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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Bone and soft tissue sarcomas, tumors of the skin</journal-id><journal-title-group><journal-title xml:lang="en">Bone and soft tissue sarcomas, tumors of the skin</journal-title><trans-title-group xml:lang="ru"><trans-title>Саркомы костей, мягких тканей и опухоли кожи</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2219-4614</issn><issn publication-format="electronic">2782-3687</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">468</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Pediatric Oncology</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ПЕДИАТРИЧЕСКАЯ ОНКОЛОГИЯ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Possibility of targeted therapy of osteosarcoma in children and adolescents (literature review)</article-title><trans-title-group xml:lang="ru"><trans-title>Возможности применения таргетной терапии при лечении остеосаркомы у детей и подростков (литературный обзор)</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Senzhapova</surname><given-names>E. R.</given-names></name><name xml:lang="ru"><surname>Сенжапова</surname><given-names>Э. Р.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>г.   Москва</p></bio><email>senzhapova@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Pediatric Oncology and Haematology Research Institute of FSBSI «N.N. Blokhin	Cancer Research Center»</institution></aff><aff><institution xml:lang="ru">НИИ ДОИГ ФГБНУ «Российский онкологический научный центр им. Н.Н. Блохина»</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2014-06-26" publication-format="electronic"><day>26</day><month>06</month><year>2014</year></pub-date><volume>6</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>34</fpage><lpage>44</lpage><history><date date-type="received" iso-8601-date="2022-01-26"><day>26</day><month>01</month><year>2022</year></date><date date-type="accepted" iso-8601-date="2022-01-26"><day>26</day><month>01</month><year>2022</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2014, Senzhapova E.R.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2014, Сенжапова Э.Р.</copyright-statement><copyright-year>2014</copyright-year><copyright-holder xml:lang="en">Senzhapova E.R.</copyright-holder><copyright-holder xml:lang="ru">Сенжапова Э.Р.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://sarbon.abvpress.ru/jour/article/view/468">https://sarbon.abvpress.ru/jour/article/view/468</self-uri><abstract xml:lang="en"><p>Osteosarcoma treatment methods have not been changed for last twenty years. There are five main drugs (such as cisplatin, doxorubicin, methotrexate, ifosfomide, etoposide) which are usually used in different combinations and doses. Results of survival are approximately similar. Five-year overall survival of patients with localized osteosarcoma is 75% and five-year event-free survival is 62%. Survival results of patients with metastatic osteosarcoma are much worse, five-year overall survival is 34% and five-year event-free survival is 20%.Relevance topic is associated with the fact that the results of treatment osteosarcoma are not satisfactory and optimal therapeutic strategy is unknown. In this connection, new programs are developed based on the experience of pre-existing protocols, taking into molecular-biological features of osteosarcoma cells. Different studies of signaling pathways, tumor microenvironment open the way to possibility of using target therapies (small molecules inhibitors and monoclonal antibodies), cell-cytokine therapy.</p></abstract><trans-abstract xml:lang="ru"><p>Методы лечения остеосаркомы на протяжении последних двадцати лет практически не менялись. существуют пять основных препаратов (цисплатин, адриамицин, метотрексат, ифосфамид, этопозид), которые применялись в различных комбинациях и дозах. результаты выживаемости приблизительно одинаковые. У пациентов с локализованным вариантом остеосаркомы 5-летняя общая выживаемость 75%, 5-летняя бессобытийная выживаемость – 62%. У пациентов с метастатической остеосаркомой результаты намного хуже: 5-летняя общая выживаемость – 35%, 5-летняя бессобытийная выживаемость – 20%.Актуальность данной темы обусловлена тем, что результаты лечения остеосаркомы остаются неудовлетворительными, и оптимальная терапевтическая стратегия неизвестна. В связи с чем разрабатываются новые программы, опираясь на опыт применения протоколов, существовавших ранее, с учетом молекулярно-биологических особенностей опухолевых клеток. Исследование различных клеточных сигнальных путей, опухолевого микроокружения открывает путь к применению совершенно новых классов лекарственных препаратов (мультикиназных ингибиторов и моноклональных антител), клеточной и цитокиновой терапии.</p></trans-abstract><kwd-group xml:lang="en"><kwd>osteosarcoma</kwd><kwd>target therapy</kwd><kwd>children</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>остеосаркома</kwd><kwd>таргетная терапия</kwd><kwd>дети</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. By Gaetano Bacci et al. Long-Term Outcome for Patients With Nonmetastatic Osteosarcoma of the Extremity Treated at the Istituto Ortopedico Rizzoli According to the Istituto Ortopedico Rizzoli/Osteosarcoma-2 Protocol: An Updated Report. Journal of clinical oncology. 