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首页> 外文期刊>Journal of neuro-oncology. >Phase II trial of pre-irradiation and concurrent temozolomide in patients with newly diagnosed anaplastic oligodendrogliomas and mixed anaplastic oligoastrocytomas: long term results of RTOG BR0131
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Phase II trial of pre-irradiation and concurrent temozolomide in patients with newly diagnosed anaplastic oligodendrogliomas and mixed anaplastic oligoastrocytomas: long term results of RTOG BR0131

机译:新诊断的间变性少突胶质细胞瘤和间变性少突星形胶质细胞瘤患者的放疗前和同时替莫唑胺II期试验:RTOG BR0131的长期结果

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We report on the long-term results of a phase II study of pre-irradiation temozolomide followed by concurrent temozolomide and radiotherapy (RT) in patients with newly diagnosed anaplastic oligodendroglioma (AO) and mixed anaplastic oligoastrocytoma. Pre-RT temozolomide was given for up to 6 cycles. RT with concurrent temozolomide was administered to patients with less than a complete radiographic response. Forty eligible patients were entered and 32 completed protocol treatment. With a median follow-up time of 8.7 years (range 1.1-10.1), median progression-free survival (PFS) is 5.8 years (95 % CI 2.0, NR) and median overall survival (OS) has not been reached (5.9, NR). 1p/19q data are available in 37 cases; 23 tumors had codeletion while 14 tumors had no loss or loss of only 1p or 19q (non-codeleted). In codeleted patients, 9 patients have progressed and 4 have died; neither median PFS nor OS have been reached and two patients who received only pre-RT temozolomide and no RT have remained progression-free for over 7 years. 3-year PFS and 6-year OS are 78 % (95 % CI 61-95 %) and 83 % (95 % CI 67-98 %), respectively. Codeleted patients show a trend towards improved 6-year survival when compared to the codeleted procarbazine/CCNU/vincristrine (PCV) and RT cohort in RTOG 9402 (67 %, 95 % CI 55-79 %). For non-codeleted patients, median PFS and OS are 1.3 and 5.8 years, respectively. These updated results suggest that the regimen of dose intense, pre-RT temozolomide followed by concurrent RT/temozolomide has significant activity, particularly in patients with 1p/19q codeleted AOs and MAOs.
机译:我们报告了新诊断的间变性少突胶质细胞瘤(AO)和混合间变性少突星形胶质细胞瘤患者接受放疗前替莫唑胺,同时进行替莫唑胺和放疗(RT)的II期研究的长期结果。给予RT前的替莫唑胺长达6个周期。并发替莫唑胺的放疗对放射学反应不完全的患者进行。入组40名合格患者,完成32例治疗方案。中位随访时间为8.7年(范围为1.1-10.1),中位无进展生存期(PFS)为5.8年(95%CI 2.0,未治疗),而未达到中位总体生存期(OS)(5.9, NR)。 1p / 19q数据可用于37个案例中; 23个肿瘤具有代码缺失,而14个肿瘤没有丢失或仅丢失1p或19q(非代码删除)。在无密码的患者中,有9例进展,4例死亡。既未达到中位PFS,也未达到OS,并且仅接受RT前替莫唑胺且未接受RT的两名患者在超过7年内无进展。 3年PFS和6年OS分别为78%(95%CI 61-95%)和83%(95%CI 67-98%)。与RTOG 9402中的普卡巴嗪/ CCNU /长春新碱(PCV)和RT队列相比,加密码的患者显示出改善的6年生存率的趋势(67%,95%CI 55-79%)。对于非无密码患者,中位PFS和OS分别为1.3岁和5.8岁。这些最新结果表明,剂量密集型,放疗前的替莫唑胺,同时放疗/替莫唑胺的治疗方案具有显着活性,特别是在使用1p / 19q编码的AO和MAO的患者中。

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