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Miller R.W., Young J.L., Novakovic B. Childhood cancer // Cancer. John Wiley & Sons, Ltd, 1995. Vol. 75, № S1. P. 395–405.
Doyle L.A. Sarcoma classiﬁcation: An update based on the 2013 World Health Organization Classiﬁcation of Tumors of Soft Tissue and Bone // Cancer. John Wiley and Sons Inc., 2014. Vol. 120, № 12. P. 1763–1774.
Gurney J.G., Young J.L., Roffers S.D. Soft tissue sarcomas // Cancer Incidence and Survival among Children and Adolescents: United States SEER Program 1975-1995, National Cancer Institute, SEER Program. 1999. P. 111–124.
Stiller C.A., Parkint D.M. International variations in the incidence of childhood soft‐tissue sarcomas // Paediatr. Perinat. Epidemiol. Paediatr Perinat Epidemiol, 1994. Vol. 8, № 1. P. 107–119.
Weihkopf T. et al. Incidence and time trends of soft tissue sarcomas in German children 1985-2004 - A report from the population-based German Childhood Cancer Registry // Eur. J. Cancer. Eur J Cancer, 2008. Vol. 44, № 3. P. 432–440.
Pastore G. et al. Childhood soft tissue sarcomas incidence and survival in European children (1978-1997): Report from the Automated Childhood Cancer Information System project // Eur. J. Cancer. Elsevier Ltd, 2006. Vol. 42, № 13. P. 2136–2149.
Koscielniak E., Klingebiel T. CWS-guidance for risk adapted treatment of soft tissue sarcoma (STS) and soft tissue tumours in children, adolescents, and young adults [Electronic resource]. URL: https://www.kinderkrebsinfo.de/health_professionals/clinical_trials/pohkinderkrebsinfotherapiestud
Детская онкология. Национальное руководство. Под ред. М.Д. Алиева, В.Г. Полякова, Г.Л. Менткевича, С.А. Маяковой. М.: Издательская группа РОНЦ. Практическая медицина, 2012. 684 p.
Туктабаева Р.Р. et al. Клинический протокол диагностики и лечения саркомы мягких тканей (рабдомиосаркома и нерабдомиосаркома). 2016. P. 117.
Schiavetti A. et al. Long-term renal function and hypertension in adult survivors of childhood sarcoma: Single center experience // Pediatric Hematology and Oncology. Taylor and Francis Ltd, 2018. Vol. 35, № 3. P. 167–176.
Brecelj J., Stirn-Kranjc B., krbec M. Visual electrophysiology in children with tumours affecting the visual pathway: Case reports // Doc. Ophthalmol. Springer, 2000. Vol. 101, № 2. P. 125–154.
Nitz A. et al. Prospective evaluation of cisplatin- and carboplatin-mediated ototoxicity in paediatric and adult soft tissue and osteosarcoma patients // Oncol. Lett. Oncol Lett, 2012. Vol. 5, № 1. P. 311–315.
Rodeberg D.A. et al. Prognostic signiﬁcance and tumor biology of regional lymph node disease in patients with rhabdomyosarcoma: A report from the children’s oncology group // J. Clin. Oncol. J Clin Oncol, 2011. Vol. 29, № 10. P. 1304–1311.
Быстрова О.В. et al. Способы восстановления фертильности у онкологических больных // Практическая онкология. 2009. Vol. 10, № 4. P. 245–253.
Williamson D. et al. Fusion gene-negative alveolar rhabdomyosarcoma is clinically and molecularly indistinguishable from embryonal rhabdomyosarcoma // J. Clin. Oncol. J Clin Oncol, 2010. Vol. 28, № 13. P. 2151–2158.
Саркомы мягких тканей // Стандарты оказания специализированной помощи детям и подросткам с гематологическими и онкологическими заболеваниями. Медпрактика-М, Москва, 2009. P. 462–482.
Borinstein S.C. et al. Consensus and controversies regarding the treatment of rhabdomyosarcoma // Pediatric Blood and Cancer. John Wiley and Sons Inc., 2018. Vol. 65, № 2.
