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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">Oncohematology</journal-id><journal-title-group><journal-title xml:lang="en">Oncohematology</journal-title><trans-title-group xml:lang="ru"><trans-title>Онкогематология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1818-8346</issn><issn publication-format="electronic">2413-4023</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">176</article-id><article-id pub-id-type="doi">10.17650/1818-8346-2016-11-1-8-13</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>HEMATOLOGIC MALIGNANCIES: DIAGNOSIS, TREATMENT, SUPPORTIVE CARE</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ГЕМОБЛАСТОЗЫ: ДИАГНОСТИКА, ЛЕЧЕНИЕ, СОПРОВОДИТЕЛЬНАЯ ТЕРАПИЯ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Brentuximab vedotin in children and adolescents with Hodgkin’s lymphoma and anaplastic large cell lymphoma – literature review and own experience</article-title><trans-title-group xml:lang="ru"><trans-title>Применение брентуксимаба ведо тина у детей и подростков с лимфомой Ходжкина и анапластической крупноклеточной лимфомой – обзор литературы и собственные наблюдения</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Myakova</surname><given-names>N. V.</given-names></name><name xml:lang="ru"><surname>Мякова</surname><given-names>Н. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>nmiakova@mail.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Evstratov</surname><given-names>D. A.</given-names></name><name xml:lang="ru"><surname>Евстратов</surname><given-names>Д. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Abramov</surname><given-names>D. S.</given-names></name><name xml:lang="ru"><surname>Абрамов</surname><given-names>Д. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Konovalov</surname><given-names>D. M.</given-names></name><name xml:lang="ru"><surname>Коновалов</surname><given-names>Д. М.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Pshonkin</surname><given-names>A. V.</given-names></name><name xml:lang="ru"><surname>Пшонкин</surname><given-names>А. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Litvinov</surname><given-names>D. V.</given-names></name><name xml:lang="ru"><surname>Литвинов</surname><given-names>Д. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Federal Research Institute of Pediatric Hematology, Oncology and Immunology named after Dmitry Rogachev, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГБУ «Федеральный научно-клинический центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">1 Samory Mashela St., Moscow, 117198, Russia</institution></aff><aff><institution xml:lang="ru">Россия, 117198, Москва, ул. Саморы Машела, 1</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2016-03-31" publication-format="electronic"><day>31</day><month>03</month><year>2016</year></pub-date><volume>11</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>8</fpage><lpage>13</lpage><history><date date-type="received" iso-8601-date="2016-03-31"><day>31</day><month>03</month><year>2016</year></date><date date-type="accepted" iso-8601-date="2016-03-31"><day>31</day><month>03</month><year>2016</year></date></history><permissions><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://oncohematology.abvpress.ru/ongm/article/view/176">https://oncohematology.abvpress.ru/ongm/article/view/176</self-uri><abstract xml:lang="en"><p>Despite significant advances in the treatment of lymphomas in children remain a small proportion of patients with refractory or recurrent disease. An effective approach to the treatment of such patients – not only is the second line chemotherapy, but the use of the new targeted therapies. An example of this approach is the use of brentuximab vedotin (antibody-drug conjugate directed to the CD30) in relapsed Hodgkin’s lymphoma and anaplastic large cell lymphoma. Literature review and own experience of using this drug in children are describes in this article.</p></abstract><trans-abstract xml:lang="ru"><p>Несмотря на значительные успехи в лечении лимфом у детей, у небольшой части пациентов заболевание остается рефрактерным или рецидивирует. Эффективный подход к лечению таких больных – это не только 2-я линия химиотерапии, но и применение новых таргетных препаратов. Примером такой тактики является использование брентуксимаба ведотина – химиоиммуноконъюгата CD30 – при рецидивах лимфомы Ходжкина и анапластической крупноклеточной лимфомы. В статье приводится описание опыта применения этого препарата у детей и обзор литературы.