针对新确诊胶质母细胞瘤的肿瘤治疗场和替莫唑胺化疗放疗并用的 1 期研究

IF 3.7 Q1 CLINICAL NEUROLOGY
S. Goldlust, Samuel Singer, Lori Cappello, A. K. Almekkawi, Kangmin D Lee, Anthony C Ingenito, Brett E Lewis, Themba Nyirenda, Hooman Azmi, G. Kaptain
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引用次数: 0

摘要

胶质母细胞瘤(GBM)是最常见的侵袭性原发性脑肿瘤,有效的治疗方法有限。肿瘤治疗场(TTF;Optune Gio®)是美国食品及药物管理局(FDA)批准的一种设备,其数据支持在维持性化疗中加入该设备可显著提高生存率,且毒性极低。但在临床实践中的应用并不普遍,如果能缩短治疗时间,情况可能会有所改善。这项 1 期试验旨在确定在化疗的同时使用 TTF 的安全性和初步疗效。 经组织学确诊的新确诊 GBM 患者符合条件。手术后,患者在接受标准化疗的同时接受 TTF 治疗。该装置每月使用两个周期的替莫唑胺维持治疗,并定期进行成像和临床评估,以评估毒性和反应。主要终点是根据不良事件的发生率和严重程度确定联合模式治疗的安全性和耐受性。次要终点是总生存期(OS)和无进展生存期(PFS)。 共有 13 名患者入组。皮肤科不良事件频发,但仅限于1/2级。只有一起严重不良事件可能与TTF有关,没有患者因TTF相关毒性而无法完成规定的多模式治疗疗程。12名患者的中位生存期和6个月无进展生存期分别为8.5个月和66.7%。中位生存期和12个月总生存期分别为16.0个月和83.3%。 TTF可以安全地与化疗同时进行。有限TTF疗程的潜力值得进一步评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phase 1 Study of Concomitant Tumor Treating Fields and Temozolomide Chemoradiation for Newly Diagnosed Glioblastoma
Glioblastoma (GBM) is the most common and aggressive primary brain tumor and has limited effective therapies. Tumor treating fields (TTF; Optune Gio®) is an FDA- approved device with data supporting a significant survival benefit and minimal toxicity when added to maintenance chemotherapy. Uptake in clinic practice is not universal and might improve if a shorter duration of treatment is feasible. This phase 1 trial was designed to determine the safety and preliminary efficacy of TTF concomitant to chemoradiation. Patients with newly diagnosed, histologically confirmed GBM were eligible. Following surgery, patients were treated with TTF concomitant to standard chemoradiation. The device continued through two monthly cycles of maintenance temozolomide with imaging and clinical assessments at regular intervals to assess toxicity and response. The primary endpoint was safety and tolerability of combined modality treatment based upon the incidence and severity of adverse events. Secondary endpoints were overall survival (OS) and progression free survival (PFS). Thirteen patients were enrolled. Dermatologic adverse events were frequent but limited to grade 1/2. There was only one serious adverse event possibly related to TTF and no patients were unable to complete the prescribed course of multimodality treatment due to TTF -associated toxicity. Twelve patients were evaluable for median and six-month progression free survival which were 8.5 months (mo) and 66.7% respectively. Median and 12 mo overall survival were 16.0 mo and 83.3% respectively. TTF can be safely delivered in conjunction with chemoradiation. The potential for a finite TTF course merits further evaluation.
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来源期刊
CiteScore
6.20
自引率
0.00%
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12 weeks
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