Stevens M.C.G. Treatment for childhood rhabdomyosarcoma: The cost of cure // Lancet Oncology. Lancet Oncol, 2005. Vol. 6, № 2. P. 77–84.
Breneman J.C. et al. Prognostic factors and clinical outcomes in children and adolescents with metastatic rhabdomyosarcoma-a report from the intergroup rhabdomyosarcoma study IV // J. Clin. Oncol. American Society of Clinical Oncology, 2003. Vol. 21, № 1. P. 78–84.
Puri D.R. et al. The challenging role of radiation therapy for very young children with rhabdomyosarcoma // Int. J. Radiat. Oncol. Biol. Phys. Int J Radiat Oncol Biol Phys, 2006. Vol. 65, № 4. P. 1177–1184.
Rodeberg D.A. et al. Surgical principles for children/adolescents with newly diagnosed rhabdomyosarcoma: A report from the Soft Tissue Sarcoma Committee of the Children’s Oncology Group // Sarcoma. Hindawi Limited, 2002. Vol. 6, № 4. P. 111–122.
Dantonello T.M. et al. Cooperative trial CWS-91 for localized soft tissue sarcoma in children, adolescents, and young adults. // J. Clin. Oncol. American Society of Clinical Oncology, 2009. Vol. 27, № 9. P. 1446–1455.
Koscielniak E. et al. Results of treatment for soft tissue sarcoma in childhood and adolescence: A ﬁnal report of the German cooperative soft tissue sarcoma study CWS-86 // J. Clin. Oncol. American Society of Clinical Oncology, 1999. Vol. 17, № 12. P. 3706–3719.
Bisogno G. et al. The IVADo regimen - A pilot study with ifosfamide, vincristine, actinomycin D, and doxorubicin in children with metastatic soft tissue sarcoma: A pilot study on behalf of the European pediatric soft tissue sarcoma study group // Cancer. Cancer, 2005. Vol. 103, № 8. P. 1719– 1724.
Minard-Colin V. et al. Phase II study of vinorelbine and continuous low doses cyclophosphamide in children and young adults with a relapsed or refractory malignant solid tumour: Good tolerance proﬁle and efﬁcacy in rhabdomyosarcoma - A report from the Société Française des Cancers et leucémies de l’Enfant et de l’adolescent (SFCE) // Eur. J. Cancer. Eur J Cancer, 2012. Vol. 48, № 15. P. 2409–2416.
Breneman J. et al. Local control with reduced-dose radiotherapy for low-risk rhabdomyosarcoma: A report from the Children’S Oncology Group D9602 study // Int. J. Radiat. Oncol. Biol. Phys. Int J Radiat Oncol Biol Phys, 2012. Vol. 83, № 2. P. 720–726.
Chisholm J.C. et al. Open-label, multicentre, randomised, phase II study of the EpSSG and the ITCC evaluating the addition of bevacizumab to chemotherapy in childhood and adolescent patients with metastatic soft tissue sarcoma (the BERNIE study) // Eur. J. Cancer. Elsevier Ltd, 2017. Vol. 83. P. 177–184.
Klingebiel T. et al. Treatment of children with metastatic soft tissue sarcoma with oral maintenance compared to high dose chemotherapy: Report of the HD CWS-96 trial // Pediatr. Blood Cancer. Pediatr Blood Cancer, 2008. Vol. 50, № 4. P. 739–745.
Klingebiel T. et al. Treatment of Children With Relapsed Soft Tissue Sarcoma: Report of the German CESS/CWS REZ 91 Trial // Med. Pediatr. Oncol. Med Pediatr Oncol, 1998. Vol. 30, № 5.
Koscielniak E., Klingebiel T. CWS-guidance for risk adapted treatment of soft tissue sarcoma and soft tissue tumours in children, adolescents, and young adults [Electronic resource]. 2009. P. 252. URL: http://www.fnkc.ru/docs/CWS-2009.pdf.