</p></trans-abstract><kwd-group xml:lang="en"><kwd>Hodgkin’s lymphoma</kwd><kwd>immunohistochemistry</kwd><kwd>refractory</kwd><kwd>CD30</kwd><kwd>brentuximab vedotin</kwd><kwd>anaplastic large cell lymphoma</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>лимфома Ходжкина</kwd><kwd>иммуногистохимия</kwd><kwd>рефрактерность</kwd><kwd>CD30</kwd><kwd>брентуксимаб ведотин</kwd><kwd>анапластическая крупноклеточная лимфома</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. Khouri I. F., Saliba R. M., Hosing C. et al. Concurrent administration of high-dose rituximab before and after autologous stemcell transplantation for relapsed aggressive B- cell non-Hodgkin’s lymphomas. J Clin Oncol 2005;23(10):2240–7.</mixed-citation><mixed-citation xml:lang="ru">Khouri I. F., Saliba R. M., Hosing C. et al. Concurrent administration of high-dose rituximab before and after autologous stemcell transplantation for relapsed aggressive B- cell non-Hodgkin’s lymphomas. J Clin Oncol 2005;23(10):2240–7.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Ansell S. M., Geyer S. M., Maurer M. J. et al. Randomized phase II study of interleukin-12 in combination with rituximab in previously treated non- Hodgkin’s lymphoma patients. Clin Cancer Res 2006;12(20 Pt 1):6056–63.</mixed-citation><mixed-citation xml:lang="ru">Ansell S. M., Geyer S. M., Maurer M. J. et al. Randomized phase II study of interleukin-12 in combination with rituximab in previously treated non- Hodgkin’s lymphoma patients. Clin Cancer Res 2006;12(20 Pt 1):6056–63.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3. Khan K. D., Emmanouilides C., Benson D. M. Jr et al. A phase 2 study of rituximab in combination with recombinant interleukin-2 for rituximabrefractory indolent non-Hodgkin’s lymphoma. Clin Cancer Res 2006;12(23):7046–53.</mixed-citation><mixed-citation xml:lang="ru">Khan K. D., Emmanouilides C., Benson D. M. Jr et al. A phase 2 study of rituximab in combination with recombinant interleukin-2 for rituximabrefractory indolent non-Hodgkin’s lymphoma. Clin Cancer Res 2006;12(23):7046–53.</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4. Teicher B. A., Chari R. V. Antibody conjugate therapeutics: challenges and potential. Clin Cancer Res 2011;17(20):6389–97.</mixed-citation><mixed-citation xml:lang="ru">Teicher B. A., Chari R. V. Antibody conjugate therapeutics: challenges and potential. Clin Cancer Res 2011;17(20):6389–97.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5. Fisher R. I., Kaminski M. S., Wahl R. L. et al. Tositumomab and iodine-131 tositumomab produces durable complete remissions in a subset of heavily pretreated patients with low-grade and transformed non-Hodgkin’s lymphomas. J Clin Oncol 2005;23(30):7565–73.</mixed-citation><mixed-citation xml:lang="ru">Fisher R. I., Kaminski M. S., Wahl R. L. et al. Tositumomab and iodine-131 tositumomab produces durable complete remissions in a subset of heavily pretreated patients with low-grade and transformed non-Hodgkin’s lymphomas. J Clin Oncol 2005;23(30):7565–73.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6. Morschhauser F., Radford J., Van Hoof A. et al. Phase III trial of consolidation therapy with yttrium-90-ibritumomab tiuxetan compared with no additional therapy after first remission in advanced follicular lymphoma. J Clin Oncol 2008;26(32): 5156–64.</mixed-citation><mixed-citation xml:lang="ru">Morschhauser F., Radford J., Van Hoof A. et al. Phase III trial of consolidation therapy with yttrium-90-ibritumomab tiuxetan compared with no additional therapy after first remission in advanced follicular lymphoma. J Clin Oncol 2008;26(32): 5156–64.</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7. Locksley R. M., Killeen N., Lenardo M. J. The TNF and TNF receptor superfamilies: integrating mammalian biology. Cell 2001;104(4):487–501.</mixed-citation><mixed-citation xml:lang="ru">Locksley R. M., Killeen N., Lenardo M. J. The TNF and TNF receptor superfamilies: integrating mammalian biology. Cell 2001;104(4):487–501.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8. Younes A., Kadin M. E. Emerging applications of the tumor necrosis factor family of ligands and receptors in cancer therapy. J Clin Oncol 2003;21(18): 3526–34.</mixed-citation><mixed-citation xml:lang="ru">Younes A., Kadin M. E. Emerging applications of the tumor necrosis factor family of ligands and receptors in cancer therapy. J Clin Oncol 2003;21(18): 3526–34.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9. Wang C. Y., Mayo M. W., Korneluk R. G. et al. NF-kappaB antiapoptosis: induction of TRAF1 and TRAF2 and c-IAP1 and c-IAP2 to suppress caspase-8 activation. Science 1998;281(5383):1680–3.