ORCID https://orcid.org/0000-0003-2197-2477
Takuya KoieDepartment of Urology, Gifu University Graduate School of Medicine, Gifu, Japan.ORCID https://orcid.org/0000-0002-2980-127X
Kiyoshi TakaharaDepartment of Urology, Fujita Health University School of Medicine, Toyoake, Japan.ORCID https://orcid.org/0000-0002-4766-2074

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesMetastatic castration-resistant prostate cancer has a poor prognosis. Although olaparib has demonstrated efficacy in patients with BRCA1/2 mutations, real-world data in Japanese patients remain limited. We aimed to evaluate the efficacy and safety of olaparib in patients with BRCA-mutated metastatic castration-resistant prostate cancer and explore the association of BRCA2 loss and microsatellite instability status with treatment outcomes.

methodsWe conducted a multicenter retrospective study of 34 patients with BRCA-mutated metastatic castration-resistant prostate cancer treated with olaparib between December 2020 and December 2024. The primary endpoint was progression-free survival. Secondary endpoints included overall survival, prostate-specific antigen-50 response rate, and safety. Exploratory analyses were performed.

resultsAmong the 34 patients, 33 had a BRCA2 mutation and one had a BRCA1 mutation. Prostate-specific antigen reduction was observed in 76.4% of patients; prostate-specific antigen-50 response rate was 58.8%. Median progression-free and overall survival were 15.8 and 35.1 months, respectively. Grade ≥ 3 adverse events (most commonly anemia) occurred in 17.6% of patients. Treatment discontinuation due to adverse events occurred in one patient. Exploratory analyses were performed in 23 BRCA2-mutated patients who underwent comprehensive genomic profiling. BRCA2 loss was observed in 39.1% of patients and showed a trend toward prolonged progression-free survival, whereas microsatellite instability-high status was observed in 13.0% and was associated with shorter progression-free survival.

conclusionsOlaparib demonstrated efficacy and safety in Japanese patients with BRCA-mutated metastatic castration-resistant prostate cancer. Exploratory analyses revealed that BRCA2 loss may be associated with prolonged progression-free survival, whereas microsatellite instability-high status may be associated with shorter progression-free survival. These findings require validation in larger cohorts.

Indexed as

BRCA2 ProteinMicrosatellite InstabilityPhthalazinesPiperazinesPoly(ADP-ribose) Polymerase InhibitorsProstatic Neoplasms, Castration-ResistantAgedAged, 80 and overBRCA1 ProteinEast Asian PeopleHumansJapanMaleMiddle AgedMutationProgression-Free SurvivalBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanolaparibPhthalazinesPiperazinesPoly(ADP-ribose) Polymerase InhibitorsProstate-Specific AntigenBRCA mutationcomprehensive genomic profilingmetastatic castration‐resistant prostate cancerolaparibpoly (ADP‐ribose) polymerase inhibitor

Identifiers

PMID42661511
PMCPMC13522863

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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.