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成神经管细胞瘤颅外转移后的预后因素。

Prognostic factors after extraneural metastasis of medulloblastoma.

机构信息

Department of Radiology, Section of Radiation Oncology, The Methodist Hospital, Houston, Texas 77030, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2010 Sep 1;78(1):72-8. doi: 10.1016/j.ijrobp.2009.07.1729. Epub 2010 Feb 3.

Abstract

PURPOSE

To review the existing literature regarding the characteristics, prognostic factors, treatment, and survival of patients with medulloblastoma, who develop extraneural metastasis (ENM).

METHODS AND MATERIALS

A PubMed search of English language articles from 1961 to 2007 was performed, yielding 47 articles reporting on 119 patients. Factors analyzed included age, time interval to development of ENM, ENM location, central nervous system (CNS) involvement, treatment, and outcome.

RESULTS

Sites of ENM included bone in 84% of patients, bone marrow in 27% of patients, lymph nodes in 15% of patients, lung in 6% of patients, and liver in 6% of patients. Median survival was 8 months after diagnosis of ENM. The 1-, 2-, and 5-year overall survival (OS) rates after diagnosis of ENM were 41.9%, 31.0%, and 26.0%, respectively. The 1-, 2-, and 5-year progression-free survival (PFS) rates after diagnosis of ENM were 34.5%, 23.2%, and 13.4%, respectively. For patients without CNS involvement at the time of ENM diagnosis, the 1-, 2-, and 5-year OS rates for those treated with and without radiotherapy (RT) were 82.4%, 64.8%, and 64.8% vs. 51.0%, 36.6%, and 30.5%, respectively (p = 0.03, log-rank test). RT did not significantly improve OS or PFS rates for those with CNS involvement. Concurrent CNS involvement, ENM in the lung or liver, a time interval of <18 months to development of ENM, and a patient age of <16 years at ENM diagnosis were found to be negative prognostic factors for both OS and PFS.

CONCLUSIONS

Several prognostic factors were identified for patients with ENM from medulloblastoma. Patients without concurrent CNS involvement, who received RT after ENM diagnosis had an OS and PFS benefit compared to those who did not receive RT.

摘要

目的

回顾有关发生颅外转移(ENM)的髓母细胞瘤患者的特征、预后因素、治疗方法和生存情况的现有文献。

方法和材料

对 1961 年至 2007 年发表的英文文献进行了 PubMed 检索,共获得 47 篇报道 119 例患者的文章。分析的因素包括年龄、发生 ENM 的时间间隔、ENM 部位、中枢神经系统(CNS)受累、治疗方法和结局。

结果

ENM 的部位包括 84%的患者骨骼、27%的患者骨髓、15%的患者淋巴结、6%的患者肺和 6%的患者肝。ENM 诊断后中位生存时间为 8 个月。ENM 诊断后 1 年、2 年和 5 年的总生存率(OS)分别为 41.9%、31.0%和 26.0%。ENM 诊断后 1 年、2 年和 5 年无进展生存率(PFS)分别为 34.5%、23.2%和 13.4%。对于 ENM 诊断时无 CNS 受累的患者,接受和未接受放疗(RT)的患者的 1 年、2 年和 5 年 OS 率分别为 82.4%、64.8%和 64.8%比 51.0%、36.6%和 30.5%(p=0.03,对数秩检验)。CNS 受累的患者,接受 RT 并未显著提高 OS 或 PFS 率。同时性 CNS 受累、肺或肝的 ENM、ENM 发生至诊断的时间间隔<18 个月以及 ENM 诊断时患者年龄<16 岁被认为是 OS 和 PFS 的负预后因素。

结论

确定了几个与髓母细胞瘤发生颅外转移的患者相关的预后因素。未同时性 CNS 受累、ENM 诊断后接受 RT 的患者的 OS 和 PFS 获益高于未接受 RT 的患者。

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