Bone and soft tissue sarcomas, tumors of the skinBone and soft tissue sarcomas, tumors of the skinСаркомы костей, мягких тканей и опухоли кожи2219-46142782-3687Publishing House ABV Press410Pediatric OncologyПЕДИАТРИЧЕСКАЯ ОНКОЛОГИЯEwings sarcoma treatmentЛечение опухолей семейства саркомы ЮингаNisichenkoO. A.НисиченкоО. А.
Russian Federation

Moscow

г.Москва

nisichenko@gmail.comKubirovM. S.КубировМ. С.
Russian Federation

Moscow

г.Москва

MichailovaS. N.МихайловаС. Н.
Russian Federation

Moscow

г.Москва

N.N. Blokhin Russian Cancer Research CenterФГБУ «Российский онкологический научный центр им. Н.Н. Блохина», МЗ РФ230920157340482301202223012022Copyright ©; 2015, Nisichenko O.A., Kubirov M.S., Michailova S.N.Copyright ©; 2015, Нисиченко О.А., Кубиров М.С., Михайлова С.Н.2015Nisichenko O.A., Kubirov M.S., Michailova S.N.Нисиченко О.А., Кубиров М.С., Михайлова С.Н.https://creativecommons.org/licenses/by/4.0https://sarbon.abvpress.ru/jour/article/view/410

Combined approach is a standard of treatment of Ewing sarcoma patients. Chemotherapy, radiotherapy, surgery and possible targeted therapy are the main steps of successful treatment. Evolution of chemotherapy is discussed in this literature review.

В настоящее время стандартом является комбинированный подход в лечении опухолей семейства саркомы Юинга. Полихимиотерапия, лучевая терапия, хирургическое лечение, а с недавнего времени использование таргетных препаратов являются залогом успешного лечения. Мы попытались отразить периоды становления химиотерапии в лечении опухолей семейства саркомы Юинга и зависимость выживаемости пациентов от применения различных подходов в терапии.

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