Progress Update in Pediatric Renal Tumors

Author:

Jain Juhi,Sutton Kathryn S.,Hong Andrew L.ORCID

Publisher

Springer Science and Business Media LLC

Subject

Oncology

Reference100 articles.

1. Surveillance, Epidemiology, and End Results (SEER) Program (www.seer.cancer.gov) SEER*Explorer database: incidence - SEER research data, kidney and renal pelvis cancer SEER incidence rates by age at diagnosis, Sub (2013-2017), National Cancer Institute, DCCPS, Surveillance Research Program. https://seer.cancer.gov/explorer/application.html?site = 72&data_type = 1&graph_type = 3&compareBy = sex&chk_sex_1 = 1&chk_sex_3 = 3&chk_sex_2 = 2&race = 1&rate_type = 1&advopt_precision = 1&advopt_display = 2. Accessed 7 Aug 2020

2. Dome JS, Fernandez CV, Mullen EA, Kalapurakal JA, Geller JI, Huff V, et al. Children’s Oncology Group’s 2013 blueprint for research: renal tumors. Pediatr Blood Cancer. 2013;60:994–1000.

3. D’Angio GJ. The National Wilms tumor study: a 40 year perspective. Lifetime Data Anal. 2007;13:463–70.

4. Scott RH, Stiller CA, Walker L, Rahman N. Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour. J Med Genet. 2006;43:705–15.

5. Chagtai T, Zill C, Dainese L, Wegert J, Savola S, Popov S, et al. Gain of 1q as a prognostic biomarker in Wilms tumors (WTs) treated with preoperative chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 trial: a SIOP renal tumours biology consortium study. J Clin Oncol Off J Am Soc Clin Oncol. 2016;34:3195–203.

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