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加拿大36个月以下儿童的胚胎性肿瘤:来自加拿大儿童脑肿瘤协作组(CPBTC)的结果。

Embryonal tumors in Canadian children less than 36 months of age: results from the Canadian Pediatric Brain Tumor Consortium (CPBTC).

作者信息

Story E, Johnston D L, Bartels U, Carret A S, Crooks B, Eisenstat D D, Fryer C, Lafay-Cousin L, Larouche V, Wilson B, Zelcer S, Silva M, Brossard J, Bouffet E, Keene D L

机构信息

Division of Pediatric Hematology/Oncology, Children's Hospital of Eastern Ontario, 401 Smyth Road, Ottawa, ON, K1H 8L1, Canada.

Division of Pediatric Hematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada.

出版信息

J Neurooncol. 2017 Jul;133(3):581-587. doi: 10.1007/s11060-017-2468-y. Epub 2017 May 16.

Abstract

Embryonal tumors are a heterogeneous group of central nervous system (CNS) tumors whose subgroups have varying incidence and outcome. Despite these differences, they are often grouped as a single entity for study purposes. To date, there are no Canadian multi-institutional studies examining the incidence and outcome of all embryonal subtypes. The current study is an observational study reviewing embryonal tumors in all patients less than 36 months of age diagnosed with a CNS tumor in Canada from 1990 to 2005. Embryonal tumors accounted for 26.9% of all CNS tumors. Medulloblastomas were the highest proportion of the embryonal tumors at 61.5%. Atypical teratoid/rhabdoid tumors (AT/RT) had the second highest proportion of embryonal tumors at 18%. The proportion of primitive neuroectodermal tumors (PNET) was 16%, with 2.6 and 1.9% for congenital medulloepithelioma and ependymoblastoma tumors, respectively. AT/RT and PNET were more common in younger age groups. Medulloblastoma became more prevalent with increasing age, with its highest prevalence in the 25 to 36 month age group. Survival rates for our Canadian population at 18 and 24 months were 0.74 and 0.68 for medulloblastoma, 0.64 and 0.60 for PNET, and 0.36 and 0.29 for AT/RT, respectively. Overall, our data are comparable with published international rates for embryonal tumors. These incidence and outcome figures can guide future research into these rare tumors.

摘要

胚胎性肿瘤是中枢神经系统(CNS)肿瘤的一个异质性群体,其子组的发病率和预后各不相同。尽管存在这些差异,但为了研究目的,它们通常被归为一个单一的实体。迄今为止,尚无加拿大多机构研究对所有胚胎性亚型的发病率和预后进行调查。本研究是一项观察性研究,回顾了1990年至2005年在加拿大诊断为中枢神经系统肿瘤的所有36个月以下患者中的胚胎性肿瘤。胚胎性肿瘤占所有中枢神经系统肿瘤的26.9%。髓母细胞瘤在胚胎性肿瘤中所占比例最高,为61.5%。非典型畸胎样/横纹肌样肿瘤(AT/RT)在胚胎性肿瘤中所占比例次之,为18%。原始神经外胚层肿瘤(PNET)的比例为16%,先天性髓上皮瘤和室管膜母细胞瘤的比例分别为2.6%和1.9%。AT/RT和PNET在较年轻的年龄组中更为常见。髓母细胞瘤的患病率随着年龄的增长而增加,在25至36个月龄组中患病率最高。我们加拿大人群中髓母细胞瘤在18个月和24个月时的生存率分别为0.74和0.68,PNET为0.64和0.60,AT/RT为0.36和0.29。总体而言,我们的数据与已发表的国际胚胎性肿瘤发病率相当。这些发病率和预后数据可为今后对这些罕见肿瘤的研究提供指导。

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