Management of BRCA-associated breast cancer patients in low and middle-income countries: a review.

IF 1.2 Q4 ONCOLOGY ecancermedicalscience Pub Date : 2024-08-22 eCollection Date: 2024-01-01 DOI:10.3332/ecancer.2024.1744
Fen Saj, Shona Nag, Nita Nair, Bhawna Sirohi
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Abstract

Breast cancer poses a significant global health challenge, with higher incidence rates in developed countries. However, low- and middle-income countries (LMICs) suffer from higher mortality rates due to various factors, including limited screening programs, delayed diagnosis and inadequate access to healthcare and advanced treatments. Approximately 5%-10% of breast cancer cases stem from germline mutations in BRCA-1/2 genes. A positive BRCA1/2 status obtained through genetic testing significantly influences surgical and medical treatment decisions. Therefore, genetic counseling, proper surveillance and customized interventions for BRCA1/2 carriers are essential to maximizing the benefits of monitoring, chemoprevention and risk-reducing surgeries for breast and ovarian cancers. Identification of BRCA mutations also impacts treatment strategies, leading to the integration of chemotherapeutic agents like platinum-based chemotherapy and PARP inhibitors. However, implementing these advanced treatment guidelines in LMICs with complex, fragmented and underfunded healthcare systems presents numerous challenges. In this review, we explore the current status and obstacles associated with managing BRCA1/2-associated breast cancer in LMICs.

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中低收入国家对 BRCA 相关乳腺癌患者的管理:综述。
乳腺癌对全球健康构成重大挑战,发达国家的发病率较高。然而,中低收入国家(LMICs)由于筛查项目有限、诊断延迟、医疗保健和先进治疗手段不足等各种因素,死亡率较高。大约 5%-10%的乳腺癌病例源于 BRCA-1/2 基因的种系突变。通过基因检测获得的 BRCA1/2 阳性状态会对手术和药物治疗决策产生重大影响。因此,为 BRCA1/2 基因携带者提供遗传咨询、适当的监测和量身定制的干预措施,对于最大限度地发挥乳腺癌和卵巢癌监测、化学预防和降低风险手术的益处至关重要。BRCA 基因突变的鉴定也会影响治疗策略,导致化疗药物(如铂类化疗和 PARP 抑制剂)的整合。然而,在医疗保健系统复杂、分散且资金不足的低收入国家和地区实施这些先进的治疗指南面临着诸多挑战。在这篇综述中,我们探讨了在低收入国家和地区管理 BRCA1/2 相关乳腺癌的现状和障碍。
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来源期刊
CiteScore
3.80
自引率
5.60%
发文量
138
审稿时长
27 weeks
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