儿科胶质母细胞瘤的临床行为和结果:目前的情况。

IF 1.8 Q3 ONCOLOGY
Radiation Oncology Journal Pub Date : 2021-03-01 Epub Date: 2021-03-30 DOI:10.3857/roj.2020.00591
Aditya Kumar Singla, Renu Madan, Kirti Gupta, Shikha Goyal, Narendra Kumar, Sushant Kumar Sahoo, Deepak K Uppal, Chirag K Ahuja
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引用次数: 4

摘要

小儿胶质母细胞瘤(pGBM)是一种罕见的实体,仅占所有儿童脑肿瘤的约3%。pGBM的治疗指南是从成人胶质母细胞瘤的治疗指南中推断出来的。在主要研究中,pGBM的罕见性和儿科人群的代表性不足妨碍了为这些患者确定理想的治疗方案。在大多数情况下,3岁以上的儿童在术后放疗后进行最大限度的安全切除。替莫唑胺对这些患者的益处尚不清楚。在这里,我们报告了2018-2019年在我所治疗的6例pGBM患者的临床病理细节和结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical behaviour and outcome in pediatric glioblastoma: current scenario.

Clinical behaviour and outcome in pediatric glioblastoma: current scenario.

Clinical behaviour and outcome in pediatric glioblastoma: current scenario.

Clinical behaviour and outcome in pediatric glioblastoma: current scenario.

Pediatric glioblastoma (pGBM) is a rare entity accounting for only approximately 3% of all childhood brain tumors. Treatment guidelines for pGBM have been extrapolated from those in adult glioblastoma. Rarity of pGBM and underrepresentation of pediatric population in major studies precludes from defining the ideal treatment protocol for these patients. Maximum safe resection is performed in most of the cases followed by postoperative radiotherapy in children over 3 years of age. Benefit of temozolomide is unclear in these patients. Here, we present the clinicopathological details and outcome of six pGBM patients treated at our institute in 2018-2019.

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来源期刊
CiteScore
3.50
自引率
4.30%
发文量
24
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