Galimberti Sara, Cervetti Giulia, Cecconi Nadia, Fazzi Rita, Pacini Simone, Guerrini Francesca, Manetti Chiara, Caracciolo Francesco, Petrini Mario
Department of Oncology, Transplant and Advances in Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
J Immunother. 2004 Sep-Oct;27(5):389-93. doi: 10.1097/00002371-200409000-00007.
Although novel therapies for chronic lymphocytic leukemia have resulted in higher hematologic response rates, the complete eradication of disease rarely occurs. Alemtuzumab (Campath-1H) seems to be extremely effective in this role in pretreated patients. The authors used a molecular semiquantitative polymerase chain reaction (PCR) method to assess the ability of alemtuzumab to induce PCR negativity in eight patients pretreated with fludarabine. IgH rearrangement was coamplified with a housekeeping gene and fluorescent PCR products were analyzed on a DNA automatic sequencer. Each patient was evaluated at diagnosis, after fludarabine, and after Campath-1H. The median interval between the last therapy course with fludarabine and the start of Campath-1H was 14 weeks. Patients received subcutaneous doses up to 10 mg, three times a week, for 12 weeks, with a median dose of 190 mg. After six cycles with fludarabine, only one patient (12.5%) achieved molecular remission, and in three other patients IgH levels decreased by 0.5 to 1 log. At the beginning of Campath-1H administration, all patients were PCR positive, including the one previously found to be negative. At the end of treatment, five patients achieved molecular remission (62.5%), four of them within 1 month after the end of therapy. Seventy-two percent of responses, with 43% of complete responses, were documented on bone marrow smears. A significant reduction of lymph node and spleen diameters was noted in 50% and 33% of patients, respectively. Four patients showed grade 2 skin reaction at the site of the subcutaneous injection and grade 1 or 2 fever. Two patients developed neutropenia (grade 2 and 3) and two hemolytic episodes. Three patients showed cytomegalovirus and one herpes zoster and Epstein-Barr virus reactivation. These results show that Campath-1H represents an efficacious in vivo purging tool with a safe profile.
尽管慢性淋巴细胞白血病的新型疗法已带来更高的血液学缓解率,但疾病的完全根除却很少发生。阿仑单抗(Campath-1H)在预处理患者中似乎在这方面极为有效。作者采用分子半定量聚合酶链反应(PCR)方法,评估阿仑单抗在8例接受过氟达拉滨预处理的患者中诱导PCR阴性的能力。IgH重排与一个管家基因共同扩增,荧光PCR产物在DNA自动测序仪上进行分析。每位患者在诊断时、接受氟达拉滨治疗后以及接受Campath-1H治疗后均接受评估。最后一次氟达拉滨治疗疗程与开始Campath-1H治疗之间的中位间隔为14周。患者接受皮下注射剂量高达10 mg,每周3次,共12周,中位剂量为190 mg。接受6个周期的氟达拉滨治疗后,仅有1例患者(12.5%)实现分子缓解,另外3例患者的IgH水平下降了0.5至1个对数。在开始使用Campath-1H时,所有患者PCR均为阳性,包括之前被发现为阴性的那例患者。治疗结束时,5例患者实现分子缓解(62.5%),其中4例在治疗结束后1个月内实现。骨髓涂片记录到72%的缓解,其中43%为完全缓解。分别有50%和33%的患者淋巴结和脾脏直径显著缩小。4例患者在皮下注射部位出现2级皮肤反应和1级或2级发热。2例患者出现中性粒细胞减少(2级和3级)以及2次溶血发作。3例患者出现巨细胞病毒感染,1例出现带状疱疹以及EB病毒再激活。这些结果表明,Campath-1H是一种有效的体内净化工具,安全性良好。