Juravinski Cancer Centre, McMaster University, Hamilton, ON, Canada.
Department of Internal Medicine, Center of Integrated Oncology and German CLL Study Group, University of Cologne, Cologne, Germany.
Leukemia. 2019 Apr;33(4):969-980. doi: 10.1038/s41375-018-0276-9. Epub 2018 Oct 12.
We report follow-up results from the randomized, placebo-controlled, phase 3 HELIOS trial of ibrutinib+bendamustine and rituximab (BR) for previously treated chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL) without deletion 17p. Overall, 578 patients were randomized 1:1 to either ibrutinib (420 mg daily) or placebo, in combination with 6 cycles of BR, followed by ibrutinib or placebo alone. Median follow-up was 34.8 months (range: 0.1-45.8). Investigator-assessed median progression-free survival (PFS) was not reached for ibrutinib+BR, versus 14.3 months for placebo+BR (hazard ratio [HR] [95% CI], 0.206 [0.159-0.265]; P < 0.0001); 36-month PFS rates were 68.0% versus 13.9%, respectively. The results are consistent with the primary analysis findings (HR = 0.203, as assessed by independent review committee, with 17-month median follow-up). Median overall survival was not reached in either arm; HR (95% CI) for ibrutinib+BR versus placebo: 0.652 (0.454-0.935; P = 0.019). Minimal residual disease (MRD)-negative response rates were 26.3% for ibrutinib+BR and 6.2% for placebo+BR (P < 0.0001). Incidence of treatment-emergent adverse events (including grades 3-4) were generally consistent with the initial HELIOS report. These long-term data support improved survival outcomes and deepening responses with ibrutinib+BR compared with BR in relapsed CLL/SLL.
我们报告了ibrutinib+bendamustine 和利妥昔单抗(BR)治疗先前未经治疗的慢性淋巴细胞白血病(CLL)/小淋巴细胞淋巴瘤(SLL)且无 17p 缺失的随机、安慰剂对照、3 期 HELIOS 试验的随访结果。总体而言,578 名患者按 1:1 随机分配至ibrutinib(每天 420mg)或安慰剂组,联合 6 个周期的 BR,然后单独使用 ibrutinib 或安慰剂。中位随访时间为 34.8 个月(范围:0.1-45.8)。研究者评估的无进展生存期(PFS)ibrutinib+BR 未达到,而安慰剂+BR 为 14.3 个月(风险比 [HR] [95%CI],0.206 [0.159-0.265];P<0.0001);36 个月 PFS 率分别为 68.0%和 13.9%。结果与主要分析结果一致(独立审查委员会评估的 HR=0.203,中位随访 17 个月)。两个治疗组的中位总生存期均未达到;ibrutinib+BR 与安慰剂的 HR(95%CI):0.652(0.454-0.935;P=0.019)。ibrutinib+BR 的微小残留病(MRD)阴性反应率为 26.3%,安慰剂+BR 为 6.2%(P<0.0001)。治疗中出现的不良事件(包括 3-4 级)的发生率与 HELIOS 初始报告基本一致。与 BR 相比,ibrutinib+BR 可改善复发 CLL/SLL 的生存结果并加深缓解。