Wuraola Funmilola Olanike, Dare Anna, Ramruthan Jenine, Reel Emma, Santiago Anna T, Sharif Folorunso, Olayide Agodirin, Sunday-Nweke Nneka, Alatise Olusegun, Cil Tulin D
Department of Surgery, Obafemi Awolowo University, Ile-Ife, Nigeria.
Department of Surgery and Dalla Lana School of Public Health, University of Toronto, Toronto, Canada.
Hered Cancer Clin Pract. 2025 May 19;23(1):16. doi: 10.1186/s13053-025-00315-w.
The 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.
In 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.
The 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.
This 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.
在撒哈拉以南非洲(SSA),遗传学在乳腺癌管理中的作用变得越来越重要。美国国立综合癌症网络(NCCN)为SSA制定的统一指南概述了作为治疗计划一部分需要进行遗传性乳腺癌基因检测的患者子集。然而,在尼日利亚等低收入和中等收入国家(LMICs),获得遗传咨询和检测的机会仍然有限。此外,从医疗服务提供者(HCP)的角度来看,这些现有服务的知识水平和可接受性在很大程度上尚不清楚。本研究旨在评估尼日利亚HCPs对遗传性乳腺癌检测的知识和看法。
2022年6月,我们对549名尼日利亚HCPs进行了一项调查。这份包含35个条目的调查问卷通过谷歌表单进行管理,并通过WhatsApp分发。该调查收集了人口统计学数据,包括关于乳腺癌患者基因检测的三个部分,重点是知识、看法和培训。
使用R版本4.4.1(R核心团队)对结果进行分析。共有121名HCPs做出回应(回复率为22%):54名(44.6%)普通外科医生、4名(3.3%)乳腺外科肿瘤学家、29名(24.0%)临床和放射肿瘤学家、31名(25.6%)肿瘤护士以及3名(2.5%)乳腺放射科医生。调查结果表明,尼日利亚HCPs对遗传性乳腺癌遗传学有一定了解,但咨询和检测的实施率较低。只有32.2%的受访者为其患者申请过基因检测,所有检测均通过私人实验室进行。只有9.9%的人接受过正规的临床遗传学培训,13.2%的人报告称其所在医院有遗传咨询师。对未来使用面对面和在线教学模式的遗传学培训项目有相当大的兴趣。
这项调查强调了为尼日利亚HCPs量身定制专门的乳腺癌基因培训的必要性,这对于实现乳腺癌治疗公平至关重要。应对尼日利亚在扩大基因检测能力方面的重大挑战对未来的进展是必要的。