Evidence map›Paper›PMID 42766234›Full record

SynthesisJournal of the Egyptian National Cancer Institute2026

Male breast cancer in Arab populations: a systematic review of molecular, genetic, and clinicopathologic characteristics.

Shaden Abunasser, Raghad Al-Taweel, Shahrazad Elnatsheh, Areej Baraka, Muna Al-Ismail, Waad Rashid Aldosari, Baraah A Alquran, Atiyeh M Abdallah, Amal Al-Haidose

Abstract readSystematic Review
In one paragraph

Synthesis in Journal of the Egyptian National Cancer Institute, 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

9 authors.

Shaden AbunasserQatar University, Doha, Qatar.
Raghad Al-TaweelQatar University, Doha, Qatar.
Shahrazad ElnatshehQatar University, Doha, Qatar.
Areej BarakaQatar University, Doha, Qatar.
Muna Al-IsmailQatar University, Doha, Qatar.
Waad Rashid AldosariMinistry of Interior, Doha, Qatar.
Baraah A AlquranJordan University of Science and Technology, Irbid, Jordan.
Atiyeh M AbdallahQatar University, Doha, Qatar.ORCID https://orcid.org/0000-0003-4812-956X
Amal Al-HaidoseQatar University, Doha, Qatar. amalah@qu.edu.qa.

Funding

Qatar University QUCG-CHS-25/26-716Qatar University QUCG-CHS-25/26-736
6 · The paper itself

Abstract

backgroundMale breast cancer (MBC) accounts for less than 1% of all breast cancer cases, yet its incidence is increasing worldwide. Research on MBC remains limited, particularly in Arab populations, where molecular and genetic characteristics are poorly characterized. Improved understanding of MBC biology is essential to support region-specific, biology-driven management strategies.

methodsThis systematic review was registered in PROSPERO (CRD42024607019) and conducted according to PRISMA guidelines. PubMed, Embase, and Scopus were searched from inception to 28 December 2025. Eligible studies reported MBC cases from Arab countries and included data on molecular subtypes, receptor status, genetic alterations, and/or clinicopathologic characteristics. Data were extracted independently by four reviewers. Risk of bias was assessed using the Joanna Briggs Institute (JBI) critical appraisal tool, and findings were synthesized narratively with harmonization of tumor grade and stage where applicable.

resultsFrom 9,337 records, 54 studies comprising 1,534 MBC patients met the inclusion criteria. Invasive ductal carcinoma was the predominant histological subtype (92.6%). Among patients with reported intrinsic subtypes (n = 335), luminal A (45.7%) and luminal B (40.9%) accounted for over 86% of cases, whereas HER2-positive (4.8%) and triple-negative (8.4%) tumors were uncommon and triple-positive disease was rare (0.3%). Receptor status was reported for 1,031 patients, with high ER (71.5%) and PR (71.6%) positivity and low HER2 positivity (12.6%), alongside substantial heterogeneity in testing and reporting. Genetic data were available for 59 patients, most frequently identifying pathogenic truncating BRCA2 variants, although BRCA-negative cases were also reported. Surgery was the most reported treatment modality (n = 856), predominantly mastectomy-based, while endocrine therapy was frequently used and HER2-targeted therapy was infrequently reported.

conclusionMBC in Arab populations is predominantly hormone receptor-driven, characterized by luminal subtypes, high ER/PR positivity, and low HER2 expression. Genetic evidence, though limited, implicates BRCA2 as the most frequently reported susceptibility gene. These findings highlight the need for standardized molecular reporting and broader access to receptor profiling and genetic testing to support personalized, region-specific MBC management.

Indexed as

ArabsBreast Neoplasms, MaleBiomarkers, TumorBRCA2 ProteinErb-b2 Receptor Tyrosine KinasesHumansMaleReceptors, EstrogenReceptors, ProgesteroneBiomarkers, TumorBRCA2 ProteinERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, ProgesteroneArab regionBRCA2Genetic alterationsHormone receptor statusMale breast cancerMolecular subtypes

Identifiers

PMID42766234
PMCPMC13594001

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.