4.2 Article

Neuroblastoma Paradigm for Precision Medicine

Journal

PEDIATRIC CLINICS OF NORTH AMERICA
Volume 62, Issue 1, Pages 225-+

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.pcl.2014.09.015

Keywords

Neuroblastoma; Risk stratification; MYCN; Segmental chromosome aberrations (SCA); ALK (anaplastic lymphoma kinase); Phox2B; Myeloablative therapy (MAT); Immunotherapy

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Neuroblastoma (NB) is the third most common pediatric cancer. Although NB accounts for 7% of pediatric malignancies, it is responsible for more than 10% of childhood cancer-related mortality. Prognosis and treatment are determined by clinical and biological risk factors. Estimated 5-year survival rates for patients with non-high-risk and high-risk NB are more than 90% and less than 50%, respectively. Recent clinical trials have continued to reduce therapy for patients with non-high-risk NB, including the most favorable subsets who are often followed with observation approaches. In contrast, high-risk patients are treated aggressively with chemotherapy, radiation, surgery, and myeloablative and immunotherapies.

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