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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">Advances in Molecular Oncology</journal-id><journal-title-group><journal-title xml:lang="en">Advances in Molecular Oncology</journal-title><trans-title-group xml:lang="ru"><trans-title>Успехи молекулярной онкологии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2313-805X</issn><issn publication-format="electronic">2413-3787</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">812</article-id><article-id pub-id-type="doi">10.17650/2313-805X-2025-12-3-8-25</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>REVIEW ARTICLES</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОРНЫЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Multiple aspects of the chemotherapy effect on immune response</article-title><trans-title-group xml:lang="ru"><trans-title>Множественные аспекты влияния противоопухолевой химиотерапии на иммунный ответ</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3297-1680</contrib-id><name-alternatives><name xml:lang="en"><surname>Fedorenko</surname><given-names>A. A.</given-names></name><name xml:lang="ru"><surname>Федоренко</surname><given-names>А. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Anastasia Alekseevna Fedorenko</p><p>5 Kooperativny Line, Tomsk 634009, Russia; 36 Lenin Prospekt, Tomsk 634050, Russia</p></bio><bio xml:lang="ru"><p>Анастасия Алексеевна Федоренко </p><p>Россия, 634009 Томск, пер. Кооперативный, 5; Россия, 634050 Томск, пр-кт Ленина, 36</p></bio><email>aafedorenko@onco.tnimc.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2865-7576</contrib-id><name-alternatives><name xml:lang="en"><surname>Patysheva</surname><given-names>M. R.</given-names></name><name xml:lang="ru"><surname>Патышева</surname><given-names>М. Р.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>5 Kooperativny Line, Tomsk 634009, Russia</p></bio><bio xml:lang="ru"><p>Россия, 634009 Томск, пер. Кооперативный, 5</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Fedorov</surname><given-names>A. A.</given-names></name><name xml:lang="ru"><surname>Федоров</surname><given-names>А. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>5 Kooperativny Line, Tomsk 634009, Russia</p></bio><bio xml:lang="ru"><p>Россия, 634009 Томск, пер. Кооперативный, 5</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0601-2240</contrib-id><name-alternatives><name xml:lang="en"><surname>Stakheyeva</surname><given-names>M. N.</given-names></name><name xml:lang="ru"><surname>Стахеева</surname><given-names>М. Н.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>5 Kooperativny Line, Tomsk 634009, Russia</p></bio><bio xml:lang="ru"><p>Россия, 634009 Томск, пер. Кооперативный, 5</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1526-9013</contrib-id><name-alternatives><name xml:lang="en"><surname>Cherdyntseva</surname><given-names>N. V.</given-names></name><name xml:lang="ru"><surname>Чердынцева</surname><given-names>Н. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>5 Kooperativny Line, Tomsk 634009, Russia; 36 Lenin Prospekt, Tomsk 634050, Russia</p></bio><bio xml:lang="ru"><p>Россия, 634009 Томск, пер. Кооперативный, 5; Россия, 634050 Томск, пр-кт Ленина, 36</p></bio><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7283-0092</contrib-id><name-alternatives><name xml:lang="en"><surname>Gerashchenko</surname><given-names>T. S.</given-names></name><name xml:lang="ru"><surname>Геращенко</surname><given-names>Т. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>5 Kooperativny Line, Tomsk 634009, Russia</p></bio><bio xml:lang="ru"><p>Россия, 634009 Томск, пер. Кооперативный, 5</p></bio><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Cancer Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences</institution></aff><aff><institution xml:lang="ru">Научно-исследовательский институт онкологии ФГБНУ «Томский национальный исследовательский медицинский центр Российской академии наук»</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">National Research Tomsk State University</institution></aff><aff><institution xml:lang="ru">ФГАОУ ВО «Национальный исследовательский Томский государственный университет»</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2025-10-06" publication-format="electronic"><day>06</day><month>10</month><year>2025</year></pub-date><volume>12</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>8</fpage><lpage>25</lpage><history><date date-type="received" iso-8601-date="2025-10-05"><day>05</day><month>10</month><year>2025</year></date><date date-type="accepted" iso-8601-date="2025-10-05"><day>05</day><month>10</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2025, Fedorenko A.A., Patysheva M.R., Fedorov A.A., Stakheyeva M.N., Cherdyntseva N.V., Gerashchenko T.S.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2025, Федоренко А.А., Патышева М.Р., Федоров А.А., Стахеева М.Н., Чердынцева Н.В., Геращенко Т.С.</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="en">Fedorenko A.A., Patysheva M.R., Fedorov A.A., Stakheyeva M.N., Cherdyntseva N.V., Gerashchenko T.S.</copyright-holder><copyright-holder xml:lang="ru">Федоренко А.А., Патышева М.Р., Федоров А.А., Стахеева М.Н., Чердынцева Н.В., Геращенко Т.С.</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://umo.abvpress.ru/jour/article/view/812">https://umo.abvpress.ru/jour/article/view/812</self-uri><abstract xml:lang="en"><p>Suppression of tumor cell growth and proliferation is the main goal of chemotherapy which is an integral part of the treatment for cancer patients. In addition to high antitumor activity, the cytotoxic effects of chemotherapeutic agents also extend to immune cells, resulting in pancytopenia and weakened immune response. Nevertheless, the effect of chemotherapy on the immune system is multifaceted, as it simultaneously exerts a suppressive influence while also stimulating the antitumor activity of lymphoid and myeloid populations. This review focuses on the analysis and generalization of modern data regarding the effects of chemotherapeutic drugs used in standard antitumor therapy regimens on the functioning of the immune system. The suppressive mechanisms of chemotherapy, including the development of cytopenia, are reviewed. Special attention is paid to the analysis of data on modulation of antitumor immune response depending on the class of chemotherapeutic agent. Mechanisms enhancing immune recognition and stimulating immune cells in response to increased expression of tumor antigens are described. The data regarding the effects of chemotherapy on the tumor microenvironment, including the reprogramming of immunosuppressive profiles and the activation of immune effectors, is presented. The summarized data underscore the dual nature of chemotherapy’s effects on the state of the immune system and its influence on the formation of antitumor immune responses.</p></abstract><trans-abstract xml:lang="ru"><p>Химиотерапия злокачественных новообразований направлена на подавление процессов роста и пролиферации опухолевых клеток и является неотъемлемой частью лечения онкологических больных. Наряду с высокой противоопухолевой активностью, цитотоксическое действие химиопрепаратов распространяется и на иммунные клетки, приводя к панцитопении и, как следствие, к ослаблению иммунного ответа. Тем не менее действие химиотерапии на иммунную систему носит комплексный характер, поскольку одновременно с супрессивным влиянием вызывает стимуляцию противоопухолевой активности лимфоидных и миелоидных популяций.