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Список литературы

  1. Алиев М.Д., Сушенцов Е.А. Cовременная онкоортопедия. Саркомы костей, мягких тканей и опухоли кожи. 2012 - №4. – стр. 3-10.
  2. Горбунова В.А., Феденко А.А., Истомин И.А., Бохян Б.Ю., Губина Г.И. Высокодозный ифосфамид в комбинации с доксорубицином в лечении сарком мягких тканей. Саркомы костей, мягких тканей и опухоли кожи. 2010 - №1. – стр. 26-31
  3. ТепляковВ.В., КарпенкоВ.Ю., Франк Г.А., Буланова А.А., Бондарев А.В., Дрошева И.В., Державин В.А., Бухаров А.В., Епифанова С.В.. Влияние ширины края резекции на частоту локальных рецидивов при комбинированном и комплексном лечении пациентов саркомами мягких тканей. Саркомы костей, мягких тканей и опухоли кожи. 2009 - №1. – стр. 28-33
  4. Зубарев А.Л. Кудрявцева Г.Т., Курильчик А.А., Курпешев О.К., Стародубцев А.Л. Комбинированное лечение распространенных сарком мягких тканей. . Саркомы костей, мягких тканей и опухоли кожи. 2010 - №2. – стр. 35-38
  5. Pervaiz N., Colterjohn N., Farrokhyar F. et al. А systematic meta-analysis of randomized controlled trials of adjuvant chemotherapy for localized resectable soft-tissue sarcoma. Cancer. 2008; 113: 573-581.
  6. Ravi V., Patel S., Benjamin R.S. Chemotherapy for Soft-Tissue Sarcomas. Oncology (Williston Park). 2015 Jan 15; 29 (1)..
  7. Nielsen O.S., Dombernowsky P., Mouridsen H. et al. High-dose epirubicin is not an alternative to standard-dose doxorubicin in the treatment of advanced soft tissue sarcomas. A study of the EORTC Soft Tissue and Bone Sarcoma Group. Br. J. Cancer. 1999; 78: 1634–1639.
  8. Mouridsen H.T., Bastholt L., Somers R. et al. Аdriamycin versus epirubicin in advanced soft tissue sarcomas. A randomized phase II/phase III study of the EORTC Soft Tissue and Bone Sarcoma Group. Eur. J. Cancer Clin. Oncol. 1987; 23: 1477–1483.
  9. Lorigan P., Verweij J., Papai Z. et al. Phase III trial of two investigational schedules of ifosfamide compared with standard-dose doxorubicin in advanced or metastatic soft tissue sarcoma: a European Organization for Research and Treatment of Cancer Soft Tissue and Bone Sarcoma Group Study. J. Clin. Oncol. 2007; 25: 3144–3150.
  10. Edmonson J.H., Ryan L.M., Blum R.H. et al. Randomized comparison of doxorubicin alone versus ifosfamide plus doxorubicin or mitomycin, doxorubicin, and cisplatin against advanced soft tissue sarcomas. J. Clin. Oncol. 1993; 11: 1269–75.
  11. Antman K., Crowley J., Balcerzak S.P. et al. An intergroup phase III randomized study of doxorubicin and dacarbazine with or without ifosfamide and mesna in advanced soft tissue and bone sarcomas. J. Clin. Oncol. 1993; 11: 1276–85.
  12. Alamanda VK, Crosby SN, Archer KR, et al. Predictors and clinical significance of local recurrence in extremity soft tissue sarcoma. Acta Oncol 2013;52:793-802.
  13. Alamanda VK, Crosby SN, Archer KR, et al. Amputation for extremity soft tissue sarcoma does not increase overall survival: a retrospective cohort study. Eur J Surg Oncol 2012;38:1178- 1183
  14. O"Donnell PW, Griffin AM, Eward WC, et al. The effect of the setting of a positive surgical margin in soft tissue sarcoma. Cancer 2014;120:2866-2875.
  15. Brady MS1, Gaynor JJ, Brennan MF. Radiation-associated sarcoma of bone and soft tissue. Arch Surg. 1992 Dec; 127(12):1379-85.
  16. Peng PD, Hyder O, Mavros MN. et al.Management and recurrence patterns of desmoids tumors: a multi-institutional analysis of 211 patients. Ann Surg Oncol. 2012 Dec;19(13):4036- 42
  17. Edmonson JH, Petersen IA, Shives TC. et al. Chemotherapy, irradiation, and surgery for function-preserving therapy of primary extremity soft tissue sarcomas: initial treatment with ifosfamide, mitomycin, doxorubicin, and cisplatin plus granulocyte macrophage-colony- stimulating factor. Cancer. 2002 Feb 1; 94 (3):786-92.
  18. Al-Refaie WB1, Andtbacka RH, Ensor J. et al. Lymphadenectomy for isolated lymph node metastasis from extremity soft-tissue sarcomas. Cancer. 2008 Apr 15; 112 (8):1821-6.
  19. Calvo FA1, Sole CV, Polo A. et al. Limb-sparing management with surgical resection, external- beam and intraoperative electron-beam radiation therapy boost for patients with primary soft tissue sarcoma of the extremity: a multicentric pooled analysis of long-term outcomes. Strahlenther Onkol. 2014 Oct; 190 (10):891-8.
  20. Coffin C.M.1, Davis J.L., Borinstein S.C. Syndromeassociated soft tissue tumours. Histopathology. 2014 Jan; 64 (1): 68–87.
  21. Enzinger F.M., Weiss S.W. Soft Tissue Tumors. 5. St. Louis: Mosby. Angiosarcoma. 2008, p. 703–720.
  22. Stewart F.W., Treves N. Lymphangiosarcoma in postmastectomy lymphedema; a report of six cases in elephantiasis chirurgica. Cancer. 1948; 1: 64–81.
  23. Inoue Y.Z., Frassica F.J., Sim F.H., Unni K.K., Petersen I.A., McLeod R.A. Clinicopathologic features and treatment of postirradiation sarcoma of bone and soft tissue. J. Surg. Oncol. 2000; 75: 42–50.
  24. Rubino C., Shamsaldin A., Lê M.G., Labbé M., Guinebretière J.M., Chavaudra J., de Vathaire F. Radiation dose and risk of soft tissue and bone sarcoma after breast cancer treatment. Breast Cancer Res. Treat. 2005; 89: 277–288.
  25. Blauvelt A., Sei S., Cook P.M., Schulz T.F., Jeang K.T. Human herpesvirus 8 infection occurs following adolescence in the united states. J. Infect. Dis. 1997; 176: 771–774.
  26. Martro E., Bulterys M., Stewart J.A., Spira T.J., Cannon M.J., Thacher T.D., Bruns R., Pellett P.E., Dollard S.C. Comparison of human herpesvirus 8 and epstein-barr virus seropositivity among children in areas endemic and non-endemic for kaposi’s sarcoma. J. Med. Virol. 2004; 72: 126–131.
  27. Каприн АД, Старинский ВВ, Петрова ГВ (eds.): Злокачественные новообразования в России в 2018 году (заболеваемость и смертность). М.: МНИОИ им. П.А. Герцена − филиал ФГБУ «НМИЦ радиологии» Минздрава России; 2019..
  28. Каприн АД, Старинский ВВ, Петрова ГВ (eds.): Состояние онкологической помощи населению России в 2018 году. М.: МНИОИ им. П.А. Герцена − филиал ФГБУ «НМИЦ радиологии» Минздрава России; 2019.