</mixed-citation><mixed-citation xml:lang="ru">Wang C. Y., Mayo M. W., Korneluk R. G. et al. NF-kappaB antiapoptosis: induction of TRAF1 and TRAF2 and c-IAP1 and c-IAP2 to suppress caspase-8 activation. Science 1998;281(5383):1680–3.</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10. Younes A., Aggarwall B. B. Clinical implications of the tumor necrosis factor family in benign and malignant hematologic disorders. Cancer 2003;98(3):458–67.</mixed-citation><mixed-citation xml:lang="ru">Younes A., Aggarwall B. B. Clinical implications of the tumor necrosis factor family in benign and malignant hematologic disorders. Cancer 2003;98(3):458–67.</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11. Nadali G., Tavecchia L., Zanolin E. et al. Serum level of the soluble form of the CD30 molecule identifies patients with Hodgkin’s disease at high risk of unfavorable outcome. Blood 1998;91(8):3011–6.</mixed-citation><mixed-citation xml:lang="ru">Nadali G., Tavecchia L., Zanolin E. et al. Serum level of the soluble form of the CD30 molecule identifies patients with Hodgkin’s disease at high risk of unfavorable outcome. Blood 1998;91(8):3011–6.</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12. Katz J., Janik J. E., Younes A. Brentuximab vedotin(SGN-35). Clin Cancer Res 2011;17(20):6428–36.</mixed-citation><mixed-citation xml:lang="ru">Katz J., Janik J. E., Younes A. Brentuximab vedotin(SGN-35). Clin Cancer Res 2011;17(20):6428–36.</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">13. Younes A. CD30-targeted antibody therapy. Curr Opin Oncol 2011;23(6): 587–93.</mixed-citation><mixed-citation xml:lang="ru">Younes A. CD30-targeted antibody therapy. Curr Opin Oncol 2011;23(6): 587–93.</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">14. Edinger J. T., Clark B. Z., Pucevich B. E. et al. CD30 expression and proliferative fraction in nontransformed mycosis fungoides. Am J Surg Pathol 2009;33(12):1860–8.</mixed-citation><mixed-citation xml:lang="ru">Edinger J. T., Clark B. Z., Pucevich B. E. et al. CD30 expression and proliferative fraction in nontransformed mycosis fungoides. Am J Surg Pathol 2009;33(12):1860–8.</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">15. Küppers R. The biology of Hodgkin’s lymphoma. Nat Rev Cancer 2009;9(1): 15–27.</mixed-citation><mixed-citation xml:lang="ru">Küppers R. The biology of Hodgkin’s lymphoma. Nat Rev Cancer 2009;9(1): 15–27.</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">16. Schmitz N., Pfistner B., Sextro M. et al. Aggressive conventional chemotherapy compared with high-dose chemotherapy with autologous haemopoietic stem-cell transplantation for relapsed chemosensitive Hodgkin’s disease: a randomised trial. Lancet 2002;359(9323):2065–71.</mixed-citation><mixed-citation xml:lang="ru">Schmitz N., Pfistner B., Sextro M. et al. Aggressive conventional chemotherapy compared with high-dose chemotherapy with autologous haemopoietic stem-cell transplantation for relapsed chemosensitive Hodgkin’s disease: a randomised trial. Lancet 2002;359(9323):2065–71.</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">17. Kuruvilla J., Keating A., Crump M. How I treat relapsed and refractory Hodgkin lymphoma. Blood 2011;117(16):4208–17.</mixed-citation><mixed-citation xml:lang="ru">Kuruvilla J., Keating A., Crump M. How I treat relapsed and refractory Hodgkin lymphoma. Blood 2011;117(16):4208–17.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">18. Burroughs L. M., O’Donnell P. V., Sandmaier B. M. et al. Comparison of outcomes of HLA-matched related, unrelated, or HLA-haploidentical related hematopoietic cell transplantation following nonmyeloablative conditioning for relapsed or refractory Hodgkin lymphoma. Biol Blood Marrow Transplant 2008;14(11):1279–87.</mixed-citation><mixed-citation xml:lang="ru">Burroughs L. M., O’Donnell P. V., Sandmaier B. M. et al. Comparison of outcomes of HLA-matched related, unrelated, or HLA-haploidentical related hematopoietic cell transplantation following nonmyeloablative conditioning for relapsed or refractory Hodgkin lymphoma. Biol Blood Marrow Transplant 2008;14(11):1279–87.</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">19. Merkel O., Hamacher F., Sifft E. et al. Novel therapeutic options in anaplastic large cell lymphoma: molecular targets and immunological tools. Mol Cancer Ther 2011;10(7):1127–36.