<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<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="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Journal of Modern Oncology</journal-id><journal-title-group><journal-title xml:lang="en">Journal of Modern Oncology</journal-title><trans-title-group xml:lang="ru"><trans-title>Современная онкология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1815-1434</issn><issn publication-format="electronic">1815-1442</issn><publisher><publisher-name xml:lang="en">LLC Obyedinennaya Redaktsiya</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">80647</article-id><article-id pub-id-type="doi">10.26442/18151434.2021.3.201138</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>CLINICAL ONCOLOGY</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>КЛИНИЧЕСКАЯ ОНКОЛОГИЯ</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Antiangiogenic therapy in pretreated patients with lung adenocarcinoma without activating mutations: new features</article-title><trans-title-group xml:lang="ru"><trans-title>Антиангиогенная терапия у предлеченных больных с аденокарциномой легкого без активирующих мутаций: новые возможности</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2154-3376</contrib-id><name-alternatives><name xml:lang="en"><surname>Reutova</surname><given-names>Elena V.</given-names></name><name xml:lang="ru"><surname>Реутова</surname><given-names>Елена Валерьевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Cand. Sci. (Med.)</p></bio><bio xml:lang="ru"><p>канд. мед. наук, ст. науч. сотр. онкологического отд-ния лекарственных методов лечения (химиотерапевтическое) №17</p></bio><email>reutova.ev@bk.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4469-502X</contrib-id><name-alternatives><name xml:lang="en"><surname>Laktionov</surname><given-names>Konstantin K.</given-names></name><name xml:lang="ru"><surname>Лактионов</surname><given-names>Константин Константинович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>D. Sci. (Med.), Prof.</p></bio><bio xml:lang="ru"><p>д-р мед. наук, проф., зав. онкологическим отд-нием лекарственных методов лечения (химиотерапевтическое) №17</p></bio><email>lkoskos@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Blokhin National Medical Research Center of Oncology</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр онкологии им. Н.Н. Блохина» Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2021-11-19" publication-format="electronic"><day>19</day><month>11</month><year>2021</year></pub-date><volume>23</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>425</fpage><lpage>427</lpage><history><date date-type="received" iso-8601-date="2021-09-20"><day>20</day><month>09</month><year>2021</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2021, Consilium Medicum</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2021, ООО "Консилиум Медикум"</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="en">Consilium Medicum</copyright-holder><copyright-holder xml:lang="ru">ООО "Консилиум Медикум"</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-nc/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://modernonco.orscience.ru/1815-1434/article/view/80647">https://modernonco.orscience.ru/1815-1434/article/view/80647</self-uri><abstract xml:lang="en"><p>The possibilities of treatment of patients with metastatic non-small cell lung cancer have significantly expanded in the recent years. Several combined regimens of chemoimmunotherapy are currently being proposed as the first line, some patients with PD-L1 overexpression may be prescribed pembrolizumab or atezolizumab in monotherapy. Standard platinum-containing chemotherapy (PCT) has lost its position and is relevant only for contraindications to immuno-oncological (IO) drugs. The change in the standart of the first line inevitably led to the search for new optimal modes of the second line. The strategy of "angio-immunogenic switching" is promising – after progression on the regimens with IO, anti-angiogenic drugs are used. Nintedanib – a multikinase angiogenesis inhibitor in combination with docetaxel is a standard second-line therapy option in patients with lung adenocarcinoma after progression on PCT. The effectiveness of this regimen is being studied in a prospective non-interventional VARGADO study. The patients were divided into 3 cohorts, depending on which regimen was used earlier – one line of PCT or PCT, followed by IO or chemoimmunotherapy. The results showed that the combination of docetaxel + nintedanib was effective both as a third line (after PCT and IO), and in the second – after chemoimmunotherapy. The research is ongoing.