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首页> 外文期刊>Journal of Neuro-Oncology >Radiotherapy and concomitant temozolomide during the first and last weeks in high grade gliomas: long-term analysis of a phase II study
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Radiotherapy and concomitant temozolomide during the first and last weeks in high grade gliomas: long-term analysis of a phase II study

机译:放疗和伴替莫唑胺在高级别神经胶质瘤的最初和最后几周:II期研究的长期分析

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We tested the efficacy and safety of temozolomide (TMZ) when given concomitantly to radiotherapy only in the first and last weeks of treatment to patients affected by high grade gliomas. Conformal radiotherapy (CTV1: tumor bed + residual tumor if present + 1.5 cm, 5,940 cGy, 180 cGy/day; CTV2: oedema, 3,960 cGy, 180 cGy/day) was associated with TMZ, 75 mg/m2 × 5 days, the first and last weeks of radiotherapy. Adjuvant chemotherapy with TMZ (150 mg/mq daily × 5 days, q28 on the first cycle, 200 mg/mq daily × 5 days, q28 for the following cycles) was given, after chemoradiation, until disease progression or up to 6 cycles. From October 2000 to December 2003, 29 patients (25 GBL, 86.2%; 4 AA, 13.8%) were enrolled in this study. Twenty-two patients (75.8%) received a median 6 cycles of adjuvant chemotherapy with TMZ (range 1–20). Hematological toxicity was absent during concomitant chemoradiation and mild in adjuvant therapy, while neurological toxicity (seizures) was observed only in one case. At a median follow-up of 66 months (range 3–96), median progression-free survival (PFS) was 8 months, with a 1- and 2-year PFS of 46.7 and 28.7%, respectively; median overall survival (OS) time was 21 months, with a 1- and 2-year OS of 69.2 and 42.3%, respectively. In our experience, TMZ proved to be effective even when given only during the first and the last week of radiotherapy, with lower hematological toxicity. Keywords Chemoradiation - Glioblastoma - Schedule - Temozolomide
机译:我们仅在受高度神经胶质瘤影响的患者治疗的最初和最后几周中,与替莫唑胺(TMZ)一起进行放疗时,测试了替莫唑胺(TMZ)的疗效和安全性。适形放疗(CTV1:肿瘤床+残留肿瘤(如果存在)+ 1.5 cm,5,940 cGy,180 cGy /天; CTV2:水肿,3,960 cGy,180 cGy /天)与TMZ相关联,75 mg / m 2 < / sup>×5天,放疗的第一周和最后一周。在化学放疗后,给予TMZ辅助化疗(每天150 mg / mq×5天,第一个周期q28,每天200 mg / mq×5天,随后的周期q28),直到疾病进展或最多6个周期。从2000年10月至2003年12月,本研究共纳入29例患者(25 GBL,86.2%; 4 AA,13.8%)。 22名患者(75.8%)接受了TMZ辅助化疗的中位数6个周期(范围1-20)。伴随化学放疗期间无血液学毒性,辅助治疗中血液学毒性较轻,而仅一例观察到神经系统毒性(癫痫发作)。在中位随访66个月(范围3–96)中,无进展生存期(PFS)中位数为8个月,其中1年和2年PFS分别为46.7和28.7%。中位总生存时间为21个月,一年和两年OS分别为69.2%和42.3%。根据我们的经验,即使仅在放疗的第一周和最后一周使用TMZ,也证明TMZ是有效的,并且血液学毒性较低。化学放疗-胶质母细胞瘤-时间表-替莫唑胺

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