2000, v. 18, p. 4016-4027.</mixed-citation><mixed-citation xml:lang="ru">By Gaetano Bacci et al. Long-Term Outcome for Patients With Nonmetastatic Osteosarcoma of the Extremity Treated at the Istituto Ortopedico Rizzoli According to the Istituto Ortopedico Rizzoli/Osteosarcoma-2 Protocol: An Updated Report. Journal of clinical oncology. 2000, v. 18, p. 4016-4027.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Stefano Ferrari et al. Neoadjuvant Chemotherapy With Methotrexate, Cisplatin, and Doxorubicin With or Without Ifosfamide in Nonmetastatic Osteosarcoma of the Extremity: An Italian Sarcoma Group Trial ISG/OS-1. Journal of clinical oncology. 2012, v. 30, No. 17, p. 2112-2118.</mixed-citation><mixed-citation xml:lang="ru">Stefano Ferrari et al. Neoadjuvant Chemotherapy With Methotrexate, Cisplatin, and Doxorubicin With or Without Ifosfamide in Nonmetastatic Osteosarcoma of the Extremity: An Italian Sarcoma Group Trial ISG/OS-1. Journal of clinical oncology. 2012, v. 30, No. 17, p. 2112-2118.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3. Stefano Ferrari et al. Neoadjuvant Chemotherapy With HighDose Ifosfamide, High-Dose Methotrexate, Cisplatin, and Doxorubicin for Patients With Localized Osteosarcoma of the Extremity: A Joint Study by the Italian and Scandinavian Sarcoma Groups. Journal of clinical oncology. 2005, v. 23, No. 34, p. 8845-8852.</mixed-citation><mixed-citation xml:lang="ru">Stefano Ferrari et al. Neoadjuvant Chemotherapy With HighDose Ifosfamide, High-Dose Methotrexate, Cisplatin, and Doxorubicin for Patients With Localized Osteosarcoma of the Extremity: A Joint Study by the Italian and Scandinavian Sarcoma Groups. Journal of clinical oncology. 2005, v. 23, No. 34, p. 8845-8852.</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4. Marta Hegyi et al. Good Prognosis of Localized Osteosarcoma in Young Patients Treated With Limb-Salvage Surgery and Chemotherapy. Pediatric Blood Cancer. 2011, v. 57, p. 415-422.</mixed-citation><mixed-citation xml:lang="ru">Marta Hegyi et al. Good Prognosis of Localized Osteosarcoma in Young Patients Treated With Limb-Salvage Surgery and Chemotherapy. Pediatric Blood Cancer. 2011, v. 57, p. 415-422.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5. Sigbjørn Smeland et al. Results of the Scandinavian Sarcoma Group XIV protocol for classical osteosarcoma. Acta Orthopaedica. 2011, v. 82 (2), p. 211-216.</mixed-citation><mixed-citation xml:lang="ru">Sigbjørn Smeland et al. Results of the Scandinavian Sarcoma Group XIV protocol for classical osteosarcoma. Acta Orthopaedica. 2011, v. 82 (2), p. 211-216.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6. Yukihide Iwamoto et al. Multiinstitutional phase II study of neoadjuvant chemotherapy for osteosarcoma (NECO study) in Japan: NECO-93J and NECO-95J. Journal of orthopedic science. 2009, v. 14, p. 397-404.</mixed-citation><mixed-citation xml:lang="ru">Yukihide Iwamoto et al. Multiinstitutional phase II study of neoadjuvant chemotherapy for osteosarcoma (NECO study) in Japan: NECO-93J and NECO-95J. Journal of orthopedic science. 2009, v. 14, p. 397-404.</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7. A. Sérgio Petrilli et al. Results of the Brazilian Osteosarcoma Treatment Group Studies III and IV: Prognostic Factors and Impact on Survival. Journal of clinical oncology. 2006, v. 24, No. 7, p. 1161-1168.</mixed-citation><mixed-citation xml:lang="ru">A. Sérgio Petrilli et al. Results of the Brazilian Osteosarcoma Treatment Group Studies III and IV: Prognostic Factors and Impact on Survival. Journal of clinical oncology. 2006, v. 24, No. 7, p. 1161-1168.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8. By Allen M. Goorin et al. Presurgical Chemotherapy Compared With Immediate Surgery and Adjuvant Chemotherapy for Nonmetastatic Osteosarcoma: Pediatric Oncology Group Study POG-8651. Journal of clinical oncology. 2003, v. 21, p. 1574-1580.</mixed-citation><mixed-citation xml:lang="ru">By Allen M. Goorin et al. Presurgical Chemotherapy Compared With Immediate Surgery and Adjuvant Chemotherapy for Nonmetastatic Osteosarcoma: Pediatric Oncology Group Study POG-8651. Journal of clinical oncology. 2003, v. 21, p. 1574-1580.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9. Marie-Cécile Le Deley et al. SFOP OS94: A randomized trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. European journal of cancer. 2007, v. 43, p. 752-761.</mixed-citation><mixed-citation xml:lang="ru">Marie-Cécile Le Deley et al. SFOP OS94: A randomized trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. European journal of cancer. 2007, v. 43, p. 752-761.</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10. Pamela S. Hinds et al. Aggressive treatment of non-metastatic osteosarcoma improves health-related quality of life in children and adolescents. European journal of cancer. 