  29. International Statistical Classification of Diseases and Related Health Problems 10th Revision [http://apps.who.int/classifications/icd10/browse/2016/en
  30. Amin MB, Edge SB, Greene FL, et al. AJCC Cancer Staging Manual, 8th edition. New York: Springer; 2017
  31. Fanburg-Smith J.C., Dal Cin P. Angiomatoid fibrous histiocytoma. In: C.D.M. Fletcher, Unni K.K., Mertens F., editors. World Health Organization Classification of Tumors: Pathology and Genetics of Tumors of Soft Tissue and Bone. Lyon, France: IARC Press. 2002. p. 194–195. In. Eds
  32. Перельмутер В.М., Васильев Н.В., Таширева Л.А., Савенкова О.В., Кайгородова Е.В., Жамгарян Г.С. Экспрессионный профиль и молекулярно-генетический анализ синовиальной саркомы и саркомы Юинга/PNET Сибирский онкологический журнал. 2014;(2):19-23
  33. Pérez-Mancera PA, Sánchez-García IUnderstanding mesenchymal cancer: the liposarcoma- associated FUS-DDIT3 fusion gene as a model. Semin Cancer Biol. 2005 Jun;15(3):206-14
  34. Pérez-Losada J, Sánchez-Martín M, Rodríguez-García MA, Pérez-Mancera PA, Pintado B, Flores T, Battaner E, Sánchez-Garćia I Liposarcoma initiated by FUS/TLS-CHOP: the FUS/TLS domain plays a critical role in the pathogenesis of liposarcoma. Oncogene. 2000 Dec 7; 19(52):6015-22.
  35. Todorov SS, Kit OI Current idea of the morphogenetic features of liposarcomas]. Arkh Patol. 2012 Nov-Dec; 74(6):61-3
  36. Italiano A, Di Mauro I, Rapp J, Pierron G, Auger N, Alberti L, Chibon F, Escande F, Voegeli AC, Ghnassia JP, Keslair F, Laé M, Ranchère-Vince D, Terrier P, Baffert S, Coindre JM, Pedeutour F Clinical effect of molecular methods in sarcoma diagnosis (GENSARC): a prospective, multicentre, observational study. Lancet Oncol. 2016 Apr;17(4):532-538.
  37. Merkelbach-Bruse S, Wardelmann E, Künstlinger H, Büttner R, Schildhaus HU [Molecular methods in the diagnosis of sarcoma]. . Pathologe. 2011 Feb; 32(1):24-31
  38. Asif A, Mushtaq S, Hassan U, Akhtar N, Hussain M, Azam M, Qazi R. Fluorescence in Situ Hybridization (FISH) for Differential Diagnosis of Soft Tissue Sarcomas Asian Pac J Cancer Prev. 2018 Mar 27; 19(3):655-660. Epub 2018 Mar 27
  39. Asif A, Mushtaq S, Hassan U, Akhtar N, Hussain M, Azam M, Qazi R. Fluorescence in Situ Hybridization (FISH) for Differential Diagnosis of Soft Tissue Sarcomas Asian Pac J Cancer Prev. 2018 Mar 27; 19(3):655-660.
  40. Pritchard DJ, Nascimento AG, Petersen IA. Local control of extra- abdominal desmoid tumors. J Bone Joint Surg Am 1996;78:848-854.
  41. Tateishi U, Hosono A, Makimoto A, et al. Comparative study of FDG PET/CT and conventional imaging in the staging of rhabdomyosarcoma. Ann Nucl Med 2009;23:155-161.
  42. Tateishi U, Hasegawa T, Beppu Y, et al. Prognostic significance of MRI findings in patients with myxoid-round cell liposarcoma. AJR Am J Roentgenol 2004;182:725-731.
  43. Karakousis CP, Emrich LJ, Rao U, Khalil M. Limb salvage in soft tissue sarcomas with selective combination of modalities. Eur J Surg Oncol 1991;17:71-80.
  44. Замогильная Янна Александровна- Современные методы лучевой диагностики в оценке эффекта предоперационной химиотерапии у больных с саркомами мягких тканей конечностей Диссертация на соискание ученой степени кандидата медицинских наук Москва 2014г.
  45. Suh CH, Jung SC, Kim KW, Pyo J: The detectability of brain metastases using contrast- enhanced spin-echo or gradient-echo images: a systematic review and meta-analysis. Journal of neuro-oncology 2016, 129(2):363-371
  46. Fletcher CDM, Bridge JA, Hogendoorn P, Mertens F. World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone, Fourth Edition. IARC, Lyon, 2013.
  47. Alektiar KM, Leung D, Zelefsky MJ, et al. Adjuvant brachytherapy for primary high-grade soft tissue sarcoma of the extremity. Ann Surg Oncol 2002;9:48-56.
  48. Alektiar KM, Brennan MF, Singer S. Local control comparison of adjuvant brachytherapy to intensity-modulated radiotherapy in primary high-grade sarcoma of the extremity. Cancer 2011;117:3229-3234
  49. Wang D, Zhang Q, Eisenberg BL, et al. Significant reduction of late toxicities in patients with extremity sarcoma treated with image-guided radiation therapy to a reduced target volume: Results of Radiation Therapy Oncology Group RTOG-0630 Trial. J Clin Oncol 2015;33:2231- 2238.
  50. O’Bryan R.M., Baker L.H., Gottlieb J.E. et al. Dose response evaluation of Adriamycin in human neoplasia. Cancer. 1977; 39: 1940–8
  51. Benjamin R.S., Legha S.S., Patel S.R., Nicaise C. Single-agent ifosfamide studies in sarcomas of soft tissue and bone: the M.D. Anderson experience. Cancer Chemother. Pharmacol. 1993; 31 (Suppl 2): S174–9.
  52. Patel S.R., Vadhan-Raj S., Papadopolous N. et al. High-dose ifosfamide in bone and soft tissue sarcomas: results of phase II and pilot studies--dose-response and schedule dependence. J. Clin. Oncol. 1997; 15: 2378–84
  53. Lorigan P., Verweij J., Papai Z. et al. Phase III trial of two investigational schedules of ifosfamide compared with standard-dose doxorubicin in advanced or metastatic soft tissue sarcoma: a European Organisation for Research and Treatment of Cancer Soft Tissue and Bone Sarcoma Group Study. J. Clin. Oncol. 2007; 25: 3144–50
  54. Феденко, Александр Александрович. Стратегия лекарственного лечения сарком мягких тканей : автореферат дис. ... доктора медицинских наук : 14.01.12 / Феденко Александр Александрович; [Место защиты: Рос. онкол. науч. центр им. Н.Н. Блохина РАМН]. - Москва, 2016. - 41 с
  55. Le Cesne A., Antoine E., Spielmann M. et al. High-dose ifosfamide: circumvention of resistance to standard-dose ifosfamide in advanced soft tissue sarcomas. J. Clin. Oncol. 1995; 13: 1600–8
  56. Patel S.R., Gandhi V., Jenkins J. et al. Phase II clinical investigation of gemcitabine in advanced soft tissue sarcomas and window evaluation of dose rate on gemcitabine triphosphate accumulation. J. Clin. Oncol. 2001; 19: 3483–9.
  57. Stacchiotti S., Palassini E., Sanfilippo R. et al. Gemcitabine in advanced angiosarcoma: a retrospective case series analysis from the Italian Rare Cancer Network. Ann. Oncol. 2012; 23: 501–8
  58. Gottlieb J.A., Benjamin R.S., Baker L.H. et al. Role of DTIC (NSC-45388) in the chemotherapy of sarcomas. Cancer Treat. Rep. 1976; 60: 199–203
  59. Buesa J.M., Mouridsen H.T., van Oosterom A.T. et al. High-dose DTIC in advanced soft-tissue sarcomas in the adult. A phase II study of the E.O.R.T.C. Soft Tissue and Bone Sarcoma Group. Ann. Oncol. 1991; 2: 307–9
  60. Garcia del Muro X., Lopez-Pousa A., Martin J. et al. A phase II trial of temozolomide as a 6- week, continuous, oral schedule in patients with advanced soft tissue sarcoma: a study by the Spanish Group for Research on Sarcomas. Cancer. 2005; 104: 1706–12.
  61. Casper E.S., Waltzman R.J., Schwartz G.K. et al. Phase II trial of paclitaxel in patients with soft-tissue sarcoma. Cancer Invest. 1998; 16: 442–6
  62. Fata F., O’Reilly E., Ilson D. et al. Paclitaxel in the treatment of patients with angiosarcoma of the scalp or face. Cancer. 1999; 86: 2034–7.
  63. Italiano A., Cioffi A., Penel N. et al. Comparison of doxorubicin and weekly paclitaxel efficacy in metastatic angiosarcomas. Cancer. 2012; 118: 3330–6.
