Evidence map›Paper›PMID 40390103›Full record

ArticleHereditary cancer in clinical practice2025

Knowledge and perceptions of genetic testing for patients with breast cancer in Nigeria: a survey of healthcare providers.

Funmilola Olanike Wuraola, Anna Dare, Jenine Ramruthan, Emma Reel, Anna T Santiago, Folorunso Sharif, Agodirin Olayide, Nneka Sunday-Nweke, Olusegun Alatise, Tulin D Cil

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Article in Hereditary cancer in clinical practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Funmilola Olanike WuraolaDepartment of Surgery, Obafemi Awolowo University, Ile-Ife, Nigeria.
Anna DareDepartment of Surgery and Dalla Lana School of Public Health, University of Toronto, Toronto, Canada.
Jenine RamruthanDepartment of General Surgery, University Health Network, Toronto, Canada.
Emma ReelDepartment of General Surgery, University Health Network, Toronto, Canada.
Anna T SantiagoDepartment of Biostatistics, University Health Network, Toronto, Canada.
Folorunso SharifDepartment of Radiology, Obafemi Awolowo University Teaching Hospitals Complex, Ile-Ife, Nigeria.
Agodirin OlayideDepartment of Surgery, University of Ilorin, Ilorin, Nigeria.
Nneka Sunday-NwekeDepartment of Surgery, Alex Ekwueme Federal University Teaching Hospital, Abakaliki, Nigeria.
Olusegun AlatiseDepartment of Surgery, Obafemi Awolowo University, Ile-Ife, Nigeria.
Tulin D CilDepartment of General Surgery, University Health Network, Toronto, Canada. Tulin.Cil@uhn.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe role of genetics in breast cancer management is becoming increasingly essential in sub-Saharan Africa (SSA). Harmonized Guidelines by the National Comprehensive Cancer Network (NCCN) for SSA outline the subset of patients requiring genetic testing for hereditary breast cancer as part of their treatment plan. However, in low-and middle-income countries (LMICs) like Nigeria, access to genetic counselling and testing remains limited. Additionally, the knowledge and acceptability of these available services from the healthcare provider (HCP) perspective are largely unknown. This study aimed to assess the knowledge and perceptions of hereditary breast cancer testing among HCPs in Nigeria.

methodsIn June 2022, we conducted a survey among 549 Nigerian HCPs. The 35-item survey was administered using Google Forms and distributed via WhatsApp. The survey collected demographic data and included three sections on genetic testing in breast cancer patients, focusing on knowledge, perceptions, and training.

resultsThe results were analyzed using R Version 4.4.1 (R Core Team). Altogether 121 HCPs responded (22% response rate): 54 (44.6%) general surgeons, 4 (3.3%) breast surgical oncologists, 29 (24.0%) clinical and radiation oncologists, 31(25.6%) oncology nurses, and 3 (2.5%) breast radiologists. The survey results indicate that Nigerian HCPs were knowledgeable about hereditary breast cancer genetics, but the implementation of counselling and testing was low. Only 32.2% of respondents had requested genetic testing for their patients, and all testing was done through private laboratories. Only 9.9% had received formal clinical genetics training, and 13.2% reported having a genetic counsellor in their hospital. There was considerable interest in future genetics training programs using in person and online teaching modalities.

conclusionThis survey highlights the need for specialized breast cancer genetic training tailored for Nigerian HCPs, which is essential in achieving breast cancer treatment parity. Addressing the substantial challenges in expanding genetic testing capacity in Nigeria is warranted for future progress.

Indexed as

Breast cancerHealthcare providersHereditary genetic testingLow-and middle-income countries

Identifiers

PMID40390103
PMCPMC12087218

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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.