</mixed-citation><mixed-citation xml:lang="ru">Merkel O., Hamacher F., Sifft E. et al. Novel therapeutic options in anaplastic large cell lymphoma: molecular targets and immunological tools. Mol Cancer Ther 2011;10(7):1127–36.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">20. Amin H. M., Lai R. Pathobiology of ALK+ anaplastic large-cell lymphoma. Blood 2007;110(7):2259–67.</mixed-citation><mixed-citation xml:lang="ru">Amin H. M., Lai R. Pathobiology of ALK+ anaplastic large-cell lymphoma. Blood 2007;110(7):2259–67.</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">21. Vaklavas C., Forero-Torres A. Safety and efficacy of brentuximab vedotin in patients with Hodgkin lymphoma or systemic anaplastic large cell lymphoma. Ther Adv Hematol 2012;3(4):209–25.</mixed-citation><mixed-citation xml:lang="ru">Vaklavas C., Forero-Torres A. Safety and efficacy of brentuximab vedotin in patients with Hodgkin lymphoma or systemic anaplastic large cell lymphoma. Ther Adv Hematol 2012;3(4):209–25.</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">22. Wahl A. F., Klussman K., Thompson J. D. et al. The anti-CD30 monoclonal antibody SGN- 30 promotes growth arrest and DNA fragmentation in vitro and affects antitumor activity in models of Hodgkin’s disease. Cancer Res 2002;62(13): 3736–42.</mixed-citation><mixed-citation xml:lang="ru">Wahl A. F., Klussman K., Thompson J. D. et al. The anti-CD30 monoclonal antibody SGN- 30 promotes growth arrest and DNA fragmentation in vitro and affects antitumor activity in models of Hodgkin’s disease. Cancer Res 2002;62(13): 3736–42.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">23. Oflazoglu E., Kissler K. M., Sievers E. L. et al. Combination of the anti-CD30- auristatin-E antibody-drug conjugate (SGN-35) with chemotherapy improves antitumour activity in Hodgkin lymphoma. Br J Haematol 2008;142(1):69–73.</mixed-citation><mixed-citation xml:lang="ru">Oflazoglu E., Kissler K. M., Sievers E. L. et al. Combination of the anti-CD30- auristatin-E antibody-drug conjugate (SGN-35) with chemotherapy improves antitumour activity in Hodgkin lymphoma. Br J Haematol 2008;142(1):69–73.</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">24. Sutherland M. S., Sanderson R. J., Gordon K. A. et al. Lysosomal trafficking and cysteine protease metabolism confer targetspecific cytotoxicity by peptide-linked anti- CD30-auristatin conjugates. J Biol Chem 2006;281(15):10540–7.</mixed-citation><mixed-citation xml:lang="ru">Sutherland M. S., Sanderson R. J., Gordon K. A. et al. Lysosomal trafficking and cysteine protease metabolism confer targetspecific cytotoxicity by peptide-linked anti- CD30-auristatin conjugates. J Biol Chem 2006;281(15):10540–7.</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">25. Younes A., Bartlett N. L., Leonard J. P. et al. Brentuximab vedotin (SGN-35) for relapsed CD30-positive lymphomas. N Engl J Med 2010;363(19):1812–21.</mixed-citation><mixed-citation xml:lang="ru">Younes A., Bartlett N. L., Leonard J. P. et al. Brentuximab vedotin (SGN-35) for relapsed CD30-positive lymphomas. N Engl J Med 2010;363(19):1812–21.</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">26. Chen R. W., Gopal A. K., Smith S. E. et al. Results of a pivotal phase II study of brentuximab vedotin (SGN-35) in patients with relapsed or refractory Hodgkin lymphoma (HL). J Clin Oncol 2011;29:8031.</mixed-citation><mixed-citation xml:lang="ru">Chen R. W., Gopal A. K., Smith S. E. et al. Results of a pivotal phase II study of brentuximab vedotin (SGN-35) in patients with relapsed or refractory Hodgkin lymphoma (HL). J Clin Oncol 2011;29:8031.</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">27. Pro B., Advani R., Brice P. et al. Brentuximab vedotin (SGN-35) in patients with relapsed or refractory systemic anaplastic large-cell lymphoma: results of a phase II study. J Clin Oncol 2012;30(18):2190–6.</mixed-citation><mixed-citation xml:lang="ru">Pro B., Advani R., Brice P. et al. Brentuximab vedotin (SGN-35) in patients with relapsed or refractory systemic anaplastic large-cell lymphoma: results of a phase II study. J Clin Oncol 2012;30(18):2190–6.</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">28. Kelly K. M., Hodgson D., Appel B. et al. Children’s Oncology Group’s 2013 blueprint for research: Hodgkin lymphoma. Pediatr Blood Cancer 2013;60(6):972–8.</mixed-citation><mixed-citation xml:lang="ru">Kelly K. M., Hodgson D., Appel B. et al. Children’s Oncology Group’s 2013 blueprint for research: Hodgkin lymphoma. Pediatr Blood Cancer 2013;60(6):972–8.</mixed-citation></citation-alternatives></ref></ref-list></back></article>
