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神经母细胞瘤:生物学、预后及治疗

Neuroblastoma: biology, prognosis, and treatment.

作者信息

Park Julie R, Eggert Angelika, Caron Huib

机构信息

Division of Hematology and Oncology, University of Washington School of Medicine and Children's Hospital and Regional Medical Center, Seattle, WA 98105-0371, USA.

出版信息

Pediatr Clin North Am. 2008 Feb;55(1):97-120, x. doi: 10.1016/j.pcl.2007.10.014.

Abstract

Neuroblastoma, a neoplasm of the sympathetic nervous system, is the second most common extracranial malignant tumor of childhood and the most common solid tumor of infancy. Neuroblastoma is a heterogeneous malignancy with prognosis ranging from near uniform survival to high risk for fatal demise. Neuroblastoma serves as a paradigm for the prognostic utility of biologic and clinical data and the potential to tailor therapy for patient cohorts at low, intermediate, and high risk for recurrence. This article summarizes our understanding of neuroblastoma biology and prognostic features and discusses their impact on current and proposed risk stratification schemas, risk-based therapeutic approaches, and the development of novel therapies for patients at high risk for failure.

摘要

神经母细胞瘤是一种交感神经系统肿瘤,是儿童期第二常见的颅外恶性肿瘤,也是婴儿期最常见的实体瘤。神经母细胞瘤是一种异质性恶性肿瘤,预后范围从几乎一致的生存到致命死亡的高风险。神经母细胞瘤是生物学和临床数据预后效用以及为复发低、中、高风险患者群体量身定制治疗方案潜力的范例。本文总结了我们对神经母细胞瘤生物学和预后特征的理解,并讨论了它们对当前和提议的风险分层方案、基于风险的治疗方法以及针对高失败风险患者的新型疗法发展的影响。

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