Evidence map›Paper›PMID 38027092›Full record

ArticleFrontiers in endocrinology2023

Immunohistochemistry-derived subtypes of breast cancer distribution in four regions of Ethiopia.

Esmael Besufikad Belachew, Adey Feleke Desta, Tewodros Yalew Gebremariam, Dinikisira Bekele Deneke, Senait Ashenafi, Melisachew Mulatu Yeshi, Bizunesh Dires Fenta, Alemwosen T/Hayimanot Alem, Addisu Alemu, Abdo Kedir Abafogi and 11 more

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. RSC advances · 2024
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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

21 authors.

Esmael Besufikad BelachewBiology Department, College of Natural and Computational Sciences, Mizan Tepi University, Mizan, Ethiopia.
Adey Feleke Desta *Department of Microbial, Cellular and Molecular Biology, College of Natural and Computational Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
Tewodros Yalew GebremariamDepartment of Pathology, School of Medicine, College of Health Sciences, Tikur Anbessa Specialized Hospital and Addis Ababa University, Addis Ababa, Ethiopia.
Dinikisira Bekele DenekeDepartment of Pathology, School of Medicine, College of Health Sciences, Tikur Anbessa Specialized Hospital and Addis Ababa University, Addis Ababa, Ethiopia.
Senait AshenafiDepartment of Pathology, School of Medicine, College of Health Sciences, Tikur Anbessa Specialized Hospital and Addis Ababa University, Addis Ababa, Ethiopia.
Melisachew Mulatu YeshiDepartment of Pathology, School of Medicine, College of Health Sciences, Mekelle University, Mekelle, Ethiopia.
Bizunesh Dires FentaPathology Department, Hawassa Referral Hospital, Hawassa, Ethiopia.
Alemwosen T/Hayimanot AlemPathology Department, Hawassa Referral Hospital, Hawassa, Ethiopia.
Addisu AlemuCollege of Health and Medical Sciences, Haramaya University, Harar, Ethiopia.
Abdo Kedir AbafogiPathology Department, Jimma University Specialized Hospital, Jimma, Ethiopia.
Tigist DestaNon-Communicable Diseases (NCD) Research Directorate, Armauer Hansen Research Institute, Addis Ababa, Ethiopia.
Menberework ChanyalewNon-Communicable Diseases (NCD) Research Directorate, Armauer Hansen Research Institute, Addis Ababa, Ethiopia.
Daniel BeshahDepartment of Diagnostic Laboratory, Tikur Anbessa Specialized Hospital, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
Lesley TaylorCity of Hope National Medical Center, Duarte, CA, United States.
Marcus BauerGlobal Health Working Group, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany.
Dareskedar TsehayNon-Communicable Diseases (NCD) Research Directorate, Armauer Hansen Research Institute, Addis Ababa, Ethiopia.
Selfu GirmaNon-Communicable Diseases (NCD) Research Directorate, Armauer Hansen Research Institute, Addis Ababa, Ethiopia.
Daniel Seifu MelkaDepartment of Biochemistry, Division of Basic Sciences, University of Global Health Equity, Kigali, Rwanda.
Tesfaye Sisay TessemaInstitute of Biotechnology, Addis Ababa University, Addis Ababa, Ethiopia.
Eva J Kantelhardt *Department of Gynecology, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany.
Rawleigh Howe *Non-Communicable Diseases (NCD) Research Directorate, Armauer Hansen Research Institute, Addis Ababa, Ethiopia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Different biological characteristics, therapeutic responses, and disease-specific outcomes are associated with different molecular subtypes of breast cancer (BC). Although there have been different studies on BC in the Ethiopian capital city of Addis Ababa, there have been few studies in other parts of the nation, and none have evaluated biological characteristics in other locations in the context of the extensive ethnic and genetic diversity found in Ethiopia. This study was carried out to evaluate the distribution of immunohistochemistry (IHC) subtypes of BCs throughout four Ethiopian regions. Methods: A total of 227 formalin-fixed paraffin-embedded (FFPE) tissue blocks were collected from tertiary hospitals in four Ethiopian regions between 2015 and 2021. The IHC staining was performed for subtyping, ER, PR, HER2, and Ki-67 proliferation markers. Results: The mean age at diagnosis was 43.9 years. The percentage of ER and PR-negative tumors were 48.3% and 53.2%, respectively. The IHC subtypes showed the following distribution: 33.1% triple-negative breast cancer (TNBC), 27.6% luminal B, 25.2% luminal A, and 14.1% HER2 enriched. In multiple logistic regression analysis, grade III and HER2 positivity were associated with larger tumor size, and also originating from Jimma compared to Mekele. Conclusion: Patients with ER-negative, PR-negative, and TNBC were found in 48.3%, 53.2%, and 33.1% of cases, respectively, showing that half the patients could potentially benefit from endocrine treatment. A considerably high prevalence of TNBC was reported in our study, demanding additional research that includes genetic predisposition factors. Additionally, aggressive tumors were found in a high percentage of younger age groups, which must be considered when planning personalized treatment strategies.

Indexed as

Triple Negative Breast NeoplasmsAdultErb-b2 Receptor Tyrosine KinasesEthiopiaHumansImmunohistochemistryReceptors, EstrogenErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenAfricabreast cancerestrogen receptorEthiopiaimmunohistochemistrysubtype

Identifiers

PMID38027092
PMCPMC10666628

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