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单纯化疗治疗局限性髓母细胞瘤患儿:前瞻性多中心 HIT 2000 试验的结果证实了组织学对预后的影响。

Treatment of young children with localized medulloblastoma by chemotherapy alone: results of the prospective, multicenter trial HIT 2000 confirming the prognostic impact of histology.

机构信息

Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Germany, Martinistr. 52, D-20246 Hamburg, Germany.

出版信息

Neuro Oncol. 2011 Jun;13(6):669-79. doi: 10.1093/neuonc/nor025.

Abstract

This study was designed to confirm the previously observed favorable survival rates and prognostic factors in young children with nonmetastatic medulloblastoma (MB) treated with postoperative chemotherapy alone. Patients who received a diagnosis during the period January 2001 through December 2005 and who were aged <4 years received 3 cycles of postoperative systemic multiagent chemotherapy and intraventricular methotrexate. In cases of complete remission, treatment was terminated after 2 additional cycles of chemotherapy. Otherwise, secondary surgery, radiotherapy, and consolidation chemotherapy were recommended. At a median follow-up of 4.5 years, the 5-year event-free survival (EFS) and overall survival (OS) rates (± standard error) for 45 patients (median age, 2.5 years) were 57% ± 8% and 80% ± 6%, respectively. Nineteen patients with desmoplastic/nodular MB variants had better 5-year EFS and OS rates (90% ± 7% and 100% ± 0%, respectively) than did 23 patients with classic MB (30% ± 11% and 68% ± 10%, respectively; P < .001 for EFS; P = .008 for OS). Five-year EFS and OS rates for 3 children with anaplastic MB were 33% ± 27%. Desmoplastic/nodular histology was an independent prognostic factor for EFS. Twenty-nine of 30 patients without postoperative residual tumor remained in continuous complete remission. Our results confirm that histology of MB variants is a strong prognostic factor in this age group. Sustained tumor control can be achieved by this chemotherapy regimen in young children with desmoplastic/nodular MB variants. For children with non-desmoplastic/nonnodular MB variants, for which predominantly local relapses lead to less favorable survival rates, local radiotherapy has been introduced after chemotherapy since 2006.

摘要

这项研究旨在证实先前观察到的在接受单纯术后化疗的非转移性髓母细胞瘤(MB)的年轻患儿中良好的生存率和预后因素。2001 年 1 月至 2005 年 12 月期间诊断为该病且年龄<4 岁的患儿接受了 3 个周期的术后全身多药化疗和脑室甲氨蝶呤治疗。完全缓解的患者在接受 2 个周期的额外化疗后停止治疗。否则,建议进行二次手术、放疗和巩固化疗。在中位随访 4.5 年后,45 例患儿(中位年龄 2.5 岁)的 5 年无事件生存率(EFS)和总生存率(OS)分别为 57%±8%和 80%±6%。19 例促纤维增生/结节型 MB 变异型患儿的 5 年 EFS 和 OS 率(分别为 90%±7%和 100%±0%)明显优于 23 例经典型 MB 患儿(分别为 30%±11%和 68%±10%;EFS 差异有统计学意义,P<0.001;OS 差异有统计学意义,P=0.008)。3 例间变性 MB 患儿的 5 年 EFS 和 OS 率分别为 33%±27%。促纤维增生/结节型组织学是 EFS 的独立预后因素。30 例无术后残留肿瘤的患儿中有 29 例持续完全缓解。我们的研究结果证实,MB 变异型的组织学是该年龄组的一个强烈的预后因素。该化疗方案可使促纤维增生/结节型 MB 患儿持续肿瘤控制。对于非促纤维增生/非结节型 MB 变异型患儿,由于主要局部复发导致生存率较低,自 2006 年以来,化疗后已引入局部放疗。

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