  64. Demetri GD, Chawla SP, von Mehren M, et al. Efficacy and safety of trabectedin in patients with advanced or metastatic liposarcoma or leiomyosarcoma after failure of prior anthracyclines and ifosfamide: results of a randomized phase II study of two different schedules. J Clin Oncol 2009;27:4188-4196
  65. Martin-Broto J, Pousa AL, de Las Penas R, et al. Randomized Phase II Study of Trabectedin and Doxorubicin Compared With Doxorubicin Alone as First-Line Treatment in Patients With Advanced Soft Tissue Sarcomas: A Spanish Group for Research on Sarcoma Study. J Clin Oncol 2016;34:2294-2302.
  66. Gronchi A., Bui B.N., Bonvalot S. et al. Phase II clinical trial of neoadjuvant trabectedin in patients with advanced localized myxoid liposarcoma. Ann. Oncol. 2012; 23: 771–6.
  67. Schöffski P, Ray-Coquard IL, Cioffi A, et al. Activity of eribulin mesylate in patients with soft- tissue sarcoma: a phase 2 study in four independent histological subtypes. Lancet Oncology 2011;12(11):1045-1052
  68. Schöffski P, et al. Eribulin versus dacarbazine in previously treated patients with advanced liposarcoma or leiomyosarcoma: a randomised, open-label, multicentre, phase 3 trial. The Lancet. 2016;
  69. Chawla S, et al. Subtype specific activity in liposarcoma (LPS) patients (pts) from a phase 3, open label, randomised study of eribulin (ERI) versus dacarbazine (DTIC) in patients with advanced LPS and leiomyosarcoma (LMS). American Society for Clinical Oncology annual meeting 2016; Abstract # 11037
  70. Edmonson J.H., Ryan L.M., Blum R.H. et al. Randomized comparison of doxorubicin alone versus ifosfamide plus doxorubicin or mitomycin, doxorubicin, and cisplatin against advanced soft tissue sarcomas. J. Clin. Oncol. 1993; 11: 1269–75
  71. Patel S.R., Vadhan-Raj S., Burgess M.A. et al. Results of two consecutive trials of dose- intensive chemotherapy with doxorubicin and ifosfamide in patients with sarcomas. Am. J. Clin. Oncol. 1998; 21: 317–21
  72. Judson I., Verweij J., Gelderblom H. et al. Doxorubicin alone versus intensified doxorubicin plus ifosfamide for first-line treatment of advanced or metastatic soft-tissue sarcoma: a randomised controlled phase 3 trial. Lancet Oncol. 2014; 15: 415–23
  73. Borden E.C., Amato D.A., Rosenbaum C., Enterline H.T., Shiraki M.J., Creech R.H., Lerner H.J., Carbone P.P. Randomized comparison of three adriamycin regimens for metastatic soft tissue sarcomas. J. Clin. Oncol. 1987 Jun; 5 (6): 840–50
  74. Antman K.H., Ryan L., Elias A. et al. Response to ifosfamide and mesna: 124 previously treated patients with metastatic or unresectable sarcoma. J. Clin. Oncol. 1989; 7: 126–31
  75. Hensley M.L., Maki R., Venkatraman E. et al. Gemcitabine and docetaxel in patients with unresectable leiomyosarcoma: results of a phase II trial. J. Clin. Oncol. 2002; 20: 2824–31.
  76. Bay J.O., Ray-Coquard I., Fayette J. et al. Docetaxel and gemcitabine combination in 133 advanced soft-tissue sarcomas: a retrospective analysis. Int. J. Cancer. 2006; 119: 706–11.
  77. Saeter G., Talle K., Solheim O.P. Treatment of advanced, high-grade soft-tissue sarcoma with ifosfamide and continuous-infusion etoposide. Cancer Chemother. Pharmacol. 1995; 36: 172– 5
  78. Palumbo R., Palmeri S., Gatti C. et al. Combination chemotherapy using vincristine, Adriamycin, cyclophosphamide (VAC) alternating with ifosfamide and etoposide (IE) for advanced soft tissue sarcomas: a phase II study. Oncol. Rep. 1998; 5: 69–72
  79. Blanchette P., Hogg D., Ferguson P. et al. Topotecan and cyclophosphamide in adults with relapsed sarcoma. Sarcoma. 2012; 2012:749067
  80. Valentin T., Fournier C., Penel N., Bompas E., Chaigneau L., Isambert N., Chevreau C. Sorafenib in patients with progressive malignant solitary fibrous tumors: a subgroup analysis from aphase II study of the French Sarcoma Group (GSF/GETO). Invest. New Drugs. 2013 Dec; 31 (6): 1626–7.
  81. D"Adamo D.R., Anderson S.E., Albritton K., Yamada J., Riedel E., Scheu K., Schwartz G.K., Chen H., Maki R.G. Phase II study of doxorubicin and bevacizumab for patients with metastatic soft-tissue sarcomas. J. Clin. Oncol. 2005 Oct 1; 23 (28): 7135–42
  82. Park M.S., Patel S.R., Ludwig J.A., Trent J.C., Conrad C.A., Lazar A.J., Wang W.L., Boonsirikamchai P., Choi H., Wang X., Benjamin R.S., Araujo D.M. Activity of temozolomide and bevacizumab in the treatment of locally advanced, recurrent, and metastatic hemangiopericytoma and malignant solitary fibrous tumor. Cancer. 2011 Nov 1; 117 (21): 4939–47.
  83. Van der Graaf W.T., Blay J.Y., Chawla S.P., Kim D.W. et al. Pazopanib for metastatic soft-tissue sarcoma (PALETTE): a randomised, double-blind, placebo-controlled phase 3 trial. Lancet. 2012 May 19; 379 (9829): 1879–86.
  84. Frustaci S., Gherlinzoni F., De Paoli A. et al. Adjuvant chemotherapy for adult soft tissue sarcomas of the extremities and girdles: results of the Italian randomized cooperative trial. J. Clin Oncol. 2001; 19: 1238–47
  85. Look Hong N.J., Hornicek F.J., Harmon D.C. et al. Neoadjuvant chemoradiotherapy for patients with high-risk extremity and truncal sarcomas: a 10-year single institution retrospective study. Eur. J. Cancer. 2013; 49: 875–83
  86. Владимирова Л. Ю.,Гладков О. А.,Когония Л. М.,Королева И. А.,Семиглазова Т. Ю. Профилактика и лечение тошноты и рвоты. Методические рекомендацииDOI: 10.18 027/2224–5057–2018–8–3s2–502–511, https://rosoncoweb.ru/standarts/RUSSCO/2018/2018- 35.pdf
  87. МанзюкЛ. В., Багрова С. Г.,Копп М. В.,Кутукова С. И.,СемиглазоваТ . Ю. Использование остеомедифицирующих агентов для профилактики и лечения патологии костной ткани при злокачественных новообразованиях методические рекомендацииDOI:10.18027/2224–5057–2018–8–3s2–512–520, https://rosoncoweb.ru/standarts/RUSSCO/2018/2018-36.pdf
  88. Сакаева Д. Д., Орлова Р. В., Шабаева М. М. Лечение инфекционных осложнений фебрильной нейтропении и назначение КСФ Методические рекомендации DOI: 10.18/027/2224–5057–2018–8–3s2–521–530, https://rosoncoweb.ru/standarts/RUSSCO/2018/2018-37.pdf
  89. Ткаченко П. Е., Ивашкин В. Т., Маевская М. В. Корекция гепатотоксичности Методические рекомендацииDOI: 10.18 027 / 2224–5057–2018–8–3s2–531–544, https://rosoncoweb.ru/standarts/RUSSCO/2018/2018-38.pdf
  90. Виценя М. В., Агеев Ф. Т., Гиляров М. Ю., Овчинников А. Г., Орлова Р. В., Полтавская М. Г., Сычева Е. А «Практические рекомендации по коррекции кардиоваскулярной токсичности противоопухолевой лекарственной терапии » (Коллектив авторов:. DOI: 10.18 027 / 2224–5057–2018–8–3s2–545–563, https://rosoncoweb.ru/standarts/RUSSCO/2018/2018-39.pdf)
