Shmueli E, Wigler N, Inbar M
Department of Oncology, Sourasky Medical Center, 6 Weizmann St, Tel-Aviv 64239, Israel.
Eur J Cancer. 2004 Feb;40(3):379-82. doi: 10.1016/j.ejca.2003.09.018.
Central nervous system (CNS) metastases from breast cancer are common and can present as the first or solitary site of disease progression. The CNS has been reported to act as a sanctuary site that denies access to many chemotherapeutic agents. We present here, a series of 10 metastatic breast cancer patients who developed CNS metastases after an initial response to trastuzumab treatment. Forty one patients with metastatic HER2-overexpressing breast cancer, without evidence of CNS involvement prior to the initiation of trastuzumab treatment, were followed during trastuzumab treatment. A neurological evaluation was performed in those patients who developed neurological signs or symptoms during the course of treatment. The clinical course and pattern of CNS involvement in these patients are discussed. Thirty two patients (78%) showed an initial response to trastuzumab treatment. Ten (31%) of the responding patients developed either isolated CNS relapse or concurrent CNS and systemic progression at a median of 43 weeks after the initiation of trastuzumab treatment. Trastuzumab as a single agent was continued following control of brain symptoms in three patients, two showed signs of systemic disease progression at 11 and 15 weeks following the diagnosis of CNS metastases, respectively. In two other patients, trastuzumab in combination with weekly chemotherapy was continued for more than 20 weeks after CNS relapse without evidence of disease progression. The incidence of CNS involvement in our group of patients was higher than expected. With more successful and prolonged systemic anti-tumour effects achieved by novel drug combinations, the risk of developing CNS metastases might be even greater. Evaluation of prophylactic cranial irradiation strategies might be studied for high-risk patients.
乳腺癌的中枢神经系统(CNS)转移很常见,可表现为疾病进展的首发或唯一部位。据报道,中枢神经系统可作为一个庇护场所,使许多化疗药物难以进入。在此,我们报告了10例转移性乳腺癌患者,这些患者在最初对曲妥珠单抗治疗有反应后发生了中枢神经系统转移。41例转移性HER2过表达乳腺癌患者在曲妥珠单抗治疗开始前无中枢神经系统受累证据,在曲妥珠单抗治疗期间接受随访。对那些在治疗过程中出现神经体征或症状的患者进行了神经学评估。讨论了这些患者中枢神经系统受累的临床过程和模式。32例患者(78%)对曲妥珠单抗治疗最初有反应。其中10例(31%)有反应的患者在曲妥珠单抗治疗开始后中位43周时出现孤立性中枢神经系统复发或中枢神经系统与全身同时进展。3例患者在脑症状得到控制后继续使用曲妥珠单抗单药治疗,2例分别在诊断中枢神经系统转移后11周和15周出现全身疾病进展迹象。另外2例患者在中枢神经系统复发后继续使用曲妥珠单抗联合每周化疗20周以上,无疾病进展证据。我们这组患者中枢神经系统受累的发生率高于预期。随着新型药物组合实现更成功和持久的全身抗肿瘤效果,发生中枢神经系统转移的风险可能更大。对于高危患者,可能需要研究预防性颅脑照射策略的评估。