Представленный обзор посвящен анализу и обобщению современных данных о влиянии химиотерапевтических препаратов, применяемых в стандартных схемах противоопухолевой терапии, на функционирование иммунной системы. Рассмотрены супрессорные механизмы действия химиотерапии, включая развитие цитопении. Особое внимание уделено анализу данных о модуляции противоопухолевого иммунного ответа в зависимости от группы химиотерапевтического препарата. Описаны механизмы усиления иммунного распознавания и стимуляции иммунных клеток в ответ на увеличение экспрессии опухолевых антигенов. Представлены сведения о влиянии химиотерапии на опухолевое микроокружение, включая перепрограммирование иммуносупрессорного профиля и активацию эффекторов иммунитета. Обобщенные данные указывают на разнонаправленное воздействие химиотерапии на состояние иммунной системы и ее влияние на формирование противоопухолевого иммунного ответа.</p></trans-abstract><kwd-group xml:lang="en"><kwd>chemotherapy</kwd><kwd>cancer</kwd><kwd>immune system</kwd><kwd>cytotoxicity</kwd><kwd>antitumor immune response</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>химиотерапия</kwd><kwd>рак</kwd><kwd>иммунная система</kwd><kwd>цитотоксичность</kwd><kwd>противоопухолевый иммунный ответ</kwd></kwd-group><funding-group><funding-statement xml:lang="en">The work was carried out with the financial support of the Russian Science Foundation (grant No. 22-75-10128).</funding-statement><funding-statement xml:lang="ru">Работа выполнена при финансовой поддержке Российского научного фонда (грант No 22-75-10128)</funding-statement></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Anand U., Dey A., Chandel A.K.S. et al. Cancer chemotherapy and beyond: Current status, drug candidates, associated risks and progress in targeted therapeutics. Genes Dis 2023;10(4):1367–401. DOI: 10.1016/j.gendis.2022.02.007</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Albert A. Chemotherapy: history and principles. In: Selective toxicity: the physico-chemical basis of therapy. Ed. by A. Albert. Dordrecht: Springer Netherlands, 1985. Pp. 206–265.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Morrison W.B. Cancer chemotherapy: an annotated history. J Vet Intern Med 2010;24(6):1249–62. DOI: 10.1111/j.1939-1676.2010.0590.x</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Sharma A., Jasrotia S., Kumar A. Effects of chemotherapy on the immune system: implications for cancer treatment and patient outcomes. Naunyn Schmiedebergs Arch Pharmacol 2024;397(5):2551–66. DOI: 10.1007/s00210-023-02781-2</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Vorontsova A., Kan T., Raviv Z. et al. The dichotomous role of bone marrow derived cells in the chemotherapy-treated tumor microenvironment. J Clin Med 2020;9(12):3912. DOI: 10.3390/jcm9123912</mixed-citation></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">Galsky M.D., Guan X., Rishipathak D. et al. Immunomodulatory effects and improved outcomes with cisplatin- versus carboplatinbased chemotherapy plus atezolizumab in urothelial cancer. Cell Rep Med 2024;5(2):101393. DOI: 10.1016/j.xcrm.2024.101393</mixed-citation><mixed-citation xml:lang="ru">Galsky M.D., Guan X., Rishipathak D. et al. Immunomodulatory effects and improved outcomes with cisplatin- versus carboplatin-based chemotherapy plus atezolizumab in urothelial cancer. Cell Rep Med 2024;5(2):101393. DOI: 10.1016/j.xcrm.2024.101393</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><mixed-citation>Mukherjee O., Rakshit S., Shanmugam G. et al. Role of chemotherapeutic drugs in immunomodulation of cancer. Curr Res Immunol 2023;4:100068. DOI: 10.1016/j.crimmu.2023.100068</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Galluzzi L., Humeau J., Buqué A. et al. Immunostimulation with chemotherapy in the era of immune checkpoint inhibitors. Nat Rev Clin Oncol 2020;17(12):725–41. DOI: 10.1038/s41571-020-0413-z</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Shin D.S., Ribas A. The evolution of checkpoint blockade as a cancer therapy: what's here, what's next? Curr Opin Immunol 2015;33:23–35. DOI: 10.1016/j.coi.2015.01.006</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Burnet M. Cancer – a biological approach. I. The processes of control. II. The Significance of somatic mutation 1957;1(5022):779–86. DOI: 10.1136/bmj.1.5022.779</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Burnet F.M. The concept of immunological surveillance. Prog Exp Tumor Res 1970;13(1):1–27. DOI: 10.1159/000386035</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Vesely M.D., Schreiber R.D. Cancer immunoediting: antigens, mechanisms, and implications to cancer immunotherapy. Ann NY Acad Sci 2013;1284(1):1–5. DOI: 10.1111/nyas.12105</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Gerashchenko T., Frolova A., Patysheva M. et al. Breast Cancer immune landscape: interplay between systemic and local immunity. Adv Biol (Weinh) 2024;8(7):e2400140. DOI: 10.1002/adbi.202400140</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Galluzzi L., Senovilla L., Zitvogel L. et al. The secret ally: immunostimulation by anticancer drugs. Nat Rev Drug Discov 2012;11(3):215–33. DOI: 10.1038/nrd3626</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Wang L., Geng H., Liu Y. et al. Hot and cold tumors: immunological features and the therapeutic strategies. MedComm (2020) 2023;4(5):e343. DOI: 10.1002/mco2.343</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Opzoomer J.W., Sosnowska D., Anstee J.E. et al. Cytotoxic Chemotherapy as an immune stimulus: a molecular perspective on turning up the immunological heat on cancer. Front Immunol 2019;10:1654. DOI: 10.3389/fimmu.2019.01654</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Merlano M.C., Denaro N., Galizia D. et al. How chemotherapy affects the tumor immune microenvironment: a narrative review. Biomedicines 2022;10(8):1822. DOI: 10.3390/biomedicines10081822</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Zhang J., Pan S., Jian C. et al. Immunostimulatory properties of chemotherapy in breast cancer: from immunogenic modulation mechanisms to clinical practice. Front Immunol 2021;12:819405. DOI: 10.3389/fimmu.2021.819405</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Kroemer G., Galassi C., Zitvogel L. et al. Immunogenic cell stress and death. Nat Immunol 2022;23(4):487–500. DOI: 10.1038/s41590-022-01132-2</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Kroemer G., Galluzzi L., Kepp O. et al. Immunogenic cell death in cancer therapy. Annu Rev Immunol 2013;31:51–72. DOI: 10.1146/annurev-immunol-032712-100008</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Zitvogel L., Apetoh L., Ghiringhelli F. et al. The anticancer immune response: indispensable for therapeutic success? J Clin Invest 2008;118(6):1991–2001. DOI: 10.1172/jci35180</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Russo M., Panini N., Fabbrizio P. et al. Chemotherapy-induced neutropenia elicits metastasis formation in mice by promoting proliferation of