Suppr超能文献

3 期 HELIOS 研究中伊布替尼、苯达莫司汀和利妥昔单抗治疗复发慢性淋巴细胞白血病/小淋巴细胞淋巴瘤的更新结果。

Updated results from the phase 3 HELIOS study of ibrutinib, bendamustine, and rituximab in relapsed chronic lymphocytic leukemia/small lymphocytic lymphoma.

机构信息

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.

出版信息

Leukemia. 2019 Apr;33(4):969-980. doi: 10.1038/s41375-018-0276-9. Epub 2018 Oct 12.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验