<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<article article-type="research-article" dtd-version="1.3" 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" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">cancersp</journal-id><journal-title-group><journal-title xml:lang="ru">Южно-Российский онкологический журнал/ South Russian Journal of Cancer</journal-title><trans-title-group xml:lang="en"><trans-title>South Russian Journal of Cancer</trans-title></trans-title-group></journal-title-group><issn pub-type="epub">2686-9039</issn><publisher><publisher-name>АНО "Перспективы онкологии"</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.37748/2686-9039-2022-3-3-5</article-id><article-id custom-type="elpub" pub-id-type="custom">cancersp-164</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>Обзор</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEW</subject></subj-group></article-categories><title-group><article-title>Эволюция лекарственного лечения классической лимфомы Ходжкина</article-title><trans-title-group xml:lang="en"><trans-title>Evolution of drug therapy for classical Hodgkin lymphoma</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0843-6012</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Саманева</surname><given-names>Н. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Samaneva</surname><given-names>N. Y.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Саманева Наталья Юрьевна – к.м.н., младший научный сотрудник отдела лекарственного лечения опухолей, врач-онколог отделения онкогематологииSPIN: 1181-0659AuthorID: 734488ResearcherID: AAH-7905-2019Scopus Author ID: 57192874030</p><p>344037, г. Ростов-на-Дону, ул. 14-я линия, д. 63</p></bio><bio xml:lang="en"><p>Natalia Yu. Samaneva – Cand. Sci. (Med.), junior researcher of the department of medicinal treatment of tumors, oncologist of the department of oncohematologySPIN: 1181-0659AuthorID: 734488ResearcherID: AAH-7905-2019Scopus Author ID: 57192874030</p><p>344037, Rostov-on-Don, 14 line str., 63</p></bio><email xlink:type="simple">prettyfairy19@rambler.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4457-3815</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лысенко</surname><given-names>И. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Lysenko</surname><given-names>I. B.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Лысенко Ирина Борисовна – д.м.н., профессор, заведующий отделением онкогематологииSPIN: 9510-3504AuthorID: 794669</p><p>г. Ростов-на-Дону</p></bio><bio xml:lang="en"><p>Irina B. Lysenko – Dr. Sci. (Med.), professor, head of the department of oncohematologySPIN: 9510-3504AuthorID: 794669</p><p>Rostov-on-Don</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7224-3106</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Николаева</surname><given-names>Н. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Nikolaeva</surname><given-names>N. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Николаева Надежда Владимировна – д.м.н., врач-гематолог отделения онкогематологии, ведущий научный сотрудник отдела лекарственного лечения опухолейSPIN: 4295-5920AuthorID: 733869</p><p>г. Ростов-на-Дону</p></bio><bio xml:lang="en"><p>Nadezhda V. Nikolaeva – Dr. Sci. (Med.), hematologist of the department of oncohematology, leading researcher at the department of drug treatment of tumorsSPIN: 4295-5920AuthorID: 733869</p><p>Rostov-on-Don</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0761-2486</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Капуза</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kapuza</surname><given-names>E. