Bou Zerdan Maroun, Ibrahim Maryam, Nakib Clara El, Hajjar Rayan, Assi Hazem I
Department of Internal Medicine, Naef K. Basile Cancer Institute, American University of Beirut Medical Center, Beirut, Lebanon.
Division of Internal Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Front Oncol. 2021 Feb 16;10:609100. doi: 10.3389/fonc.2020.609100. eCollection 2020.
In recent years, developments in breast cancer have allowed yet another realization of individualized medicine in the field of oncology. One of these advances is genomic assays, which are considered elements of standard clinical practice in the management of breast cancer. These assays are widely used today not only to measure recurrence risk in breast cancer patients at an early stage but also to tailor treatment as well and minimize avoidable treatment side effects. At present, genomic tests are applied extensively in node negative disease. In this article, we review the use of these tests in node positive disease, explore their ramifications on neoadjuvant chemotherapy decisions, highlight sufficiently powered recent studies emphasizing their use and review the most recent guidelines.
近年来,乳腺癌领域的进展使得肿瘤学领域再次实现了个性化医疗。其中一项进展是基因组检测,它被视为乳腺癌管理标准临床实践的要素。如今,这些检测不仅广泛用于测量早期乳腺癌患者的复发风险,还用于调整治疗方案并尽量减少可避免的治疗副作用。目前,基因组检测在淋巴结阴性疾病中得到广泛应用。在本文中,我们回顾了这些检测在淋巴结阳性疾病中的应用,探讨它们对新辅助化疗决策的影响,强调近期有充分说服力的研究对其应用的重视,并回顾最新指南。