  91. Королева И. А., Болотина Л. В., Гладков О. А., Горбунова В. А., Круглова Л. С., Манзюк Л. В., Орлова Р. В. DOI: «Практические рекомендации по лекарственному лечению дерматологических реакций у пациентов получающих противоопухолевую лекарственную терапию» (Коллектив авторов: 10.18 027 / 2224–5057–2018–8–3s2–564– 574, https://rosoncoweb.ru/standarts/RUSSCO/2018/2018-40.pdf)
  92. Сытов А. В., Лейдерман И. Н., Ломидзе С. В., Нехаев И. В., Хотеев А. Ж. «Практические рекомендации по нутритивной поддержке онкологических больных (Коллектив авторов: DOI: 10.18 027 / 2224–5057–2018–8–3s2–575–583, https://rosoncoweb.ru/standarts/RUSSCO/2018/2018-41.pdf)
  93. Громова Е.Г., Бирюкова Л.С., Джумабаева Б.Т., Курмуков И.А. «Практические рекомендации по коррекции нефротоксичности противоопухолевых препаратов» (Коллектив авторов: DOI: 10.18 027 / 2224–5057–2018–8–3s2–591–603, https://rosoncoweb.ru/standarts/RUSSCO/2018/2018-44.pdf)
  94. Сомонова О. В., Антух Э. А., Елизарова А. Л., Матвеева И. И., Сельчук В. Ю., Черкасов В. А . «Практические рекомендации по профилактике тромбоэмболических осложнений у онкологических больных » (Коллектив авторов:, DOI: 10.18 027 / 2224–5057–2018–8– 3s2–604–609, https://rosoncoweb.ru/standarts/RUSSCO/2018/2018-45.pdf)
  95. Алиев М.Д. Бохян Б.Ю. Буров Д.А Прогностическая роль края резекции в хирургии сарком мягких тканей . Саркомы костей, мягких тканей и опухоли кожи №1, 2013г стр 60-66
  96. Феденко А.А. Бохяч Б.Ю. Конев А.А. Горбунова В.А. Первый Российский опыт применения пазопаниба в лечении больных саркомами мягких тканей. Саркомы костей, мягких тканей и опухоли кожи (№3-4, 2014г стр 44-51)
  97. Харатишвили Т.К. Петроченко Н.С Бохян Б.Ю. Сравнительное изучение клинической эффективности и безопасности метода изолированной перфузии конечностей с гипертермией у больных с саркомами мягких тканей Саркомы костей, мягких тканей и опухоли кожи (№4, 2016г)
  98. Бохян Б.Ю. Тепляков В.В. Онкология Национальное руководство Глава 21 Опухоли опорно-двигательного аппарата;. (Коллектив авторов под редакцией Чиссов В.И. , Давыдов М.И.) Москва ГЭОТАР-Медиа 2017г. 624стр стр535-548
  99. Буйденок Ю. В «Рекомендации по лечению последствий экстравазации противоопухолевых препаратов »:. DOI: 10.18 027 / 2224–5057–2018–8–3s2–610–616, https://rosoncoweb.ru/standarts/RUSSCO/2018/2018-46.pdf)
  100. Nicole L Stout,1 Catherine M Alfano,2 Christopher W Belter,3 Ralph Nitkin,4 Alison Cernich,4Karen Lohmann Siegel,5 and Leighton Chan1 A Bibliometric Analysis of the Landscape of Cancer Rehabilitation Research (1992–2016) J Natl Cancer Inst 2018 /08 110(8) 815-824
  101. Segal R1, Zwaal C2, Green E3, Tomasone JR4, Loblaw A5, Petrella T6; Exercise for People with Cancer Guideline Development Group. Exercise for people with cancer: a clinical practice guideline. Curr Oncol. 2017 Feb;24(1):40-46. doi: 10.3747/co.24.3376.
  102. Silver JK, Baima J: Cancer prehabilitation: an opportunity to decrease treatment-related morbidity, increase cancer treatment options, and improve physical and psychological health outcomes. Am J Phys Med Rehabil 2013, 92(8):715-727.
  103. Siegel GW, Biermann JS, Chugh R, Jacobson JA, Lucas D, Feng M, Chang AC, Smith SR, Wong SL, Hasen J: The multidisciplinary management of bone and soft tissue sarcoma: an essential organizational framework. J Multidiscip Healthc 2015, 8:109-115.
  104. Shehadeh A, El Dahleh M, Salem A, Sarhan Y, Sultan I, Henshaw RM, Aboulafia AJ: Standardization of rehabilitation after limb salvage surgery for sarcomas improves patients" outcome. Hematol Oncol Stem Cell Ther 2013, 6(3-4):105-111.
  105. Marchese VG, Spearing E, Callaway L, Rai SN, Zhang L, Hinds PS, Carlson CA, Neel MD, Rao BN, Ginsberg J: Relationships among range of motion, functional mobility, and quality of life in children and adolescents after limb-sparing surgery for lower-extremity sarcoma. Pediatr Phys Ther 2006, 18(4):238-244.
  106. Cox CL, Montgomery M, Oeffinger KC, Leisenring W, Zeltzer L, Whitton JA, Mertens AC, Hudson MM, Robison LL: Promoting physical activity in childhood cancer survivors: results from the Childhood Cancer Survivor Study. Cancer 2009, 115(3):642-654.
  107. Field T: Massage therapy research review. Complement Ther Clin Pract 2016, 24:19-31.
  108. Tantawy SA, Abdelbasset WK, Nambi G, Kamel DM: Comparative Study Between the Effects of Kinesio Taping and Pressure Garment on Secondary Upper Extremity Lymphedema and Quality of Life Following Mastectomy: A Randomized Controlled Trial. Integr Cancer Ther 2019, 18:1534735419847276.
  109. Fallon M, Giusti R, Aielli F, Hoskin P, Rolke R, Sharma M, Ripamonti CI, Committee EG: Management of cancer pain in adult patients: ESMO Clinical Practice Guidelines. Ann Oncol 2018, 29(Suppl 4):iv166-iv191.
  110. Oren R, Zagury Al, Katzir O, Kollender Y, Meller I: Musculoskeletal Cancer Surgery. In., edn. Edited by Malawer. Dordrecht: Springer; 2013: 583-593.
  111. Committee. NMA: Topic: The Diagnosis and Treatment of Lymphedema. Position Statement of the National Lymphedema Network. . In.; 2011: 1-19.
  112. Baxter GD, Liu L, Petrich S, Gisselman AS, Chapple C, Anders JJ, Tumilty S: Low level laser therapy (Photobiomodulation therapy) for breast cancer-related lymphedema: a systematic review. BMC cancer 2017, 17(1):833.
  113. Segal R, Zwaal C, Green E, Tomasone JR, Loblaw A, Petrella T, Exercise for People with Cancer Guideline Development G: Exercise for people with cancer: a systematic review. Curr Oncol 2017, 24(4):e290-e315.
  114. Nilsson H, Angeras U, Bock D, Borjesson M, Onerup A, Fagevik Olsen M, Gellerstedt M, Haglind E, Angenete E: Is preoperative physical activity related to post-surgery recovery? A cohort study of patients with breast cancer. BMJ Open 2016, 6(1):e007997
  115. Stout NL, Baima J, Swisher AK, Winters-Stone KM, Welsh J: A Systematic Review of Exercise Systematic Reviews in the Cancer Literature (2005-2017). PM R 2017, 9(9S2):S347-S384.
  116. Hu M, Lin W: Effects of exercise training on red blood cell production: implications for anemia. Acta Haematol 2012, 127(3):156-164.
  117. Bland KA, Zadravec K, Landry T, Weller S, Meyers L, Campbell KL: Impact of exercise on chemotherapy completion rate: A systematic review of the evidence and recommendations for future exercise oncology research. Crit Rev Oncol Hematol 2019, 136:79-85.
  118. Mustian KM, Alfano CM, Heckler C, Kleckner AS, Kleckner IR, Leach CR, Mohr D, Palesh OG, Peppone LJ, Piper BF et al: Comparison of Pharmaceutical, Psychological, and Exercise Treatments for Cancer-Related Fatigue: A Meta-analysis. JAMA Oncol 2017, 3(7):961-968.
  119. Streckmann F, Zopf EM, Lehmann HC, May K, Rizza J, Zimmer P, Gollhofer A, Bloch W, Baumann FT: Exercise intervention studies in patients with peripheral neuropathy: a systematic review. Sports Med 2014, 44(9):1289-1304.
