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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">Pediatric Hematology/Oncology and Immunopathology</journal-id><journal-title-group><journal-title xml:lang="en">Pediatric Hematology/Oncology and Immunopathology</journal-title><trans-title-group xml:lang="ru"><trans-title>Вопросы гематологии/онкологии и иммунопатологии в педиатрии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-1708</issn><issn publication-format="electronic">2414-9314</issn><publisher><publisher-name xml:lang="en">Fund Doctors, Innovations, Science for Children</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">78</article-id><article-id pub-id-type="doi">10.24287/1726-1708-2017-16-1-28-39</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Results of mobilization, apheresis and autoreinfusion of hematopoietic stem cells in children with neuroblastoma: role of monitoring the count of CD34+ cells in peripheral blood</article-title><trans-title-group xml:lang="ru"><trans-title>Результаты мобилизации, афереза и аутореинфузии гемопоэтических стволовых клеток у детей с нейробластомой: роль мониторинга количества CD34+ клеток в периферической крови</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kurnikova</surname><given-names>E. E.</given-names></name><name xml:lang="ru"><surname>Курникова</surname><given-names>Е. Е.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD, Department of Transfusion medicine</p><p>Russia 117997, Moscow, Samory Mashela st., 1</p><p>+7 (495) 287-6570, ext. 5223</p></bio><email>elena.kurnikova@fccho-moscow.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kumukova</surname><given-names>I. B.</given-names></name><name xml:lang="ru"><surname>Кумукова</surname><given-names>И. Б.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Guz</surname><given-names>I. V.</given-names></name><name xml:lang="ru"><surname>Гуз</surname><given-names>И. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Chismatullina</surname><given-names>R. D.</given-names></name><name xml:lang="ru"><surname>Хисматуллина</surname><given-names>Р. Д.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Shamanskaya</surname><given-names>T. V.</given-names></name><name xml:lang="ru"><surname>Шаманская</surname><given-names>Т. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Fadeeva</surname><given-names>M. S.</given-names></name><name xml:lang="ru"><surname>Фадеева</surname><given-names>М. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Glushkova</surname><given-names>S. Y.</given-names></name><name xml:lang="ru"><surname>Глушкова</surname><given-names>С. Ю.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Brilliantova</surname><given-names>V. V.</given-names></name><name xml:lang="ru"><surname>Бриллиантова</surname><given-names>В. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Varfolomeyeva</surname><given-names>S. R.</given-names></name><name xml:lang="ru"><surname>Варфоломеева</surname><given-names>С. Р.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Trakhtman</surname><given-names>P. E.</given-names></name><name xml:lang="ru"><surname>Трахтман</surname><given-names>П. Е.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">National Reseach Practicle Center of Pediatric Hematology, Oncology, and Immunology named after Dmitry Rogachev</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный научно-практический центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева» Минздрава России, Москва</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2017-02-10" publication-format="electronic"><day>10</day><month>02</month><year>2017</year></pub-date><volume>16</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>28</fpage><lpage>39</lpage><history><date date-type="received" iso-8601-date="2018-08-10"><day>10</day><month>08</month><year>2018</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2017, «D. Rogachev NMRCPHOI»</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2017, ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="en">«D. Rogachev NMRCPHOI»</copyright-holder><copyright-holder