</p></abstract><trans-abstract xml:lang="ru"><p>Возможности лекарственного лечения больных немелкоклеточным раком легкого в последние годы существенным образом расширились. В качестве 1-й линии сейчас предлагается несколько комбинированных химиоиммунотерапевтических режимов, некоторым больным с гиперэкспрессией PD-L1 могут быть назначены пембролизумаб или атезолизумаб в монотерапии. Стандартная платиносодержащая химиотерапия (ПХТ) уступила свои позиции и актуальна лишь при противопоказаниях к иммуноонкологическим (ИО) препаратам. Изменение стандартов 1-й линии неизбежно привело к поиску новых оптимальных режимов 2-й линии. Перспективной представляется стратегия «ангиоиммуногенного переключения» – после прогрессирования на режимах с ИО применить антиангиогенные препараты. Нинтеданиб – мультикиназный ингибитор ангиогенеза в комбинации с доцетакселом – является стандартной опцией 2-й линии терапии у больных с аденокарциномой легкого после прогрессирования на ПХТ. Эффективность данного режима прицельно изучается в проспективном неинтервенционном исследовании VARGADO. Пациенты распределены в 3 когорты в зависимости от того, какой режим применялся ранее, – одна линия ПХТ или ПХТ затем ИО-терапия или химиоиммунотерапия. Как показали результаты, комбинация доцетаксел + нинтеданиб оказалась эффективной как в качестве 3-й линии (после ПХТ и ИО-терапии), так и во 2-й – после химиоиммунотерапии. Исследование продолжается.</p></trans-abstract><kwd-group xml:lang="en"><kwd>non-small cell lung cancer</kwd><kwd>adenocarcinoma</kwd><kwd>chemotherapy</kwd><kwd>immunotherapy</kwd><kwd>angiogenesis inhibitors</kwd><kwd>docetaxel</kwd><kwd>nintedanib</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>немелкоклеточный рак легкого</kwd><kwd>аденокарцинома</kwd><kwd>химиотерапия</kwd><kwd>иммунотерапия</kwd><kwd>ингибиторы ангиогенеза</kwd><kwd>доцетаксел</kwd><kwd>нинтеданиб</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Jenkins RW, Barbie DA, Flaherty KT. Mechanisms of resistance to immune checkpoint inhibitors. Br J Cancer. 2018;118:9-16.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Popat S, Grohé C, Corral J, et al. Anti-angiogenic agents in the age of resistance to immune checkpoint inhibitors: do they have a role in non-oncogene-addicted non-small cell lung cancer? Lung Cancer. 2020;144:76-84.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Fukumura D, Kloepper J, Amoozgar Z, et al. Enhancing cancer immunotherapy using antiangiogenics: opportunities and challenges. Nat Rev Clin Oncol. 2018;15:325-40.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Hilberg F, Roth GJ, Krssak M, et al. BIBF 1120: Triple Angiokinase Inhibitor with Sustained Receptor Blockade and Good Antitumor Efficacy. Cancer Res. 2008;68(12):4774-82. DOI:10.1158/0008-5472.CAN-07-6307</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Режим доступа: https://www.ema.europa.eu/en/documents/product-information/vargatef-epar-product-information_en.pdf. Ссылка активна на 28.06.2021 [Available at: https://www.ema.europa.eu/en/documents/product-information/vargatef-epar-product-information_en.pdf. Accessed: 28.06.2021 (in Russian)].</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Heigener D, Gottfried M, Bennouna J, et al. Efficacy and safety of nintedanib (NIN)/docetaxel (DOC) in patients with lung adenocarcinoma: Further analyses from the LUME-Lung 1 study. Ann Oncol. 2016;27(Suppl. 6):abstract 1276P and poster.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Gottfried M, Bennouna J, Bondarenko I, et al. Efficacy and Safety of Nintedanib Plus Docetaxel in Patients with Advanced Lung Adenocarcinoma: Complementary and Exploratory Analyses of the Phase III LUME-Lung 1 Study. Target Oncol. 2017;12(4):475-85. DOI:10.1007/s11523-017-0517-2</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Grohé C, Gleiber W, Haas S, et al. Efficacy and safety of nintedanib plus docetaxel in lung adenocarcinoma patients after failure of previous immune checkpoint inhibitor therapy: updated results from the ongoing non-interventional study VARGADO (NCT02392455). ESMO 2020 Virtual, Sept 19–21, 2020.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Grohé C, Wehler T, Dechow T, et al. Second-line nintedanib plus docetaxel for patients with lung adenocarcinoma after failure on first-line immune checkpoint inhibitor combination therapy: Initial efficacy and safety results from VARGADO Cohort C. J Clin Oncol. 2021;39(Suppl. 15):9033.</mixed-citation></ref></ref-list></back></article>