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Капуза Елена Анатольевна – врач-онколог отделения онкогематологииSPIN: 4430-1151AuthorID: 794666</p><p>г. Ростов-на-Дону</p></bio><bio xml:lang="en"><p>Elena A. Kapuza – MD, oncologist of the department of oncohematologySPIN: 4430-1151AuthorID: 794666</p><p>Rostov-on-Don</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3001-0675</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Камаева</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kamaeva</surname><given-names>I. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Камаева Инна Анатольевна – врач-онколог отделения онкогематологии, младший научный сотрудник отдела лекарственного лечения опухолейSPIN: 8953-3351AuthorID: 937725</p><p>г. Ростов-на-Дону</p></bio><bio xml:lang="en"><p>Inna A. Kamaeva – MD, oncologist of the department of hematology, junior researcher of the department of drug treatment of tumorsSPIN:  8953-3351AuthorID: 937725</p><p>Rostov-on-Don</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2785-1721</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гайсултанова</surname><given-names>Я. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Gaysultanova</surname><given-names>Y. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Гайсултанова Яха Сулеймановна – врач-онколог отделения онкогематологии</p><p>г. Ростов-на-Дону</p></bio><bio xml:lang="en"><p>Yakha S. Gaysultanova – MD, oncologist of the department of oncohematology</p><p>Rostov-on-Don</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7990-8710</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Тишина</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Tishina</surname><given-names>A. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Тишина Анна Викторовна – врач-онколог отделения онкогематологииSPIN: 7686-3707AuthorID: 965165ResearcherID: H-2460-2018</p><p>г. Ростов-на-Дону</p></bio><bio xml:lang="en"><p>Anna V. Tishina – MD, oncologist of the department of oncohematologySPIN: 7686-3707AuthorID: 965165ResearcherID: H-2460-2018</p><p>Rostov-on-Don</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Пушкарева</surname><given-names>Т. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Pushkareva</surname><given-names>T. F.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Пушкарева Татьяна Федоровна – врач-онколог клинико-диагностического отделенияSPIN: 8047-6830AuthorID: 801681</p><p>г. Ростов-на-Дону</p></bio><bio xml:lang="en"><p>Tatiana F. Pushkareva – MD, oncologist of the clinical and diagnostic departmentSPIN: 8047-6830AuthorID: 801681</p><p>Rostov-on-Don</p><p> </p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>НМИЦ онкологии</institution><country>Россия</country></aff><aff xml:lang="en"><institution>National Medical Research Centre for Oncology</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2022</year></pub-date><pub-date pub-type="epub"><day>31</day><month>08</month><year>2022</year></pub-date><volume>3</volume><issue>3</issue><fpage>41</fpage><lpage>47</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Саманева Н.Ю., Лысенко И.Б., Николаева Н.В., Капуза Е.А., Камаева И.А., Гайсултанова Я.С., Тишина А.В., Пушкарева Т.Ф., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Саманева Н.Ю., Лысенко И.Б., Николаева Н.В., Капуза Е.А., Камаева И.А., Гайсултанова Я.С., Тишина А.В., Пушкарева Т.Ф.</copyright-holder><copyright-holder xml:lang="en">Samaneva N.Y., Lysenko I.B., Nikolaeva N.V., Kapuza E.A., Kamaeva I.A., Gaysultanova Y.S., Tishina A.V., Pushkareva T.F.