disseminated tumor cells. Oncoimmunology 2023;12(1):2239035. DOI: 10.1080/2162402x.2023.2239035</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Sistigu A., Yamazaki T., Vacchelli E. et al. Cancer cell–autonomous contribution of type I interferon signaling to the efficacy of chemotherapy. Nat Med 2014;20(11):1301–9. DOI: 10.1038/nm.3708</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Benson Z., Manjili S.H., Habibi M. et al. Conditioning neoadjuvant therapies for improved immunotherapy of cancer. Biochem Pharmacol 2017;145:12–7. DOI: 10.1016/j.bcp.2017.08.007</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Patysheva M., Larionova I., Stakheyeva M. et al. Effect of earlystage human breast carcinoma on monocyte programming. Front Oncol 2021;11:800235. DOI: 10.3389/fonc.2021.800235</mixed-citation></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">Romanov B.K., Dmitrieva N.B., Zatsepilova T.A. Antitumor drugs. Medical Journal of the Russian Federation, Russian Journal 2018;24(3):146–50. (In Russ.). DOI: 10.18821/0869-2106-2018-24-3-146-150</mixed-citation><mixed-citation xml:lang="ru">Романов Б.К., Дмитриева Н.Б., Зацепилова Т.А. Противоопухолевые препараты. Medical Journal of the Russian Federation, Russian Journal 2018;24(3):146–50. DOI: 10.18821/0869-2106-2018-24-3-146-150</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><mixed-citation>Wu J., Waxman D.J. Immunogenic chemotherapy: dose and schedule dependence and combination with immunotherapy. Cancer Lett 2018;419:210–21. DOI: 10.1016/j.canlet.2018.01.050</mixed-citation></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">Tryakin A.A., Besova N.S., Volkov N.M. et al. General principles of antitumor drug therapy. Zlokachestvennye opukholi = Malignant Tumors 2024;14(3s2–1):33–46. (In Russ.). DOI: 10.18027/2224-5057-2024-14-3s2-1.1-01</mixed-citation><mixed-citation xml:lang="ru">Трякин А.А., Бесова Н.С., Волков Н.М. и др. Общие принципы противоопухолевой лекарственной терапии. Злокачественные опухоли 2024;14(3s2–1):33–46. DOI: 10.18027/2224-5057-2024-14-3s2-1.1-01</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">Tryakin A.A., Besova N.S., Volkov N.M. et al. Practical recommendations on the general principles of antitumor drug therapy. Zlokachestvennye opukholi = Malignant Tumors 2020;10(3s2–1): 26–39. (In Russ.). DOI: 10.18027/2224-5057-2020-10-3s2-01</mixed-citation><mixed-citation xml:lang="ru">Трякин А.А., Бесова Н.С., Волков Н.М. и др. Практические рекомендации по общим принципам проведения противоопухолевой лекарственной терапии. Злокачественные опухоли 2020;10(3s2–1):26–39. DOI: 10.18027/2224-5057-2020-10-3s2-01</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">Laktionov K.K., Artamonova E.V., Breder V.V. et al. Non-small cell lung cancer. Zlokachestvennye opukholi = Malignant Tumors 2024;14(3s2–1):65–104. (In Russ.). DOI: 10.18027/2224-5057-2024-14-3s2-1.1-04</mixed-citation><mixed-citation xml:lang="ru">Лактионов К.К., Артамонова Е.В., Бредер В.В. и др. Немелкоклеточный рак легкого. Злокачественные опухоли 2024;14(3s2–1): 65–104. DOI: 10.18027/2224-5057-2024-14-3s2-1.1-04</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">Chubenko V.A., Bychkov M.B., Dengina N.V. et al. Small cell lung cancer. Zlokachestvennye opukholi = Malignant Tumors 2024;14(3s2–1):105–14. (In Russ.). DOI: 10.18027/2224-5057-2024-14-3s2-1.1-05</mixed-citation><mixed-citation xml:lang="ru">Чубенко В.А., Бычков М.Б., Деньгина Н.В. и др. Мелкоклеточный рак легкого. Злокачественные опухоли 2024;14(3s2–1): 105–114. DOI: 10.18027/2224-5057-2024-14-3s2-1.1-05</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">Stroyakovsky D.L., Abramov M.E., Demidov L.V. et al. Melanoma of the skin. Zlokachestvennye opukholi = Malignant Tumors 2024;14(3s2):300–29. (In Russ.). DOI: 10.18027/2224-5057-2024-14-3s2-1.2-12</mixed-citation><mixed-citation xml:lang="ru">Строяковский Д.Л., Абрамов М.Е., Демидов Л.В. и др. Меланома кожи. Злокачественные опухоли 2024;14(3s2):300–29. DOI: 10.18027/2224-5057-2024-14-3s2-1.2-12</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">Tyulandin S.A., Artamonova E.V., Zhigulev A.N. et al. Breast cancer. Zlokachestvennye opukholi = Malignant Tumors 2024;14(3s2–2):32–81. (In Russ.). DOI: 10.18027/2224-5057-2024-14-3s2-1.2-01</mixed-citation><mixed-citation xml:lang="ru">Тюляндин С.А., Артамонова Е.В., Жигулев А.Н. и др. Рак молочной железы. Злокачественные опухоли 2024;14(3s2–2):32–81. DOI: 10.18027/2224-5057-2024-14-3s2-1.2-01</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">Khokhlova S.V., Kravets O.A., Morkhov K.Yu. et al. Cervical cancer. Zlokachestvennye opukholi = Malignant Tumors 2024;14(3s2–2): 136–64. (In Russ.). DOI: 10.18027/2224-5057-2024-14-3s2-1.2-05</mixed-citation><mixed-citation xml:lang="ru">Хохлова С.В., Кравец О.А., Морхов К.Ю. и др. Рак шейки матки. Злокачественные опухоли 2024;14(3s2–2):136–64. DOI: 10.18027/2224-5057-2024-14-3s2-1.2-05</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">Pokataev I.A., Dudina I.A., Kolomiets L.A. et al. Ovarian cancer, primary peritoneal cancer, and fallopian tube cancer. Zlokachestvennye opukholi = Malignant Tumors 2024;14(3s2–2): 82–101. (In Russ.). DOI: 10.18027/2224-5057-2024-14-3s2-1.2-02</mixed-citation><mixed-citation xml:lang="ru">Покатаев И.А., Дудина И.А., Коломиец Л.А. и др. Рак яичников, первичный рак брюшины и рак маточных труб. Злокачественные опухоли 2024;14(3s2–2):82–101. DOI: 10.18027/2224-5057-2024-14-3s2-1.2-02</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">Bolotina L.V., Vladimirova L.Yu., Dengina N.V. et al. Tumors of the head and neck. Zlokachestvennye opukholi = Malignant Tumors 2024;14(3s2–1):160–82. (In Russ.). DOI: 10.18027/2224-5057-2024-14-3s2-1.1-09</mixed-citation><mixed-citation xml:lang="ru">Болотина Л.В., Владимирова Л.Ю., Деньгина Н.В. и др. Опухоли головы и шеи. Злокачественные опухоли 2024; 14(3s2–1):160–82. DOI: 10.18027/2224-5057-2024-14-3s2-1.1-09</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">Ulitin A.Yu., Zheludkova O.G., Ivanov P.I. et al. Primary tumors of the central nervous system. Zlokachestvennye opukholi = Malignant Tumors 2024;14(3s2–1):183–211. (In Russ.). DOI: 10.18027/2224-5057-2024-14-3s2-1.1-10</mixed-citation><mixed-citation xml:lang="ru">Улитин А.Ю., Желудкова О.Г., Иванов П.И. и др. Первичные опухоли центральной нервной системы. Злокачественные опухоли 2024;14(3s2–1):183–211. DOI: 10.18027/2224-5057-2024-14-3s2-1.1-10</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">Tryakin A.A., Besova N.S., Volkov N.M. et al. Cancer of the esophagus and esophageal-gastric junction. Zlokachestvennye opukholi = Malignant Tumors 2024;14(3s2–1):221–40. (In Russ.). DOI: 10.18027/2224-5057-2024-14-3s2-1.1-12</mixed-citation><mixed-citation xml:lang="ru">Трякин А.А., Бесова Н.С., Волков Н.М. и др. Рак пищевода и пищеводно-желудочного перехода. Злокачественные опухоли 2024;14(3s2-1):221–240. DOI: 10.18027/2224-5057-2024-14-3s2-1.1-12</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">Besova N.S., Bolotina L.V., Gamayunov S.V. et al. Stomach cancer. Zlokachestvennye opukholi = Malignant Tumors 2024;14(3s2–1): 241–62. (In Russ.). DOI: 10.18027/2224-5057-2024-14-3s2-1.1-13</mixed-citation><mixed-citation xml:lang="ru">Бесова Н.С., Болотина Л.В., Гамаюнов С.