xml:lang="ru">ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</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://hemoncim.com/jour/article/view/78">https://hemoncim.com/jour/article/view/78</self-uri><abstract xml:lang="en"><p>Myeloablative chemotherapy with autologous hematopoietic stem cells transplantation, can improve the results of long-term survival in patients with high-risk neuroblastoma. This treatment requires a sufficient number of autologous peripheral blood stem cells. Methods: 118 apheresis procedures was completed for 116 children with high-risk neuroblastoma, the median age was 2 years and 10 months (range, 6 months to 13 years), median body weight of 13 kg (range, 5.8 to 47 kg). Mobilization with G-CSF at a dose of 10 mg/kg was initiated at the time of incipient recovery of hematopoiesis after the last cycle of chemotherapy, monitoring of CD34+ cells in peripheral blood were started on 3rd day from the beginning of mobilization. Apheresis was performed the following day after reaching the number of CD34+ cells &gt;15 cells/μl after 4 consequent days of mobilization. Results: Modification of mobilization, based on CD34+ cells monitoring data, allowed us to reach the median number of CD34+ cells of 105,27 cells/μl (range, 14.8–714.8) at the day of apheresis. The median number of collected CD34+/kg was 14,43×106/kg b.w. (range, 2.68–74). Was revealed a significant correlation between the dose of CD34+/kg b.w in the apheresis product and the level of CD34+ cells in peripheral blood at the day of apheresis (R=0.762; р&lt;0.0001) and decrease of the results of mobilizing results and apheresis efficiency if mobilization was initiated later than after the 3rd course of chemotherapy. Conclusion: By monitoring the number of circulating CD34+ cells in peripheral blood and modification of mobilization tactic, the task to collect an adequate dose of CD34+ cells for autoSCT with one apheresis procedure was feasible. In 88 (75.86%) of the 116 patients we were able to collect 10×106/kg CD34+ cells and more, and 100% of patients collected &gt; 2.5×106/kg CD34+ cells with 1 apheresis.</p></abstract><trans-abstract xml:lang="ru"><p/></trans-abstract><kwd-group xml:lang="en"><kwd>peripheral blood stem cells</kwd><kwd>stem cell mobilization</kwd><kwd>apheresis</kwd><kwd>neuroblastoma</kwd><kwd>plerixafor</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>периферические стволовые клетки</kwd><kwd>мобилизация</kwd><kwd>аферез</kwd><kwd>лейкаферез</kwd><kwd>нейробластома</kwd><kwd>плериксафор</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. Caron H.N., Pearson A.D.J. Neuroblastoma. In: Voute P.A., Barrett A., Stevens M.C.G., Caron H.N., еds. Cancer in Сhildren. 5th еd. Oxford: Oxford University Press; 2005:337-352.</mixed-citation><mixed-citation xml:lang="ru">Caron H.N., Pearson A.D.J. Neuroblastoma. In: Voute P.A., Barrett A., Stevens M.C.G., Caron H.N., еds. Cancer in Сhildren. 5th еd. Oxford: Oxford University Press; 2005:337-352.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Brodeur G.M., Maris J.M. Neuroblastoma. In: Pizzo, D.A., Poplack, D.G., еds. Principles and Practice of Pediatric Oncology. 5th ed. Philadelphia, PA, Lippincott: Williams &amp;Wilkins; 2006:933-970.</mixed-citation><mixed-citation xml:lang="ru">Brodeur G.M., Maris J.M. Neuroblastoma. In: Pizzo, D.A., Poplack, D.G., еds. Principles and Practice of Pediatric Oncology. 5th ed. Philadelphia, PA, Lippincott: Williams &amp;Wilkins; 2006:933-970.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3. Luksch R., Castellani M. R., Collini P., De Bernardi B., Conte M., Gambini C. еt al. Neuroblastoma (Peripheral neuroblastic tumours). Crit Rev Oncol Hematol. 2016;107:163-181.</mixed-citation><mixed-citation xml:lang="ru">Luksch R., Castellani M. R., Collini P., De Bernardi B., Conte M., Gambini C. еt al. Neuroblastoma (Peripheral neuroblastic tumours). Crit Rev Oncol Hematol. 2016;107:163-181.</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4. Seeger R.C., Brodeur G.M., Sather H., Dalton A., Siegel S.E., Wong K.Y. et al. Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas. N Engl J Med. 1985;313(18):1111-1116.