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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Japanese Fdn Canc Res, Ctr Canc Chemotherapy, Tokyo 1358550, JapanJapanese Fdn Canc Res, Ctr Canc Chemotherapy, Tokyo 1358550, Japan
Katayama, Ryohei
Lovly, Christine M.
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Vanderbilt Univ, Dept Med, Nashville, TN USAJapanese Fdn Canc Res, Ctr Canc Chemotherapy, Tokyo 1358550, Japan
Lovly, Christine M.
Shaw, Alice T.
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Massachusetts Gen Hosp, Ctr Canc, Boston, MA USA
Harvard Univ, Sch Med, Dept Med, Boston, MA USAJapanese Fdn Canc Res, Ctr Canc Chemotherapy, Tokyo 1358550, Japan