2009, v. 45, p. 2007-2014.</mixed-citation><mixed-citation xml:lang="ru">Pamela S. Hinds et al. Aggressive treatment of non-metastatic osteosarcoma improves health-related quality of life in children and adolescents. European journal of cancer. 2009, v. 45, p. 2007-2014.</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11. Najat C. Daw et al. Frontline Treatment of Localized Osteosarcoma Without Methotrexate. Cancer. 2011, v. 117, p. 2770-2778.</mixed-citation><mixed-citation xml:lang="ru">Najat C. Daw et al. Frontline Treatment of Localized Osteosarcoma Without Methotrexate. Cancer. 2011, v. 117, p. 2770-2778.</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12. Paul A. Meyers et al. Osteosarcoma: the addition of muramyl tripeptide to chemotherapy improves overall survival – a report from the Children’s Oncology Group. Journal of clinical oncology. 2008, v. 28, No. 9, p. 633-638.</mixed-citation><mixed-citation xml:lang="ru">Paul A. Meyers et al. Osteosarcoma: the addition of muramyl tripeptide to chemotherapy improves overall survival – a report from the Children’s Oncology Group. Journal of clinical oncology. 2008, v. 28, No. 9, p. 633-638.</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">13. Meyersa P.A., Healeya J.H., Choua A.J. et al. Addition of pamidronate to chemotherapy for the treatment of osteosarcoma. Cancer. 2011, v. 117, 8, p. 1736-1744.</mixed-citation><mixed-citation xml:lang="ru">Meyersa P.A., Healeya J.H., Choua A.J. et al. Addition of pamidronate to chemotherapy for the treatment of osteosarcoma. Cancer. 2011, v. 117, 8, p. 1736-1744.</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">14. Michael S. Isakoff et al. Poor Survival for Osteosarcoma of the Pelvis: A Report from the Children’s Oncology Group. Clinical Orthopedics Related Research. 2012, v. 470, p. 2007-2013.</mixed-citation><mixed-citation xml:lang="ru">Michael S. Isakoff et al. Poor Survival for Osteosarcoma of the Pelvis: A Report from the Children’s Oncology Group. Clinical Orthopedics Related Research. 2012, v. 470, p. 2007-2013.</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">15. Kjetil Boye et al. High-Dose Chemotherapy with Stem Cell Rescue in the Primary Treatment of Metastatic and Pelvic Osteosarcoma: Final Results of the ISG/SSG II Study. Pediatric blood cancer. 2014, v. 61, 5, p. 840-845.</mixed-citation><mixed-citation xml:lang="ru">Kjetil Boye et al. High-Dose Chemotherapy with Stem Cell Rescue in the Primary Treatment of Metastatic and Pelvic Osteosarcoma: Final Results of the ISG/SSG II Study. Pediatric blood cancer. 2014, v. 61, 5, p. 840-845.</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">16. Najat C. Daw et al. Metastatic Osteosarcoma. Results of Two Consecutive Therapeutic Trials at St. Jude Children’s Research Hospital. Cancer. 2006, v. 106, p. 403-412.</mixed-citation><mixed-citation xml:lang="ru">Najat C. Daw et al. Metastatic Osteosarcoma. Results of Two Consecutive Therapeutic Trials at St. Jude Children’s Research Hospital. Cancer. 2006, v. 106, p. 403-412.</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">17. Ebb David, Holcombe Grier, Karen Marcus et al. Phase II Trial of Trastuzumab in Combination With Cytotoxic Chemotherapy for Treatment of Metastatic Osteosarcoma With Human Epidermal Growth Factor Receptor 2 Overexpression: A Report From the Children’s Oncology Group. Journal of clinical oncology. 2012, v. 30, No. 20, p. 2245-2551.</mixed-citation><mixed-citation xml:lang="ru">Ebb David, Holcombe Grier, Karen Marcus et al. Phase II Trial of Trastuzumab in Combination With Cytotoxic Chemotherapy for Treatment of Metastatic Osteosarcoma With Human Epidermal Growth Factor Receptor 2 Overexpression: A Report From the Children’s Oncology Group. Journal of clinical oncology. 2012, v. 30, No. 20, p. 2245-2551.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">18. Goldsby RobertE., Timothy M. Fan, Doojduen Villaluna et al. Feasibility and dose discovery analysis of zoledronic acid with concurrent hemotherapy in the treatment of newly diagnosed metastatic osteosarcoma: A report from the Children’s Oncology Group. European Journal of Cancer. 2013, v. 49, p. 2384-2391.</mixed-citation><mixed-citation xml:lang="ru">Goldsby RobertE., Timothy M. Fan, Doojduen Villaluna et al. Feasibility and dose discovery analysis of zoledronic acid with concurrent hemotherapy in the treatment of newly diagnosed metastatic osteosarcoma: A report from the Children’s Oncology Group. European Journal of Cancer. 2013, v. 49, p. 2384-2391.</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">19. Grignani G. et al. A phase II trial of sorafenib in relapsed and unresectable high-grade osteosarcoma after failure of standard multimodal therapy: an Italian Sarcoma Group study. Annals of Oncology. 2012, v. 23 (2), p. 508-516.</mixed-citation><mixed-citation xml:lang="ru">Grignani G. et al. A phase II trial of sorafenib in relapsed and unresectable high-grade osteosarcoma after failure of standard multimodal therapy: an Italian Sarcoma Group study. Annals of Oncology. 