Current standards of care and future directions for “high-risk” pediatric renal tumors: Anaplastic Wilms tumor and Rhabdoid tumor

Author:

Geller James I.

Publisher

Elsevier BV

Subject

Urology,Oncology

Reference52 articles.

1. Elizabeth Anne Mullen, James I. Geller, Eric J. Gratias, Elizabeth Jones Perlman, Peter F. Ehrlich, Geetika Khanna, et al. Comprehensive update of pediatric renal tumor epidemiology: analysis of the first 4000 patients on Children׳s Oncology Group (COG) renal Tumor Classification and Biology Protocol AREN03B2. SIOP 2014 (Abstract 364).

2. National Wilms Tumor Study Group. Loss of heterozygosity for chromosomes 1p and 16q is an adverse prognostic factor in favorable-histology Wilms tumor: a report from the National Wilms Tumor Study Group;Grundy;J Clin Oncol,2005

3. Renal tumors:;Fernandez,2011

4. Treatment of anaplastic histology Wilms׳ tumor: results from the fifth National Wilms׳ Tumor Study;Dome;J Clin Oncol,2006

5. Mutations of the p53 tumor suppressor gene occur infrequently in Wilms׳ tumor;Malkin;Cancer Res,1994

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