</mixed-citation><mixed-citation xml:lang="ru">Seeger R.C., Brodeur G.M., Sather H., Dalton A., Siegel S.E., Wong K.Y. et al. Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas. N Engl J Med. 1985;313(18):1111-1116.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5. Shimada H., Stram D.O., Chatten J., Joshi V.V., Hachitanda Y., Brodeur G.M. et al. Identification of subsets of neuroblastomas by combined histopathologic and N-myc analysis. J Natl Cancer Inst. 1995;87(19):1470-1476.</mixed-citation><mixed-citation xml:lang="ru">Shimada H., Stram D.O., Chatten J., Joshi V.V., Hachitanda Y., Brodeur G.M. et al. Identification of subsets of neuroblastomas by combined histopathologic and N-myc analysis. J Natl Cancer Inst. 1995;87(19):1470-1476.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6. Brodeur G.M., Maris J.M., Yamashiro D.J., Hogarty M.D., White P.S. Biology and genetics of human neuroblastomas. J Pediatr Hematol Oncol. 1997;19(2):93-101.</mixed-citation><mixed-citation xml:lang="ru">Brodeur G.M., Maris J.M., Yamashiro D.J., Hogarty M.D., White P.S. Biology and genetics of human neuroblastomas. J Pediatr Hematol Oncol. 1997;19(2):93-101.</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7. NB2004 protocol. Berthold F. (principal investigator) [cited 2016 March 15]. Available at: http://www.kinderkrebsinfo.de/dlja_specialistov/ protokoly_gpoh/pohkinderkrebsinfotherapiestudien/nb2004/index_rus.html.</mixed-citation><mixed-citation xml:lang="ru">NB2004 protocol. Berthold F. (principal investigator) [cited 2016 March 15]. Available at: http://www.kinderkrebsinfo.de/dlja_specialistov/ protokoly_gpoh/pohkinderkrebsinfotherapiestudien/nb2004/index_rus.html.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8. Pearson A.D., Pinkerton C.R., Lewis I.J., Imeson J., Ellershaw C., Machin D.; European Neuroblastoma Study Group; Children’s Cancer and Leukaemia Group (CCLG formerly United Kingdom Children’s Cancer Study Group). High-dose rapid and standard induction chemotherapy for patients aged over 1 year with stage 4 neuroblastoma: a randomised trial. Lancet Oncol. 2008;9(3):247-256.</mixed-citation><mixed-citation xml:lang="ru">Pearson A.D., Pinkerton C.R., Lewis I.J., Imeson J., Ellershaw C., Machin D.; European Neuroblastoma Study Group; Children’s Cancer and Leukaemia Group (CCLG formerly United Kingdom Children’s Cancer Study Group). High-dose rapid and standard induction chemotherapy for patients aged over 1 year with stage 4 neuroblastoma: a randomised trial. Lancet Oncol. 2008;9(3):247-256.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9. Park J.R., Eggert A., Caron H. Neuroblastoma: biology, prognosis, and treatment. Hematol Оncol Сlin North Am. 2010;24(1):65-86.</mixed-citation><mixed-citation xml:lang="ru">Park J.R., Eggert A., Caron H. Neuroblastoma: biology, prognosis, and treatment. Hematol Оncol Сlin North Am. 2010;24(1):65-86.</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10. Matthay K.K., Reynolds C.P., Seeger R.C., Shimada H., Adkins E.S., Haas-Kogan D. E et al. Long-term results for children with high-risk neuroblastoma treated on a randomized trial of myeloablative therapy followed by 13-cis-retinoic acid: a children’s oncology group study. J Clin Oncol. 2009;27(7):1007-1013.</mixed-citation><mixed-citation xml:lang="ru">Matthay K.K., Reynolds C.P., Seeger R.C., Shimada H., Adkins E.S., Haas-Kogan D. E et al. Long-term results for children with high-risk neuroblastoma treated on a randomized trial of myeloablative therapy followed by 13-cis-retinoic acid: a children’s oncology group study. J Clin Oncol. 2009;27(7):1007-1013.</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11. Grupp S.A., Cohn S.L., Wall D., Reynolds P.C.; Hematopoietic Stem Cell Transplant Discipline and the Neuroblastoma Disease Committee, Children’s Oncology Group. Collection, storage, and infusion of stem cells in children with high-risk neuroblastoma: saving for a rainy day. Pediatr Blood Cancer. 2006;46(7): 719-722.</mixed-citation><mixed-citation xml:lang="ru">Grupp S.A., Cohn S.L., Wall D., Reynolds P.C.; Hematopoietic Stem Cell Transplant Discipline and the Neuroblastoma Disease Committee, Children’s Oncology Group. Collection, storage, and infusion of stem cells in children with high-risk neuroblastoma: saving for a rainy day. Pediatr Blood Cancer. 