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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="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Russian Journal of Oncology</journal-id><journal-title-group><journal-title xml:lang="en">Russian Journal of Oncology</journal-title><trans-title-group xml:lang="ru"><trans-title>Российский онкологический журнал</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1028-9984</issn><issn publication-format="electronic">2412-9119</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">700721</article-id><article-id pub-id-type="doi">10.17816/onco700721</article-id><article-id pub-id-type="edn">ZROONG</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Original Study Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Оригинальные исследования</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">The level of serum soluble E-cadherin as an indicator of prognosis in patients with aggressive B-cell lymphomas</article-title><trans-title-group xml:lang="ru"><trans-title>Уровень сывороточного растворимого Е-кадгерина как показатель прогноза у пациентов с агрессивными В-клеточными лимфомами</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Komarov</surname><given-names>Andrey S.</given-names></name><name xml:lang="ru"><surname>Комаров</surname><given-names>Андрей Сергеевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>andrey_komarow@inbox.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1136-7396</contrib-id><contrib-id contrib-id-type="spin">4541-8220</contrib-id><name-alternatives><name xml:lang="en"><surname>Shestakova</surname><given-names>Valeriya G.</given-names></name><name xml:lang="ru"><surname>Шестакова</surname><given-names>Валерия Геннадьевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD, Dr. Sci. (Medicine), Assistant Professor</p></bio><bio xml:lang="ru"><p>д-р мед. наук, доцент</p></bio><email>shestvg@mail.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9777-1220</contrib-id><contrib-id contrib-id-type="spin">4312-9786</contrib-id><name-alternatives><name xml:lang="en"><surname>Dolgopolov</surname><given-names>Igor S.</given-names></name><name xml:lang="ru"><surname>Долгополов</surname><given-names>Игорь Станиславович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD, Dr. Sci. (Medicine)</p></bio><bio xml:lang="ru"><p>д-р мед. наук</p></bio><email>irdolgopolov@gmail.com</email><xref ref-type="aff" rid="aff3"/><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7865-0984</contrib-id><name-alternatives><name xml:lang="en"><surname>Slyusar</surname><given-names>Nikolai N.</given-names></name><name xml:lang="ru"><surname>Слюсарь</surname><given-names>Николай Николаевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD, Cand. Sci. (Medicine)</p></bio><bio xml:lang="ru"><p>канд. мед. наук</p></bio><email>slusar2011@rambler.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0004-5106-9582</contrib-id><name-alternatives><name xml:lang="en"><surname>Chernyayeva</surname><given-names>Elena A.</given-names></name><name xml:lang="ru"><surname>Черняева</surname><given-names>Елена Анатольевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>martus12345@yandex.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8398-7001</contrib-id><contrib-id contrib-id-type="spin">7652-0122</contrib-id><name-alternatives><name xml:lang="en"><surname>Rykov</surname><given-names>Maxim Yu.</given-names></name><name xml:lang="ru"><surname>Рыков</surname><given-names>Максим Юрьевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD, Dr. Sci. (Medicine), Assistant Professor, Head of the Department of Pediatrics</p></bio><bio xml:lang="ru"><p>д-р мед. наук, доцент, заведующий кафедрой педиатрии</p></bio><email>wordex2006@rambler.ru</email><xref ref-type="aff" rid="aff4"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Tver Regional Clinical Oncology Dispensary, Tver</institution></aff><aff><institution xml:lang="ru">Тверской областной клинический онкологический диспансер, Тверь</institution></aff><aff><institution xml:lang="kk"></institution></aff><aff><institution xml:lang="pt"></institution></aff><aff><institution xml:lang="zh"></institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Tver State Medical University, Tver</institution></aff><aff><institution xml:lang="ru">Тверской государственный медицинский университет, Тверь</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Neurovita Clinical Hospital, Moscow</institution></aff><aff><institution xml:lang="ru">Клинический госпиталь «НейроВита», Москва</institution></aff></aff-alternatives><aff-alternatives id="aff4"><aff><institution xml:lang="en">Russian State Social University, Moscow</institution></aff><aff><institution xml:lang="ru">Российский государственный социальный университет, Москва</institution></aff></aff-alternatives><pub-date date-type="preprint" iso-8601-date="2026-05-04" publication-format="electronic"><day>04</day><month>05</month><year>2026</year></pub-date><volume>31</volume><issue>1</issue><issue-title xml:lang="ru"/><history><date date-type="received" iso-8601-date="2026-01-13"><day>13</day><month>01</month><year>2026</year></date><date