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在既往治疗的 CLL/SLL 患者中,3 期 RESONATE 研究中高危预后因素的延长随访及影响。

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

机构信息

Dana-Farber Cancer Institute, Boston, MA, USA.

St James Institute of Oncology, Leeds, UK.

出版信息

Leukemia. 2018 Jan;32(1):83-91. doi: 10.1038/leu.2017.175. Epub 2017 Jun 8.

Abstract

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.

摘要

在 3 期 RESONATE 研究中,与奥法妥木单抗相比,伊布替尼在伴有高风险预后因素的复发/难治性 CLL 患者中显示出优越的无进展生存期(PFS)、总生存期(OS)和总缓解率(ORR)。我们报告了 RESONATE 研究中这些传统上对化疗耐药的高风险基因组亚组的更新结果,中位随访时间为 19 个月。突变通过 FoundationOne Heme Panel 检测。伊布替尼组的基线突变包括 TP53(51%)、SF3B1(31%)、NOTCH1(28%)、ATM(19%)和 BIRC3(14%)。中位 PFS 未达到,随机分配至伊布替尼组的 74%患者在 24 个月时仍存活且无疾病进展。伊布替尼与奥法妥木单抗相比的疗效改善在所有预后亚组中持续存在,包括 del17p 和 del11q。在大多数基因组亚型中,伊布替尼组内的 PFS 并未观察到各亚组之间的显著差异,尽管携带 TP53 突变和 del17p 的亚组与既无异常的患者相比,PFS 降低。仅携带 del17p 的患者未出现 PFS 或 OS 降低。与后线治疗相比,二线及以后治疗的伊布替尼治疗患者的 PFS 显著改善。伊布替尼的稳健临床活性持续显示出一致的疗效和可接受的安全性,与之前的报告一致,与各种已知的高风险突变无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/beb2/5770586/bbc884ec839c/leu2017175f1.jpg

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