В. и др. Рак желудка. Злокачественные опухоли 2024;14(3s2–1):241–62. DOI: 10.18027/2224-5057-2024-14-3s2-1.1-13</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">Kudashkin N.E., Gladkov O.A., Zagainov V.E. et al. Pancreatic cancer. Zlokachestvennye opukholi = Malignant Tumors 2024;14(3s2–1):404–15. (In Russ.). DOI: 10.18027/2224-5057-2024-14-3s2-1.1-18</mixed-citation><mixed-citation xml:lang="ru">Кудашкин Н.Е., Гладков О.А., Загайнов В.Е. и др. Рак поджелудочной железы. Злокачественные опухоли 2024;14(3s2–1): 404–15. DOI: 10.18027/2224-5057-2024-14-3s2-1.1-18</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">Fedyanin M.Yu., Gladkov O.A., Gordeev S.S. et al. Cancer of the colon, rectosigmoid junction and rectum. Zlokachestvennye opukholi = Malignant Tumors 2024;14(3s2–1):263–322. (In Russ.). DOI: 10.18027/2224-5057-2024-14-3s2-1.1-14</mixed-citation><mixed-citation xml:lang="ru">Федянин М.Ю., Гладков О.А., Гордеев С.С. и др. Рак ободочной кишки, ректосигмоидного соединения и прямой кишки. Злокачественные опухоли 2024;14(3s2–1):263–322. DOI: 10.18027/2224-5057-2024-14-3s2-1.1-14</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">Matveev V.B., Volkova M.I., Gladkov O.A. et al. Germinogenic tumors in men. Zlokachestvennye opukholi = Malignant Tumors 2024;14(3s2–2):267–99. (In Russ.). DOI: 10.18027/2224-5057-2024-14-3s2-1.2-11</mixed-citation><mixed-citation xml:lang="ru">Матвеев В.Б., Волкова М.И., Гладков О.А. и др. Герминогенные опухоли у мужчин. Злокачественные опухоли 2024;14(3s2–2): 267–99. DOI: 10.18027/2224-5057-2024-14-3s2-1.2-11</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">Rumyantsev A.A., Bulychkin P.V., Volkova M.I. et al. Bladder cancer. Zlokachestvennye opukholi = Malignant Tumors 2024; 14(3s2–2):221–41. (In Russ.). DOI: 10.18027/2224-5057-2024-14-3s2-1.2-09</mixed-citation><mixed-citation xml:lang="ru">Румянцев А.А., Булычкин П.В., Волкова М.И. и др. Рак мочевого пузыря. Злокачественные опухоли 2024;14(3s2–2):221–41. DOI: 10.18027/2224-5057-2024-14-3s2-1.2-09</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">Egorenkov V.V., Bokhyan A.Yu., Konev A.A. et al. Soft tissue sarcomas. Zlokachestvennye opukholi = Malignant Tumors 2024;14(3s2–2):393–413. (In Russ.). DOI: 10.18027/2224-5057-2024-14-3s2-1.2-15</mixed-citation><mixed-citation xml:lang="ru">Егоренков В.В., Бохян А.Ю., Конев А.А. и др. Саркомы мягких тканей. Злокачественные опухоли 2024;14(3s2–2):393–413. DOI: 10.18027/2224-5057-2024-14-3s2-1.2-15</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><mixed-citation>Bukowski K., Kciuk M., Kontek R. Mechanisms of multidrug resistance in cancer chemotherapy. Int J Mol Sci 2020;21(9):3233. DOI: 10.3390/ijms21093233</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Olofinsan K., Abrahamse H., George B.P. Therapeutic role of alkaloids and alkaloid derivatives in cancer management. Molecules 2023;28(14):5578. DOI: 10.3390/molecules28145578</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Ostios-Garcia L., Pérez D.M., Castelo B. et al. Classification of anticancer drugs: an update with FDA- and EMA-approved drugs. Cancer Metastasis Rev 2024;43(4):1561–71. DOI: 10.1007/s10555-024-10188-5</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Gebremeskel S., Johnston B. Concepts and mechanisms underlying chemotherapy induced immunogenic cell death: impact on clinical studies and considerations for combined therapies. Oncotarget 2015;6(39):41600–19. DOI: 10.18632/oncotarget.6113</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Gerashchenko T.S., Patysheva M.R., Fedorenko A.A. et al. Chemotherapy-induced developmental trajectories of monocytes in breast cancer. RUDN Journal of MEDICIN 2024;28(4):427–38. DOI: 10.22363/2313-0245-2024-28-4-427-438</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Karati D., Mahadik K.R., Trivedi P. et al. Alkylating agents, the road less traversed, changing anticancer therapy. Anticancer Agents Med Chem 2022;22(8):1478–95. DOI: 10.2174/1871520621666210811105344</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Khoury A., Deo K.M., Aldrich-Wright J.R. Recent advances in platinum-based chemotherapeutics that exhibit inhibitory and targeted mechanisms of action. J Inorg Biochem 2020;207:111070. DOI: 10.1016/j.jinorgbio.2020.111070</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Bayat Mokhtari R., Homayouni T.S., Baluch N. et al. Combination therapy in combating cancer. Oncotarget 2017;8(23):38022–43. DOI: 10.18632/oncotarget.16723</mixed-citation></ref><ref id="B53"><label>53.</label><citation-alternatives><mixed-citation xml:lang="en">Nikitina O.G., Valiakhmetova A.R., Gazdalieva L.M. The use of chemotherapy in the treatment of cancer patients. Mezhdunarodny studencheskiy nauchny vestnik = International Student Scientific Bulletin 2018;4(3):471–4. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Никитина О.Г., Валиахметова А.Р., Газдалиева Л.М. Применение химиотерапии при лечении онкологических больных. Международный студенческий научный вестник 2018;4(3):471–4.</mixed-citation></citation-alternatives></ref><ref id="B54"><label>54.</label><citation-alternatives><mixed-citation xml:lang="en">Orlova O.L., Nikolaeva L.L., Korol L.A. et al. Modern cancer drugs for internal use. Farmatsiya i farmakologiya = Pharmacy and Pharmacology 2018;6(5):440–61. (In Russ.). DOI: 10.19163/2307-9266-2018-6-5-440-461</mixed-citation><mixed-citation xml:lang="ru">Орлова О.Л., Николаева Л.Л., Король Л.А. и др. Современные онкопрепараты для внутреннего применения. Фармация и фармакология 2018;6(5):440–61. DOI: 10.19163/2307-9266-2018-6-5-440-461</mixed-citation></citation-alternatives></ref><ref id="B55"><label>55.</label><mixed-citation>Yoo J., Jung Y., Ahn J.H. et al. Incidence and clinical course of septic shock in neutropenic patients during chemotherapy for gynecological cancers. J Gynecol Oncol 2020;31(5):e62. DOI: 10.3802/jgo.2020.31.e62</mixed-citation></ref><ref id="B56"><label>56.</label><citation-alternatives><mixed-citation xml:lang="en">Ahlmann M., Hempel G. The effect of cyclophosphamide on the immune system: implications for clinical cancer therapy. Cancer Chemother Pharmacol 2016;78(4):661–71. DOI: 10.1007/s00280-016-3152-1</mixed-citation><mixed-citation xml:lang="ru">Ahlmann M., Hempel G. The effect of cyclophosphamide on the immune system: implications for clinical cancer therapy. Cancer Chemother Pharmacol 2016;78(4):661–71. DOI: 10.1007/s00280-016-3152-1</mixed-citation></citation-alternatives></ref><ref id="B57"><label>57.