2012, v. 23 (2), p. 508-516.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">20. Jiong Mei et al. VEGFR, RET, and RAF/MEK/ERK Pathway Take Part in the Inhibition of Osteosarcoma MG63 Cells with Sorafenib Treatment. Cell Biochem Biophys. 2014, v. 69 (1), p. 151-156.</mixed-citation><mixed-citation xml:lang="ru">Jiong Mei et al. VEGFR, RET, and RAF/MEK/ERK Pathway Take Part in the Inhibition of Osteosarcoma MG63 Cells with Sorafenib Treatment. Cell Biochem Biophys. 2014, v. 69 (1), p. 151-156.</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">21. Grignani G., Palmerini E., Dileo P. et al. A Phase I Trial and Pharmacokinetic Study of Sorafenib in Children with Refractory Solid Tumors or Leukemias: A Children’s Oncology Group Phase I Consortium Report. Clinical Cancer Research. 2012, v. 18 (21), p. 6011-6022.</mixed-citation><mixed-citation xml:lang="ru">Grignani G., Palmerini E., Dileo P. et al. A Phase I Trial and Pharmacokinetic Study of Sorafenib in Children with Refractory Solid Tumors or Leukemias: A Children’s Oncology Group Phase I Consortium Report. Clinical Cancer Research. 2012, v. 18 (21), p. 6011-6022.</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">22. Inaba Hiroto, Jeffrey E. Rubnitz et al. Phase I Pharmacokinetic and Pharmacodynamic Study of the Multikinase Inhibitor Sorafenib in Combination With Clofarabine and Cytarabine in Pediatric Relapsed/Refractory Leukemia. Journal of clinical oncology. 2011, v. 29, No. 24, p. 3293-3300.</mixed-citation><mixed-citation xml:lang="ru">Inaba Hiroto, Jeffrey E. Rubnitz et al. Phase I Pharmacokinetic and Pharmacodynamic Study of the Multikinase Inhibitor Sorafenib in Combination With Clofarabine and Cytarabine in Pediatric Relapsed/Refractory Leukemia. Journal of clinical oncology. 2011, v. 29, No. 24, p. 3293-3300.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">23. COG AAML1031: Phase III randomized trial for patients with de novo AML using bortezomib and sorafenib for high allelic ratio FLT3/ITD. Protocol Children’s Oncology Group.</mixed-citation><mixed-citation xml:lang="ru">COG AAML1031: Phase III randomized trial for patients with de novo AML using bortezomib and sorafenib for high allelic ratio FLT3/ITD. Protocol Children’s Oncology Group.</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">24. AML08: A phase III randomized trial of clofarabine plus cytarabine versus conventional induction therapy and a phase II study of natural killer cell transplantation in patients with newly diagnosed acute myeloid leukemia. Protocol St. Jude Children’s Research Hospital.</mixed-citation><mixed-citation xml:lang="ru">AML08: A phase III randomized trial of clofarabine plus cytarabine versus conventional induction therapy and a phase II study of natural killer cell transplantation in patients with newly diagnosed acute myeloid leukemia. Protocol St. Jude Children’s Research Hospital.</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">25. Schmid Irene, MD, Beate Haberle, MD, Michael H. Albert et al. Sorafenib and Cisplatin/Doxorubicin (PLADO) in Pediatric Hepatocellular Carcinoma. Pediatric Blood Cancer. 2012, v. 58, p. 539-544.</mixed-citation><mixed-citation xml:lang="ru">Schmid Irene, MD, Beate Haberle, MD, Michael H. Albert et al. Sorafenib and Cisplatin/Doxorubicin (PLADO) in Pediatric Hepatocellular Carcinoma. Pediatric Blood Cancer. 2012, v. 58, p. 539-544.</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">26. Martín-Liberal J. et al. Phase I trial of sorafenib in combination with ifosfamide in patients with advanced sarcoma: a Spanish group for research on sarcomas (GEIS) study. Invest New Drugs. 2014, v. 32, p. 287-294.</mixed-citation><mixed-citation xml:lang="ru">Martín-Liberal J. et al. Phase I trial of sorafenib in combination with ifosfamide in patients with advanced sarcoma: a Spanish group for research on sarcomas (GEIS) study. Invest New Drugs. 2014, v. 32, p. 287-294.</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">27. Pignochino Ymera, Carmine Dell’Aglio, Marco Basiricò et al. The Combination of Sorafenib and Everolimus Abrogates mTORC1 and mTORC2 Upregulation in Osteosarcoma Preclinical Models. Clinical Cancer Research. 2013, v. 19 (8), p. 2117-2131.</mixed-citation><mixed-citation xml:lang="ru">Pignochino Ymera, Carmine Dell’Aglio, Marco Basiricò et al. The Combination of Sorafenib and Everolimus Abrogates mTORC1 and mTORC2 Upregulation in Osteosarcoma Preclinical Models. Clinical Cancer Research. 2013, v. 19 (8), p. 2117-2131.</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">28. Palmerini E., Lewis Jones R., Paioli A. et al. Phase II Open Label, Non-randomized study of sorafenib and everolimus in unresectable metastatic osteosarcoma (OST) patients relapsed after standard chemotherapy. NCT01804374. http://meetinglibrary.asco.org/content/133681-144.