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Treatment of Relapsed Wilms Tumor

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Renal Tumors of Childhood

Part of the book series: Pediatric Oncology ((PEDIATRICO))

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Abstract

The outlook for children with newly diagnosed Wilms tumors (WT) has improved dramatically with the advent of multimodal therapy, which includes surgery, chemotherapy, and for some, radiation therapy, with survival rates currently approaching 90 % (Lemerle et al. 1983; D’Angio et al. 1981, 1976). Although the overall relapse rate for children with WT has decreased to less than 15 %, the overall long-term survival for patients with recurrent disease remains at approximately 50 % (Grundy et al. 1989; Pinkerton et al. 1991; Pein et al. 1998; Kremens et al. 2002; Tannous et al. 2000). Due to the small numbers of relapsed patients, advancements in the treatment of these patients have remained a challenge. Investigators from different cooperative groups have evaluated the role of different therapeutic strategies in an attempt to improve the outcomes of patients with recurrent WT. Therapy for these patients depends on characteristics of their primary disease, extent of previous therapy, and time from initial diagnosis to relapse.

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Correspondence to Filippo Spreafico .

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Spreafico, F., Malogolowkin, M.H. (2014). Treatment of Relapsed Wilms Tumor. In: Pritchard-Jones, K., Dome, J. (eds) Renal Tumors of Childhood. Pediatric Oncology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-44003-2_7

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  • DOI: https://doi.org/10.1007/978-3-662-44003-2_7

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