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首页> 外文期刊>Pediatric blood & cancer >Outcome of children less than three years old at diagnosis with non-metastatic medulloblastoma treated with chemotherapy on the 'Head Start' I and II protocols.
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Outcome of children less than three years old at diagnosis with non-metastatic medulloblastoma treated with chemotherapy on the 'Head Start' I and II protocols.

机译:根据“ Head Start” I和II方案经化学疗法治疗的非转移性髓母细胞瘤诊断为三岁以下儿童的结果。

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PURPOSE: To determine the survival of infants and young children with non-metastatic medulloblastoma using intensive myeloablative chemotherapy and autologous hematopoietic progenitor cell rescue (AuHCR). METHODS: Twenty-one children less than 3 years old at diagnosis with non-metastatic medulloblastoma were enrolled on two identical serial studies, "Head Start" I and "Head Start" II. After surgery, patients received five cycles of induction chemotherapy consisting of vincristine, cisplatin, cyclophosphamide and etoposide. Following induction, all patients underwent myeloablative chemotherapy using carboplatin, thiotepa and etoposide with AuHCR. Irradiation was used only at relapse. RESULTS: The 5-year event-free (EFS) and overall survival (OS) rates (+/-SE) for all patients, patients with gross total resection, and patients with residual tumor were 52 +/- 11% and 70 +/- 10%, 64 +/- 13% and 79 +/- 11%, and 29 +/- 17% and 57 +/- 19%, respectively. The 5-year EFS and OS ( +/- SE) for patients with desmoplastic and classical medulloblastoma were 67 +/- 16% and 78 +/- 14%, and 42 +/- 14 and 67 +/- 14%, respectively. There were four treatment related deaths. The majority of survivors (71%) avoided irradiation completely. Mean intellectual functioning and quality of life (QoL) for children surviving without irradiation was within average range for a majority of survivors tested. CONCLUSION: This strategy of brief intensive chemotherapy for young children with non-metastatic medulloblastoma eliminated the need for craniospinal irradiation 52% of the patients, and may preserve QoL and intellectual functioning. The excellent survival rates are somewhat dampened by high toxic mortality.
机译:目的:使用强化的清髓性化学疗法和自体造血祖细胞抢救(AuHCR)来确定非转移性髓母细胞瘤的婴幼儿的存活率。方法:21名诊断为非转移性髓母细胞瘤的3岁以下儿童参加了两项相同的连续研究,即“ Head Start” I和“ Head Start” II。手术后,患者接受了五个周期的诱导化疗,包括长春新碱,顺铂,环磷酰胺和依托泊苷。诱导后,所有患者均接受卡铂,thiotepa和依托泊苷联合AuHCR的清髓化疗。仅在复发时使用辐射。结果:所有患者,总全切除患者和残留肿瘤患者的5年无事件(EFS)和总生存(OS)率分别为52 +/- 11%和70 +分别为10%,64 +/- 13%和79 +/- 11%,29 +/- 17%和57 +/- 19%。增生和经典髓母细胞瘤患者的5年EFS和OS(+/- SE)分别为67 +/- 16%和78 +/- 14%,以及42 +/- 14和67 +/- 14% 。有四例与治疗有关的死亡。大多数幸存者(71%)完全避免了照射。对于未经测试幸存的儿童,其平均智力功能和生活质量(QoL)在大多数接受测试的幸存者的平均范围内。结论:这种针对非转移性髓母细胞瘤的幼儿进行短暂强化化疗的策略消除了52%的患者进行颅骨脊髓照射的需要,并且可以保留QoL和智力功能。高毒性死亡率在一定程度上削弱了优异的存活率。

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