Bisogno G. et al. Vinorelbine and continuous low-dose cyclophosphamide as maintenance chemotherapy in patients with high-risk rhabdomyosarcoma (RMS 2005): a multicentre, open- label, randomised, phase 3 trial // Lancet Oncol. Lancet Publishing Group, 2019. Vol. 20, № 11. P. 1566–1575.
August D.A., Huhmann M.B. A.S.P.E.N. Clinical guidelines: Nutrition support therapy during adult anticancer treatment and in hematopoietic cell transplantation // Journal of Parenteral and Enteral Nutrition. JPEN J Parenter Enteral Nutr, 2009. Vol. 33, № 5. P. 472–500.
Васильева Е.С., Вашура А.Ю., Литвинов Д.В. Нутритивный статус детей с онкологическими и гематологическими заболеваниями, находящихся на лечении в ФГБУ «ФНКЦ ДГОИ им. Дмитрия Рогачева» (результаты скринингового исследования) // Современная онкология. 2016. Vol. 18, № 4. P. 48–52.
Isenring E., Elia M. Which screening method is appropriate for older cancer patients at risk for malnutrition? // Nutrition. Elsevier Inc., 2015. Vol. 31, № 4. P. 594–597.
Martin L. et al. Diagnostic criteria for the classiﬁcation of cancer-associated weight loss // J. Clin. Oncol. American Society of Clinical Oncology, 2015. Vol. 33, № 1. P. 90–99.
Manary M.J., Sandige H.L. Management of acute moderate and severe childhood malnutrition // BMJ. BMJ, 2008. Vol. 337, № 7680. P. 1227–1230.
van den Broeck J., Eeckels R., Massa G. Validity of Single-Weight Measurements to Predict Current Malnutrition and Mortality in Children // J. Nutr. 1996. Vol. 126, № 1. P. 113–120.
Meijers J.M.M. et al. Nutritional care; do process and structure indicators inﬂuence malnutrition prevalence over time? // Clin. Nutr. Churchill Livingstone, 2014. Vol. 33, № 3. P. 459– 465.
Muscaritoli M. et al. Consensus deﬁnition of sarcopenia, cachexia and pre-cachexia: Joint document elaborated by Special Interest Groups (SIG) “ cachexia-anorexia in chronic wasting diseases” and “ nutrition in geriatrics” // Clin. Nutr. Clin Nutr, 2010. Vol. 29, № 2. P. 154–159.
Kondrup J. et al. ESPEN guidelines for nutrition screening 2002 // Clin. Nutr. Churchill Livingstone, 2003. Vol. 22, № 4. P. 415–421.
Joosten K.F.M., Kerklaan D., Verbruggen S.C.A.T. Nutritional support and the role of the stress response in critically ill children // Current Opinion in Clinical Nutrition and Metabolic Care. Lippincott Williams and Wilkins, 2016. Vol. 19, № 3. P. 226–233.
Arends J. et al. ESPEN guidelines on nutrition in cancer patients // Clin. Nutr. Churchill Livingstone, 2017. Vol. 36, № 1. P. 11–48.
Koletzko B. et al. Guidelines on Paediatric Parenteral Nutrition of the European Society of Paediatric Gastroenterology, Hepatology and Nutrition (ESPGHAN) and the European Society for Clinical Nutrition and Metabolism (ESPEN), Supported by the European Society of Paediatri // Journal of Pediatric Gastroenterology and Nutrition. J Pediatr Gastroenterol Nutr, 2005. Vol. 41, № SUPPL. 2. 87 p.
Tanner L. et al. Cancer Rehabilitation in the Pediatric and Adolescent/Young Adult Population // Seminars in Oncology Nursing. Elsevier Inc, 2020. Vol. 36, № 1. P. 150984.
Karnofsky D.A., Burchenal J.H. The clinical evaluation of chemotherapeutic agents in cancer. // Evaluation of chemotherapeutic agents. / ed. MacLeod C. New York: Columbia University Press, 1949. P. 191–205.
Oken M.M. et al. Toxicity and response criteria of the Eastern Cooperative Oncology Group // Am. J. Clin. Oncol. 1982. Vol. 5, № 6. P. 649–655.