</mixed-citation><mixed-citation xml:lang="ru">Palmerini E., Lewis Jones R., Paioli A. et al. Phase II Open Label, Non-randomized study of sorafenib and everolimus in unresectable metastatic osteosarcoma (OST) patients relapsed after standard chemotherapy. NCT01804374. http://meetinglibrary.asco.org/content/133681-144.</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">29. Fouladi Maryam, Fred Laningham, Jianrong Wu et al. Phase I Study of Everolimus in Pediatric Patients With Refractory Solid Tumors. Journal of clinical oncology. 2007, v. 25, No. 30, p. 4806-4812.</mixed-citation><mixed-citation xml:lang="ru">Fouladi Maryam, Fred Laningham, Jianrong Wu et al. Phase I Study of Everolimus in Pediatric Patients With Refractory Solid Tumors. Journal of clinical oncology. 2007, v. 25, No. 30, p. 4806-4812.</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">30. Franz D.N., Sparagana S., Frost M. et al. Efficacy and safety of everolimus for subependymal giant cell astrocytomas associated with tuberous sclerosis complex (EXIST-1): a multicentre, randomized, placebo-controlled phase 3 trial. Lancet. 2013, v. 381 (9861), p. 125-132.</mixed-citation><mixed-citation xml:lang="ru">Franz D.N., Sparagana S., Frost M. et al. Efficacy and safety of everolimus for subependymal giant cell astrocytomas associated with tuberous sclerosis complex (EXIST-1): a multicentre, randomized, placebo-controlled phase 3 trial. Lancet. 2013, v. 381 (9861), p. 125-132.</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">31. Phase II Study of Everolimus in Children and Adolescents With Refractory or Relapsed Osteosarcoma. http://clinicaltrial.gov/show/NCT01216826.</mixed-citation><mixed-citation xml:lang="ru">Phase II Study of Everolimus in Children and Adolescents With Refractory or Relapsed Osteosarcoma. http://clinicaltrial.gov/show/NCT01216826.</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">32. By Richard Gorlick et al. Expression of HER2/erbB-2 Correlates With Survival in Osteosarcoma. Journal of clinical oncology. 1999, v. 17, p. 2781-2788.</mixed-citation><mixed-citation xml:lang="ru">By Richard Gorlick et al. Expression of HER2/erbB-2 Correlates With Survival in Osteosarcoma. Journal of clinical oncology. 1999, v. 17, p. 2781-2788.</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">33. Tomohiro Akatsuka et al. ErbB2 Expression Is Correlated with Increased Survival of Patients with Osteosarcoma. Cancer. 2002, v. 94, p. 1397-1404.</mixed-citation><mixed-citation xml:lang="ru">Tomohiro Akatsuka et al. ErbB2 Expression Is Correlated with Increased Survival of Patients with Osteosarcoma. Cancer. 2002, v. 94, p. 1397-1404.</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">34. Sarah Gorlick et al. HER-2 Expression is Not Prognostic in Osteosarcoma; A Children’s Oncology Group Prospective Biology Study. Pediatric blood cancer. 2014, v. 69.</mixed-citation><mixed-citation xml:lang="ru">Sarah Gorlick et al. HER-2 Expression is Not Prognostic in Osteosarcoma; A Children’s Oncology Group Prospective Biology Study. Pediatric blood cancer. 2014, v. 69.</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">35. Melinda S. Merchant at al. Phase 1 trial and pharmacokinetic study of Lexatumumab in pediatric patients with solid tumor. Journal of clinical oncology. 2012, v. 30, No. 33, p. 4141-4147.</mixed-citation><mixed-citation xml:lang="ru">Melinda S. Merchant at al. Phase 1 trial and pharmacokinetic study of Lexatumumab in pediatric patients with solid tumor. Journal of clinical oncology. 2012, v. 30, No. 33, p. 4141-4147.</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">36. Michal Roth et al. Ganglioside GD2 as a therapeutic target for antibody-mediated therapy in patients with osteosarcoma. Cancer. 2014, v. 120, p. 548-554.</mixed-citation><mixed-citation xml:lang="ru">Michal Roth et al. Ganglioside GD2 as a therapeutic target for antibody-mediated therapy in patients with osteosarcoma. Cancer. 2014, v. 120, p. 548-554.</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">37. A Phase I trial of humanized Anti-GD2 Monoclonal Antibody (Hu14.18K322A) in children and adolescents with neuroblastoma, osteosarcoma and melanoma. http://clinicaltrial.gov/show/NCT00743496.</mixed-citation><mixed-citation xml:lang="ru">A Phase I trial of humanized Anti-GD2 Monoclonal Antibody (Hu14.18K322A) in children and adolescents with neuroblastoma, osteosarcoma and melanoma. http://clinicaltrial.gov/show/NCT00743496.</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">38. Alice L.Yu, MD, Andrew L. Gilman et al. Anti-GD2 Antibody with GM-CSF, Interleukin-2, and Isotretinoin for Neuroblastoma. New English Journal of Medicine. 2010, v. 363 (14), p. 1324-1334.</mixed-citation><mixed-citation xml:lang="ru">Alice L.Yu, MD, Andrew L. Gilman et al. Anti-GD2 Antibody with GM-CSF, Interleukin-2, and Isotretinoin for Neuroblastoma. New English Journal of Medicine. 2010, v. 363 (14), p. 1324-1334.</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">39. Suzanne S. Shusterman, Wendy B. London, Stephen D. Gillies et al. Antitumor Activity of Hu14.18-IL2 in Patients With Relapsed/Refractory Neuroblastoma: A Children’s Oncology Group (COG) Phase II Study. Journal of clinical oncology. 