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儿童 3 岁以下恶性脑肿瘤的串联大剂量化疗和自体外周血干细胞移植。

Tandem high-dose chemotherapy and auto-SCT for malignant brain tumors in children under 3 years of age.

机构信息

Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.

出版信息

Bone Marrow Transplant. 2013 Jul;48(7):932-8. doi: 10.1038/bmt.2012.263. Epub 2013 Jan 14.

Abstract

In an effort to improve survival and reduce late adverse effects of radiation therapy (RT), 25 children <3 years of age with malignant brain tumors received tandem high-dose chemotherapy (HDCT) and auto-SCT following six cycles of induction chemotherapy. RT was either not given or deferred until 3 years of age if the patient was in CR after tandem HDCT/auto-SCT. Tumors relapsed or progressed in nine patients (five during induction treatment), and two of these patients survived after receiving salvage treatment, including RT. Two patients died due to toxicities during tandem HDCT/auto-SCT. A total of 16 patients survived to a median follow-up period of 52 months (range 18-96) from the time of diagnosis. Four of these patients did not receive RT, two received local RT (L-RT), three received craniospinal RT (CSRT), and seven received both L-RT and CSRT. The 5-year OS and EFS rates were 67.8±9.4% and 55.5±10.0%, respectively. Neuroendocrine and neurocognitive functions evaluated 3 years after tandem HDCT/auto-SCT were acceptable. Our results indicate that tandem HDCT/auto-SCT may improve survival in young children with malignant brain tumors with an acceptable level of risk of long-term toxicity.

摘要

为了提高生存率并减少放疗的晚期不良反应,25 名年龄<3 岁的恶性脑肿瘤患儿在接受六周期诱导化疗后接受了串联高剂量化疗(HDCT)和自体造血干细胞移植(auto-SCT)。如果患者在串联 HDCT/auto-SCT 后处于完全缓解(CR),则不给予放疗或推迟至 3 岁以后。9 名患者(5 名在诱导治疗期间)肿瘤复发或进展,其中 2 名患者在接受挽救治疗(包括放疗)后存活。2 名患者因串联 HDCT/auto-SCT 期间的毒性而死亡。从诊断到随访中位数 52 个月(18-96 个月)的时间,共有 16 名患者存活。其中 4 名患者未接受放疗,2 名患者接受局部放疗(L-RT),3 名患者接受颅脊髓放疗(CSRT),7 名患者接受 L-RT 和 CSRT。5 年总生存率(OS)和无事件生存率(EFS)分别为 67.8±9.4%和 55.5±10.0%。在接受串联 HDCT/auto-SCT 治疗 3 年后评估的神经内分泌和神经认知功能可接受。我们的结果表明,串联 HDCT/auto-SCT 可能改善恶性脑肿瘤患儿的生存率,同时长期毒性风险可接受。

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