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.cancersp.com/jour/article/view/164">https://www.cancersp.com/jour/article/view/164</self-uri><abstract><p>Лимфома Ходжкина – злокачественное заболевание лимфатической системы. Лимфома Ходжкина была впервые описана доктором Томасом Ходжкином в 1832 г., а позже названа «болезнью Ходжкина» Сэмюэлем Уилксом. Лимфома Ходжкина составляет около 24 % среди всех лимфом. Лимфома Ходжкина классифицируют как классическую и нодулярную с лимфоидным преобладанием (нодулярный тип лимфоидного преобладания лимфомы Ходжкина). Классическая лимфома Ходжкина включает следующие гистологические варианты: вариант с нодулярным склерозом (I и II типа), смешанно-клеточный вариант, классический вариант с большим количеством лимфоцитов и редко встречающийся вариант с лимфоидным истощением. Эпидемиологические и серологические исследования выявили причастность вируса Эпштейна-Барр к этиологии лимфомы Ходжкина: геном вируса Эпштейна-Барр был обнаружен при исследовании образцов биопсийного материала пациентов с лимфомой Ходжкина. Также выявлена связь с вирусом иммунодефицита человека (ВИЧ), заключающаяся в том, что пациенты, инфицированные ВИЧ, имеют значительно повышенный риск развития лимфомы Ходжкина по сравнению со здоровыми людьми. Углубленное изучение патофизиологии лимфомы Ходжкина позволило найти новые терапевтические мишени в лечении данного заболевания. Все эти открытия принесли изменения в понимании патогенеза данной патологии, и имеют важное значение в разработках новых методов лечения. История терапии начинается на рубеже XIX и XX вв. За последние четыре десятилетия достижения в лучевой терапии и использование комбинированной химиотерапии, значительно повысили уровень общей выживаемости пациентов с лимфомой Ходжкина. В настоящее время более 80 % пациентов моложе 60 лет с впервые диагностированной лимфомой Ходжкина могут быть излечены от данного заболевания после проведения первой линии химиотерапии.</p></abstract><trans-abstract xml:lang="en"><p>Hodgkin's lymphoma is a malignant disease of the lymphatic system. Hodgkin's lymphoma was first described by Dr. Thomas Hodgkin in 1832 and later named “Hodgkin's disease” by Samuel Wilkes. Hodgkin's lymphoma accounts for about 24 % of all lymphomas. Hodgkin's lymphoma is classified as classical and nodular lymphoid-predominant (Nodular type of lymphoidpredominant Hodgkin's lymphoma). Classical Hodgkin's lymphoma includes the following histologic variants: nodular sclerosis variant (types I and II), mixed cell variant, classic lymphocyte-rich variant, and rare lymphoid depletion variant. Epidemiological and serological studies showed the involvement of the Epstein-Barr virus into Hodgkin's lymphoma etiology, since its genome was found in the study of the biopsy material samples from patients with Hodgkin's lymphoma. A relationship with the human immunodeficiency virus (HIV) was revealed as well, and patients infected with HIV have a significantly increased risk of developing Hodgkin's lymphoma compared to healthy people. An in-depth study of the Hodgkin's lymphoma pathophysiology revealed new therapeutic targets in the treatment of this disease. All these discoveries changed the understanding of the Hodgkin's lymphoma pathogenesis, and were important for the development of new methods of treatment. The history of therapy begins on the cusp of the 19th and 20th centuries. Over the past four decades, achievements in radiation therapy and combined chemotherapy have significantly improved overall survival of patients with Hodgkin's lymphoma. Currently, more than 80 % of patients under 60 years old with first diagnosed Hodgkin's lymphoma can be cured from this disease after first-line chemotherapy.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>лимфома Ходжкина</kwd><kwd>ВИЧ</kwd><kwd>вирус Эпштейна-Барр</kwd><kwd>ИГХ</kwd><kwd>ремиссия</kwd><kwd>прогрессирование</kwd><kwd>резистентность к&#13;