2010, v. 28 (33), p. 4969-4975.</mixed-citation><mixed-citation xml:lang="ru">Suzanne S. Shusterman, Wendy B. London, Stephen D. Gillies et al. Antitumor Activity of Hu14.18-IL2 in Patients With Relapsed/Refractory Neuroblastoma: A Children’s Oncology Group (COG) Phase II Study. Journal of clinical oncology. 2010, v. 28 (33), p. 4969-4975.</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">40. Fariba Navid, Barry L. Shulkin, Robert A. Kaufman et al. Phase I Trial of a Novel Anti-GD2 Monoclonal Antibody, Hu14.18K322A, Designed to Decrease Toxicity in Children With Refractory or Recurrent Neuroblastoma. Journal of clinical oncology. 2014, v. 10, No. 11.</mixed-citation><mixed-citation xml:lang="ru">Fariba Navid, Barry L. Shulkin, Robert A. Kaufman et al. Phase I Trial of a Novel Anti-GD2 Monoclonal Antibody, Hu14.18K322A, Designed to Decrease Toxicity in Children With Refractory or Recurrent Neuroblastoma. Journal of clinical oncology. 2014, v. 10, No. 11.</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">41. Philippe Clézardin et al. Bisphosphonates in preclinical bone oncology. Bone. 2011, v. 49, p. 66-70.</mixed-citation><mixed-citation xml:lang="ru">Philippe Clézardin et al. Bisphosphonates in preclinical bone oncology. Bone. 2011, v. 49, p. 66-70.</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">42. Jun Ah Lee, Jun Soo Jung, Dong Ho Kim. RANKL Expression Is Related to Treatment Outcome of Patients With Localized, High-Grade Osteosarcoma. Pediatric Blood Cancer. 2010, v. 56, p. 738-743.</mixed-citation><mixed-citation xml:lang="ru">Jun Ah Lee, Jun Soo Jung, Dong Ho Kim. RANKL Expression Is Related to Treatment Outcome of Patients With Localized, High-Grade Osteosarcoma. Pediatric Blood Cancer. 2010, v. 56, p. 738-743.</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">43. Toru Akiyama, Crispin R. Dass et al. Novel therapeutic strategy for osteosarcoma targeting osteoclast differentiation, boneresorbing activity, and apoptosis pathway. Molecular Cancer Therapy. 2008, v. 7, p. 11.</mixed-citation><mixed-citation xml:lang="ru">Toru Akiyama, Crispin R. Dass et al. Novel therapeutic strategy for osteosarcoma targeting osteoclast differentiation, boneresorbing activity, and apoptosis pathway. Molecular Cancer Therapy. 2008, v. 7, p. 11.</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">44. Zhaoxu Li et al. Potential of human γδ T-cells for immunotherapy of osteosarcoma. Molecular Biology Reports. 2013, v. 40, p. 427-437.</mixed-citation><mixed-citation xml:lang="ru">Zhaoxu Li et al. Potential of human γδ T-cells for immunotherapy of osteosarcoma. Molecular Biology Reports. 2013, v. 40, p. 427-437.</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><citation-alternatives><mixed-citation xml:lang="en">45. Maria Serena Benassi, Francesca Ponticelli et al. Growth inhibition and sensitization to cisplatin by zoledronic acid in osteosarcoma cells. Cancer Letters. 2007, v. 250, p. 194-205.</mixed-citation><mixed-citation xml:lang="ru">Maria Serena Benassi, Francesca Ponticelli et al. Growth inhibition and sensitization to cisplatin by zoledronic acid in osteosarcoma cells. Cancer Letters. 2007, v. 250, p. 194-205.</mixed-citation></citation-alternatives></ref><ref id="B46"><label>46.</label><citation-alternatives><mixed-citation xml:lang="en">46. Meyersa P.A., Healeya J.H., Choua A.J. et al. Addition of pamidronate to chemotherapy for the treatment of osteosarcoma. Cancer. 2011, v. 117 (8), p. 1736-1744.</mixed-citation><mixed-citation xml:lang="ru">Meyersa P.A., Healeya J.H., Choua A.J. et al. Addition of pamidronate to chemotherapy for the treatment of osteosarcoma. Cancer. 2011, v. 117 (8), p. 1736-1744.</mixed-citation></citation-alternatives></ref><ref id="B47"><label>47.</label><citation-alternatives><mixed-citation xml:lang="en">47. Goldsby Robert E., Timothy M. Fan, Doojduen Villaluna et al. Feasibility and dose discovery analysis of zoledronic acid with concurrent hemotherapy in the treatment of newly diagnosed metastatic osteosarcoma: A report from the Children’s Oncology Group. European Journal of Cancer. 2013, v. 49, p. 2384-2391.</mixed-citation><mixed-citation xml:lang="ru">Goldsby Robert E., Timothy M. Fan, Doojduen Villaluna et al. Feasibility and dose discovery analysis of zoledronic acid with concurrent hemotherapy in the treatment of newly diagnosed metastatic osteosarcoma: A report from the Children’s Oncology Group. European Journal of Cancer. 2013, v. 49, p. 2384-2391.</mixed-citation></citation-alternatives></ref><ref id="B48"><label>48.</label><citation-alternatives><mixed-citation xml:lang="en">48. Gatien Moriceau et al. Zoledronic acid potentiates mTOR inhibition and abolishes the resistance of osteosarcoma cells to RAD001 (Everolimus): pivotal role of the prenylation process. Cancer Reserch. 2010, v. 70 (24), p. 10329-10339.</mixed-citation><mixed-citation xml:lang="ru">Gatien Moriceau et al. Zoledronic acid potentiates mTOR inhibition and abolishes the resistance of osteosarcoma cells to RAD001 (Everolimus): pivotal role of the prenylation process. Cancer Reserch. 