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Review

High-Risk Neuroblastoma Treatment Review

Baylor College of Medicine Department of Pediatrics, Texas Children’s Cancer and Hematology Center, Houston, TX 77030, USA
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Children 2018, 5(9), 114; https://doi.org/10.3390/children5090114
Received: 30 June 2018 / Revised: 18 August 2018 / Accepted: 20 August 2018 / Published: 28 August 2018
(This article belongs to the Special Issue Recent Advances in Diagnosis and Treatment of Neuroblastoma)
Neuroblastoma is the most common extracranial solid tumor in children. One subset, high-risk neuroblastoma, is very difficult to treat and requires multi-modal therapy. Intensification of therapy has vastly improved survival rates, and research is focused on novel treatments to further improve survival rates. The current treatment schema is divided into three stages—induction, consolidation, and maintenance. This review serves as an overview of the current treatment for high-risk neuroblastoma and a glimpse at current research for future therapy. View Full-Text
Keywords: neuroblastoma; high-risk neuroblastoma; diagnosis; treatment neuroblastoma; high-risk neuroblastoma; diagnosis; treatment
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MDPI and ACS Style

Smith, V.; Foster, J. High-Risk Neuroblastoma Treatment Review. Children 2018, 5, 114. https://doi.org/10.3390/children5090114

AMA Style

Smith V, Foster J. High-Risk Neuroblastoma Treatment Review. Children. 2018; 5(9):114. https://doi.org/10.3390/children5090114

Chicago/Turabian Style

Smith, Valeria, and Jennifer Foster. 2018. "High-Risk Neuroblastoma Treatment Review" Children 5, no. 9: 114. https://doi.org/10.3390/children5090114

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