</label><mixed-citation>Kim C.G., Sohn J., Chon H. et al. Incidence of febrile neutropenia in korean female breast cancer patients receiving preoperative or postoperative doxorubicin/cyclophosphamide followed by docetaxel chemotherapy. J Breast Cancer 2016;19(1):76–82. DOI: 10.4048/jbc.2016.19.1.76</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Lyman G.H., Michels S.L., Reynolds M.W. et al. Risk of mortality in patients with cancer who experience febrile neutropenia. Cancer 2010;116(23):5555–63. DOI: 10.1002/cncr.25332</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Uitdehaag B.M., Nillesen W.M., Hommes O.R. Long-lasting effects of cyclophosphamide on lymphocytes in peripheral blood and spinal fluid. Acta Neurol Scand 1989;79(1):12–7. DOI: 10.1111/j.1600-0404.1989.tb03702.x</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Emadi A., Jones R.J., Brodsky R.A. Cyclophosphamide and cancer: golden anniversary. Nat Rev Clin Oncol 2009;6(11):638–47. DOI: 10.1038/nrclinonc.2009.146</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>Ghiringhelli F., Menard C., Puig P.E. et al. Metronomic cyclophosphamide regimen selectively depletes CD4+CD25+regulatory T cells and restores T and NK effector functions in end stage cancer patients. Cancer Immunol Immunother 2007;56(5):641–8. DOI: 10.1007/s00262-006-0225-8</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>Dimeloe S., Frick C., Fischer M. et al. Human regulatory T cells lack the cyclophosphamide-extruding transporter ABCB1 and are more susceptible to cyclophosphamide-induced apoptosis. Eur J Immunol 2014;44(12):3614–20. DOI: 10.1002/eji.201444879</mixed-citation></ref><ref id="B63"><label>63.</label><mixed-citation>Huijts C.M., Lougheed S.M., Bodalal Z. et al. The effect of everolimus and low-dose cyclophosphamide on immune cell subsets in patients with metastatic renal cell carcinoma: results from a phase I clinical trial. Cancer Immunol Immunother 2019;68(3):503–15. DOI: 10.1007/s00262-018-2288-8</mixed-citation></ref><ref id="B64"><label>64.</label><mixed-citation>Nakahara T., Uchi H., Lesokhin A.M. et al. Cyclophosphamide enhances immunity by modulating the balance of dendritic cell subsets in lymphoid organs. Blood 2010;115(22):4384–92. DOI: 10.1182/blood-2009-11-251231</mixed-citation></ref><ref id="B65"><label>65.</label><mixed-citation>Bao L., Hao C., Wang J. et al. High-dose cyclophosphamide administration orchestrates phenotypic and functional alterations of immature dendritic cells and regulates th cell polarization. Front Pharmacol 2020;11:775. DOI: 10.3389/fphar.2020.00775</mixed-citation></ref><ref id="B66"><label>66.</label><mixed-citation>Larionova I., Cherdyntseva N., Liu T. et al. Interaction of tumorassociated macrophages and cancer chemotherapy. Oncoimmunology 2019;8(7):1596004. DOI: 10.1080/2162402x.2019.1596004</mixed-citation></ref><ref id="B67"><label>67.</label><mixed-citation>Bart V.M.T., Pickering R.J., Taylor P.R. et al. Macrophage reprogramming for therapy. Immunology 2021;163(2):128–44. DOI: 10.1111/imm.13300</mixed-citation></ref><ref id="B68"><label>68.</label><mixed-citation>Heath O., Berlato C., Maniati E. et al. Chemotherapy induces tumor-associated macrophages that aid adaptive immune responses in ovarian cancer. Cancer Immunol Res 2021;9(6):665–81. DOI: 10.1158/2326-6066.Cir-20-0968</mixed-citation></ref><ref id="B69"><label>69.</label><mixed-citation>Sevko A., Sade-Feldman M., Kanterman J. et al. Cyclophosphamide promotes chronic inflammation-dependent immunosuppression and prevents antitumor response in melanoma. J Invest Dermatol 2013;133(6):1610–1619. DOI: 10.1038/jid.2012.444</mixed-citation></ref><ref id="B70"><label>70.</label><mixed-citation>Longley D.B., Harkin D.P., Johnston P.G. 5-fluorouracil: mechanisms of action and clinical strategies. Nat Rev Cancer 2003;3(5):330–8. DOI: 10.1038/nrc1074</mixed-citation></ref><ref id="B71"><label>71.</label><mixed-citation>Cavalcanti I.D.L., Soares J.C.S. Conventional cancer treatment. In: Advances in Cancer Treatment: From Systemic Chemotherapy to Targeted Therapy. Ed. by I.D.L. Cavalcanti, J.C.S. Soares. Cham: Springer International Publishing, 2021. Pp. 29–56.</mixed-citation></ref><ref id="B72"><label>72.</label><mixed-citation>Al-Shammary E.H., Mohammed D.J. Chemotherapy-induced neutropenia after initial and subsequent chemotherapy cycle of non-Hodgkin lymphoma. Mustansiriya Med J 2020;19(1):16–9. DOI: 10.4103/mj.Mj_4_20</mixed-citation></ref><ref id="B73"><label>73.</label><mixed-citation>Bracci L., Schiavoni G., Sistigu A. et al. Immune-based mechanisms of cytotoxic chemotherapy: implications for the design of novel and rationale-based combined treatments against cancer. Cell Death Differ 2014;21(1):15–25. DOI: 10.1038/cdd.2013.67</mixed-citation></ref><ref id="B74"><label>74.</label><mixed-citation>Nowak A.K., Robinson B.W., Lake R.A. Gemcitabine exerts a selective effect on the humoral immune response: implications for combination chemo-immunotherapy. Cancer Res 2002;62(8):2353–8</mixed-citation></ref><ref id="B75"><label>75.</label><mixed-citation>Herman S., Zurgil N., and Deutsch M. Low dose methotrexate induces apoptosis with reactive oxygen species involvement in T lymphocytic cell lines to a greater extent than in monocytic lines. Inflamm Res 2005;54(7):273–80. DOI: 10.1007/s00011-005-1355-8</mixed-citation></ref><ref id="B76"><label>76.</label><mixed-citation>Eriksson E., Wenthe J., Irenaeus S. et al. Gemcitabine reduces MDSCs, tregs and TGFβ-1 while restoring the teff/treg ratio in patients with pancreatic cancer. J Transl Med 2016;14(1):282. DOI: 10.1186/s12967-016-1037-z</mixed-citation></ref><ref id="B77"><label>77.</label><mixed-citation>Sawasdee N., Thepmalee C., Sujjitjoon J. et al. Gemcitabine enhances cytotoxic activity of effector T-lymphocytes against chemo-resistant cholangiocarcinoma cells. Int Immunopharmacol 2020;78:106006. DOI: 10.1016/j.intimp.2019.106006</mixed-citation></ref><ref id="B78"><label>78.</label><mixed-citation>Szczygieł A., Węgierek-Ciura K., Mierzejewska J. et al. The modulation of local and systemic anti-tumor immune response induced by methotrexate nanoconjugate in murine MC38 colon carcinoma and B16 F0 melanoma tumor models. Am J Cancer Res 2023;13(10):4623–43.</mixed-citation></ref><ref id="B79"><label>79.</label><mixed-citation>Ma G., Zhang Z., Li P. et al. Reprogramming of glutamine metabolism and its impact on immune response in the tumor microenvironment. Cell Commun Signal 2022;20(1):114. DOI: 10.1186/s12964-022-00909-0</mixed-citation></ref><ref id="B80"><label>80.</label><mixed-citation>Cerezo M., Rocchi S. Cancer cell metabolic reprogramming: a keystone for the response to immunotherapy. Cell Death Disease 2020;11(11):964. DOI: 10.1038/s41419-020-03175-5</mixed-citation></ref><ref id="B81"><label>81.</label><mixed-citation>Fang H., Ang B., Xu X. et al. TLR4 is essential for dendritic cell activation and anti-tumor T-cell response enhancement by DAMPs released from chemically stressed cancer cells. Cell Mol Immunol 2014;11(2):150–9. DOI: 10.1038/cmi.2013.59</mixed-citation></ref><ref id="B82"><label>82.</label><mixed-citation>Apetoh L., Ladoire S., Coukos G. et al. Combining immunotherapy and anticancer agents: the right path to achieve cancer cure? Ann Oncol 2015;26(9):1813–23. DOI: 10.1093/annonc/mdv209</mixed-citation></ref><ref id="B83"><label>83.</label><mixed-citation>Püschel F., Favaro F., Redondo-Pedraza J. et al. Starvation and antimetabolic therapy promote cytokine release and recruitment of immune cells. Proc Natl Acad Sci USA 2020;117(18):9932–41. DOI: 10.1073/pnas.1913707117</mixed-citation></ref><ref id="B84"><label>84.</label><mixed-citation>Malesci A., Bianchi P., Celesti G. et al. Tumor-associated macrophages and response to 5-fluorouracil adjuvant therapy in stage III colorectal cancer. Oncoimmunology 2017;6(12):e1342918. DOI: 10.1080/2162402x.2017.1342918</mixed-citation></ref><ref id="B85"><label>85.