  120. Kleckner IR, Kamen C, Gewandter JS, Mohile NA, Heckler CE, Culakova E, Fung C, Janelsins MC, Asare M, Lin PJ et al: Effects of exercise during chemotherapy on chemotherapy-induced peripheral neuropathy: a multicenter, randomized controlled trial. Support Care Cancer 2018, 26(4):1019-1028.
  121. Lee JM, Look RM, Turner C, Gardiner SK, Wagie T, Douglas J, Sorenson L, Evans L, Kirchner S, Dashkoff C et al: Low-level laser therapy for chemotherapy-induced peripheral neuropathy. Journal of Clinical Oncology 2012, 30(15_suppl):9019-9019.
  122. Rick O, von Hehn U, Mikus E, Dertinger H, Geiger G: Magnetic field therapy in patients with cytostatics-induced polyneuropathy: A prospective randomized placebo-controlled phase-III study. Bioelectromagnetics 2017, 38(2):85-94.
  123. Kilinc M, Livanelioglu A, Yildirim SA, Tan E: Effects of transcutaneous electrical nerve stimulation in patients with peripheral and central neuropathic pain. J Rehabil Med 2014, 46(5):454-460.
  124. Oberoi S, Zamperlini-Netto G, Beyene J, Treister NS, Sung L: Effect of prophylactic low level laser therapy on oral mucositis: a systematic review and meta-analysis. PLoS One 2014, 9(9):e107418.
  125. Westphal JG, Schulze PC: Exercise training in cancer related cardiomyopathy. J Thorac Dis 2018, 10(Suppl 35):S4391-S4399.
  126. Ross M, Fischer-Cartlidge E: Scalp Cooling: A Literature Review of Efficacy, Safety, and Tolerability for Chemotherapy-Induced Alopecia. Clin J Oncol Nurs 2017, 21(2):226-233.
  127. Kessels E, Husson O, van der Feltz-Cornelis CM: The effect of exercise on cancer-related fatigue in cancer survivors: a systematic review and meta-analysis. Neuropsychiatr Dis Treat 2018, 14:479-494.
  128. Rief H, Omlor G, Akbar M, Welzel T, Bruckner T, Rieken S, Haefner MF, Schlampp I, Gioules A, Habermehl D et al: Feasibility of isometric spinal muscle training in patients with bone metastases under radiation therapy - first results of a randomized pilot trial. BMC cancer 2014, 14:67.
  129. Bensadoun RJ, Nair RG: Low-Level Laser Therapy in the Management of Mucositis and Dermatitis Induced by Cancer Therapy. Photomed Laser Surg 2015, 33(10):487-491..
  130. Folkman S, Lazarus RS, Gruen RJ, DeLongis A: Appraisal, coping, health status, and psychological symptoms. J Pers Soc Psychol 1986, 50(3):571-579.
  131. Беляев АМ, Чулкова ВА, Семиглазова ТЮ, Рогачев МВ (eds.): Онкопсихология для врачей-онкологов и медицинских психологов. Руководство. СПб: Любавич; 2017.
  132. Fawzy FI, Cousins N, Fawzy NW, Kemeny ME, Elashoff R, Morton D: A structured psychiatric intervention for cancer patients. I. Changes over time in methods of coping and affective disturbance. Arch Gen Psychiatry 1990, 47(8):720-725.
  133. Fawzy FI, Kemeny ME, Fawzy NW, Elashoff R, Morton D, Cousins N, Fahey JL: A structured psychiatric intervention for cancer patients. II. Changes over time in immunological measures. Arch Gen Psychiatry 1990, 47(8):729-735.
  134. Karnofsky DA, Burchenal JH: The clinical evaluation of chemotherapeutic agents in cancer. In: Evaluation of chemotherapeutic agents. edn. Edited by MacLeod C. New York: Columbia University Press; 1949: 191-205
  135. Oken MM, Creech RH, Tormey DC, Horton J, Davis TE, McFadden ET, Carbone PP: Toxicity and response criteria of the Eastern Cooperative Oncology Group. Am J Clin Oncol 1982, 5(6):649-655
  136. Therasse P., Arbuck S.G., Eisenhauer E.A. et al. New guidelines to evaluate the response to treatment in solid tumors. J. Natl. Cancer. Inst. 2000; 92 (3): 205–216.
  137. Eisenhauer EA, Therasse P, Bogaerts J, Schwartz LH, Sargent D, Ford R, Dancey J, Arbuck S, Gwyther S, Mooney M et al: New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer 2009, 45(2):228-247
  138. Choi H., Charnsangavej C., Faria S.C. et al. Correlation of computed tomography and positron emission tomography in patients with metastatic gastrointestinal stromal tumor treated at a single institution with imatinib mesylate: proposal of new computed tomography response criteria. J. Clin. Oncol. 2007; 25 (13): 1753–1759
  139. Thway K., Fisher C. Synovial sarcoma: defining features and diagnostic evolution. Ann. Diagn. Pathol. 2014 Dec; 18 (6): 369–80
  140. Nielsen T.O., Poulin N.M., Ladanyi M. Synovial Sarcoma: Recent Discoveries as a Roadmap to New Avenues for Therapy. Cancer Discov. 2015 Feb; 5 (2): 124–134.
  141. Saeter G., Talle K., Solheim O.P. Treatment of advanced, high-grade soft-tissue sarcoma with ifosfamide and continuous-infusion etoposide. Cancer Chemother. Pharmacol. 1995; 36: 172– 5.
  142. Blay J.Y., van Glabbeke M., Verweij J. et al. Advanced soft-tissue sarcoma: a disease that is potentially curable for a subset of patients treated with chemotherapy. Eur. J. Cancer. 2003; 39: 64–69.
  143. Fayette J., Martin E., Piperno-Neumann S., Le Cesne A., Robert C., Bonvalot S. Angiosarcoma: a heterogeneous group of sarcomas with specific behavior depending on primary site: a retrospective study of 161 cases. Ann. Oncol. 2007; 18: 2030–2036.
  144. Abrahamson T.G., Stone M.S., Piette W.W. Cutaneous angiosarcoma. Adv. Dermatol. 2001; 17: 279–299.
  145. hePenel N., Bui B.N., Bay J.O. et al. Phase II trial of weekly paclitaxel for unresectable angiosarcoma: the ANGIOTAX Study. J. Clin. Oncol. 2008; 26: 5269–74.
  146. Hensley M.L., Sill M.W., Scribner D.R. Jr. et al. Sunitinib malate in the treatment of recurrent or persistent uterine leiomyosarcoma: a Gynecologic Oncology Group phase II study. Gynecol. Oncol. 2009; 115: 460–465
  147. Stiller C.A., Irama A., Serraino D. et al. Descriptive epidemiology of sarcoma Europe: report from the RARECARE project. Eur. J. Cancer. 2013; 49 (3): 68–1 9
  148. Coffin C.M., Patel A., Perkins S. et al. ALK1 and p80 expression and chromosomal rearrangements involving 2p23 in inflammatory myofibroblastic tumor. Mod. Pathol. 2001; 14: 569–76
  149. Rodig S.J., Shapiro G.l. Crizotinib, a small-molecule dual inhibitor of thec-Met and ALK receptor tyrosine kinases. Curr. Opin. Investig. Drugs. 2010; 11: 1477–90.
  150. Butrynski J.E., D’Adamo D.R., Hornick J.L. et al. Crizotinib in ALK-rearranged inflammatory myofibroblastic tumor. N. Engl. J. Med. 2010; 363: 1727–33.
  151. Bisogno G., Rosolen A., Carli M. Interferon alpha for alveolar soft part sarcoma. Pediatr. Blood Cancer. 2005; 44: 687–8.
  152. Roozendaal K.J., de Valk B., ten Velden J.J. et al. Alveolar soft-part sarcoma responding to interferon alpha-2b. Br. J. Cancer. 2003; 89: 243–5.
  153. Azizi A.A., Haberler C., Czech T. et al. Vascular-endothelial-growth-factor (VEGF) expression and possible response to angiogenesis inhibitor bevacizumab in metastatic alveolar soft part sarcoma. Lancet Oncol. 2006; 7: 521–3.
