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Nathalie Gaspar, Douglas S Hawkins, Uta Dirksen, Ian J Lewis, Stefano Ferrari, Marie-Cecile Le Deley, Heinrich Kovar, Robert Grimer, Jeremy Whelan, Line Claude, Olivier Delattre, Michael Paulussen, Piero Picci, Kirsten Sundby Hall, Hendrik van den Berg, Ruth Ladenstein, Jean Michon, Lars Hjorth, Ian Judson, Roberto Luksch, Mark L Bernstein, Perrine Marec-BĂ©rard, Bernadette Brennan, Alan W Craft, Richard B Womer, Heribert Juergens, Odile Oberlin
Ewing sarcoma (ES) is an aggressive sarcoma of bone and soft tissue occurring at any age with a peak incidence in adolescents and young adults. The treatment of ES relies on a multidisciplinary approach, coupling risk-adapted intensive neoadjuvant and adjuvant chemotherapies with surgery and/or radiotherapy for control of the primary site and possible metastatic disease. The optimization of ES multimodality therapeutic strategies has resulted from the efforts of several national and international groups in Europe and North America and from cooperation between pediatric and medical oncologists...
September 20, 2015: Journal of Clinical Oncology: Official Journal of the American Society of Clinical Oncology
Aimee M Crago, Murray F Brennan
No abstract text is available yet for this article.
2015: Advances in Surgery
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