激素受体阳性、人类表皮生长因子受体 2 阴性转移性乳腺癌的现有治疗方案和新型治疗方案

IF 4.7 3区 医学 Q1 ONCOLOGY JCO oncology practice Pub Date : 2024-08-21 DOI:10.1200/OP.23.00830
Nerea Lopetegui-Lia, Revati Varma, Jame Abraham, Erin Roesch
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引用次数: 0

摘要

转移性乳腺癌(mBC)仍然是一种无法治愈的疾病,大多数患者在治疗过程中会出现疾病进展。尽管内分泌治疗仍是激素受体阳性/人表皮生长因子受体 2 阴性 mBC 的主要治疗方法,但在治疗这一 BC 亚型方面已经取得了重大进展,并将继续取得进展。分子标记物、关键细胞通路突变和基因组特征的发现促进了新型靶向药物的开发,如抗体药物共轭物、口服选择性雌激素受体下调剂和 PI3K/AKT/mTOR 通路抑制剂。这大大提高了患者的生存率和生活质量。随着患者可选择的治疗方案越来越多,适当的药物排序仍然是一项挑战。在讨论治疗方案时,患者和医生应共同做出决定,并考虑基因组数据、既往治疗方案、副作用以及临床试验注册情况。
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Current and Novel Treatment Options in Hormone Receptor-Positive, Human Epidermal Growth Factor Receptor 2-Negative Metastatic Breast Cancer.

Metastatic breast cancer (mBC) remains an incurable disease, and most patients will experience disease progression during their treatment course. Although endocrine therapy remains the mainstay of treatment for hormone receptor-positive/human epidermal growth factor receptor 2-negative mBC, significant progress has been and continues to be made in the treatment of this BC subtype. The discovery of molecular markers, mutations in key cellular pathways, and genomic signatures have led to the development of novel and targeted agents, such as antibody-drug conjugates, oral selective estrogen receptor downregulators, and inhibitors of the PI3K/AKT/mTOR pathway. This has resulted in significant improvements in the survival and quality of life of patients. With the increasing number of treatment options for patients, appropriate drug sequencing remains a challenge. Treatment discussions should involve patient-physician shared decision making, with consideration of genomic data, previous lines of therapy, side effect profiles, and clinical trial enrollment.

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CiteScore
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7.50%
发文量
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