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Cited by 332

The DOI matches its Crossref record; 96 of the 96 references it cites were found in a registry or an index.

Children's Oncology Group's 2013 blueprint for research: Neuroblastoma

Park, Julie R., Bagatell, Rochelle, London, Wendy B., Maris, John M., Cohn, Susan L., Mattay, Katherine M., Hogarty, Michael, on behalf of the COG Neuroblastoma Committee·2013·Pediatric Blood & Cancer

Abstract

Estimated 5‐year survival rates for patients with non‐high‐risk and high‐risk neuroblastoma are 90% and 50%, respectively. Recent clinical trials have shown excellent outcomes with reduced therapy for non‐high‐risk disease. For patients with high‐risk neuroblastoma treated with chemoradiotherapy, surgery, and stem cell transplantation, the addition of anti‐disialoganglioside (GD2) immunotherapy plus cytokines improves survival. Upcoming trials will study the incorporation of targeted radionuclide therapy prior to myeloablative chemotherapy into high‐risk treatment. Phase 2 trials will investigate druggable target(s) including mTOR inhibition and GD2‐directed therapy in combination with chemotherapy for patients with recurrent neuroblastoma, and ALK inhibition for those with ALK‐aberrant tumors. Pediatr Blood Cancer 2013; 60: 985–993. © 2013 Wiley Periodicals, Inc.

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Crossref · 10.1002/pbc.24433

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Metadata

Authors
Park, J. R., Bagatell, R., London, W. B., Maris, J. M., Cohn, S. L., Mattay, K. M., Hogarty, M., & on behalf of the COG Neuroblastoma Committee
Venue
Pediatric Blood & Cancer
Publisher
Wiley
Published
2012-12-19
Volume
60
Issue
6
Pages
985-993
ISSN
  • 1545-5009 (ISSN-L)
  • 1545-5017
OpenAlex
W2064013031
Cited by
332
References
96
FWCI
9.72
Type
journal article
Language
en
Open access
closed

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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