2010, v. 70 (24), p. 10329-10339.</mixed-citation></citation-alternatives></ref><ref id="B49"><label>49.</label><citation-alternatives><mixed-citation xml:lang="en">49. Emilie P. Buddingh et al. Tumor-infiltrating macrophages are associated with metastasis suppression in high-grade osteosarcoma: a rationale for treatment with macrophage activating agents. Clinical cancer research. 2011, v. 17, 8, p. 2110-2019.</mixed-citation><mixed-citation xml:lang="ru">Emilie P. Buddingh et al. Tumor-infiltrating macrophages are associated with metastasis suppression in high-grade osteosarcoma: a rationale for treatment with macrophage activating agents. Clinical cancer research. 2011, v. 17, 8, p. 2110-2019.</mixed-citation></citation-alternatives></ref><ref id="B50"><label>50.</label><citation-alternatives><mixed-citation xml:lang="en">50. Carola A.S. Arndt et al. Inhaled granulocyte-macrophage colony stimulating factor for first pulmonary recurrence of osteosarcoma: effects on disease-free survival and immunomodulation. A report from the Children’s Oncology Group. Clinical cancer research. 2010, v. 16, 15, p. 4024-4030.</mixed-citation><mixed-citation xml:lang="ru">Carola A.S. Arndt et al. Inhaled granulocyte-macrophage colony stimulating factor for first pulmonary recurrence of osteosarcoma: effects on disease-free survival and immunomodulation. A report from the Children’s Oncology Group. Clinical cancer research. 2010, v. 16, 15, p. 4024-4030.</mixed-citation></citation-alternatives></ref><ref id="B51"><label>51.</label><citation-alternatives><mixed-citation xml:lang="en">51. By Tadahiko Kubo et al. Interferon-α/β receptor as a prognostic marker in osteosarcoma. Journal Bone Joint Surg. Am. 2011, v. 93, p. 519-526.</mixed-citation><mixed-citation xml:lang="ru">By Tadahiko Kubo et al. Interferon-α/β receptor as a prognostic marker in osteosarcoma. Journal Bone Joint Surg. Am. 2011, v. 93, p. 519-526.</mixed-citation></citation-alternatives></ref><ref id="B52"><label>52.</label><citation-alternatives><mixed-citation xml:lang="en">52. Stefan S. Bielack et al. MAP plus maintenance pegylated interferon α 2b (MAPInf) versus MAP alone in patients with resectable high-grade osteosarcoma and good histologic response to preoperative MAP: first results of the EURAMOS1 «good response» randomization. Journal of clinical oncology. 2013, v. 31, No. 18.</mixed-citation><mixed-citation xml:lang="ru">Stefan S. Bielack et al. MAP plus maintenance pegylated interferon α 2b (MAPInf) versus MAP alone in patients with resectable high-grade osteosarcoma and good histologic response to preoperative MAP: first results of the EURAMOS1 «good response» randomization. Journal of clinical oncology. 2013, v. 31, No. 18.</mixed-citation></citation-alternatives></ref><ref id="B53"><label>53.</label><citation-alternatives><mixed-citation xml:lang="en">53. Kosei Ando et al. Mifamurtide for the treatment of nonmetastatic osteosarcoma. Expert Opin. Pharmacotherapy. 2011, v. 12, 2, p. 285-292.</mixed-citation><mixed-citation xml:lang="ru">Kosei Ando et al. Mifamurtide for the treatment of nonmetastatic osteosarcoma. Expert Opin. Pharmacotherapy. 2011, v. 12, 2, p. 285-292.</mixed-citation></citation-alternatives></ref><ref id="B54"><label>54.</label><citation-alternatives><mixed-citation xml:lang="en">54. Paul A. Meyers et al. Osteosarcoma: a randomized, prospective trial of the addition of ifosfamide and/or muramyl tripeptide to cisplatin, doxorubicin, and high dose methotrexate. Journal of clinical oncology. 2005, v. 23, No. 9, p. 2004-2011.</mixed-citation><mixed-citation xml:lang="ru">Paul A. Meyers et al. Osteosarcoma: a randomized, prospective trial of the addition of ifosfamide and/or muramyl tripeptide to cisplatin, doxorubicin, and high dose methotrexate. Journal of clinical oncology. 2005, v. 23, No. 9, p. 2004-2011.</mixed-citation></citation-alternatives></ref><ref id="B55"><label>55.</label><citation-alternatives><mixed-citation xml:lang="en">55. Paul A. Meyers et al. Osteosarcoma: the addition of muramyl tripeptide to chemotherapy improves overall survival – a report from the Children’s Oncology Group. Journal of clinical oncology. 2008, v. 28, No. 9, p. 633-638.</mixed-citation><mixed-citation xml:lang="ru">Paul A. Meyers et al. Osteosarcoma: the addition of muramyl tripeptide to chemotherapy improves overall survival – a report from the Children’s Oncology Group. Journal of clinical oncology. 2008, v. 28, No. 9, p. 633-638.</mixed-citation></citation-alternatives></ref><ref id="B56"><label>56.</label><citation-alternatives><mixed-citation xml:lang="en">56. Anderson P.M. et al. Mifamurtid e in metastatic and recurrent osteosarcoma: a patient access study with pharmacokinetic, pharmacodynamic and safety assessments. Pediatric blood cancer. 2014, v. 61, 2, p. 238-244.</mixed-citation><mixed-citation xml:lang="ru">Anderson P.M. et al. Mifamurtid e in metastatic and recurrent osteosarcoma: a patient access study with pharmacokinetic, pharmacodynamic and safety assessments. Pediatric blood cancer. 