Gutierrez Maya, Lyazidi Souad, Brasseur Louis, Cvitkovic Frédérique, Le Scodan Romuald
Institut Curie, hôpital René-Huguenin, 35, rue Dailly, 92210 Saint-Cloud, France.
Bull Cancer. 2011 Apr;98(4):417-24. doi: 10.1684/bdc.2011.1341.
Leptomeningeal metastases are very commonly associated with breast cancer. The prognosis is very poor in the short term with an overall median survival less than 6 months. Based on pragmatic and historical considerations intrathecal chemotherapy (IT) are considered to be the adequate treatment. However overall results are disappointing. Despite specific and symptomatic treatment, improvement in survival and quality of life remains very modest, highlighting the importance for ongoing research for developing new molecules or on improving the use a better use of those available today. The incidence of leptomeningeal metastases is particularly marked in cases of overexpression of HER2. The main hypothesis is there may be a better control of extra-cerebral localisations with trastuzumab therefore intra-cerebral recurrences may be encountered preferentially as they are not reached by this high molecular weight monoclonal antibody (148 kD). Analyses performed in the cerebrospinal fluid following intravenous trastuzumab showed extremely low levels of the antibody and support the hypothesis that leptomeningeal metastasis of HER2-overexpressing breast carcinoma remain potentially sensitive to HER2-type receptor inhibition by a target agent under the condition of by-passing the meningeal blood brain barrier. Intra-ventricular or IT administered with trastuzumab would reach high loco-regional therapeutic concentrations in the cerebro-meningeal without risk for normal non-expressing HER2 leptomeningeal tissue. This strategy has been successfully tested on several animal models. A limited number of administrations in humans have been described in the literature, with weekly doses up to 100 mg. No specific toxicity has been described and some data suggest a potential benefit in survival despite the real difficulties for adequate interpretations. Furthermore, a multicentric phase I-II clinical trial, of which the Curie institute is the sponsor and investigating the intra-thecal administration and the efficacy of the trastuzumab will begin very soon. More studies are needed to measure the exact impact of small molecule inhibitors of tyrosine kinase on the leptomeningeal localizations.
软脑膜转移非常常见于乳腺癌。短期预后很差,总体中位生存期不到6个月。基于实用和历史考量,鞘内化疗(IT)被认为是适当的治疗方法。然而,总体结果令人失望。尽管进行了特异性和对症治疗,但生存率和生活质量的改善仍然非常有限,这凸显了持续开展研究以开发新分子或改善现有药物使用方法的重要性。HER2过表达的病例中软脑膜转移的发生率尤为显著。主要假说是,曲妥珠单抗可能更好地控制脑外转移灶,因此可能会优先出现脑内复发,因为这种高分子量单克隆抗体(148 kD)无法到达脑内复发部位。静脉注射曲妥珠单抗后在脑脊液中进行的分析显示抗体水平极低,这支持了以下假说:在绕过脑膜血脑屏障的情况下,HER2过表达乳腺癌的软脑膜转移可能对靶向药物抑制HER2型受体仍具有潜在敏感性。脑室内或鞘内给予曲妥珠单抗可在脑脊膜达到高局部治疗浓度,而对正常不表达HER2的软脑膜组织无风险。该策略已在多个动物模型上成功测试。文献中描述了在人类中的有限次数给药,每周剂量高达100 mg。未描述特定毒性,一些数据表明尽管难以进行充分解读,但可能对生存有益。此外,一项多中心I-II期临床试验即将开始,居里研究所是该试验的发起者,正在研究鞘内给药和曲妥珠单抗的疗效。还需要更多研究来衡量酪氨酸激酶小分子抑制剂对软脑膜转移灶的确切影响。