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儿童颅内室管膜瘤:长期预后及预后因素

Intracranial ependymomas of childhood: long-term outcome and prognostic factors.

作者信息

Pollack I F, Gerszten P C, Martinez A J, Lo K H, Shultz B, Albright A L, Janosky J, Deutsch M

机构信息

Department of Neurosurgery, University of Pittsburgh School of Medicine, Children's Hospital of Pittsburgh, Pennsylvania, USA.

出版信息

Neurosurgery. 1995 Oct;37(4):655-66; discussion 666-7. doi: 10.1227/00006123-199510000-00008.

Abstract

A detailed outcome analysis was performed on 40 children with intracranial ependymomas treated at our institution between 1975 and 1993 to identify those factors that were predictive of overall and progression-free survival. Three patients (7.5%) who were treated in the first 5 years of the study died within 3 months of surgery and were excluded from further outcome assessments. Eight (22%) of the 37 patients who survived the perioperative period had evidence of leptomeningeal dissemination at presentation, on the basis of either imaging (three children) and/or cytological (six children) results. The 5- and 10-year progression-free survival rates among these 37 patients were 45.1 and 36.1%, respectively; overall survival rates were 57.1 and 45.0%, respectively. The site of progression was local in 17 of 19 patients with progressive disease. Three factors were found to have a significant association (P < or = 0.05) with the outcome on both univariate and multivariate analyses: 1) the extent of the resection, 2) the age of the patient at diagnosis, and 3) the duration of the symptoms before diagnosis. The 5-year progression-free and overall survivals were 8.9 and 22%, respectively, among patients who had evidence of residual disease on postoperative imaging studies, compared with 68 and 80% rates among patients with no apparent residual disease (P = 0.0001 and P < 0.0001, respectively). Patients younger than 3 years fared significantly worse than older children (5-year progression-free and overall survival rates of 12 and 22%, respectively, in the younger children versus 60 and 75% in older children (P = 0.003 and P = 0.01, respectively). In addition, patients with a duration of symptoms before diagnosis of < 1 month had a worse outcome than those with a more protracted course (5-year progression-free and overall survival rates of 33 and 33%, respectively, versus rates of 53 and 64%, respectively (P = 0.02 for both). Neither the finding of evidence for dissemination at presentation nor the detection of anaplastic histological features (e.g., dense cellularity or high numbers of mitoses) were associated with a significantly worse outcome in this series. The combination of variables that had the strongest association with both favorable and unfavorable outcomes was the combination of the age of the patient and the resection extent. Only 2 of 17 patients older than 3 years with gross total resections have died, whereas 13 of 20 children who were either younger than 3 years or had radiologically incomplete resections have died (P < 0.0001).(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

对1975年至1993年间在我们机构接受治疗的40例儿童颅内室管膜瘤患者进行了详细的预后分析,以确定那些可预测总生存期和无进展生存期的因素。在研究的前5年接受治疗的3例患者(7.5%)在手术后3个月内死亡,被排除在进一步的预后评估之外。37例围手术期存活的患者中有8例(22%)在就诊时根据影像学(3例儿童)和/或细胞学(6例儿童)结果有软脑膜播散的证据。这37例患者的5年和10年无进展生存率分别为45.1%和36.1%;总生存率分别为57.1%和45.0%。19例疾病进展患者中有17例进展部位在局部。在单因素和多因素分析中均发现有3个因素与预后有显著相关性(P≤0.05):1)切除范围,2)诊断时患者年龄,3)诊断前症状持续时间。术后影像学检查有残留疾病证据的患者,其5年无进展生存率和总生存率分别为8.9%和22%,而无明显残留疾病的患者这两个比率分别为68%和80%(分别为P = 0.0001和P < 0.0001)。3岁以下的患者比年龄较大的儿童预后明显更差(3岁以下儿童的5年无进展生存率和总生存率分别为12%和22%,而年龄较大儿童分别为60%和7%(分别为P = 0.003和P = 0.01)。此外,诊断前症状持续时间<1个月的患者比病程较长的患者预后更差(5年无进展生存率和总生存率分别为33%和33%,而后者分别为53%和64%(两者均为P = 0.02)。在本系列中,就诊时发现播散证据或检测到间变组织学特征(如细胞密集或有大量有丝分裂)与明显更差的预后均无相关性。与良好和不良预后关联最强的变量组合是患者年龄和切除范围的组合。17例3岁以上行全切术的患者中只有2例死亡,而20例3岁以下或影像学切除不完全的儿童中有13例死亡(P < 0.0001)。(摘要截断于400字)

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