肿瘤细胞治疗研究
英文原题:Biomarkers in breast cancer 2024: an updated consensus statement by the Spanish Society of Medical Oncology and the Spanish Society of Pathology.
Biomarkers in breast cancer 2024: an updated consensus statement by the Spanish Society of Medical Oncology and the Spanish Society of Pathology.
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西班牙肿瘤内科学会(SEOM)和西班牙病理解剖学会(SEAP)的这份修订版共识声明更新了我们在2018年首次发表的关于乳腺癌诊断和治疗中生物标志物使用的建议。专家组建议,在早期乳腺癌中检测雌激素受体(ER)、孕激素受体(PR)、Ki-67和人表皮生长因子受体2(HER2),以及在高风险HER2阴性乳腺癌中检测BRCA基因,以协助预后判断并帮助指示治疗选择,包括激素治疗、化疗、抗HER2治疗和其他靶向治疗。在ER阳性的早期乳腺癌患者中,可使用四种可用的基因预后平台之一(Oncotype DX ®、MammaPrint ®、Prosigna ® 或EndoPredict ®)来确定预后分类,并帮助与患者共同决定辅助治疗是否可仅限于激素治疗。在二线晚期乳腺癌中,此外,应在激素敏感性病例中检测PIK3CA和ESR1,在HER2阴性癌症中检测BRCA基因突变,在三阴性乳腺癌(TNBC)中检测PD-L1。较新的生物标志物和技术,包括TIL(肿瘤浸润淋巴细胞)(TILs)、同源重组缺陷(HRD)检测、AKT通路激活和下一代测序(NGS),目前仍处于研究阶段。
This revised consensus statement of the Spanish Society of Medical Oncology (SEOM) and the Spanish Society of Pathological Anatomy (SEAP) updates the recommendations for biomarkers use in the diagnosis and treatment of breast cancer that we first published in 2018. The expert group recommends determining in early breast cancer the estrogen receptor (ER), progesterone receptor (PR), Ki-67, and Human Epidermal growth factor Receptor 2 (HER2), as well as BReast CAncer (BRCA) genes in high-risk HER2-negative breast cancer, to assist prognosis and help in indicating the therapeutic options, including hormone therapy, chemotherapy, anti-HER2 therapy, and other targeted therapies.
One of the four available genetic prognostic platforms (Oncotype DX ® , MammaPrint ® , Prosigna ® , or EndoPredict ® ) may be used in ER-positive patients with early breast cancer to establish a prognostic category and help decide with the patient whether adjuvant treatment may be limited to hormonal therapy.
In second-line advanced breast cancer, in addition, phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) and estrogen receptor 1 (ESR1) should be tested in hormone-sensitive cases, BRCA gene mutations in HER2-negative cancers, and in triple-negative breast cancer (TNBC), programmed cell death-1 ligand (PD-L1).
Newer biomarkers and technologies, including tumor-infiltrating lymphocytes (TILs), homologous recombination deficiency (HRD) testing, serine/threonine kinase (AKT) pathway activation, and next-generation sequencing (NGS), are at this point investigational.
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