Service d'Hématologie Clinique, Centre Hospitalier Universitaire (CHU) Hôtel Dieu, Université de Nantes, Centre d'Investigation Clinique en Cancerologie (CI2C) and Inserm U892, Nantes, France.
Blood. 2012 Mar 15;119(11):2474-7. doi: 10.1182/blood-2011-11-390781. Epub 2012 Jan 20.
The aim of this phase 2 study was to evaluate the efficacy and safety of trastuzumab, a humanized monoclonal antibody targeted against the human epidermal growth factor receptor 2 (HER2), for adult patients with relapsed/refractory HER2-positive B-ALL. Fifteen patients, with a median age of 62 years, received trastuzumab according to the schedule approved for breast cancer patients (ie, 4 mg/kg intravenous loading dose followed by 2 mg/kg weekly). The overall response rate was 13% with 2 patients achieving partial response and partial remission cytolytic response, respectively. Two other patients were documented with blast clearance. Only 1 reversible grade 3 cardiac toxic event occurred. This phase 2 study showed that trastuzumab monotherapy can allow for some responses in a very high-risk refractory/relapsed HER2-positive adult B-ALL population. Combination of trastuzumab with chemotherapy or other therapeutic monoclonal antibodies should be tested in the future.
本 2 期研究的目的是评估曲妥珠单抗(一种针对人表皮生长因子受体 2(HER2)的人源化单克隆抗体)治疗复发性/难治性 HER2 阳性 B-ALL 成年患者的疗效和安全性。15 名中位年龄为 62 岁的患者按照批准用于乳腺癌患者的方案(即 4 mg/kg 静脉负荷剂量,随后每周 2 mg/kg)接受曲妥珠单抗治疗。总缓解率为 13%,其中 2 例患者分别达到部分缓解和部分细胞溶解缓解,另有 2 例患者的原始细胞清除率得到确认。仅发生 1 例可逆的 3 级心脏毒性事件。这项 2 期研究表明,曲妥珠单抗单药治疗可使高危难治性/复发性 HER2 阳性成人 B-ALL 人群中的部分患者获得缓解。未来应检测曲妥珠单抗与化疗或其他治疗性单克隆抗体联合应用的效果。