Department of Internal Medicine III with Hematology and Medical Oncology, Oncologic Center, Paracelsus Medical University Salzburg, Müllner-Hauptstr. 48, 5020, Salzburg, Austria.
Salzburg Cancer Research Institute - Laboratory of Immunological and Molecular Cancer Research (SCRI-LIMCR) and Cancer Cluster Salzburg (CCS), Salzburg, Austria.
Ann Hematol. 2018 Oct;97(10):1825-1839. doi: 10.1007/s00277-018-3380-z. Epub 2018 Jun 4.
Despite recent advances, chemoimmunotherapy remains a standard for fit previously untreated chronic lymphocytic leukaemia patients. Lenalidomide had activity in early monotherapy trials, but tumour lysis and flare proved major obstacles in its development. We combined lenalidomide in increasing doses with six cycles of fludarabine and rituximab (FR), followed by lenalidomide/rituximab maintenance. In 45 chemo-naive patients, included in this trial, individual tolerability of the combination was highly divergent and no systematic toxicity determining a maximum tolerated dose was found. Grade 3/4 neutropenia (71%) was high, but only 7% experienced grade 3 infections. No tumour lysis or flare > grade 2 was observed, but skin toxicity proved dose-limiting in nine patients (20%). Overall and complete response rates after induction were 89 and 44% by intention-to-treat, respectively. At a median follow-up of 78.7 months, median progression-free survival (PFS) was 60.3 months. Minimal residual disease and immunoglobulin variable region heavy chain mutation state predicted PFS and TP53 mutation most strongly predicted OS. Baseline clinical factors did not predict tolerance to the immunomodulatory drug lenalidomide, but pretreatment immunophenotypes of T cells showed exhausted memory CD4 cells to predict early dose-limiting non-haematologic events. Overall, combining lenalidomide with FR was feasible and effective, but individual changes in the immune system seemed associated with limiting side effects. clinicaltrials.gov (NCT00738829) and EU Clinical Trials Register ( www.clinicaltrialsregister.eu , 2008-001430-27).
尽管最近取得了进展,但化疗免疫疗法仍然是适合以前未经治疗的慢性淋巴细胞白血病患者的标准治疗方法。来那度胺在早期单药治疗试验中具有活性,但肿瘤溶解和发作被证明是其发展的主要障碍。我们将来那度胺与六周期氟达拉滨和利妥昔单抗(FR)联合使用,然后进行来那度胺/利妥昔单抗维持治疗。在这项试验中,我们纳入了 45 名化疗初治患者,该组合的个体耐受性差异很大,没有发现确定最大耐受剂量的系统性毒性。3/4 级中性粒细胞减少症(71%)发生率较高,但仅有 7%的患者发生 3 级感染。未观察到 2 级以上的肿瘤溶解或发作,但皮肤毒性在 9 名患者(20%)中成为剂量限制因素。按意向治疗,诱导后的总缓解率和完全缓解率分别为 89%和 44%。在中位随访 78.7 个月时,中位无进展生存期(PFS)为 60.3 个月。微小残留病和免疫球蛋白可变区重链突变状态预测 PFS,TP53 突变最强烈地预测 OS。基线临床因素不能预测免疫调节药物来那度胺的耐受性,但 T 细胞的预处理免疫表型显示耗尽的记忆 CD4 细胞可预测早期剂量限制的非血液学事件。总的来说,将来那度胺与 FR 联合使用是可行且有效的,但免疫系统的个体变化似乎与限制副作用有关。clinicaltrials.gov(NCT00738829)和欧盟临床试验注册中心(www.clinicaltrialsregister.eu,2008-001430-27)。