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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Long-term follow-up of the RESONATE phase 3 trial of ibrutinib vs ofatumumab
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Long-term follow-up of the RESONATE phase 3 trial of ibrutinib vs ofatumumab

机译:长期随访的共鸣相3试验Ibrutinib Vs atatumumab

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摘要

Ibrutinib, a once-daily oral inhibitor of Bruton tyrosine kinase, has greatly improved outcomes for patients with chronic lymphocytic leukemia (CLL). The phase 3 RESONATE trial, which compared single-agent ibrutinib to ofatumumab in high-risk, relapsed patients with CLL, provided support for approval of ibrutinib in the United States and Europe. We describe long-term follow-up of patients treated in RESONATE, where continued superiority of progression-free survival (PFS) (hazard ratio [HR], 0.133; 95% confidence interval [CI], 0.099-0.178) was observed. Overall survival benefit continues (HR, 0.591; 95% CI, 0.378-0.926), although with decreased magnitude relative to that seen before crossover to ibrutinib was implemented for patients on ofatumumab (HR, 0.426; 95% CI, 0.220-0.823). Notably, overall response to ibrutinib increased over time, with 91% of patients attaining a response. The PFS benefit with ibrutinib was independent of baseline risk factors, although patients with >= 2 prior therapies had shorter PFS than those with = 3 adverse events generally decreased over time, causing only a small proportion of patients to cease therapy. Ibrutinib was discontinued due to progressive disease in 27% of patients. This long-term study provides support for sustained efficacy and safety of ibrutinib in relapsed/refractory CLL and consideration of study provisions that allow crossover to investigational therapy when benefit has been clearly demonstrated.
机译:伊布洛替尼(Bruton Tyrosine激酶)曾经每日口服抑制剂,对慢性淋巴细胞白血病(CLL)患者的结果大大提高了结果。第3阶段共振试验,其在高风险中与高风险,复发的CLL患者的单孕易替替尼对其进行了比较,提供了支持在美国和欧洲批准伊布鲁替尼的支持。我们描述了在共振治疗的患者的长期随访,其中延续的无进展存活(PFS)(危害比[HR],0.133; 95%置信区间[CI],0.099-0.178)。总体存活益处继续(HR,0.591; 95%CI,0.378-0.926),但对于在ofaTumumab(HR,0.426; 95%CI,0.220-0.823)上的患者实施了对Ibrutinib的交叉之前,相对于Ibrutinib的交叉进行了降低的幅度。值得注意的是,对Ibrutinib的总体反应随着时间的推移而增加,91%的患者达到了反应。与Ibrutinib的PFS益处与基线风险因素无关,尽管患者> = 2患者的患者的PFS比随着时间的推移通常降低= 3个不良事件,但甚至只有一小部分患者停止治疗。由于27%的患者患有渐进性疾病,Ibrutinib被停止。这项长期研究为伊布洛替尼对复发/难治性CLL的持续疗效和安全性提供了支持,并考虑了在清楚地证明有利时允许交叉对调查治疗的研究。

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