Evidence map›Paper›PMID 42018554›Full record

SynthesisThe Prostate2026

Human Epidermal Growth Factor Receptor 2 Expression in Prostatic Carcinomas: A Systematic Review and Meta-Analysis of a Potential Therapeutic Target.

Jacky T F Luk, Alex H Lin, Esther K C Cheung, Renald Meçani, Taulant Muka, Jana Nano, Joanna K M Ng, Matthew K L Chiu, Bryan C W Li, Rong Na and 1 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis 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

11 authors.

Jacky T F LukDepartment of Pathology, School of Clinical Medicine, The University of Hong Kong, Pokfulam, Hong Kong SAR.
Alex H LinDepartment of Pathology, School of Clinical Medicine, The University of Hong Kong, Pokfulam, Hong Kong SAR.
Esther K C CheungDepartment of Pathology, School of Clinical Medicine, The University of Hong Kong, Pokfulam, Hong Kong SAR.
Renald MeçaniEpistudia, Bern, Switzerland.
Taulant MukaEpistudia, Bern, Switzerland.ORCID 0000-0003-3235-3073
Jana NanoDepartment of Radiation Oncology, TUM School of Medicine and Health, Klinikum Rechts der Isar, Technical University of Munich, Munich, Germany.
Joanna K M NgDepartment of Pathology, School of Clinical Medicine, The University of Hong Kong, Pokfulam, Hong Kong SAR.
Matthew K L ChiuDepartment of Clinical Oncology, Queen Mary Hospital, The University of Hong Kong, Pokfulam, Hong Kong SAR.
Bryan C W LiDepartment of Medicine, Queen Mary Hospital, The University of Hong Kong, Pokfulam, Hong Kong SAR.
Rong NaDepartment of Surgery, Queen Mary Hospital, The University of Hong Kong, Pokfulam, Hong Kong SAR.
Joshua J X LiDepartment of Pathology, School of Clinical Medicine, The University of Hong Kong, Pokfulam, Hong Kong SAR.ORCID 0000-0003-2425-0314

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe clinical relevance of HER2 expression profile in solid cancers has expanded with the evolving landscape of HER2 targeting agents. This systematic review and meta-analysis aim to detail the prevalence of HER (over)expression in prostate cancer and identify patient/disease subgroups with enriched HER2 overexpression.

methodsLiterature searches of five databases were performed. HER2 scores with cross-tabulation of clinicopathological parameters were extracted for pooled prevalence and odds ratio analyses. Study quality, heterogeneity, and publication bias were assessed by the CASP checklist, I

resultsIn total, 16 studies were included with 1258 cases. There were 669 (53.18%), 269 (21.38%), 250 (19.87%), and 70 (5.56%) of HER2 Scores 0/1/2/3, respectively. Pooled analysis indicated a prevalence of 4.9% (95% CI 3.0%-7.2%) for HER2 Score 3 and 42.0% (95% CI 29.0%-55.6%) for HER2 non-negative (Scores 1-3). Subgroup analysis comparing HER2 negative (0, 1) and HER2 overexpression (3) indicated higher Gleason score (OR = 0.061, 95% CI: 0.010-0.359, p < 0.001), higher disease stage (OR = 0.063, 95% CI: 0.016-0.252, p < 0.001) and biopsies from metastatic site (OR: > 100, 95% C.I.: > 100-> 100, p < 0.001) favoring HER overexpression, without significant differences for patient age or prostate-specific antigen (PSA) level. I

conclusionsHER2 overexpression is rare in prostatic carcinomas but nearly half show HER2 expression of Score 1 or above. Cases with higher Gleason score and advanced disease stage are more likely to overexpress HER2.

Indexed as

Erb-b2 Receptor Tyrosine KinasesProstatic NeoplasmsBiomarkers, TumorHumansMaleBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesHER2immunohistochemistrymeta‐analysisprostate cancertargeted therapy

Identifiers

PMID42018554
PMCPMC13172941

What OpenQuestion holds

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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.