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一项在未经甲基化 MGMT 脑胶质母细胞瘤患者中进行的随机 II 期试验:VELIparib、放疗和替莫唑胺(VERTU 研究)。

A randomized phase II trial of veliparib, radiotherapy, and temozolomide in patients with unmethylated MGMT glioblastoma: the VERTU study.

机构信息

NHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia.

St Vincent's Clinical School, University of New South Wales, Sydney, Australia.

出版信息

Neuro Oncol. 2021 Oct 1;23(10):1736-1749. doi: 10.1093/neuonc/noab111.

Abstract

BACKGROUND

Temozolomide offers minimal benefit in patients with glioblastoma with unmethylated O6-methylguanine-DNA methyltransferase (MGMT) promoter status, hence, the need for novel therapies. This study evaluated whether veliparib, a brain-penetrant poly(ADP-ribose) polymerase (PARP) inhibitor, acts synergistically with radiation and temozolomide.

METHODS

VERTU was a multicenter 2:1 randomized phase II trial in patients with newly diagnosed glioblastoma and MGMT-unmethylated promotor status. The experimental arm consisted of veliparib and radiotherapy, followed by adjuvant veliparib and temozolomide. The standard arm consisted of concurrent temozolomide and radiotherapy, followed by adjuvant temozolomide. The primary objective was to extend the progression-free survival rate at six months (PFS-6m) in the experimental arm.

RESULTS

A total of 125 participants were enrolled, with 84 in the experimental arm and 41 in the standard arm. The median age was 61 years, 70% were male, 59% had Eastern Cooperative Oncology Group (ECOG) performance status of 0, and 87% underwent macroscopic resection. PFS-6m was 46% (95% confidence interval [CI]: 36%-57%) in the experimental arm and 31% (95% CI: 18%-46%) in the standard arm. Median overall survival was 12.7 months (95% CI: 11.4-14.5 months) in the experimental arm and 12.8 months (95% CI: 9.5-15.8 months) in the standard arm. The most common grade 3-4 adverse events were thrombocytopenia and neutropenia, with no new safety signals.

CONCLUSION

The veliparib-containing regimen was feasible and well tolerated. However, there was insufficient evidence of clinical benefit in this population. Further information from correlative translational work and other trials of PARP inhibitors in glioblastoma are still awaited.

摘要

背景

替莫唑胺在 O6-甲基鸟嘌呤-DNA 甲基转移酶(MGMT)启动子状态未甲基化的胶质母细胞瘤患者中获益甚微,因此需要新的治疗方法。本研究评估了 veliparib(一种脑穿透性聚(ADP-核糖)聚合酶(PARP)抑制剂)与放疗和替莫唑胺联合应用是否具有协同作用。

方法

VERTU 是一项多中心、2:1 随机的 II 期临床试验,纳入了新诊断的胶质母细胞瘤且 MGMT 启动子状态未甲基化的患者。实验组由 veliparib 和放疗组成,随后是辅助 veliparib 和替莫唑胺。标准组由替莫唑胺联合放疗组成,随后是辅助替莫唑胺。主要目的是延长实验组的 6 个月无进展生存期(PFS-6m)。

结果

共纳入 125 名患者,实验组 84 例,标准组 41 例。中位年龄为 61 岁,70%为男性,59%的东部肿瘤协作组(ECOG)表现状态为 0,87%行大体切除术。实验组的 6 个月无进展生存率(PFS-6m)为 46%(95%置信区间 [CI]:36%-57%),标准组为 31%(95% CI:18%-46%)。实验组的中位总生存期为 12.7 个月(95% CI:11.4-14.5 个月),标准组为 12.8 个月(95% CI:9.5-15.8 个月)。最常见的 3-4 级不良事件为血小板减少和中性粒细胞减少,无新的安全信号。

结论

含 veliparib 的方案是可行且耐受良好的。然而,在该人群中,没有足够的临床获益证据。仍需等待相关转化研究和其他 PARP 抑制剂在胶质母细胞瘤中的试验的进一步信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82c2/8485443/0eaddcd88c94/noab111f0001.jpg

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