Department of Haematology and Oncology, Göttingen Comprehensive Cancer Center (G-CCC), Georg-August-University, 37099, Goettingen, Germany.
Ann Hematol. 2013 Nov;92(11):1521-8. doi: 10.1007/s00277-013-1880-4. Epub 2013 Aug 24.
The rate of long-term remissions after treatment of peripheral T cell lymphomas (PTCL) with standard CHOP-like protocols is unsatisfactory. A prospective multicenter phase II trial was initiated in untreated patients with PTCL of all International Prognostic Index-risk groups, evaluating alemtuzumab consolidation in patients with complete or good partial remission after CHO(E)P-14 induction. Twenty-nine (70.7 %) of the 41 enrolled patients received alemtuzumab consolidation (133 mg in total). The main grades 3-4 toxicities during alemtuzumab therapy were infections and neutropenia with one potentially treatment-related death. Complete responses were seen in 58.5 %, partial responses in 2.4 % and 29.3 % had progressive disease. After a median observation time of 46 months, 19 patients have died, 16 of them due to lymphoma and/or salvage therapy complications. Event-free and overall survival at 3 years in the whole intent to treat population are 32.3 and 62.5 %, respectively, and 42.4 and 75.1 % in the patients who received alemtuzumab. In conclusion, application of a short course of alemtuzumab after CHO(E)P-14 induction is feasible although complicated by severe infections. A current phase III trial, applying alemtuzumab as part of the initial chemotherapy protocol to avoid early progression, will further clarify its significance for the therapeutic outcome.
采用标准 CHOP 样方案治疗外周 T 细胞淋巴瘤(PTCL)后的长期缓解率并不令人满意。一项针对所有国际预后指数风险组的未经治疗的 PTCL 患者的前瞻性多中心 II 期试验,评估了在 CHO(E)P-14 诱导后完全或部分缓解的患者中用阿仑单抗进行巩固治疗。41 名入组患者中有 29 名(70.7%)接受了阿仑单抗巩固治疗(总剂量为 133mg)。阿仑单抗治疗期间主要的 3-4 级毒性是感染和中性粒细胞减少症,有 1 例可能与治疗相关的死亡。完全缓解率为 58.5%,部分缓解率为 2.4%,29.3%的患者疾病进展。中位观察时间为 46 个月后,19 名患者死亡,其中 16 名死于淋巴瘤和/或挽救治疗并发症。在整个意向治疗人群中,3 年时的无事件生存和总生存分别为 32.3%和 62.5%,接受阿仑单抗治疗的患者分别为 42.4%和 75.1%。总之,在 CHO(E)P-14 诱导后应用短疗程阿仑单抗是可行的,尽管严重感染使情况复杂化。目前正在进行的 III 期试验,将阿仑单抗作为初始化疗方案的一部分来避免早期进展,将进一步明确其对治疗结果的意义。