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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Tumour Treating Fields (TTFields) in combination with lomustine and temozolomide in patients with newly diagnosed glioblastoma
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Tumour Treating Fields (TTFields) in combination with lomustine and temozolomide in patients with newly diagnosed glioblastoma

机译:肿瘤处理田地(TTFIELDS)与新诊断的胶质母细胞瘤患者中的LOMUSTINE和Temozolomide组合

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Purpose In the EF-14 trial for newly diagnosed glioblastoma (ndGBM) patients addition of Tumour Treating Fields (TTFields) to temozolomide treatment resulted in a significantly improved overall survival (OS). In the NOA-09/CeTeG trial, combination of lomustine and temozolomide was superior to temozolomide monotherapy in patients with O6-methylguanine DNA methyltransferase (MGMT) promoter methylated (MGMTm) ndGBM. We evaluated combination of these two treatment modalities in patients with MGMTm ndGBM. There have been so far no data on the combination of these two efficient regimens. Methods This bicentric retrospective analysis investigated 16 patients. Parameters evaluated included safety outcome as measured by Common Toxicity Criteria for Adverse Events (CTCAE), clinical outcomes, and compliance to treatment. Results Hematologic adverse events CTCAE >= 3 were observed in seven, hepatotoxic adverse events of CTCAE >= 3 in four patients. Mild to moderate skin toxicity was detected in six patients. At data cutoff, patients demonstrated a median progression-free survival (PFS) of 20 months. The usage rate of TTFields showed a high median adherence (83%) to the therapy. Conclusions This analysis provides first indication that the combination of TTFields/lomustine/temozolomide is safe and feasible. The observed survival outcomes might suggest potential beneficial effects.
机译:目的在EF-14试验中进行新诊断的胶质母细胞瘤(NDGBM)患者的患者加入肿瘤处理田间(TTFIELS)对替替莫唑胺治疗导致了显着改善的整体存活率(OS)。在NOA-09 / Ceteg试验中,Lomustine和Temozolomide的组合优于O6-甲基叶甲烷DNA甲基转移酶(MGMT)启动子甲基化(MgMTM)NdGBM患者的替莫唑胺单疗法。我们评估了MGMTM NDGBM患者的这两种治疗方式的组合。到目前为止没有关于这两个有效的方案组合的数据。方法该双发回图分析研究了16例。评估的参数包括通过常见毒性标准来测量的不良事件(CTCAE),临床结果和治疗依从性测量的安全结果。结果血液学不良事件CTCAE> = 3在七,肝毒性不良事件中观察到四个患者中的肝毒性不良事件> = 3。在六名患者中检测到轻度至中度皮肤毒性。在数据截止下,患者展示了20个月的中位进展生存期(PFS)。 TTFIELS的使用率显示治疗的高中粘附(83%)。结论该分析提供了第一个指示TTFIELS / LOMUSTINE / Temozolomide的组合是安全可行的。观察到的生存结果可能表明潜在的有益效果。

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