Beth Israel Comprehensive Cancer Center, New York, New York, USA,
Dana Farber Cancer Institute-ECOG-ACRIN Biostatistics Center, Boston, Massachusetts, USA.
Acta Haematol. 2019;142(4):224-232. doi: 10.1159/000500164. Epub 2019 Jul 23.
Patients with relapsed/refractory (R/R) chronic lymphocytic leukemia (CLL) may benefit from salvage chemoimmunotherapy (CIT). To explore further the use of CIT in the pre-novel agent era, ECOG-ACRIN undertook a phase 2 trial (E2903) for R/R CLL utilizing pentostatin, cyclophosphamide, and rituximab (PCR) followed by a consolidation course of alemtuzumab. This trial enrolled 102 patients with a median age of 64 years. Treatment consisted of 6 cycles of PCR followed by alemtuzumab for either 4 or 18 weeks depending on the initial response to PCR. The overall response after PCR (complete remission, CR, nodular partial remission, nPR, and partial remission, PR) was 55%. Major responses (CR or nPR) were achieved in 6%. The median overall survival (OS) and the median progression-free survival were 28 and 12 months, respectively. The most serious nonlethal adverse events were myelosuppression, febrile neutropenia, fatigue, nausea, and hyponatremia. PCR is an effective and well-tolerated nucleoside-based regimen for heavily pretreated CLL patients with R/R disease. The addition of alemtuzumab to CLL patients with a minor response (PR) or stable disease did not result in a significant number of higher responses (CR or nPR) nor an improvement in OS.
复发/难治性 (R/R) 慢性淋巴细胞白血病 (CLL) 患者可能从挽救性化疗免疫治疗 (CIT) 中获益。为了在新型药物出现之前进一步探索 CIT 的应用,ECOG-ACRIN 开展了一项针对 R/R CLL 的 2 期试验 (E2903),采用了苯达莫司汀、环磷酰胺和利妥昔单抗 (PCR),随后进行了阿仑单抗巩固治疗。该试验纳入了 102 例中位年龄为 64 岁的患者。治疗包括 6 个周期的 PCR,随后根据对 PCR 的初始反应,给予阿仑单抗 4 或 18 周的治疗。PCR 后的总体缓解率(完全缓解 (CR)、结节部分缓解 (nPR) 和部分缓解 (PR))为 55%。主要缓解(CR 或 nPR)的发生率为 6%。中位总生存期 (OS) 和中位无进展生存期分别为 28 个月和 12 个月。最严重的非致命性不良事件为骨髓抑制、发热性中性粒细胞减少、疲劳、恶心和低钠血症。PCR 是一种有效的、耐受性良好的核苷类方案,适用于 R/R 疾病的大量预处理过的 CLL 患者。在对 PCR 有轻微缓解 (PR) 或疾病稳定的 CLL 患者中添加阿仑单抗,并未导致更高比例的缓解(CR 或 nPR),也未改善 OS。