Evidence map›Paper›PMID 42559798›Full record

Observational studyInternational journal of urology : official journal of the Japanese Urological Association2026

Real-World Outcomes of Olaparib Treatment in Japanese Patients With Metastatic Castration-Resistant Prostate Cancer Harboring BRCA Pathogenic or Likely Pathogenic Variants.

Yosuke Yasuda, Soichiro Yoshida, Ichiro Yonese, Yuta Sano, Shunya Matsumoto, Tetsuya Urasaki, Takashi Tamiya, Hajime Tanaka, Masaya Ito, Yuji Miura and 5 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study 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.

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

15 authors.

Yosuke YasudaDepartment of Urology, Institute of Science Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0001-5427-1680
Soichiro YoshidaDepartment of Urology, Institute of Science Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0003-2757-8083
Ichiro YoneseDepartment of Urology, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, Tokyo, Japan.ORCID https://orcid.org/0009-0001-2607-1013
Yuta SanoDepartment of Urology, Saitama Cancer Center, Saitama, Japan.ORCID https://orcid.org/0000-0002-1033-3648
Shunya MatsumotoDepartment of Urology, Saitama Cancer Center, Saitama, Japan.ORCID https://orcid.org/0000-0003-4459-4384
Tetsuya UrasakiDepartment of Medical Oncology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Takashi TamiyaDepartment of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0009-0001-2330-6833
Hajime TanakaDepartment of Urology, Institute of Science Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0003-3632-2901
Masaya ItoDepartment of Urology, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0002-0230-6367
Yuji MiuraDepartment of Medical Oncology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0002-7091-628X
Noboru NumaoDepartment of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0003-4024-4248
Yoh MatsuokaDepartment of Urology, Saitama Cancer Center, Saitama, Japan.ORCID https://orcid.org/0000-0002-2440-5104
Fumitaka KogaDepartment of Urology, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, Tokyo, Japan.ORCID https://orcid.org/0000-0001-7888-0085
Junji YoneseDepartment of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID https://orcid.org/0000-0001-9266-4020
Yasuhisa FujiiDepartment of Urology, Institute of Science Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0002-6761-3229

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOlaparib has demonstrated clinical benefit in patients with metastatic castration-resistant prostate cancer (mCRPC) harboring BRCA pathogenic or likely pathogenic variants (PVs) in randomized clinical trials; however, multicenter real-world data in Japanese patients remain limited.

methodsThis multicenter retrospective study included Japanese patients with mCRPC who received olaparib between 2021 and 2025 at four institutions. Eligible patients had pathogenic or likely pathogenic BRCA1/2 variants identified by comprehensive genomic profiling or BRCA-specific testing (BRACAnalysis). Disease progression was defined as prostate-specific antigen (PSA) progression or radiographic progression. Overall survival (OS) and progression-free survival (PFS) were estimated using the Kaplan-Meier method.

resultsAmong 128 patients undergoing comprehensive genomic profiling, 18 (14%) were identified as having BRCA PVs, of whom 13 received olaparib. Among 239 patients tested by BRACAnalysis, 14 (6%) harbored BRCA PVs and all received olaparib. Overall, 27 patients with mCRPC harboring BRCA PVs were analyzed. The median duration of olaparib treatment was 8 months, with three patients treated for more than 30 months. One-year OS rate was 80.6%, with a median OS of 18.4 months, and 1-year PFS rate was 27.2% with a median PFS of 7.6 months. Grade 3 anemia occurred in 33% of patients and was manageable, with no grade 4 or 5 events observed.

conclusionsThis multicenter retrospective study provides real-world data on olaparib treatment in Japanese patients with mCRPC harboring BRCA PVs. The observed outcomes and safety profile were generally consistent with previous reports, although interpretation is limited by the small sample size, retrospective design, and heterogeneity of prior treatments.

Indexed as

BRCA1 ProteinBRCA2 ProteinPhthalazinesPiperazinesPoly(ADP-ribose) Polymerase InhibitorsProstatic Neoplasms, Castration-ResistantAgedAged, 80 and overDisease ProgressionHumansJapanMaleMiddle AgedProgression-Free SurvivalRetrospective StudiesTreatment OutcomeBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanolaparibPhthalazinesPiperazinesPoly(ADP-ribose) Polymerase InhibitorsBRCAmetastatic castration‐resistant prostate cancerolaparib

Identifiers

PMID42559798
PMCPMC13445535

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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.