2006;46(7): 719-722.</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12. Cheung N.K., Kushner B.H., La Quaglia M., Kramer K., Gollamudi S., Heller G. et al. N7: а novel multi-modality therapy of high risk neuroblastoma (NB) in children diagnosed over 1 year of age. Med Pediatr Oncol. 2001;36(1):227-230.</mixed-citation><mixed-citation xml:lang="ru">Cheung N.K., Kushner B.H., La Quaglia M., Kramer K., Gollamudi S., Heller G. et al. N7: а novel multi-modality therapy of high risk neuroblastoma (NB) in children diagnosed over 1 year of age. Med Pediatr Oncol. 2001;36(1):227-230.</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">13. Donzella G.A., Schols D., Lin S.W., Esté J.A., Nagashima K.A., Maddon P.J. et al. AMD3100, a small molecule inhibitor of HIV-1 entry via the CXCR4 co-receptor. Nat Med 1998;4(1):72-77.</mixed-citation><mixed-citation xml:lang="ru">Donzella G.A., Schols D., Lin S.W., Esté J.A., Nagashima K.A., Maddon P.J. et al. AMD3100, a small molecule inhibitor of HIV-1 entry via the CXCR4 co-receptor. Nat Med 1998;4(1):72-77.</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">14. Liles W.C., Broxmeyer H.E., Rodger E., Wood B., Hübel K., Cooper S. et al. Mobilization of hematopoietic progenitor cells in healthy volunteers by AMD3100, a CXCR4 antagonist. Blood. 2003;102(8):2728-2730.</mixed-citation><mixed-citation xml:lang="ru">Liles W.C., Broxmeyer H.E., Rodger E., Wood B., Hübel K., Cooper S. et al. Mobilization of hematopoietic progenitor cells in healthy volunteers by AMD3100, a CXCR4 antagonist. Blood. 2003;102(8):2728-2730.</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">15. Flatt T., Lewing K., Gonzalez C., Anthony K., Ryan R., Jones R. et al. Successful mobilization with AMD3100 and filgrastim with engraftment of autologous peripheral blood stem cells in a heavily pretreated pediatric patient with recurrent Burkitt lymphoma. Pediatr Hematol Oncol. 2010;27(2):138-149.</mixed-citation><mixed-citation xml:lang="ru">Flatt T., Lewing K., Gonzalez C., Anthony K., Ryan R., Jones R. et al. Successful mobilization with AMD3100 and filgrastim with engraftment of autologous peripheral blood stem cells in a heavily pretreated pediatric patient with recurrent Burkitt lymphoma. Pediatr Hematol Oncol. 2010;27(2):138-149.</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">16. Toledano H., Yahel A., Cohen I.J., Yaniv I., Stein J. Successful mobilization, harvest and transplant of peripheral blood stem cells using AMD3100 and G-CSF following high dose craniospinal irradiation for medulloblastoma in a young child. Pediatr Blood Cancer. 2010;54(4):613-615.</mixed-citation><mixed-citation xml:lang="ru">Toledano H., Yahel A., Cohen I.J., Yaniv I., Stein J. Successful mobilization, harvest and transplant of peripheral blood stem cells using AMD3100 and G-CSF following high dose craniospinal irradiation for medulloblastoma in a young child. Pediatr Blood Cancer. 2010;54(4):613-615.</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">17. Sutherland D.R., Anderson L., Keeney M., Nayar R., Chin-Yee I. The ISHAGE guidelines for CD34+ cell determination by flow cytometry. International Society of Hemototherapy and Graft Engineering. J Hematother. 1996;5(3):213-226.</mixed-citation><mixed-citation xml:lang="ru">Sutherland D.R., Anderson L., Keeney M., Nayar R., Chin-Yee I. The ISHAGE guidelines for CD34+ cell determination by flow cytometry. International Society of Hemototherapy and Graft Engineering. J Hematother. 1996;5(3):213-226.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">18. Dubrovsky L., Wong E.C., Perez-Albuerne E., Loechelt B., Kamani N., Sande J. et al. CD34+ Collection efficiency as a function of blodd volumes processed in Pediatric autologous peripheral blood stem cell collection. J Clini Apher. 2011;26(3):131-137.</mixed-citation><mixed-citation xml:lang="ru">Dubrovsky L., Wong E.C., Perez-Albuerne E., Loechelt B., Kamani N., Sande J. et al. CD34+ Collection efficiency as a function of blodd volumes processed in Pediatric autologous peripheral blood stem cell collection. J Clini Apher. 