</label><mixed-citation>Yokoyama C., Sueyoshi Y., Ema M. et al. Induction of oxidative stress by anticancer drugs in the presence and absence of cells. Oncol Lett 2017;14(5):6066–70. DOI: 10.3892/ol.2017.6931</mixed-citation></ref><ref id="B86"><label>86.</label><mixed-citation>Mordente A., Meucci E., Silvestrini A. et al. Anthracyclines and Mitochondria. In: Advances in mitochondrial medicine. Ed. by R. Scatena, P. Bottoni, B. Giardina. Dordrecht: Springer Netherlands, 2012. Pp. 385–419.</mixed-citation></ref><ref id="B87"><label>87.</label><citation-alternatives><mixed-citation xml:lang="en">Steele T.A. Chemotherapy-induced immunosuppression and reconstitution of immune function. Leuk Res 2002;26(4):411–4. DOI: 10.1016/S0145-2126(01)00138-2</mixed-citation><mixed-citation xml:lang="ru">Steele T.A. Chemotherapy-induced immunosuppression and reconstitution of immune function. Leuk Res 2002;26(4):411–4. DOI: 10.1016/S0145-2126(01)00138-2</mixed-citation></citation-alternatives></ref><ref id="B88"><label>88.</label><mixed-citation>Krysko D.V., Kaczmarek A., Krysko O. et al. TLR-2 and TLR-9 are sensors of apoptosis in a mouse model of doxorubicin-induced acute inflammation. Cell Death Differ 2011;18(8):1316–25. DOI: 10.1038/cdd.2011.4</mixed-citation></ref><ref id="B89"><label>89.</label><mixed-citation>Ghiringhelli F., Apetoh L., Tesniere A. et al. Activation of the NLRP3 inflammasome in dendritic cells induces IL-1β-dependent adaptive immunity against tumors. Nat Med 2009;15(10):1170–8. DOI: 10.1038/nm.2028</mixed-citation></ref><ref id="B90"><label>90.</label><mixed-citation>Obeid M., Tesniere A., Ghiringhelli F. et al. Calreticulin exposure dictates the immunogenicity of cancer cell death. Nat Med 2007;13(1):54–61. DOI: 10.1038/nm1523</mixed-citation></ref><ref id="B91"><label>91.</label><mixed-citation>Giglio P., Mara G., Nicola T. et al. PKR and GCN2 stress kinases promote an ER stress-independent eIF2α phosphorylation responsible for calreticulin exposure in melanoma cells. OncoImmunology 2018;7(8):e1466765. DOI: 10.1080/2162402X.2018.1466765</mixed-citation></ref><ref id="B92"><label>92.</label><mixed-citation>Hodge J.W., Garnett C.T., Farsaci B. et al. Chemotherapy-induced immunogenic modulation of tumor cells enhances killing by cytotoxic T lymphocytes and is distinct from immunogenic cell death. Int J Cancer 2013;133(3):624–36. DOI: 10.1002/ijc.28070</mixed-citation></ref><ref id="B93"><label>93.</label><mixed-citation>Alizadeh D., Larmonier N. Chemotherapeutic targeting of cancerinduced immunosuppressive cells. Cancer Res 2014;74(10):2663–8. DOI: 10.1158/0008-5472.Can-14-0301</mixed-citation></ref><ref id="B94"><label>94.</label><mixed-citation>Park J.Y., Jang M.J., Chung Y.H. et al. Doxorubicin enhances CD4+ T-cell immune responses by inducing expression of CD40 ligand and 4-1BB. Int Immunopharmacol 2009;9(13):1530–9. DOI: 10.1016/j.intimp.2009.09.008</mixed-citation></ref><ref id="B95"><label>95.</label><mixed-citation>Mattarollo S.R., Loi S., Duret H. et al. Pivotal role of innate and adaptive immunity in anthracycline chemotherapy of established tumors. Cancer Res 2011;71(14):4809–20. DOI: 10.1158/0008-5472.Can-11-0753</mixed-citation></ref><ref id="B96"><label>96.</label><mixed-citation>Huang J., Wu R., Chen L. et al. Understanding anthracycline cardiotoxicity from mitochondrial aspect. Front Pharmacol 2022;13:811406. DOI: 10.3389/fphar.2022.811406</mixed-citation></ref><ref id="B97"><label>97.</label><mixed-citation>Ocadlikova D., Lecciso M., Isidori A. et al. Chemotherapy-induced tumor cell death at the crossroads between immunogenicity and immunotolerance: focus on acute myeloid leukemia. Front Oncol 2019;9:1004. DOI: 10.3389/fonc.2019.01004</mixed-citation></ref><ref id="B98"><label>98.</label><mixed-citation>Wijayahadi N., Haron M.R., Stanslas J. et al. Changes in cellular immunity during chemotherapy for primary breast cancer with anthracycline regimens. J Chemother 2007;19(6):716–23. DOI: 10.1179/joc.2007.19.6.716</mixed-citation></ref><ref id="B99"><label>99.</label><mixed-citation>Elsea C.R., Roberts D.A., Druker B.J. et al. Inhibition of p38 MAPK suppresses inflammatory cytokine induction by etoposide, 5-fluorouracil, and doxorubicin without affecting tumoricidal activity. PLoS One 2008;3(6):e2355. DOI: 10.1371/journal.pone.0002355</mixed-citation></ref><ref id="B100"><label>100.</label><mixed-citation>Sauter K.A., Wood L.J., Wong J. et al. Doxorubicin and daunorubicin induce processing and release of interleukin-1β through activation of the NLRP3 inflammasome. Cancer Biol Ther 2011;11(12):1008–16. DOI: 10.4161/cbt.11.12.15540</mixed-citation></ref><ref id="B101"><label>101.</label><mixed-citation>Wang L., Chen Q., Qi H. et al. Doxorubicin-induced systemic inflammation is driven by upregulation of toll-like receptor TLR4 and endotoxin leakage. Cancer Res 2016;76(22):6631–42. DOI: 10.1158/0008-5472.Can-15-3034</mixed-citation></ref><ref id="B102"><label>102.</label><mixed-citation>Singh A., Kaur N., Singh G. et al. Topoisomerase I and II inhibitors: a patent review. Recent Pat Anticancer Drug Discov 2016;11(4):401–23. DOI: 10.2174/0929866523666160720095940</mixed-citation></ref><ref id="B103"><label>103.</label><mixed-citation>Yakkala P.A., Penumallu N.R., Shafi S. et al. Prospects of topoisomerase inhibitors as promising anti-cancer agents. Pharmaceuticals (Basel) 2023;16(10):1456. DOI: 10.3390/ph16101456</mixed-citation></ref><ref id="B104"><label>104.</label><mixed-citation>Kim G.M., Kim Y.S., Ae Kang Y. et al. Efficacy and toxicity of belotecan for relapsed or refractory small cell lung cancer patients. J Thorac Oncol 2012;7(4):731–6. DOI: 10.1097/JTO.0b013e31824b23cb</mixed-citation></ref><ref id="B105"><label>105.</label><mixed-citation>Dang X., Ogbu S.C., Zhao J. et al. Inhibition of topoisomerase IIA (Top2α) induces telomeric DNA damage and T cell dysfunction during chronic viral infection. Cell Death Dis 2020;11(3):196. DOI: 10.1038/s41419-020-2395-2</mixed-citation></ref><ref id="B106"><label>106.</label><mixed-citation>Rialdi A., Campisi L., Zhao N. et al. Topoisomerase 1 inhibition suppresses inflammatory genes and protects from death by inflammation. Science 2016;352(6289):aad7993. DOI: 10.1126/science.aad7993</mixed-citation></ref><ref id="B107"><label>107.</label><mixed-citation>Haggerty T.J., Dunn I.S., Rose L.B. et al. Topoisomerase inhibitors modulate expression of melanocytic antigens and enhance T cell recognition of tumor cells. Cancer Immunol Immunother 2011;60(1):133–44. DOI: 10.1007/s00262-010-0926-x</mixed-citation></ref><ref id="B108"><label>108.</label><mixed-citation>Wan S., Pestka S., Jubin R.G. et al. Chemotherapeutics and radiation stimulate MHC class I expression through elevated interferon-beta signaling in breast cancer cells. PLoS One 2012;7(3):e32542. DOI: 10.1371/journal.pone.0032542</mixed-citation></ref><ref id="B109"><label>109.</label><mixed-citation>Mckenzie J.A., Mbofung R.M., Malu S. et al. The effect of topoisomerase i inhibitors on the efficacy of T-cell-based cancer immunotherapy. J Natl Cancer Inst 2018;110(7):777–86. DOI: 10.1093/jnci/djx257</mixed-citation></ref><ref id="B110"><label>110.</label><mixed-citation>Lee J.-M., Shin K.-S., Koh C.-H. et al. Inhibition of topoisomerase I shapes antitumor immunity through the induction of monocyte-derived dendritic cells. Cancer Lett 2021;520:38–47. DOI: 10.1016/j.canlet.2021.06.031</mixed-citation></ref><ref id="B111"><label>111.