химиотерапии</kwd><kwd>общая выживаемость</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Hodgkin lymphoma</kwd><kwd>HIV</kwd><kwd>Epstein-Barr virus</kwd><kwd>IHC</kwd><kwd>remission</kwd><kwd>progression</kwd><kwd>chemotherapy resistance</kwd><kwd>overall survival</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Hodgkin null. On some Morbid Appearances of the Absorbent Glands and Spleen. Med Chir Trans. 1832;17:68–114. https://doi.org/10.1177/095952873201700106</mixed-citation><mixed-citation xml:lang="en">Hodgkin null. On some Morbid Appearances of the Absorbent Glands and Spleen. Med Chir Trans. 1832;17:68–114. https://doi.org/10.1177/095952873201700106</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Gemici A, Aydogdu I, Terzi H, Sencan M, Aslan A, Kaya AH, et al. Nodular lymphocyte predominant Hodgkin’s lymphoma in daily practice: A multicenter experience. Hematol Oncol. 2018 Feb;36(1):116–120. https://doi.org/10.1002/hon.2460</mixed-citation><mixed-citation xml:lang="en">Gemici A, Aydogdu I, Terzi H, Sencan M, Aslan A, Kaya AH, et al. Nodular lymphocyte predominant Hodgkin’s lymphoma in daily practice: A multicenter experience. Hematol Oncol. 2018 Feb;36(1):116–120. https://doi.org/10.1002/hon.2460</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Злокачественные новообразования в России в 2017 году (заболеваемость и смертность). Под ред. А. Д. Каприна, В. В. Старинского, Г. В. Петровой. М.: МНИОИ им. П. А. Герцена – филиал ФГБУ «НМИЦ радиологии» Минздрава России, 2018, 250 с.</mixed-citation><mixed-citation xml:lang="en">Malignant neoplasms in Russia in 2017 (morbidity and mortality). Ed. by A. D. Kaprin, V. V. Starinsky, G. V. Petrova. Moscow: P. A. Herzen Moscow State Medical Research Institute – Branch of the Federal State Budgetary Institution "NMIC of Radiology" of the Ministry of Health of Russia, 2018, 250 p. (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, et al. WHO classification of tumours of haematopoietic and lymphoid tissues. Revised 4th ed. Lyon, France: International Agency for Research in Cancer (IARC). 2017, 585 p.</mixed-citation><mixed-citation xml:lang="en">Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, et al. WHO classification of tumours of haematopoietic and lymphoid tissues. Revised 4th ed. Lyon, France: International Agency for Research in Cancer (IARC). 2017, 585 p.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Devita VT, Serpick AA, Carbone PP. Combination chemotherapy in the treatment of advanced Hodgkin’s disease. Ann Intern Med. 1970 Dec;73(6):881–895. https://doi.org/10.7326/0003-4819-73-6-881</mixed-citation><mixed-citation xml:lang="en">Devita VT, Serpick AA, Carbone PP. Combination chemotherapy in the treatment of advanced Hodgkin’s disease. Ann Intern Med. 1970 Dec;73(6):881–895. https://doi.org/10.7326/0003-4819-73-6-881</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Horning SJ, Rosenberg SA, Hoppe RT. Brief chemotherapy (Stanford V) and adjuvant radiotherapy for bulky or advanced Hodgkin’s disease: an update. Ann Oncol. 1996;7 Suppl 4:105–108. https://doi.org/10.1093/annonc/7.suppl_4.s105</mixed-citation><mixed-citation xml:lang="en">Horning SJ, Rosenberg SA, Hoppe RT. Brief chemotherapy (Stanford V) and adjuvant radiotherapy for bulky or advanced Hodgkin’s disease: an update. Ann Oncol. 1996;7 Suppl 4:105–108. https://doi.org/10.1093/annonc/7.suppl_4.s105</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Merli F, Luminari S, Gobbi PG, Cascavilla N, Mammi C, Ilariucci F, et al. Long-Term Results of the HD2000 Trial Comparing ABVD Versus BEACOPP Versus COPP-EBV-CAD in Untreated Patients With Advanced Hodgkin Lymphoma: A Study by Fondazione Italiana Linfomi. J Clin Oncol. 2016 Apr 10;34(11):1175–1181. https://doi.org/10.1200/JCO.2015.62.4817</mixed-citation><mixed-citation xml:lang="en">Merli F, Luminari S, Gobbi PG, Cascavilla N, Mammi C, Ilariucci F, et al. Long-Term Results of the HD2000 Trial Comparing AB-VD Versus BEACOPP Versus COPP-EBV-CAD in Untreated Patients With Advanced Hodgkin Lymphoma: A Study by Fondazione Italiana Linfomi. J Clin Oncol. 