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神经母细胞瘤:生物学、预后和治疗。

Neuroblastoma: biology, prognosis, and treatment.

机构信息

Division of Hematology and Oncology, University of Washington School of Medicine and Seattle Children's Hospital, 4800 Sand Point Way NE, Seattle, WA 98105-0371, USA.

出版信息

Hematol Oncol Clin North Am. 2010 Feb;24(1):65-86. doi: 10.1016/j.hoc.2009.11.011.

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

神经母细胞瘤是交感神经系统的一种肿瘤,是儿童期第二大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,其预后从近乎一致的存活率到高风险的致命性死亡率不等。神经母细胞瘤是生物学和临床数据预后效用的典范,以及为低、中、高危复发风险的患者群体定制治疗的潜力。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拟议的风险分层方案、基于风险的治疗方法以及高危失败患者的新型治疗方法的影响。

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