  154. Stacchiotti S., Tamborini E., Marrari A. et al. Response to sunitinib malate in advanced alveolar soft part sarcoma. Clin. Cancer Res. 2009; 15: 1096–104.
  155. Stacchiotti S., Negri T., Zaffaroni N. et al. Sunitinib in advanced alveolar soft part sarcoma: evidence of a direct antitumor effect. Ann. Oncol. 2011; 22: 1682–90.
  156. Stacchiotti S., Libertini M., Negri T. et al. Response to chemotherapy of solitary fibrous tumor: a retrospective study. Eur. J. Cancer. 2013; 49 (10): 2376–83.
  157. Park M.S., Patel S.R., Ludwig J.A. et al. Activity of temozolomide and bevacizumab in the treatment of locally advanced, recurrent, and metastatic hemangiopericy-toma and malignant solitary fibrous tumor. Cancer. 2011; 117: 4939–47.
  158. Domont J., Massard C., Lassau N. et al. Hemangiopericytoma and antiangio-genic therapy: clinical benefit of antiangiogenic therapy (sorafenib and sunitinib) in relapsed malignant haemangioperyctoma/solitary fibrous tumour. Invesl New Drugs. 2010; 28: 199–202.
  159. Mulamalla K., Truskinovsky A.M., Dudek A.Z. Rare case of hemangiopericytoma responds to sunitinib. Transl. Res. 2008; 151: 129–33.
  160. Stacchiotti S., Negri T., Libertini M. et al. Sunitinib in solitary fibrous tumor. Ann. Oncol. 2012; 23: 3171–9.
  161. Van der Graaf W.T., Blay J.Y., Chawla S.P. et al. Pazopanib for metastatic soft-tissue sarcoma (PALETTE): a randomized, double-blind, placebo-controlled phase trial. Lancet. 2012; 379: 1879–86.
  162. Sleijfer S., Ray-Coquard I., Papai Z. et al. Pazopanib, a multikinase angiogenesis inhibitor, in patients with relapsed or refractory advanced soft tissue sarcoma 11 phase II study from the European Organization for Research and Treatment of Cancer-Soft Tissue and Bone Sarcoma Group (EORTC study 62043). J. Clin. Oncol. 2009; 27: 3126–32
  163. Marrari A., Hornick J.L., Butrynski J.E. et al. Malignant perivascular epithelioid cell tumors (PEComas): a retrospective analysis el 24 patients to define clinical history and response to therapy [abstract 39396]. Presented ay the Connective Tissue Oncology Society (CTOS) 16th annual meeting, Chicago, November, 2011.]
  164. Stacchiotti S., Grosso F., Negri T. et al. Tumor response to sunitinib malate observed in clear- cell sarcoma. Ann. Oncol. 2010; 21: 1130–1.
  165. Stacchiotti S., Palassini E., Negri T. et al. Sunitinib malate in clear cell sarcoma [abstract 1496P]. Presented at ESMO annual meeting, Prague, September, 2012.
  166. Mir O., Boudou-Rouquette P., Larousserie F. et al. Objective response to sorafenib in advanced clear-cell sarcoma. Ann. Oncol. 2012; 23: 807–9
  167. Hasskarl J. Sorafenib: targeting multiple tyrosine kinases in cancer. Recent Results Cancer Res. 2014; 201: 145–164.
  168. Von Mehren M., Rankin C., Goldblum J.R., Demetri G.D., Bramwell V., Ryan C.W., Borden E. Phase 2 Southwest Oncology Group-directed intergroup trial (S0505) of sorafenib in advanced soft tissue sarcomas. Cancer. 2012; 118 (3): 770–776.
  169. Maki R.G., D’Adamo D.R., Keohan M.L., Saulle M., Schuetze S.M., Undevia S.D., Livingston M.B., Cooney M.M., Hensley M.L., Mita M.M., Takimoto C.H., Kraft A.S., Elias A.D., Brockstein B., Blachère N.E., Edgar M.A., Schwartz L.H., Qin L.X., Antonescu C.R., Schwartz G.K. Phase II study of sorafenib in patients with metastatic or recurrent sarcomas. Clin. Cancer Res. 2009; 27 (19): 3133–3140.
  170. Valentin T., Fournier C., Penel N., Bompas E., Chaigneau L., Isambert N., Chevreau C. Sorafenib in patients with progressive malignant solitary fibrous tumors: a subgroup analysis from aphase II study of the French Sarcoma Group (GSF/GETO). Invest. New Drugs. 2013 Dec; 31 (6): 1626–7.
  171. Онкология. Национальное руководство. Краткое издание / под ред. В. И. Чиссова, М. И. Давыдова. - М. : ГЭОТАР-Медиа, 2014. - 576 с. - ISBN 978-5-9704-3153-5.
  172. Von Mehren M. et al. Soft tissue sarcoma, version 2.2018, NCCN clinical practice guidelines in oncology //Journal of the National Comprehensive Cancer Network. – 2018. – Т. 16. – №. 5. – С. 536-563
  173. Casali P. G. et al. Soft tissue and visceral sarcomas: ESMO–EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up //Annals of Oncology. – 2018. – Т. 29. – №. Supplement_4. – С. iv51-iv67
  174. Chan J. Y. et al. Biological significance and prognostic relevance of peripheral blood neutrophil-to-lymphocyte ratio in soft tissue sarcoma //Scientific reports. – 2018. – Т. 8. – №. 1. – С. 11959
  175. Asanuma K. et al. Impact of plasma fibrinogen levels in benign and malignant soft tissue tumors //Cancer Biomarkers. – 2016. – Т. 16. – №. 3. – С. 453-458
  176. Szkandera J. et al. Uric acid levels in blood are associated with clinical outcome in soft-tissue sarcoma patients //Clinical Chemistry and Laboratory Medicine (CCLM). – 2015. – Т. 53. – №. 3. – С. 493-497
  177. Liang Y. et al. Prognostic value of the fibrinogen/albumin ratio (FAR) in patients with operable soft tissue sarcoma //BMC cancer. – 2018. – Т. 18. – №. 1. – С. 942
  178. Nakamura T. et al. Clinical significance of pretreatment serum C‐reactive protein level in soft tissue sarcoma //Cancer. – 2012. – Т. 118. – №. 4. – С. 1055-1061
  179. Kirchner P. T., Simon M. A. The clinical value of bone and gallium scintigraphy for soft-tissue sarcomas of the extremities //The Journal of bone and joint surgery. American volume. – 1984. – Т. 66. – №. 3. – С. 319-327
  180. Szkandera J. et al. The derived neutrophil/lymphocyte ratio predicts poor clinical outcome in soft tissue sarcoma patients //The American Journal of Surgery. – 2015. – Т. 210. – №. 1. – С. 111-116
  181. Swanson E L et al. Comparison of Three-Dimensional (3D) Conformal Proton Radiotherapy (RT), 3D Conformal Photon RT, and Intensity-Modulated RT for Retroperitoneal and Intra- Abdominal Sarcomas. International Journal of Radiation Oncology • Biology • Physics, Volume 83, Issue 5, 1549 - 1557.
  182. Brierley J, Gospodarowicz MK, Wittekind Ch TNM classification of malignant tumours. 8th edition Chichester, West Sussex, UK; Hoboken, NJ: John Wiley & Sons, Inc., 2017; 253
  183. Eggermont AM , de Wilt JH, ten Hagen TL. Current uses of isolated limb perfusion in the clinic and model system for new strategies . Lancet Oncol 2003, 4, 429-437
  184. Grunhagen DJ, de Wilt JH et al Ouctome and prognostic factor analysis of 217 consecutive isolated limb perfusions with tumor necrosis factor alpha and melphalan for limb-threating soft tissue sarcoma. Cancer 2006, 106, 1776-1784
  185. Ji T., Guo W., Yang RL., Tang XD., Wang YF. Modular hemipelvic endoprosthesis reconstruction--experience in 100 patients with mid-term follow-up results. Eur J Surg Oncol. 2013 Jan;39(1):53-60.