2014, v. 61, 2, p. 238-244.</mixed-citation></citation-alternatives></ref><ref id="B57"><label>57.</label><citation-alternatives><mixed-citation xml:lang="en">57. Jens H.W. Pahl et al. Macrophages inhibit human osteosarcoma cell growth after activation with the bacterial cell wall derivative liposomal muramyl tripeptide in combination with interferon-γ. Journal of experimental and clinical cancer research. 2014, 27-33.</mixed-citation><mixed-citation xml:lang="ru">Jens H.W. Pahl et al. Macrophages inhibit human osteosarcoma cell growth after activation with the bacterial cell wall derivative liposomal muramyl tripeptide in combination with interferon-γ. Journal of experimental and clinical cancer research. 2014, 27-33.</mixed-citation></citation-alternatives></ref><ref id="B58"><label>58.</label><citation-alternatives><mixed-citation xml:lang="en">58. Sergei R. Guma et al. Natural killer sell therapy and aerosol interleukin-2 for the treatment of osteosarcoma lung metastasis. Pediatric blood cancer. 2014, v. 61, p. 618-626.</mixed-citation><mixed-citation xml:lang="ru">Sergei R. Guma et al. Natural killer sell therapy and aerosol interleukin-2 for the treatment of osteosarcoma lung metastasis. Pediatric blood cancer. 2014, v. 61, p. 618-626.</mixed-citation></citation-alternatives></ref><ref id="B59"><label>59.</label><citation-alternatives><mixed-citation xml:lang="en">59. Emilie P. Beddingh et al. Chemotherapy-resistant osteosarcoma is highly susceptible to IL-15 – activated allogenic and autologous NK-cells. Cancer Immunology Immunotherapy. 2011, v. 60, p. 575-586.</mixed-citation><mixed-citation xml:lang="ru">Emilie P. Beddingh et al. Chemotherapy-resistant osteosarcoma is highly susceptible to IL-15 – activated allogenic and autologous NK-cells. Cancer Immunology Immunotherapy. 2011, v. 60, p. 575-586.</mixed-citation></citation-alternatives></ref><ref id="B60"><label>60.</label><citation-alternatives><mixed-citation xml:lang="en">60. Haploidentical Donor natural killer cell infusion with intravenous recombinant human IL-15 (rhIL-15) in adults with refractory or relapsed acute myelogenous leukemia. Protocol University of Minesota.</mixed-citation><mixed-citation xml:lang="ru">Haploidentical Donor natural killer cell infusion with intravenous recombinant human IL-15 (rhIL-15) in adults with refractory or relapsed acute myelogenous leukemia. Protocol University of Minesota.</mixed-citation></citation-alternatives></ref><ref id="B61"><label>61.</label><citation-alternatives><mixed-citation xml:lang="en">61. Jens H.W. Pahl et al. Anti-EGFR antibody cetuximab enhances the cytolytic activity of natural killer cells toward osteosarcoma. Clinical cancer research. 2012, v. 18, p. 432-441.</mixed-citation><mixed-citation xml:lang="ru">Jens H.W. Pahl et al. Anti-EGFR antibody cetuximab enhances the cytolytic activity of natural killer cells toward osteosarcoma. Clinical cancer research. 2012, v. 18, p. 432-441.</mixed-citation></citation-alternatives></ref><ref id="B62"><label>62.</label><citation-alternatives><mixed-citation xml:lang="en">62. David Delgado et al. KIR receptor-ligand incompatibility predicts killing of osteosarcoma cell lines by allogenic NKcells. Pediatric blood cancer. 2010, v. 55, 7, p. 1300-1305.</mixed-citation><mixed-citation xml:lang="ru">David Delgado et al. KIR receptor-ligand incompatibility predicts killing of osteosarcoma cell lines by allogenic NKcells. Pediatric blood cancer. 2010, v. 55, 7, p. 1300-1305.</mixed-citation></citation-alternatives></ref><ref id="B63"><label>63.</label><citation-alternatives><mixed-citation xml:lang="en">63. Jeffrey E. Rubnitz et al. NKAML: a pilot study to determine the safety and feasibility of haploidentical natural killer cell transplantation in childhood acute myeloid leukemia. Journal of clinical oncology. 2010, v. 28, No. 6, p. 955-959.</mixed-citation><mixed-citation xml:lang="ru">Jeffrey E. Rubnitz et al. NKAML: a pilot study to determine the safety and feasibility of haploidentical natural killer cell transplantation in childhood acute myeloid leukemia. Journal of clinical oncology. 2010, v. 28, No. 6, p. 955-959.</mixed-citation></citation-alternatives></ref><ref id="B64"><label>64.</label><citation-alternatives><mixed-citation xml:lang="en">64. GD2NK: A safety/feasibility trial of the addition of the humanized anti-GD2 antibody (hu14.18K322A) with and without natural killer cells to chemotherapy in children and adolescents with recurrent/refractory neuroblastoma. Protocol St. Jude Children’s Research Hospital.</mixed-citation><mixed-citation xml:lang="ru">GD2NK: A safety/feasibility trial of the addition of the humanized anti-GD2 antibody (hu14.18K322A) with and without natural killer cells to chemotherapy in children and adolescents with recurrent/refractory neuroblastoma. Protocol St. Jude Children’s Research Hospital.</mixed-citation></citation-alternatives></ref></ref-list></back></article>