2011;26(3):131-137.</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">19. Reinhardt P., Brauninger S., Bialleck H., Thorausch K., Smith R., Schrezenmeier H. et al. Automatic interface-controlled apheresis collection of stem/progenitor cells: results from an autologus donor validation trial of a novel stem cell apheresis device. Transfusion. 2010;51(6):1321-1330.</mixed-citation><mixed-citation xml:lang="ru">Reinhardt P., Brauninger S., Bialleck H., Thorausch K., Smith R., Schrezenmeier H. et al. Automatic interface-controlled apheresis collection of stem/progenitor cells: results from an autologus donor validation trial of a novel stem cell apheresis device. Transfusion. 2010;51(6):1321-1330.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">20. Lie A.K., To L.B. Peripheral Blood Stem Cells: Transplantation and Beyond. Oncologist. 1997;2(1):40-49.</mixed-citation><mixed-citation xml:lang="ru">Lie A.K., To L.B. Peripheral Blood Stem Cells: Transplantation and Beyond. Oncologist. 1997;2(1):40-49.</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">21. Modak S., Cheung I.Y., Kushner B.H., Kramer K., Reich L., Cheung N.K. Plerixafor plus granulocyte-colony stimulating factor for autologous hematopoietic stem cell mobilization in patients with metastatic neuroblastoma. Pediatr Blood Cancer. 2012;58(3):469-471.</mixed-citation><mixed-citation xml:lang="ru">Modak S., Cheung I.Y., Kushner B.H., Kramer K., Reich L., Cheung N.K. Plerixafor plus granulocyte-colony stimulating factor for autologous hematopoietic stem cell mobilization in patients with metastatic neuroblastoma. Pediatr Blood Cancer. 2012;58(3):469-471.</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">22. Maschan A.A., Balashov D.N., Kurnikova E.E., Trakhtman P.E., Boyakova E.V., еt al. Efficacy of plerixafor in children with malignant tumors failing to mobilize a sufficient number of hematopoietic progenitors with G-CSF. Bone Marrow Transplant. 2015;50(8):1089-1091.</mixed-citation><mixed-citation xml:lang="ru">Maschan A.A., Balashov D.N., Kurnikova E.E., Trakhtman P.E., Boyakova E.V., еt al. Efficacy of plerixafor in children with malignant tumors failing to mobilize a sufficient number of hematopoietic progenitors with G-CSF. Bone Marrow Transplant. 2015;50(8):1089-1091.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">23. Sevilla J., Gonzalez-Vicent M., Madero L., Garcia-Sanchez F., Diaz M.A. Granulocytecolony stimulating factor alone at 12 microg/kg twice a day for 4 days for peripheral blood progenitor cell priming in pediatric patients. Bone Marrow Transplant. 2002;30(7):417-420.</mixed-citation><mixed-citation xml:lang="ru">Sevilla J., Gonzalez-Vicent M., Madero L., Garcia-Sanchez F., Diaz M.A. Granulocytecolony stimulating factor alone at 12 microg/kg twice a day for 4 days for peripheral blood progenitor cell priming in pediatric patients. Bone Marrow Transplant. 2002;30(7):417-420.</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">24. Bensinger W., Appelbaum F., Rowley S., Storb R., Sanders J., Lilleby K. et al. Factors that influence collection and engraftment of autologous peripheral blood stem cells. J Clin Oncol. 1995;13(10):2547-2555.</mixed-citation><mixed-citation xml:lang="ru">Bensinger W., Appelbaum F., Rowley S., Storb R., Sanders J., Lilleby K. et al. Factors that influence collection and engraftment of autologous peripheral blood stem cells. J Clin Oncol. 1995;13(10):2547-2555.</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">25. Giralt S., Costa L., Schriber J., Dipersio J., Maziarz R., McCarty J. et al. Optimizing autologous stem cell mobilization strategies to improve patient outcomes: consensus guidelines and recommendations. Biol Blood Marrow Transplant. 2014;20(3):295-308.</mixed-citation><mixed-citation xml:lang="ru">Giralt S., Costa L., Schriber J., Dipersio J., Maziarz R., McCarty J. et al. Optimizing autologous stem cell mobilization strategies to improve patient outcomes: consensus guidelines and recommendations. Biol Blood Marrow Transplant. 2014;20(3):295-308.