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精准导航:下一代测序复发风险评估在定制激素受体阳性、人表皮生长因子受体 2 阴性早期乳腺癌辅助治疗中的关键作用。

Navigating precision: the crucial role of next-generation sequencing recurrence risk assessment in tailoring adjuvant therapy for hormone receptor-positive, human epidermal growth factor Receptor2-negative early breast cancer.

机构信息

Department of Obestetrics and Gynecology, Xiangyang Central Hospital, Affiliated Hospital of Hubei University of Arts and Science, Xiangyang, China.

The Medical Department, Jiangsu Simcere Diagnostics Co. Ltd. Nanjing Simcere Medical Laboratory Science Co. Ltd., The State Key Laboratory of Neurology and Oncology Drug Development, Nanjing, China.

出版信息

Cancer Biol Ther. 2024 Dec 31;25(1):2405060. doi: 10.1080/15384047.2024.2405060. Epub 2024 Sep 20.

Abstract

Hormone receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (HER2-) breast cancer is the most common subtype, representing over two-thirds of new diagnoses. Adjuvant therapy, which encompasses various medications and treatment durations, is the standard approach for managing early stage HR+ HER2- breast cancer. Optimizing treatment is essential to minimize unnecessary side effects while addressing the biological variability inherent in HR+/HER2- breast cancers. Incorporating biological biomarkers into treatment decisions, alongside traditional clinical factors, is vital. Gene expression assays can identify patients unlikely to benefit from adjuvant chemotherapy, thereby refining treatment strategies and improving risk assessment. This paper reviews evidence for several genomic tests, including Oncotype DX, MammaPrint, Breast Cancer Index, RucurIndex, and EndoPredict, which assist in tailoring adjuvant therapy. Additionally, we explore the role of liquid biopsies in personalizing treatment, emphasizing the importance of considering late relapse risks and potential benefits of extended systemic therapy for HR+/HER2- breast cancer patients.

摘要

激素受体阳性(HR+)/人表皮生长因子受体 2 阴性(HER2-)乳腺癌是最常见的亚型,占新诊断病例的三分之二以上。辅助治疗包括各种药物和治疗持续时间,是管理早期 HR+HER2-乳腺癌的标准方法。优化治疗对于最大限度地减少不必要的副作用并解决 HR+/HER2-乳腺癌固有的生物学变异性至关重要。将生物标志物纳入治疗决策,与传统的临床因素一起,是至关重要的。基因表达检测可以识别不太可能从辅助化疗中获益的患者,从而完善治疗策略并改善风险评估。本文回顾了几种基因组检测的证据,包括 Oncotype DX、MammaPrint、Breast Cancer Index、RucurIndex 和 EndoPredict,这些检测有助于定制辅助治疗。此外,我们还探讨了液体活检在个体化治疗中的作用,强调考虑 HR+/HER2-乳腺癌患者的晚期复发风险和延长系统治疗的潜在获益的重要性。

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