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氯丙嗪作为未甲基化基因启动子的胶质母细胞瘤患者辅助治疗的疗效和安全性:II期多中心试验RACTAC

Efficacy and safety of chlorpromazine as an adjuvant therapy for glioblastoma in patients with unmethylated gene promoter: RACTAC, a phase II multicenter trial.

作者信息

Pace Andrea, Lombardi Giuseppe, Villani Veronica, Benincasa Dario, Abbruzzese Claudia, Cestonaro Ilaria, Corrà Martina, Padovan Marta, Cerretti Giulia, Caccese Mario, Silvani Antonio, Gaviani Paola, Giannarelli Diana, Ciliberto Gennaro, Paggi Marco G

机构信息

IRCCS - Regina Elena National Cancer Institute, Rome, Italy.

Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.

出版信息

Front Oncol. 2023 Dec 14;13:1320710. doi: 10.3389/fonc.2023.1320710. eCollection 2023.

Abstract

INTRODUCTION

Drug repurposing is a promising strategy to develop new treatments for glioblastoma. In this phase II clinical trial, we evaluated the addition of chlorpromazine to temozolomide in the adjuvant phase of the standard first-line therapeutic protocol in patients with unmethylated gene promoter.

METHODS

This was a multicenter phase II single-arm clinical trial. The experimental procedure involved the combination of CPZ with standard treatment with TMZ in the adjuvant phase of the Stupp protocol in newly-diagnosed GBM patients carrying an unmethylated gene promoter. Progression-free survival was the primary endpoint. Secondary endpoints were overall survival and toxicity.

RESULTS

Forty-one patients were evaluated. Twenty patients (48.7%) completed 6 cycles of treatment with TMZ+CPZ. At 6 months, 27 patients (65.8%) were without progression, achieving the primary endpoint. Median PFS was 8.0 months (95% CI: 7.0-9.0). Median OS was 15.0 months (95% CI: 13.1-16.9). Adverse events led to reduction or interruption of CPZ dosage in 4 patients (9.7%).

DISCUSSION

The addition of CPZ to standard TMZ in the first-line treatment of GBM patients with unmethylated gene promoter was safe and led to a longer PFS than expected in this population of patients. These findings provide proof-of-concept for the potential of adding CPZ to standard TMZ treatment in GBM patients with unmethylated gene promoter.

CLINICAL TRIAL REGISTRATION

https://clinicaltrials.gov/study/NCT04224441, identifier NCT04224441.

摘要

引言

药物重新利用是开发胶质母细胞瘤新疗法的一种有前景的策略。在这项II期临床试验中,我们评估了在未甲基化基因启动子的患者的标准一线治疗方案的辅助阶段,将氯丙嗪添加到替莫唑胺中。

方法

这是一项多中心II期单臂临床试验。实验程序包括在新诊断的携带未甲基化基因启动子的胶质母细胞瘤患者的Stupp方案辅助阶段,将CPZ与TMZ标准治疗相结合。无进展生存期是主要终点。次要终点是总生存期和毒性。

结果

评估了41名患者。20名患者(48.7%)完成了TMZ+CPZ的6个周期治疗。在6个月时,27名患者(65.8%)无进展,达到主要终点。中位无进展生存期为8.0个月(95%CI:7.0-9.0)。中位总生存期为15.0个月(95%CI:13.1-16.9)。不良事件导致4名患者(9.7%)的CPZ剂量减少或中断。

讨论

在未甲基化基因启动子的胶质母细胞瘤患者的一线治疗中,将CPZ添加到标准TMZ中是安全的,并且在该患者群体中导致了比预期更长的无进展生存期。这些发现为在未甲基化基因启动子的胶质母细胞瘤患者的标准TMZ治疗中添加CPZ的潜力提供了概念验证。

临床试验注册

https://clinicaltrials.gov/study/NCT04224441,标识符NCT04224441。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf9/10755935/22e245c13ee9/fonc-13-1320710-g001.jpg

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