The diagnosis and treatment of osteosarcoma and Ewing’s sarcoma in children and adolescents

Author:

Zarghooni Kourosh,Bratke Grischa,Landgraf Pablo,Simon Thorsten,Maintz David,Eysel Peer

Publisher

Deutscher Arzte-Verlag GmbH

Subject

General Medicine

Reference65 articles.

1. Erdmann FKP, Grabow D, Spix C: German Childhood Cancer Registry—Annual Report 2019 (1980–2018). Institute of Medical Biostatistics, Epidemiology and Informatics (IMBEI) at the University Medical Center of the Johannes Gutenberg University: 2020.

2. (WHO) WHOCoTEB: WHO classification of tumours. Soft tissue and bone tumors. 5th edition Volume 3. International Agency for Research on Cancer. Lyon, France: WHO 2020.

3. Esiashvili N, Goodman M, Marcus RB Jr.: Changes in incidence and survival of Ewing sarcoma patients over the past 3 decades: surveillance epidemiology and end results data. J Pediatr Hematol Oncol 2008; 30: 425–30.

4. Bielack SS, Kempf-Bielack B, Delling G, et al.: Prognostic factors in high-grade osteosarcoma of the extremities or trunk: an analysis of 1,702 patients treated on neoadjuvant cooperative osteosarcoma study group protocols. J Clin Oncol 2002; 20: 776–90.

5. Le Deley MC, Delattre O, Schaefer KL, et al.: Impact of EWS-ETS fusion type on disease progression in Ewing‘s sarcoma/peripheral primitive neuroectodermal tumor: prospective results from the cooperative Euro-E.W.I.N.G. 99 trial. J Clin Oncol 2010; 28: 1982–8.

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