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首页> 外文期刊>Journal of neuro-oncology. >Phase II study of temozolomide and cisplatin as primary treatment prior to radiotherapy in newly diagnosed glioblastoma multiforme patients with measurable disease. A study of the Spanish Medical Neuro-Oncology Group (GENOM).
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Phase II study of temozolomide and cisplatin as primary treatment prior to radiotherapy in newly diagnosed glioblastoma multiforme patients with measurable disease. A study of the Spanish Medical Neuro-Oncology Group (GENOM).

机译:在新诊断的多形性胶质母细胞瘤患者中,替莫唑胺和顺铂作为放疗前主要治疗方法的II期研究。西班牙医学神经肿瘤学小组(GENOM)的研究。

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This phase II study evaluates the activity of temozolomide and cisplatin administered before radiation therapy in newly diagnosed glioblastoma multiforme patients, in terms of response, time to progression and survival. PATIENTS AND METHODS: Forty patients with measurable disease after surgery, a Karnofsky status > 60, and Barthel Index > 10 were included. They were treated with three cycles of temozolomide 200 mg/m2/day for 5 days and cisplatin 100 mg/m2 on day 1. Conventional focal radiation therapy to 60 Gy was administered after response evaluation. RESULTS: Three patients were not evaluable for central reviewed response but all 40 were evaluable for toxicity, time to progression and survival. Objective responses by Macdonald criteria on an intent to treat basis were 45% including complete response in three patients (7.5%), and partial response in 15 patients (37.5%). Responses were seen in biopsy-only patients (33.4%) as well as in partial surgery patients (52%). Median survival for all patients was 12.5 months. Biopsy-only patients had a median survival of 12.8 months. Grade 3 to 4 neutropenia was the most important toxicity, and occurred in 37.5% of patients. A delay in 18.2% and a dose reduction in 9.6% of cycles were necessary due to myelosuppression on day 28. Two patients had neutropenic fever resulting in one treatment-related death. Eighty-two percent of patients received radiotherapy. CONCLUSION: This regimen has significant activity, as it induces objective responses even in biopsy-only patients, appearing to improve their median survival. A better combination schedule is needed to improve the toxicity profile.
机译:这项II期研究评估了新诊断的成胶质母细胞瘤患者放疗前替莫唑胺和顺铂的活性,包括反应,进展时间和生存率。患者与方法:包括40例术后可测量的疾病,卡诺夫斯基状态> 60,巴特尔指数> 10的患者。他们分别接受3个周期的替莫唑胺200 mg / m2 /天的治疗,共5天,顺铂100 mg / m2在第1天的治疗。在反应评估后,常规放疗至60 Gy。结果:三例患者的中枢性评估反应未得到评估,但所有40例患者的毒性,进展时间和生存率均得到了评估。以治疗意图为基础的麦克唐纳德标准的客观缓解为45%,包括三位患者的完全缓解(7.5%)和15位患者的部分缓解(37.5%)。仅活检患者(33.4%)和部分手术患者(52%)观察到反应。所有患者的中位生存期为12.5个月。仅活检的患者中位生存期为12.8个月。 3至4级中性粒细胞减少是最重要的毒性反应,发生在37.5%的患者中。由于第28天的骨髓抑制,必须延迟18.2%的剂量并减少9.6%的周期。两名患者出现中性粒细胞减少症,导致一名与治疗有关的死亡。 82%的患者接受了放射治疗。结论:该方案具有显着的活性,因为它甚至在仅活检的患者中也能引起客观反应,从而似乎改善了其中位生存期。需要更好的组合方案以改善毒性。

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