</label><mixed-citation>Iwai T., Sugimoto M., Wakita D. et al. Topoisomerase I inhibitor, irinotecan, depletes regulatory T cells and up-regulates MHC class I and PD-L1 expression, resulting in a supra-additive antitumor effect when combined with anti-PD-L1 antibodies. Oncotarget 2018;9(59):31411–21. DOI: 10.18632/oncotarget.25830</mixed-citation></ref><ref id="B112"><label>112.</label><mixed-citation>Matsuura H.N., Fett-Neto A.G. Plant alkaloids: main features, toxicity, and mechanisms of action. In: Plant toxins. Ed. by P. Gopalakrishnakone, C.R. Carlini, R. Ligabue-Braun. Dordrecht: Springer Netherlands, 2015. Pp. 1–15.</mixed-citation></ref><ref id="B113"><label>113.</label><mixed-citation>Khan H., Alam W., Alsharif K.F. et al. Alkaloids and colon cancer: molecular mechanisms and therapeutic implications for cell cycle arrest. Molecules 2022;27(3):920. DOI: 10.3390/molecules27030920</mixed-citation></ref><ref id="B114"><label>114.</label><mixed-citation>Taub J.W., Buck S.A., Xavier A.C. et al. The evolution and history of vinca alkaloids: from the big bang to the treatment of pediatric acute leukemia. Pediatr Blood Cancer 2024;71(11):e31247. DOI: 10.1002/pbc.31247</mixed-citation></ref><ref id="B115"><label>115.</label><mixed-citation>Markman J., Zanotti K., Webster K. et al. Experience with the management of neutropenia in gynecologic cancer patients receiving carboplatin-based chemotherapy. Gynecol Oncol 2004;92(2):592–5. DOI: 10.1016/j.ygyno.2003.11.005</mixed-citation></ref><ref id="B116"><label>116.</label><mixed-citation>Markman M. Management of toxicities associated with the administration of taxanes. Exp Opin Drug Saf 2003;2(2):141–6. DOI: 10.1517/14740338.2.2.141</mixed-citation></ref><ref id="B117"><label>117.</label><mixed-citation>Beretta G.L., Cassinelli G., Rossi G. et al. Novel insights into taxane pharmacology: An update on drug resistance mechanisms, immunomodulation and drug delivery strategies. Drug Resist Updates 2025;81:101223. DOI: 10.1016/j.drup.2025.101223</mixed-citation></ref><ref id="B118"><label>118.</label><mixed-citation>Serpico A.F., Pisauro C., Grieco D. cGAS-dependent proinflammatory and immune homeostatic effects of the microtubule-targeting agent paclitaxel. Front Immunol 2023;14:1127623. DOI: 10.3389/fimmu.2023.1127623</mixed-citation></ref><ref id="B119"><label>119.</label><mixed-citation>Kaneno R., Shurin G.V., Tourkova I.L. et al. Chemomodulation of human dendritic cell function by antineoplastic agents in low noncytotoxic concentrations. J Translat Med 2009;7(1):58. DOI: 10.1186/1479-5876-7-58</mixed-citation></ref><ref id="B120"><label>120.</label><mixed-citation>Pfannenstiel L.W., Lam S.S., Emens L.A. et al. Paclitaxel enhances early dendritic cell maturation and function through TLR4 signaling in mice. Cell Immunol 2010;263(1):79–87. DOI: 10.1016/j.cellimm.2010.03.001</mixed-citation></ref><ref id="B121"><label>121.</label><mixed-citation>Ramakrishnan R., Assudani D., Nagaraj S. et al. Chemotherapy enhances tumor cell susceptibility to CTL-mediated killing during cancer immunotherapy in mice. J Clin Invest 2010;120(4):1111–24. DOI: 10.1172/jci40269</mixed-citation></ref><ref id="B122"><label>122.</label><mixed-citation>Pellicciotta I., Yang C.P., Goldberg G.L. et al. Epothilone B enhances class I HLA and HLA-A2 surface molecule expression in ovarian cancer cells. Gynecol Oncol 2011;122(3):625–31. DOI: 10.1016/j.ygyno.2011.05.007</mixed-citation></ref><ref id="B123"><label>123.</label><mixed-citation>Wanderley C.W., Colón D.F., Luiz J.P.M. et al. Paclitaxel reduces tumor growth by reprogramming tumor-associated macrophages to an M1 profile in a TLR4-dependent manner. Cancer Res 2018;78(20):5891–900. DOI: 10.1158/0008-5472.Can-17-3480</mixed-citation></ref><ref id="B124"><label>124.</label><mixed-citation>Dos Santos Guimarães I., Ladislau-Magescky T., Tessarollo N.G. et al. Chemosensitizing effects of metformin on cisplatin- and paclitaxelresistant ovarian cancer cell lines. Pharmacol Rep 2018;70(3):409–17. DOI: 10.1016/j.pharep.2017.11.007</mixed-citation></ref><ref id="B125"><label>125.</label><mixed-citation>Pusztai L., Mendoza T.R., Reuben J.M. et al. Changes in plasma levels of inflammatory cytokines in response to paclitaxel chemotherapy. Cytokine 2004;25(3):94–102. DOI: 10.1016/j.cyto.2003.10.004</mixed-citation></ref><ref id="B126"><label>126.</label><mixed-citation>Laha D., Grant R., Mishra P. et al. The role of tumor necrosis factor in manipulating the immunological response of tumor microenvironment. Front Immunol 2021;12:656908. DOI: 10.3389/fimmu.2021.656908</mixed-citation></ref><ref id="B127"><label>127.</label><mixed-citation>Tsavaris N., Kosmas C., Vadiaka M. et al. Immune changes in patients with advanced breast cancer undergoing chemotherapy with taxanes. Br J Cancer 2002;87(1):21–7. DOI: 10.1038/sj.bjc.6600347</mixed-citation></ref><ref id="B128"><label>128.</label><mixed-citation>Sun Y., Ma X., Hu H. Application of nano-drug delivery system based on cascade technology in cancer treatment. Int J Mol Sci 2021;22(11):5698. DOI: 10.3390/ijms22115698</mixed-citation></ref><ref id="B129"><label>129.</label><mixed-citation>D’incalci M., Badri N., Galmarini C.M. et al. Trabectedin, a drug acting on both cancer cells and the tumour microenvironment. Br J Cancer 2014;111(4):646–50. DOI: 10.1038/bjc.2014.149</mixed-citation></ref><ref id="B130"><label>130.</label><mixed-citation>Germano G., Frapolli R., Belgiovine C. et al. Role of macrophage targeting in the antitumor activity of trabectedin. Cancer Cell 2013;23(2):249–62. DOI: 10.1016/j.ccr.2013.01.008</mixed-citation></ref><ref id="B131"><label>131.</label><mixed-citation>Blackburn G.L. Metabolic considerations in management of surgical patients. Surg Clin North Am 2011;91(3):467–80. DOI: 10.1016/j.suc.2011.03.001</mixed-citation></ref><ref id="B132"><label>132.</label><citation-alternatives><mixed-citation xml:lang="en">Kadagidze Z.G., Chertkova A.I. The immune system and cancer. Prakticheskaya onkologiya = Practical Oncology 2016;17(2):62–73. (In Russ.). DOI: 10.31917/1702062</mixed-citation><mixed-citation xml:lang="ru">Кадагидзе З.Г., Черткова А.И. Иммунная система и рак. Практическая онкология 2016;17(2):62–73. DOI: 10.31917/1702062</mixed-citation></citation-alternatives></ref><ref id="B133"><label>133.</label><mixed-citation>Hiam-Galvez K.J., Allen B.M., Spitzer M.H. Systemic immunity in cancer. Nat Rev Cancer 2021;21(6):345–59. DOI: 10.1038/s41568-021-00347-z</mixed-citation></ref><ref id="B134"><label>134.</label><mixed-citation>Zou W., Wolchok J.D., Chen L. PD-L1 (B7-H1) and PD-1 pathway blockade for cancer therapy: mechanisms, response biomarkers, and combinations. Sci Transl Med 2016;8(328):328rv324. DOI: 10.1126/scitranslmed.aad7118</mixed-citation></ref><ref id="B135"><label>135.</label><mixed-citation>Tilsed C.M., Fisher S.A., Nowak A.K. et al. Cancer chemotherapy: insights into cellular and tumor microenvironmental mechanisms of action. Front Oncol 2022;12:960317. DOI: 10.3389/fonc.2022.960317</mixed-citation></ref><ref id="B136"><label>136.