Evidence map›Paper›PMID 41524484›Full record

ArticleThe Prostate2026

Post Hoc Subgroup Analysis of Clinical Outcomes in Patients With High-Risk Metastatic Hormone-Naïve Prostate Cancer: Results From a 3-Year Interim Analysis of the J-ROCK Study.

Atsushi Mizokami, Rikiya Matsumoto, Hideaki Miyake, Hiroji Uemura, Hirotsugu Uemura, Satoru Kawakami, Kazuyoshi Nakamura, Shigekatsu Maekawa, Hiroaki Tsuchiya, Sachie Okazaki and 5 more

Abstract read
In one paragraph

Article in The Prostate, 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.

Atsushi MizokamiDepartment of Urology, Kanazawa University Hospital, Ishikawa, Japan.ORCID https://orcid.org/0000-0002-5643-2182
Rikiya MatsumotoDepartment of Urology, Chutoen General Medical Center, Shizuoka, Japan.
Hideaki MiyakeDivision of Urology, Kobe University Graduate School of Medicine, Hyogo, Japan.ORCID https://orcid.org/0000-0003-0563-4160
Hiroji UemuraDepartment of Urology, Yokohama City University Graduate School of Medical Science, Kanagawa, Japan.ORCID https://orcid.org/0000-0001-7943-1564
Hirotsugu UemuraDepartment of Urology, Kindai University Hospital, Osaka, Japan.ORCID https://orcid.org/0000-0002-3665-9523
Satoru KawakamiDepartment of Urology, Saitama Medical Center, Saitama Medical University, Saitama, Japan.ORCID https://orcid.org/0000-0001-6319-3821
Kazuyoshi NakamuraDepartment of Urology, Kimitsu Chuo Hospital, Chiba, Japan.ORCID https://orcid.org/0009-0001-8308-921X
Shigekatsu MaekawaDepartment of Urology, Iwate Medical University Hospital, Iwate, Japan.ORCID https://orcid.org/0000-0003-4620-2831
Hiroaki TsuchiyaDepartment of Medical Affairs, Johnson & Johnson, Tokyo, Japan.ORCID https://orcid.org/0000-0001-6530-7298
Sachie OkazakiMedical Affairs Delivery Unit, Global Development, Johnson & Johnson R&D, Tokyo, Japan.
Eri AdachiDepartment of Medical Affairs, Johnson & Johnson, Tokyo, Japan.ORCID https://orcid.org/0009-0007-2684-3873
Ryo YanoDepartment of Medical Affairs, Johnson & Johnson, Tokyo, Japan.ORCID https://orcid.org/0009-0001-9800-2105
Yohei TajimaDepartment of Medical Affairs, Johnson & Johnson, Tokyo, Japan.ORCID https://orcid.org/0000-0001-6818-1424
Kiyohide FujimotoDepartment of Urology, Nara Medical University Hospital, Nara, Japan.ORCID https://orcid.org/0000-0003-1507-2464
Hideyasu MatsuyamaDepartment of Urology, Nagato General Hospital, Yamaguchi, Japan.ORCID https://orcid.org/0000-0001-5607-7769

Funding

Johnson & Johnson
6 · The paper itself

Abstract

introductionIn real-world practice in Japan, standard treatment for metastatic hormone-naïve prostate cancer (mHNPC) is androgen deprivation therapy (ADT), administered as monotherapy, combined androgen blockade (CAB), ADT plus androgen receptor pathway inhibitors (ARPIs), or ADT plus docetaxel. In a previous interim analysis of the large-scale, longitudinal, multicentre, J-ROCK registry study of real-world clinical and patient-reported outcomes, ADT plus ARPI or ADT plus docetaxel was used more frequently than ADT/CAB in patients (aged ≥ 20 years) with newly diagnosed LATITUDE-criteria high-risk mHNPC.

methodsThis post hoc analysis of the J-ROCK study evaluated prostate-specific antigen (PSA) response, progression-free survival (PFS), time to castration-resistant prostate cancer (CRPC), overall survival (OS) and safety in patients with high-risk mHNPC who received ADT/CAB (cohort 1) or ADT plus ARPI (cohort 2B) in subgroups were defined according to the following known prognostic factors at baseline: age, Gleason Grade Group (GGG), alkaline phosphatase (ALP), hemoglobin (Hb) and lactate dehydrogenase (LDH).

resultsThis analysis included 947 evaluable patients (371 in cohort 1 and 576 in cohort 2B). PSA response rates remained similar among age and GGG subgroups in both cohorts, but were reduced in cohort 2B patients with elevated ALP, low Hb, and elevated LDH. Time to CRPC and OS were longer in cohort 2B than in cohort 1, regardless of prognostic factors. Among patients with poor prognosis (older, high GGG, low Hb, elevated LDH), OS decline occurred earlier in cohort 1 versus cohort 2B. A trend towards a plateau in the time to CRPC curve was observed in both cohorts, even in patients with poor prognosis. Safety data were not affected by prognostic factors or treatment.

conclusionsThese findings suggest that novel ADT plus ARPI regimens for LATITUDE-criteria high-risk mHNPC may improve real-world outcomes compared with ADT monotherapy or CAB, particularly among patients with poor prognosis.

Indexed as

androgen deprivation therapyandrogen receptor pathway inhibitorcombined androgen blockadeJ‐ROCK studymetastatic hormone‐naïve prostate cancerprognostic factors

Identifiers

PMID41524484
PMCPMC12935391

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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.