首页> 外文期刊>Pediatric blood & cancer >Outcome for children <4 years of age with malignant central nervous system tumors treated with high-dose chemotherapy and autologous stem cell rescue.
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Outcome for children <4 years of age with malignant central nervous system tumors treated with high-dose chemotherapy and autologous stem cell rescue.

机译:大剂量化疗和自体干细胞抢救治疗的<4岁儿童恶性中枢神经系统肿瘤的结果。

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摘要

BACKGROUND: Children <4 years of age (yo) with malignant central nervous system (CNS) tumors have a dismal prognosis. In an attempt to delay or obviate radiation therapy (XRT) and improve outcome, our institution has treated children <4 yo with newly diagnosed malignant CNS tumors with high-dose chemotherapy (HDC) and autologous stem cell rescue (ASCR) followed by selective XRT. PROCEDURE: Fifteen children (age 4-38 months) with malignant CNS tumors have completed treatment with HDC/ASCR. All patients received three cycles of induction chemotherapy (cisplatin 3.5 mg/kg- day 0, cyclophosphamide 60 mg/kg- day 1 and 2, etoposide 2.5 mg/kg- day 0-2, vincristine 0.05 mg/kg, day 0, 7, 14) followed by three cycles of HDC (carboplatin 17 mg/kg and thiotepa 6 mg/kg, day 0 and 1) with ASCR. Histology included five medulloblastomas, four primitive neuroectodermal tumors (PNET), five malignant gliomas, and one ependymoma. Outcome and treatment toxicities were evaluated by retrospective chart review. RESULTS: Median follow-up time of the 15 patients is 22 months (range 8-82 months). The 1- and 2-year progression-free survival (PFS) is 86.1% and 52.2% and overall survival (OS) 91.6% and 72.1%, respectively. Ten patients are alive and disease free 3-77 months (median 18 months) after having completed HDC/ASCR, thereoff five received XRT. Toxicity was primarily myelosuppression. There was no treatment mortality. CONCLUSIONS: We are encouraged by the outcome of 15 children <4 yo with malignant CNS tumors treated with tandem cycles of HDC and ASCR at our institution. The treatment regimen is relatively well tolerated.
机译:背景:<4岁(yo)患恶性中枢神经系统(CNS)肿瘤的儿童预后不良。为了延缓或消除放射治疗(XRT)并改善结局,我们的机构对4岁以下患有新诊断为恶性中枢神经系统肿瘤的儿童进行了大剂量化疗(HDC)和自体干细胞抢救(ASCR),然后进行选择性XRT 。程序:15名儿童(4-38个月)患有恶性中枢神经系统肿瘤,已完成HDC / ASCR治疗。所有患者均接受三个周期的诱导化疗(顺铂3.5 mg / kg-第0天,环磷酰胺60 mg / kg-第1和2天,依托泊苷2.5 mg / kg-第0-2天,长春新碱0.05 mg / kg,第0、7天) ,14),然后进行3个周期的HDC(卡铂17 mg / kg和thiotepa 6 mg / kg,第0和1天)。组织学包括5个髓母细胞瘤,4个原始神经外胚层肿瘤(PNET),5个恶性神经胶质瘤和1个室管膜瘤。通过回顾性图表审查评估结果和治疗毒性。结果:15名患者的中位随访时间为22个月(8-82个月)。 1年和2年无进展生存期(PFS)分别为86.1%和52.2%,总生存期(OS)为91.6%和72.1%。完成HDC / ASCR后10例患者存活3-77个月(中位18个月),无疾病,其中5例接受了XRT。毒性主要是骨髓抑制。没有治疗死亡率。结论:我们的机构接受了HDC和ASCR串联治疗的15名4岁以下儿童恶性CNS肿瘤的治疗结果令我们感到鼓舞。该治疗方案的耐受性相对较好。

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