</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">26. Kroger N., Renges H., Kruger W., Gutensohn K., Löliger C., Carrero I. et al. A randomized comparison of once versus twice daily recombinant human granulocyte colony stimulating factor (filgrastim) for stem cell mobilization in healthy donors for allogeneic transplantation. Br J Haematol. 2000;111(3):761-765.</mixed-citation><mixed-citation xml:lang="ru">Kroger N., Renges H., Kruger W., Gutensohn K., Löliger C., Carrero I. et al. A randomized comparison of once versus twice daily recombinant human granulocyte colony stimulating factor (filgrastim) for stem cell mobilization in healthy donors for allogeneic transplantation. Br J Haematol. 2000;111(3):761-765.</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">27. Meier R., Mühlethaler-Mottet A., Flahaut М., Coulon A., Fusco C., Louache F. et al. The chemokine receptor CXCR4 strongly promotes neuroblastoma primary tumour, metastatic growth, but not invasion. PLoS One. 2007;2(10):e1016.</mixed-citation><mixed-citation xml:lang="ru">Meier R., Mühlethaler-Mottet A., Flahaut М., Coulon A., Fusco C., Louache F. et al. The chemokine receptor CXCR4 strongly promotes neuroblastoma primary tumour, metastatic growth, but not invasion. PLoS One. 2007;2(10):e1016.</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">28. Geminder H., Sagi-Assif O., Goldberg L., Meshel T., Rechavi G., Witz I.P. et al. A possible role for CXCR4 and its ligand, the CXC chemokine stromal cell-derived factor-1, in the development of bone marrow metastases in neuroblastoma. J Immunol. 2001;167(8):4747-4757.</mixed-citation><mixed-citation xml:lang="ru">Geminder H., Sagi-Assif O., Goldberg L., Meshel T., Rechavi G., Witz I.P. et al. A possible role for CXCR4 and its ligand, the CXC chemokine stromal cell-derived factor-1, in the development of bone marrow metastases in neuroblastoma. J Immunol. 2001;167(8):4747-4757.</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">29. Airoldi I., Raffaghello L., Piovan E., Cocco C., Carlini B., Amadori A. CXCL12 does not attract CXCR4þ human metastatic neuroblastoma cells: clinical implications. Clin Cancer Res. 2006;12(1):77-82.</mixed-citation><mixed-citation xml:lang="ru">Airoldi I., Raffaghello L., Piovan E., Cocco C., Carlini B., Amadori A. CXCL12 does not attract CXCR4þ human metastatic neuroblastoma cells: clinical implications. Clin Cancer Res. 2006;12(1):77-82.</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">30. Carlisle A.J., Lyttle C.A., Carlisle R.Y., Maris J.M. CXCR4 expression heterogeneity in neuroblastoma cells due to ligand-independent regulation. Mol Cancer. 2009;8:126.</mixed-citation><mixed-citation xml:lang="ru">Carlisle A.J., Lyttle C.A., Carlisle R.Y., Maris J.M. CXCR4 expression heterogeneity in neuroblastoma cells due to ligand-independent regulation. Mol Cancer. 2009;8:126.</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">31. Bensimhon P., Villablanca J.G., Sender L.S., Matthay K.K., Park J.R., Seeger R. et al. Peripheral blood stem cell support for multiple cycles of dose intensive induction therapy is feasible with little risk of tumor contamination in advanced stage neuroblastoma: a report from the Children’s Oncology Group. Pediatr Blood Cancer. 2010;54(4):596-602.</mixed-citation><mixed-citation xml:lang="ru">Bensimhon P., Villablanca J.G., Sender L.S., Matthay K.K., Park J.R., Seeger R. et al. Peripheral blood stem cell support for multiple cycles of dose intensive induction therapy is feasible with little risk of tumor contamination in advanced stage neuroblastoma: a report from the Children’s Oncology Group. Pediatr Blood Cancer. 2010;54(4):596-602.</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">32. Kreissman S.G., Seeger R.C., Matthay K.K., London W.B., Sposto R., Grupp S.A. Purged versus non-purged peripheral blood stem-cell transplantation for high-risk neuroblastoma (COG A3973): a randomised phase 3 trial. Lancet Oncol. 2013;14(10):999-1008.</mixed-citation><mixed-citation xml:lang="ru">Kreissman S.G., Seeger R.C., Matthay K.K., London W.B., Sposto R., Grupp S.A. Purged versus non-purged peripheral blood stem-cell transplantation for high-risk neuroblastoma (COG A3973): a randomised phase 3 trial. Lancet Oncol. 