  186. Daniel Müller, Dominik Kaiser, Kati Sairanen, Thorsten Studhalter, İlker Uçkay Antimicrobial Prophylaxis for the Prevention of Surgical Site Infections in Orthopaedic Oncology - A Narrative Review of Current Concepts J Bone Jt Infect 2019; 4(6):254-263.
  187. T.Baad Hansen et al Is there consensus regarding surgical treatment of bone sarcomas September 2018 World Journal of Orthopaedics 9(9):173-179
  188. Patil N, Ahmed Kabeer Rasheed S, Abba M, Hendrik Leupold J, Schwarzbach M, Allgayer H. A mechanistic study on the metastasis inducing function of FUS-CHOP fusion protein in liposarcoma. Int J Cancer. 2014 Jun 15;134(12):2808-19. doi: 10.1002/ijc.28638. Epub 2013 Dec 7
  189. Constantine Gennatas, Vasiliki Michalaki, Paraskevi Vasilatou Kairi, Agathi Kondi-Paphiti, and Dionysios Voros Successful treatment with the mTOR inhibitor everolimus in a patient with Perivascular epithelioid cell tumor World J Surg Oncol. 2012; 10: 181.
  190. Falk Roeder and Robert Krempien Intraoperative radiation therapy (IORT) in soft-tissue sarcoma. Radiat Oncol. 2017; 12: 20
  191. Casper ES, Gaynor JJ, Hajdu SI, Magill GB, Tan C, Friedrich C, Brennan MF A prospective randomized trial of adjuvant chemotherapy with bolus versus continuous infusion of doxorubicin in patients with high-grade extremity soft tissue sarcoma and an analysis of prognostic factors. Cancer. 1991 Sep 15;68(6):1221-9.
  192. Woll PJ, Reichardt P, Le Cesne A, Bonvalot S, Azzarelli A, Hoekstra HJ, Leahy M, Van Coevorden F, Verweij J, Hogendoorn PC, Ouali M, Marreaud S, Bramwell VH, Hohenberger P; EORTC Soft Tissue and Bone Sarcoma Group and the NCIC Clinical Trials Group Sarcoma Disease Site Committee.Adjuvant chemotherapy with doxorubicin, ifosfamide, and lenograstim for resected soft-tissue sarcoma (EORTC 62931): a multicentre randomised controlled trial. Lancet Oncol. 2012 Oct;13(10):1045-54. doi: 10.1016/S1470-2045(12)70346-7. Epub 2012 Sep 4.
  193. Palumbo R, Palmeri S, Gatti C, Villani G, Cesca A, Toma S. Combination chemotherapy using vincristine, adriamycin, cyclophosphamide (VAC) alternating with ifosfamide and etoposide (IE) for advanced soft tissue sarcomas: a phase II study. Oncol Rep. 1998 Jan-Feb;5(1):69-72.
  194. Judson I, Verweij J, Gelderblom H, Hartmann JT, Schöffski P, Blay JY, Kerst JM, Sufliarsky J, Whelan J, Hohenberger P, Krarup-Hansen A, Alcindor T, Marreaud S, Litière S, Hermans C, Fisher C Hogendoorn PC, dei Tos AP, van der Graaf WT; European Organisation and Treatment of Cancer Soft Tissue and Bone Sarcoma Group Doxorubicin alone versus intensified doxorubicin plus ifosfamide for first-line treatment of advanced or metastatic soft- tissue sarcoma: a randomised controlled phase 3 trial. Lancet Oncol. 2014 Apr;15(4):415-23. doi: 10.1016/S1470-2045(14)70063-4. Epub 2014 Mar 5.
  195. Maki RG1, Wathen JK, Patel SR, Priebat DA, Okuno SH, Samuels B, Fanucchi M, Harmon DC, Schuetze SM, Reinke D, Thall PF, Benjamin RS, Baker LH, Hensley ML. Randomized phase II study of gemcitabine and docetaxel compared with gemcitabine alone in patients with metastatic soft tissue sarcomas: results of sarcoma alliance for research through collaboration study 002 [corrected]. J Clin Oncol. 2007 Jul 1;25(19):2755-63.
  196. Davis EJ, Chugh R, Zhao L, Lucas DR, Biermann JS, Zalupski MM, Feng M, Wong SL, Jacobson J, Zyczynski L, Reinke D, Metko G, Baker LH, Schuetze SMA randomised, open-label, phase II study of neo/adjuvant doxorubicin and ifosfamide versus gemcitabine and docetaxel in patients with localised, high-risk, soft tissue sarcoma. Eur J Cancer. 2015 Sep;51(13):1794- 802. doi: 10.1016/j.ejca.2015.05.010. Epub 2015 Jun 9.
  197. D"Ambrosio L, Touati N, Blay JY, Grignani G, Flippot R, Czarnecka AM, Piperno-Neumann S, Martin-Broto J, Sanfilippo R, Katz D, Duffaud F, Vincenzi B, Stark DP, Mazzeo F, Tuchscherer A, Chevreau C, Sherriff J, Estival A, Litière S, Sents W, Ray-Coquard I, Tolomeo F, Le Cesne A, Rutkowski P, Stacchiotti S, Kasper B, Gelderblom H, Gronchi A; European Organization for Research and Treatment of Cancer Soft Tissue and Bone Sarcoma Group Doxorubicin plus dacarbazine, doxorubicin plus ifosfamide, or doxorubicin alone as a first- line treatment for advanced leiomyosarcoma: A propensity score matching analysis from the European Organization for Research and Treatment of Cancer Soft Tissue and Bone Sarcoma Group. Cancer. 2020 Mar 4. doi: 10.1002/cncr.32795. [Epub ahead of print]
  198. Alexander Rehders 1 , Stefan B Hosch, Peter Scheunemann, Nikolas H Stoecklein, Wolfram T Knoefel, Matthias PeiperBenefit of Surgical Treatment of Lung Metastasis in Soft Tissue Sarcoma Arch Surg 142 (1), 70-5; discission 76Jan 2007
  199. Juneko E Grilley-Olson , Nicholas P Webber , David S Demos , Jared D Christensen David G Kirsch 1Multidisciplinary Management of Oligometastatic Soft Tissue Sarcoma Am Soc Clin Oncol Educ Book 38, 939-948 2018 May 23
  200. E Palmerini , R L Jones , E Setola , P Picci , E Marchesi , R Luksch , G Grignani , M Cesari A Longhi , M E Abate A Paioli , Z Szucs , L D"ambrosio , K Scotlandi F Fagioli , S Asaftei , S Ferrari Irinotecan and Temozolomide in Recurrent Ewing Sarcoma: An Analysis in 51 Adult and Pediatric Patients Acta Oncol, 57 (7), 958-964Jul 2018
  201. Cristian Navarrete-Dechent 1 2, Shoko Mori 2, Christopher A Barker 3, Mark A Dickson 4, Kishwer S Nehal Imatinib Treatment for Locally Advanced or Metastatic Dermatofibrosarcoma Protuberans: A Systematic Review MA Dermatol, 155 (3), 361-369 2019 Mar 1
  202. Sibyl Anderson , Carol Aghajanian Temozolomide in Uterine Leiomyosarcomas Gynecol Oncol, 98 (1), 99-103 Jul 2005
  203. Miso Kim , Tae Min Kim , Bhumsuk Keam , Yu Jung Kim , Jin Chul Paeng, Kyung Chul Moon , Dong-Wan Kim, Dae Seog HeoA Phase II Trial of Pazopanib in Patients With Metastatic Alveolar Soft Part Sarcoma Oncologist, 24 (1), 20-e29 Jan 2019
  204. S R Patel , S Vadhan-Raj, M A Burgess, C Plager, N Papadopolous, J Jenkins, R S Benjamin Results of Two Consecutive Trials of Dose-Intensive Chemotherapy With Doxorubicin and Ifosfamide in Patients With Sarcomas Am J Clin Oncol, 21 (3), 317-21 Jun 1998
  205. Alexander Kreuter , Heinrich Rasokat, Mariam Klouche, Stefan Esser, Armin Bader, Thilo Gambichler, Peter Altmeyer, Norbert H BrockmeyerLiposomal Pegylated Doxorubicin Versus Low-Dose Recombinant Interferon Alfa-2a in the Treatment of Advanced Classic Kaposi"s Sarcoma; Retrospective Analysis of Three German Centers Cancer Invest, 23 (8), 653-92005
  206. Timothy Cooley David Henry, Margaret Tonda, Steven Sun, Martin O"Connell, Wayne Rackoff A Randomized, Double-Blind Study of Pegylated Liposomal Doxorubicin for the Treatment of AIDS-related Kaposi"s Sarcoma Oncologist, 12 (1), 114-23 Jan 2007
  207. Larrier N. A., Czito B. G., Kirsch D. G. Radiation therapy for soft tissue sarcoma: indications and controversies for neoadjuvant therapy, adjuvant therapy, intraoperative radiation therapy, and brachytherapy //Surgical Oncology Clinics. – 2016. – Т. 25. – №. 4. – С. 841-860.
