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Extended follow-up and impact of high-risk prognostic factors from the phase 3 RESONATE study in patients with previously treated CLL/SLL

机译:RESONATE 3期研究对先前接受过CLL / SLL治疗的患者的后续随访和高危预后因素的影响

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摘要

In the phase 3 RESONATE study, ibrutinib demonstrated superior progression-free survival (PFS), overall survival (OS) and overall response rate (ORR) compared with ofatumumab in relapsed/refractory CLL patients with high-risk prognostic factors. We report updated results from RESONATE in these traditionally chemotherapy resistant high-risk genomic subgroups at a median follow-up of 19 months. Mutations were detected by Foundation One Heme Panel. Baseline mutations in the ibrutinib arm included TP53 (51%), SF3B1 (31%), NOTCH1 (28%), ATM (19%) and BIRC3 (14%). Median PFS was not reached, with 74% of patients randomized to ibrutinib alive and progression-free at 24 months. The improved efficacy of ibrutinib vs ofatumumab continues in all prognostic subgroups including del17p and del11q. No significant difference within the ibrutinib arm was observed for PFS across most genomic subtypes, although a subset carrying both TP53 mutation and del17p had reduced PFS compared with patients with neither abnormality. Reduced PFS or OS was not evident in patients with only del17p. PFS was significantly better for ibrutinib-treated patients in second-line vs later lines of therapy. The robust clinical activity of ibrutinib continues to show ongoing efficacy and acceptable safety consistent with prior reports, independent of various known high-risk mutations.
机译:在RESONATE的3期研究中,依法鲁替尼在具有高风险预后因素的复发/难治性CLL患者中显示出优于ofatumumab的无进展生存期(PFS),总生存期(OS)和总缓解率(ORR)。我们报告了RESONATE在这些传统上具有化疗耐药性的高风险基因组亚组中的最新结果,中位随访时间为19个月。基金会一血红素检测小组检测到突变。依鲁替尼组的基线突变包括TP53(51%),SF3B1(31%),NOTCH1(28%),ATM(19%)和BIRC3(14%)。未达到中位PFS,有74%的患者在24个月时随机接受了ibrutinib的存活和无进展治疗。在包括del17p和del11q在内的所有预后亚组中,依鲁替尼和ofatumumab的疗效持续改善。在大多数基因组亚型中,依鲁替尼组内的PFS均未观察到显着差异,尽管与没有异常的患者相比,同时携带TP53突变和del17p的亚组降低了PFS。仅del17p患者的PFS或OS降低并不明显。在二线治疗中,依鲁替尼治疗的患者的PFS明显优于后期治疗。依鲁替尼的强劲临床活性继续显示出持续的疗效和可接受的安全性,与先前的报道一致,而与各种已知的高风险突变无关。

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