Department of Medicine I, Clinical Division of Oncology, Comprehensive Cancer Centre, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
CNS Drugs. 2013 Feb;27(2):121-34. doi: 10.1007/s40263-012-0024-z.
The incidence of brain metastases (BM) in breast cancer patients has increased over the last decade, presumably due to advances in systemic treatment. Today, breast cancer is the second most common cause of BM among all solid malignancies, second only to lung cancer; furthermore, it is the most common cause of leptomeningeal carcinomatosis. The HER2-positive subtype was consistently shown to have a higher risk for BM as compared with HER2-negative disease. More recently, however, it was shown that a similar incidence exists in triple-negative tumours. Local treatment options, radiotherapy and neurosurgical resection, remain the mainstay of therapy for BM. While some studies have suggested a direct effect of conventional chemotherapy on BM, the main beneficial aspect of systemic treatment is rather due to control of non-CNS systemic disease. Importantly, in patients with HER2-positive breast cancer receiving HER2-targeted therapy after local treatment for BM, superior survival outcomes were reported. Leptomeningeal carcinomatosis has a dismal prognosis. Survival with whole brain radiotherapy alone remains short and the potential additional benefit of intrathecal chemotherapy is still disputed. According to case reports, intrathecal administration of trastuzumab appears to be a promising strategy in patients with HER2-positive leptomeningeal carcinomatosis. In conclusion, while the outcome of breast cancer patients with BM has improved especially in the HER2-positive subtype, the prognosis for the majority of patients remains poor. Therefore, development of novel systemic treatment options offering activity within the brain is urgently warranted. Novel insights into the pathobiology of BM formation may offer the possibility for targeted drug prophylaxis of CNS involvement in high-risk patients.
脑转移(BM)在乳腺癌患者中的发病率在过去十年中有所增加,这可能是由于系统治疗的进步。如今,乳腺癌是所有实体恶性肿瘤中 BM 的第二大常见原因,仅次于肺癌;此外,它是软脑膜癌病最常见的原因。HER2 阳性亚型与 HER2 阴性疾病相比,BM 的风险始终更高。然而,最近的研究表明,三阴性肿瘤也存在类似的发病率。局部治疗选择,放疗和神经外科切除术,仍然是 BM 治疗的主要方法。虽然一些研究表明常规化疗对 BM 有直接影响,但系统治疗的主要益处主要是由于控制非中枢神经系统全身疾病。重要的是,HER2 阳性乳腺癌患者在接受局部治疗后接受 HER2 靶向治疗,报告了更好的生存结果。软脑膜癌病预后不良。单独接受全脑放疗的生存时间仍然较短,鞘内化疗的潜在额外益处仍有争议。根据病例报告,曲妥珠单抗鞘内给药似乎是 HER2 阳性软脑膜癌病患者的一种有前途的策略。总之,尽管 BM 乳腺癌患者的预后,尤其是 HER2 阳性亚型,有所改善,但大多数患者的预后仍然较差。因此,迫切需要开发在大脑中具有活性的新型系统治疗选择。对 BM 形成的病理生物学的新见解可能为高危患者的 CNS 受累提供靶向药物预防的可能性。