Oncology Department, Instituto Alexander Fleming, Cramer 1180, zip code 1426 ANZ, Ciudad Autonoma de Buenos Aires, Argentina.
Breast Cancer Res. 2010;12 Suppl 2(Suppl 2):S3. doi: 10.1186/bcr2574. Epub 2010 Oct 22.
Perou's molecular classification defines tumors that neither express hormone receptors nor overexpress HER2 as triple-negative (TN) tumors. These tumors account for approximately 15% of breast cancers. The so-called basaloid tumors are not always synonymous with TN tumors; they differ in the fact that they express different molecular markers, have a higher histologic grade, and have a worse prognosis. Clinically they occur in younger women as interval cancer, and the risk of recurrence is higher within the first 3 years. Distant recurrences in the brain and visceral metastases are more common than in hormone receptor-positive tumors. Therapeutically, despite being highly chemosensitive, their progression-free time is generally short. In terms of chemotherapeutic treatment, anthracyclines and taxanes are useful drugs, and high response rates have been described for the combination of ixabepilone-capecitabine and platinums. The combination with antiangiogenic drugs has also proven useful. A group of new drugs, poly-(ADP-ribose)-polymerase inhibitors, showed favorable results in TN tumors with BRCA mutation. There are currently several ongoing studies with new drugs including epidermal growth factor receptor inhibitors, c-kit inhibitors, Raf/Mek/Map kinase inhibitors and mTOR inhibitors.
佩鲁的分子分类将既不表达激素受体也不过表达 HER2 的肿瘤定义为三阴性(TN)肿瘤。这些肿瘤约占乳腺癌的 15%。所谓的基底样肿瘤并不总是与 TN 肿瘤同义;它们的区别在于它们表达不同的分子标志物,具有更高的组织学分级,并且预后更差。临床上,它们作为间隔癌发生在年轻女性中,并且在前 3 年内复发的风险更高。脑内远处复发和内脏转移比激素受体阳性肿瘤更常见。在治疗方面,尽管具有高度的化疗敏感性,但它们的无进展时间通常较短。在化疗治疗方面,蒽环类药物和紫杉烷类药物是有用的药物,并且已经描述了伊沙匹隆-卡培他滨和铂类联合治疗的高反应率。联合使用抗血管生成药物也被证明是有用的。一组新型药物,聚(ADP-核糖)聚合酶抑制剂,在具有 BRCA 突变的 TN 肿瘤中显示出良好的结果。目前正在进行几项新药物的研究,包括表皮生长因子受体抑制剂、c-kit 抑制剂、Raf/Mek/Map 激酶抑制剂和 mTOR 抑制剂。