2016 Apr 10;34(11):1175–1181. https://doi.org/10.1200/JCO.2015.62.4817</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Gordon LI, Hong F, Fisher RI, Bartlett NL, Connors JM, Gascoyne RD, et al. Randomized phase III trial of ABVD versus Stanford V with or without radiation therapy in locally extensive and advanced-stage Hodgkin lymphoma: an intergroup study coordinated by the Eastern Cooperative Oncology Group (E2496). J Clin Oncol. 2013 Feb 20;31(6):684–691. https://doi.org/10.1200/JCO.2012.43.4803</mixed-citation><mixed-citation xml:lang="en">Gordon LI, Hong F, Fisher RI, Bartlett NL, Connors JM, Gascoyne RD, et al. Randomized phase III trial of ABVD versus Stanford V with or without radiation therapy in locally extensive and advanced-stage Hodgkin lymphoma: an intergroup study coordinated by the Eastern Cooperative Oncology Group (E2496). J Clin Oncol. 2013 Feb 20;31(6):684–691. https://doi.org/10.1200/JCO.2012.43.4803</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Viviani S, Zinzani PL, Rambaldi A, Brusamolino E, Levis A, Bonfante V, et al. ABVD versus BEACOPP for Hodgkin’s lymphoma when high-dose salvage is planned. N Engl J Med. 2011 Jul 21;365(3):203–212. https://doi.org/10.1056/NEJMoa1100340</mixed-citation><mixed-citation xml:lang="en">Viviani S, Zinzani PL, Rambaldi A, Brusamolino E, Levis A, Bonfante V, et al. ABVD versus BEACOPP for Hodgkin’s lymphoma when high-dose salvage is planned. N Engl J Med. 2011 Jul 21;365(3):203–212. https://doi.org/10.1056/NEJMoa1100340</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Eichenauer DA, Engert A. The evolving role of targeted drugs in the treatment of Hodgkin lymphoma. Expert Rev Hematol. 2017 Sep;10(9):775–782. https://doi.org/10.1080/17474086.2017.1350167</mixed-citation><mixed-citation xml:lang="en">Eichenauer DA, Engert A. The evolving role of targeted drugs in the treatment of Hodgkin lymphoma. Expert Rev Hematol. 2017 Sep;10(9):775–782. https://doi.org/10.1080/17474086.2017.1350167</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Moskowitz AJ, Schöder H, Yahalom J, McCall SJ, Fox SY, Gerecitano J, et al. PET-adapted sequential salvage therapy with brentuximab vedotin followed by augmented ifosamide, carboplatin, and etoposide for patients with relapsed and refractory Hodgkin’s lymphoma: a non-randomised, open-label, single-centre, phase 2 study. Lancet Oncol. 2015 Mar;16(3):284–292. https://doi.org/10.1016/S1470-2045(15)70013-6</mixed-citation><mixed-citation xml:lang="en">Moskowitz AJ, Schöder H, Yahalom J, McCall SJ, Fox SY, Gerecitano J, et al. PET-adapted sequential salvage therapy with brentuximab vedotin followed by augmented ifosamide, carboplatin, and etoposide for patients with relapsed and refractory Hodgkin’s lymphoma: a non-randomised, open-label, single-centre, phase 2 study. Lancet Oncol. 2015 Mar;16(3):284–292. https://doi.org/10.1016/S1470-2045(15)70013-6</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Kumar A, Casulo C, Yahalom J, Schöder H, Barr PM, Caron P, et al. Brentuximab vedotin and AVD followed by involved-site radiotherapy in early stage, unfavorable risk Hodgkin lymphoma. Blood. 2016 Sep 15;128(11):1458–1464. https://doi.org/10.1182/blood-2016-03-703470</mixed-citation><mixed-citation xml:lang="en">Kumar A, Casulo C, Yahalom J, Schöder H, Barr PM, Caron P, et al. Brentuximab vedotin and AVD followed by involved-site radiotherapy in early stage, unfavorable risk Hodgkin lymphoma. Blood. 2016 Sep 15;128(11):1458–1464. https://doi.org/10.1182/blood-2016-03-703470</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Böll B, Borchmann P, Topp MS, Hänel M, Reiners KS, Engert A, et al. Lenalidomide in patients with refractory or multiple relapsed Hodgkin lymphoma. Br J Haematol. 