  208. Dao A. et al. Five years of local control of subscapularis aggressive fibromatosis managed by surgery and imatinib: a case report //Journal of medical case reports. – 2014. – Т. 8. – №. 1. – С. 416.
  209. Практические рекомендации по лекарственному лечению сарком мягких тканей. Рекомендации восточно-европейской группы по изучению сарком https://rosoncoweb.ru/standarts/RUSSCO/2019/2019-17.pdf
  210. Tap W. D. et al. Doxorubicin plus evofosfamide versus doxorubicin alone in locally advanced, unresectable or metastatic soft-tissue sarcoma (TH CR-406/SARC021): an international, multicentre, open-label, randomised phase 3 trial //The lancet oncology. – 2017. – Т. 18. – №. 8. – С. 1089-1103.
  211. Wagner M. J. et al. Vincristine, ifosfamide, and doxorubicin for initial treatment of Ewing sarcoma in adults //The oncologist. – 2017. – Т. 22. – №. 10. – С. 1271.
  212. Stacchiotti S. et al. Sunitinib malate in solitary fibrous tumor (SFT) //Annals of oncology. – 2012.–Т.23.–№.12.–С.3171-3179.
  213. Ye C. et al. Effective treatment of advanced alveolar soft part sarcoma with sunitinib: A case report //Medicine. – 2018. – Т. 97. – №. 51.
  214. Adjuvant chemotherapy for localized resectable soft-tissue sarcoma of adults: Meta-analysis of individual data. Sarcoma Meta-analysis Collaboration. Lancet. 1997;350:1647–1654.
  215. Pervaiz N, Colterjohn N, Farrokhyar F, et al. A systematic meta-analysis of randomized controlled trials of adjuvant chemotherapy for localized resectable soft-tissue sarcoma. Cancer. 2008;113:573–581.
  216. Grobmyer SR, Maki RG, Demetri GD, et al. Neo-adjuvant chemotherapy for primary high- grade extremity soft tissue sarcoma. Ann Oncol. 2004;15:1667–1672.
  217. Edmonson J, Ryan L, Blum R, et al. Randomized comparison of doxorubicin alone versus ifosfamide plus doxorubicin or mitomycin, doxorubicin, and cisplatin against advanced soft tissue sarcomas. J Clin Oncol. 1993;11:1269–1275.
  218. Soft Tissue Sarcoma Treatment Regimens April 20, 2018 https://www.cancertherapyadvisor.com/home/cancer-topics/sarcoma/soft-tissue-sarcoma-treatment-regimens/
  219. Mack LA, Crowe PJ, Yang JL, et al. Preoperative chemoradiotherapy (modified Eilber protocol) provides maximum local control and minimal morbidity in patients with soft tissue sarcoma. Ann Surg Oncol. 2005;12:646–653.
  220. Judson I, Radford J, Harris M, et al. Randomized phase II trial of pegylated liposomal doxorubicin versus doxorubicin in the treatment of advanced or metastatic soft tissue sarcoma: a study by the EORTC Soft Tissue and Bone Sarcoma Group. Eur J Cancer. 2001; 37:870–877
  221. Holcombe E. Grier, M.D., Mark D. Krailo, Ph.D., Nancy J. Tarbell, M.D., Michael P. Link, M.D., Christopher J.H. Fryer, M.D., Douglas J. Pritchard, M.D., Mark C. Gebhardt, M.D., Paul S. Dickman, M.D., Elizabeth J. Perlman, M.D., Paul A. Meyers, M.D., Sarah S. Donaldson, M.D., Sheila Moore, M.D., et al. Addition of Ifosfamide and Etoposide to Standard Chemotherapy for Ewing"s Sarcoma and Primitive Neuroectodermal Tumor of BoneFebruary20,2003N.EnglJMed2003;348:694-701
  222. Kirill I. Kirsanov ,Ekaterina A. Lesovaya ,Timur I. Fetisov,Beniamin Yu Bokhyan ,Gennady A. Belitsky , and Marianna G. Yakubovskaya Current Approaches for Personalized Therapy of Soft Tissue Sarcomas SarcomaVolume 2020, Article ID 6716742, 15 pages
  223. Alexandros Diamantis, M.D., M.Sc., Ph.D., Ioannis Baloyiannis,Dimitrios E. Magouliotis,Maria Tolia,Dimitrios Symeonidis,Effrosyni Bompou,Georgios Polymeneas and Konstantinos TepetesPerioperative Radiotherapy Versus Surgery Alone for Retroperitoneal Sarcomas: A Systematic Review and Meta-analysis Radiol Oncol. 2020 Mar; 54(1): 14–21. Published online 2020 Feb 29
  224. O"Sullivan B, Davis AM, Turcotte R, Bell R, Catton C, Chabot P, Wunder J, Kandel R, Goddard K, Sadura A, Pater J, Zee B Preoperative versus postoperative radiotherapy in soft-tissue sarcoma of the limbs: a randomised trial. Lancet. 2002 Jun 29; 359(9325):2235-41
  225. Adam Dangoor,Beatrice Seddon, Craig Gerrand, Robert Grimer,Jeremy Whelan, and Ian JudsonUK guidelines for the management of soft tissue sarcomas Clin Sarcoma Res. 2016; 6: 20. Published online 2016 Nov 15
  226. Seddon B. et al. Gemcitabine and docetaxel versus doxorubicin as first-line treatment in previously untreated advanced unresectable or metastatic soft-tissue sarcomas (GeDDiS): a randomised controlled phase 3 trial //The lancet oncology. – 2017. – Т. 18. – №. 10. – С. 1397- 1410.
  227. Röper B. et al. Study of preoperative radiotherapy for sarcomas of the extremities with intensity-modulation, image-guidance and small safety-margins (PREMISS) //BMC cancer. – 2015. – Т. 15. – №. 1. – С. 904.
  228. Prosnitz L. R. et al. The treatment of high-grade soft tissue sarcomas with preoperative thermoradiotherapy //International Journal of Radiation Oncology* Biology* Physics. – 1999. – Т. 45. – №. 4. – С. 941-949.
  229. Feyerabend T. et al. Local hyperthermia, radiation, and chemotherapy in locally advanced malignancies //Oncology. – 1996. – Т. 53. – №. 3. – С. 214-220.
  230. Brenda J. Weigel, Elizabeth Lyden, James R. Anderson, William H. Meyer, David M. Parham, David A. Rodeberg, Jeff M. Michalski, Douglas S. Hawkins, and Carola A.S. ArndtIntensive Multiagent Therapy, Including Dose-Compressed Cycles of Ifosfamide/Etoposide and Vincristine/Doxorubicin/Cyclophosphamide, Irinotecan, and Radiation, in Patients With High-Risk Rhabdomyosarcoma: A Report From the Children"s Oncology Group J Clin Oncol.2016Jan10; 34(2): 117–122.doi: 10.1200/JCO.2015.63.4048
  231. Seddon BM, Whelan J, Strauss SJ et al. GeDDiS: a prospective random controlled phase III trial of gemcitabine and docetaxel compared with doxorubicin as first-line treatment in previously untreated advanced unresectable or metastatic soft tissue sarcomas (EudraCT 2009-014907- 29). J Clin Oncol 2015; 33(Suppl 15); Abstr 10500
  232. Anderton J. et al. International randomised controlled trial for the treatment of newly diagnosed EWING sarcoma family of tumours–EURO EWING 2012 Protocol //Trials. – 2020. – Т. 21. – №. 1. – С. 1-9.

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