Thieblemont Catherine, Bouafia Fadhela, Hornez Emmanuel, Dumontet Charles, Tartas Sophie, Antal Daciana, Lemieux Bernard, Traullé Catherine, Espinouse Daniel, Salles Gilles, Coiffier Bertrand
Hematology Departement, Hospices civils de Lyon, Claude Bernard University, 69495 Pierre-Benite, France.
Leuk Lymphoma. 2004 Apr;45(4):711-4. doi: 10.1080/10428190310001615675.
Alemtuzumab, the monoclonal anti-CD52 antibody, has clinical activity in B-cell and T-cell malignancies at the dose of 30 mg three times weekly for 9-12 weeks. This standard regimen induced responses usually shorter than 6 months. To prolong time to progression, we initialized a phase II study with an identical initial scheme until partial response, followed by a maintenance therapy lasting at least 4 months. Eleven heavily pretreated patients (8 with B-chronic lymhocytic leukemia (B-CLL) and 3 with small lymphoctyic lymphoma (SLL)) have been treated with this maintenance regimen (MR patients) and were retrospectively compared to 5 patients (3 B-CLL and 2 SLL) treated with the standard regimen (SR patients). Patients characteristics before treatment were identical in both groups. Objective response was reached by 9 (82%) MR patients and 3 (60%) SR patients (p NS). After the treatment, 8 (73%) MR patients and all SR patients progressed with a median time at 12.2 months and 3 months respectively. Survival time from alemtuzumab was significatively different (P < 0.005). None of the patients died in the MR group with a median follow-up at 16 months. In the SR group, the median survival from alemtuzumab was 5.9 months. We did not observe any differences in terms of hematological toxicites and infections between the two groups. In conclusion, maintenance alemtuzumab therapy seems to increase the time to progression and the survival, without adding hematological toxicities and infectious complications. More patients are needed to confirm this observation.
阿仑单抗,一种单克隆抗CD52抗体,以每周三次、每次30毫克的剂量给药9至12周,对B细胞和T细胞恶性肿瘤具有临床活性。这种标准方案诱导的缓解通常短于6个月。为了延长疾病进展时间,我们启动了一项II期研究,采用相同的初始方案直至出现部分缓解,随后进行至少持续4个月的维持治疗。11例经过大量预处理的患者(8例B细胞慢性淋巴细胞白血病(B-CLL)和3例小淋巴细胞淋巴瘤(SLL))接受了这种维持方案治疗(MR组患者),并与5例接受标准方案治疗的患者(3例B-CLL和2例SLL,SR组患者)进行回顾性比较。两组治疗前的患者特征相同。9例(82%)MR组患者和3例(60%)SR组患者达到客观缓解(p无统计学意义)。治疗后,8例(73%)MR组患者和所有SR组患者病情进展,中位进展时间分别为12.2个月和3个月。阿仑单抗治疗后的生存时间有显著差异(P<0.005)。MR组患者在中位随访16个月时均未死亡。在SR组,阿仑单抗治疗后的中位生存期为5.9个月。我们未观察到两组在血液学毒性和感染方面存在任何差异。总之,阿仑单抗维持治疗似乎能延长疾病进展时间和生存期,且不增加血液学毒性和感染并发症。需要更多患者来证实这一观察结果。