2010 Feb;148(3):480–482. https://doi.org/10.1111/j.1365-2141.2009.07963.x</mixed-citation><mixed-citation xml:lang="en">Böll B, Borchmann P, Topp MS, Hänel M, Reiners KS, Engert A, et al. Lenalidomide in patients with refractory or multiple relapsed Hodgkin lymphoma. Br J Haematol. 2010 Feb;148(3):480–482. https://doi.org/10.1111/j.1365-2141.2009.07963.x</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Johnston PB, Inwards DJ, Colgan JP, Laplant BR, Kabat BF, Habermann TM, et al. A Phase II trial of the oral mTOR inhibitor everolimus in relapsed Hodgkin lymphoma. Am J Hematol. 2010 May;85(5):320–324. https://doi.org/10.1002/ajh.21664</mixed-citation><mixed-citation xml:lang="en">Johnston PB, Inwards DJ, Colgan JP, Laplant BR, Kabat BF, Habermann TM, et al. A Phase II trial of the oral mTOR inhibitor everolimus in relapsed Hodgkin lymphoma. Am J Hematol. 2010 May;85(5):320–324. https://doi.org/10.1002/ajh.21664</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Horie R, Watanabe T. CD30: expression and function in health and disease. Semin Immunol. 1998 Dec;10(6):457–470. https://doi.org/10.1006/smim.1998.0156</mixed-citation><mixed-citation xml:lang="en">Horie R, Watanabe T. CD30: expression and function in health and disease. Semin Immunol. 1998 Dec;10(6):457–470. https://doi.org/10.1006/smim.1998.0156</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Younes A, Santoro A, Shipp M, Zinzani PL, Timmerman JM, Ansell S, et al. Nivolumab for classical Hodgkin’s lymphoma after failure of both autologous stem-cell transplantation and brentuximab vedotin: a multicentre, multicohort, single-arm phase 2 trial. Lancet Oncol. 2016 Sep;17(9):1283–1294. https://doi.org/10.1016/S1470-2045(16)30167-X</mixed-citation><mixed-citation xml:lang="en">Younes A, Santoro A, Shipp M, Zinzani PL, Timmerman JM, Ansell S, et al. Nivolumab for classical Hodgkin’s lymphoma af- ter failure of both autologous stem-cell transplantation and brentuximab vedotin: a multicentre, multicohort, single-arm phase 2 trial. Lancet Oncol. 2016 Sep;17(9):1283–1294. https://doi.org/10.1016/S1470-2045(16)30167-X</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Ansell S, Bröckelmann P, Keudell G von, Lee HJ, Santoro A, Zinzani PL, et al. HL-398: Five-Year Overall Survival from the CheckMate 205 Study of Nivolumab for Relapsed or Refractory (R/R) Classical Hodgkin Lymphoma (cHL). Clinical Lymphoma, Myeloma and Leukemia. 2021 Sep 1;21:S373–S374. https://doi.org/10.1016/S2152-2650(21)01854-1</mixed-citation><mixed-citation xml:lang="en">Ansell S, Bröckelmann P, Keudell G von, Lee HJ, Santoro A, Zinzani PL, et al. HL-398: Five-Year Overall Survival from the CheckMate 205 Study of Nivolumab for Relapsed or Refractory (R/R) Classical Hodgkin Lymphoma (cHL). Clinical Lymphoma, Myeloma and Leukemia. 2021 Sep 1;21:S373–S374. https://doi.org/10.1016/S2152-2650(21)01854-1</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Ilcus C, Bagacean C, Tempescul A, Popescu C, Parvu A, Cenariu M, et al. Immune checkpoint blockade: the role of PD-1-PD-L axis in lymphoid malignancies. Onco Targets Ther. 2017;10:2349–2363. https://doi.org/10.2147/OTT.S133385</mixed-citation><mixed-citation xml:lang="en">Ilcus C, Bagacean C, Tempescul A, Popescu C, Parvu A, Cenariu M, et al. Immune checkpoint blockade: the role of PD-1-PD-L axis in lymphoid malignancies. Onco Targets Ther. 2017;10:2349–2363. https://doi.org/10.2147/OTT.S133385</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Killock D. CAR T cells are active in Hodgkin lymphoma. Nat Rev Clin Oncol. 2020 Oct;17(10):592. https://doi.org/10.1038/s41571-020-0425-8</mixed-citation><mixed-citation xml:lang="en">Killock D. CAR T cells are active in Hodgkin lymphoma. Nat Rev Clin Oncol. 2020 Oct;17(10):592. https://doi.org/10.1038/s41571-020-0425-8</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