</label><citation-alternatives><mixed-citation xml:lang="en">Novik A.V., Protsenko S.A., Baldueva I.A. The use of assessment of the state of the adaptive immune system in patients with malignant solid tumors as predictive or prognostic factors: a systematic review. Effektivnaya farmakoterapiya = Effective Pharmacotherapy 2020;16(33): 58–75. (In Russ.). DOI: 10.33978/2307-3586-2020-16-33-58-75</mixed-citation><mixed-citation xml:lang="ru">Новик А.В., Проценко С.А., Балдуева И.А. Использование оценки состояния адаптивной иммунной системы у больных со злокачественными солидными опухолями в качестве предиктивных или прогностических факторов: систематический обзор. Эффективная фармакотерапия 2020;16(33):58–75. DOI: 10.33978/2307-3586-2020-16-33-58-75</mixed-citation></citation-alternatives></ref><ref id="B137"><label>137.</label><citation-alternatives><mixed-citation xml:lang="en">Artamonova E.V. The place of immunomodulators in breast cancer therapy. Opukholi zhenskoy reproduktivnoy sistemy = Tumors of the Female Reproductive System 2007;1(2):23–6. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Артамонова Е.В. Место иммуномодуляторов в терапии рака молочной железы. Опухоли женской репродуктивной системы 2007;1(2):23–6.</mixed-citation></citation-alternatives></ref><ref id="B138"><label>138.</label><citation-alternatives><mixed-citation xml:lang="en">Sagakyants A.B., Belyakova L.I., Shevchenko A.N. et al. Features of local immunity in patients with noninvasive muscular bladder cancer of varying degrees of malignancy. Yuzhno-Rossiyskiy onkologicheskiy zhurnal = South Russian Journal of Oncology 2022;3(4):58–66. (In Russ.). DOI: 10.37748/2686-9039-2022-3-4-6</mixed-citation><mixed-citation xml:lang="ru">Сагакянц А.Б., Белякова Л.И., Шевченко А.Н. и др. Особенности локального иммунитета у пациентов с неинвазивномышечным раком мочевого пузыря различной степени злокачественности. Южно-Российский онкологический журнал 2022;3(4):58–66. DOI: 10.37748/2686-9039-2022-3-4-6</mixed-citation></citation-alternatives></ref><ref id="B139"><label>139.</label><citation-alternatives><mixed-citation xml:lang="en">Staheeva M.N., Eidenzon D., Slonimskaya E.M. et al. The relationship of the state of the immune system as an integrated whole with the clinical course of breast cancer. Sibirskiy onkologicheskiy zhurnal = Siberian Journal of Oncology 2011;2(44):11–9. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Стахеева М.Н., Эйдензон Д., Слонимская Е.М. и др. Взаимосвязь состояния иммунной системы как интегрированного целого с клиническим течением рака молочной железы. Сибирский онкологический журнал 2011;2(44):11–9.</mixed-citation></citation-alternatives></ref><ref id="B140"><label>140.</label><mixed-citation>Stakheyeva M., Eidenzon D., Slonimskaya E. et al. Integral characteristic of the immune system state predicts breast cancer outcome. Exp Oncol 2019;41(1):32–8.</mixed-citation></ref><ref id="B141"><label>141.</label><mixed-citation>Adhikary S., Pathak S., Palani V. et al. Current technologies and future perspectives in immunotherapy towards a clinical oncology approach. Biomedicines 2024;12(1):217. DOI: 10.3390/biomedicines12010217</mixed-citation></ref><ref id="B142"><label>142.</label><citation-alternatives><mixed-citation xml:lang="en">Rybkina V.L., Adamova G.V., Oslina D.S. The role of cytokines in the pathogenesis of malignant neoplasms. Sibirskiy onkologicheskiy zhurnal = Siberian Journal of Oncology 2023;43(2):15–28. DOI: 10.18699/SSMJ20230202</mixed-citation><mixed-citation xml:lang="ru">Рыбкина В.Л., Адамова Г.В., Ослина Д.С. Роль цитокинов в патогенезе злокачественных новообразований. Сибирский научный медицинский журнал 2023;43(2):15–28. DOI: 10.18699/SSMJ20230202</mixed-citation></citation-alternatives></ref><ref id="B143"><label>143.</label><mixed-citation>Fu Y., Tang R., Zhao X. Engineering cytokines for cancer immunotherapy: a systematic review. Front Immunol 2023;14:1218082. DOI: 10.3389/fimmu.2023.1218082</mixed-citation></ref><ref id="B144"><label>144.</label><citation-alternatives><mixed-citation xml:lang="en">Vladimirova L.Yu., Nepomnyashchaya E.M., Podzorova N.A. et al. Recombinant tumor necrosis factor-thymosin-a1: effect on the effectiveness of neoadjuvant chemotherapy and neoangiogenesis in breast cancer. Voprosy onkologii = Oncology Issues 2017;63(1):76–81. (In Russ.). DOI: 10.37469/0507-3758-2017-63-1-76-81</mixed-citation><mixed-citation xml:lang="ru">Владимирова Л.Ю., Непомнящая Е.М., Подзорова Н.А. и др. Рекомбинантный фактор некроза опухоли-тимозин-α1: влияние на эффективность неоадъювантной химиотерапии и неоангиогенез при раке молочной железы. Вопросы онкологии 2017;63(1):76–81. DOI: 10.37469/0507-3758-2017-63-1-76-81</mixed-citation></citation-alternatives></ref><ref id="B145"><label>145.</label><citation-alternatives><mixed-citation xml:lang="en">Ilyushin A.L., Bogdashin I.V., Aleksanyan A.Z. et al. Interferon-γ and tumor growth. Sibirskiy onkologicheskiy zhurnal = Siberian Journal of Oncology 2023;22(4):118–27. (In Russ.). DOI: 10.21294/1814-4861-2023-22-4-118-127</mixed-citation><mixed-citation xml:lang="ru">Илюшин А.Л., Богдашин И.В., Алексанян А.З. и др. Интерферон-γ и опухолевый рост. Сибирский онкологический журнал 2023;22(4):118–27. DOI: 10.21294/1814-4861-2023-22-4-118-127</mixed-citation></citation-alternatives></ref><ref id="B146"><label>146.</label><citation-alternatives><mixed-citation xml:lang="en">Isaeva V.G., Grivtsova L.Y., Zhovtun L.P. et al. Antitumor effect of recombinant interferon-gamma in an experimental model of Ehrlich’s bilateral solid carcinoma. Uspekhi molekulyarnoy onkologii = Advances in Molecular Oncology 2022;9(2):111–9. (In Russ.). DOI: 10.17650/2313-805X-2022-9-2-111-119</mixed-citation><mixed-citation xml:lang="ru">Исаева В.Г., Гривцова Л.Ю., Жовтун Л.П. и др. Противоопухолевый эффект рекомбинантного интерферона гамма в экспериментальной модели билатеральной солидной карциномы Эрлиха. Успехи молекулярной онкологии 2022;9(2):111–9. DOI: 10.17650/2313-805X-2022-9-2-111-119</mixed-citation></citation-alternatives></ref><ref id="B147"><label>147.</label><citation-alternatives><mixed-citation xml:lang="en">Staheeva M.N., Bogdashin I.V., Tarabanovskaya N.A. et al. A clinical case of inhaled cytokines in a breast cancer patient with lung tumors of unknown origin. Immunologiya = Immunology 2024;45(3):321–8. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Стахеева М.Н., Богдашин И.В., Тарабановская Н.А. и др. Клинический случай ингаляционного применения цитокинов у больной раком молочной железы с образованиями в легком неясного генеза. Иммунология 2024;45(3):321–8.</mixed-citation></citation-alternatives></ref><ref id="B148"><label>148.</label><mixed-citation>Galluzzi L., Vitale I., Warren S. et al. Consensus guidelines for the definition, detection and interpretation of immunogenic cell death. J Immunother Cancer 2020;8(1):e000337. DOI: 10.1136/jitc-2019-000337</mixed-citation></ref><ref id="B149"><label>149.</label><mixed-citation>Galluzzi L., Buqué A., Kepp O. et al. Immunological effects of conventional chemotherapy and targeted anticancer agents. Cancer Cell 2015;28(6):690–714. DOI: 10.1016/j.ccell.2015.10.012</mixed-citation></ref><ref id="B150"><label>150.</label><mixed-citation>Bailly C., Thuru X., Quesnel B. Combined cytotoxic chemotherapy and immunotherapy of cancer: modern times. NAR Cancer 2020;2(1):zcaa002. DOI: 10.1093/narcan/zcaa002</mixed-citation></ref></ref-list></back></article>