2013;14(10):999-1008.</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">33. Chambon F., Tchirkov A., Pereira B., Rochette E., Demeocq F., Kanold J. Molecular assessment of minimal residual disease in PBSC harvests provides prognostic information in neuroblastoma. Pediatr Blood Cancer. 2013; published online March 21.</mixed-citation><mixed-citation xml:lang="ru">Chambon F., Tchirkov A., Pereira B., Rochette E., Demeocq F., Kanold J. Molecular assessment of minimal residual disease in PBSC harvests provides prognostic information in neuroblastoma. Pediatr Blood Cancer. 2013; published online March 21.</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">34. Burchill S.A., Kinsey S.E., Picton S., Roberts P., Pinkerton C.R., Selby P. et al. Minimal residual disease at the time of peripheral blood stem cell harvest in patients with advanced neuroblastoma. Med Pediatr Oncol. 2001;36(1):213-219.</mixed-citation><mixed-citation xml:lang="ru">Burchill S.A., Kinsey S.E., Picton S., Roberts P., Pinkerton C.R., Selby P. et al. Minimal residual disease at the time of peripheral blood stem cell harvest in patients with advanced neuroblastoma. Med Pediatr Oncol. 2001;36(1):213-219.</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">35. Corrias M.V., Haupt R., Carlini B., Parodi S., Rivabella L., Garaventa A. et al. Peripheral blood stem cell tumor cell contamination and survival of neuroblastoma patients. Clin Cancer Res. 2006;12(19):5680-5685.</mixed-citation><mixed-citation xml:lang="ru">Corrias M.V., Haupt R., Carlini B., Parodi S., Rivabella L., Garaventa A. et al. Peripheral blood stem cell tumor cell contamination and survival of neuroblastoma patients. Clin Cancer Res. 2006;12(19):5680-5685.</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">36. Reynolds C.P., Seeger R.C., Vo D.D., Black A.T., Wells J., Ugelstad J. Model system for removing neuroblastoma cells from bone marrow using monoclonal antibodies and magnetic immunobeads. Cancer Res. 1986;46(11):5882-5886.</mixed-citation><mixed-citation xml:lang="ru">Reynolds C.P., Seeger R.C., Vo D.D., Black A.T., Wells J., Ugelstad J. Model system for removing neuroblastoma cells from bone marrow using monoclonal antibodies and magnetic immunobeads. Cancer Res. 1986;46(11):5882-5886.</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">37. Cherqaoui B., Rouel N., Defachelles A.S., Auvrignon A., Demeocq F., Merlin E. Peripheral blood stem cell collection in low-weight children: retrospective comparison of two apheresis devices. Transfusion. 2014;54(5):1371-1378.</mixed-citation><mixed-citation xml:lang="ru">Cherqaoui B., Rouel N., Defachelles A.S., Auvrignon A., Demeocq F., Merlin E. Peripheral blood stem cell collection in low-weight children: retrospective comparison of two apheresis devices. Transfusion. 2014;54(5):1371-1378.</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">38. Ravagnani F., Coluccia P., Notti P., Arienti F., Bompadre A., Avella M. et al. Peripheral blood stem cell collection in pediatric patients: feasibility of leukapheresis under anesthesia in uncompliant small children with solid tumors. J Clin Apher. 2006;21(2):85-91.</mixed-citation><mixed-citation xml:lang="ru">Ravagnani F., Coluccia P., Notti P., Arienti F., Bompadre A., Avella M. et al. Peripheral blood stem cell collection in pediatric patients: feasibility of leukapheresis under anesthesia in uncompliant small children with solid tumors. J Clin Apher. 2006;21(2):85-91.</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">39. Delgado J., Fernandez-Jimenez M.C., Martinez A., Sastre A., Garcia-Miguel P., Hernandez-Navarro F., et al. Analysis of factors affecting PBPC collection in low-weight children with malignant disorders. Cytotherapy. 2004;6(1):43-49</mixed-citation><mixed-citation xml:lang="ru">Delgado J., Fernandez-Jimenez M.C., Martinez A., Sastre A., Garcia-Miguel P., Hernandez-Navarro F., et al. Analysis of factors affecting PBPC collection in low-weight children with malignant disorders. Cytotherapy. 2004;6(1):43-49</mixed-citation></citation-alternatives></ref></ref-list></back></article>