date-type="accepted" iso-8601-date="2026-03-25"><day>25</day><month>03</month><year>2026</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; , Eco-Vector</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; , Эко-Вектор</copyright-statement><copyright-holder xml:lang="en">Eco-Vector</copyright-holder><copyright-holder xml:lang="ru">Эко-Вектор</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/" start_date="2029-03-27"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://eco-vector.com/for_authors.php#07</ali:license_ref></license></permissions><self-uri xlink:href="https://rjonco.com/1028-9984/article/view/700721">https://rjonco.com/1028-9984/article/view/700721</self-uri><abstract xml:lang="en"><p><bold>Introduction. </bold>Criteria for the effectiveness of therapy and the prognosis of disease development remain an urgent problem in oncology. The study of prognostic markers in blood serum is a promising way to track the dynamics of B—cell lymphomas during therapy..</p> <p><bold>Aim.</bold> To analyze the relationship between the presence of a tumor process and the level of the marker E-cadherin.</p> <p><bold>Materials and Methods. </bold>The study included 53 patients (30 men, 23 women) with B-cell lymphomas (stage 1 — 1 patient, stage 2A/2B — 9, 3A/3B — 9, 4A/4B — 34 patients). The level of soluble E-cadherin (sEcad) was determined before the start of treatment, after the third and sixth courses of CT. The dynamics of sEcad levels were performed both in the general group of patients and separately in subgroups of patients without and with recurrent lymphomas. The subgroups were comparable in age and stages of the disease. The control group consisted of 25 people (18 men, 7 women) without oncological pathology. The average age in the study and control groups was 61.2±2.1 (95% CI 57.1–65.3) versus 60.0±2.6 years (95% CI 49.7–60.3), p=0.08. As a normal value (in patients without tumor disease), we assumed a sEcad level of 1.0 ng/ml..</p> <p><bold>Results. </bold>Lymphoma recurrence was observed in 22 (42%) of 53 patients. Seven (13%) patients died of other non-tumor related causes, 1 (2%) patient lost to follow-up. E-cadherin level in the general group before the start of treatment was 3.7 ± 0.4 ng/ml, compared with 0.9 ± 0.1 ng/ml in the control group, p &lt;0.0001. During the therapy, a decrease in the level of E-cadherin was observed after the third and sixth courses of CT to 2.8 ± 0.3 ng/ml and 2.4 ± 0.4 ng/ml, respectively. In the subgroups without relapse (n = 31) and with relapse of lymphomas (n = 22), serum E-cadherin levels before therapy, after three and six courses of chemotherapy were 3.5 ± 0.4, 2.4 ± 0.3 and 1.5 ± 0.2 ng/ml versus 4.1 ± 0.9, 3.4 ± 0.5 and 3.5 ± 0.7 ng/ml, p = 0.5, p = 0.1 and p = 0.003, respectively. Serum E-cadherin level in patients without relapse significantly decreased after 6 courses of CT compared to the time of diagnosis (p = 0.0001). Relapse-free survival (RFS) in the overall patient group was 50.3 ± 8%, with a median follow-up of 43.9 ± 5.2 months. RFS at E-cadherin levels ≤ 1.0 ng/mL and&gt; 1.0 ng/mL after six courses of chemotherapy was 58.3 ± 16% versus 43.3 ± 11% with a mean follow-up of 46.4 ± 10.3 months versus 28.2 ± 4.1 months, respectively (p = 0.045).</p> <p><bold>Conclusions.</bold> The risk of B-lymphoma recurrence is lower at sEcad &lt;1.0 ng/ml after six courses of therapy than at higher values of this marker. A decrease in this marker during treatment indicates a good response to therapy. For further research, it is necessary to expand the observation groups and standardize methods for determining the sEcad level.</p></abstract><trans-abstract xml:lang="ru"><p><bold>Обоснование. </bold>Критерии эффективности терапии и прогноз развития болезни остаются актуальной проблемой онкологии. Изучение прогностических маркёров в сыворотке крови — перспективный способ отслеживания динамики В-клеточных лимфом на фоне терапии.</p> <p><bold>Цель. </bold>Проанализировать<bold> </bold>связь между наличием опухолевого процесса и уровнем маркёра Е-кадгерина.</p> <p><bold>Методы. </bold>В исследование вошли 53 пациента (30 мужчин, 23 женщины) с В-клеточными лимфомами (1 стадия — 1 пациент, 2А/2В стадия — 9, 3А/3В — 9, 4А/4В — 34 пациента). Уровень растворимого Е-кадгерина (sEcad) определяли перед началом лечения, после третьего и шестого курсов ХТ. Динамику уровня sEcad осуществляли как в общей группе пациентов, так и раздельно в подгруппах пациентов без рецидива и с рецидивом лимфом. Подгруппы были сравнимы по возрасту и стадиям заболевания. Группу контроля составили 25 человек (18 мужчин, 7 женщин) без онкологической патологии. В качестве нормального значения (у пациентов без опухолевого заболевания) принимали уровень sEcad ≤1,0 нг/мл.</p> <p><bold>Результаты. </bold>Рецидив лимфомы наблюдался у 22-х (42%) из 53-х пациентов. Умерло от других причин, не связанных с опухолью, — 7 (13%) пациентов, один (2%) пациент потерян из наблюдения. Уровень sEcad в общей группе пациентов до начала лечения составил 3,7±0,4 нг/мл по сравнению с 0,9±0,1 нг/мл в контрольной группе, <italic>р </italic>&lt;0,0001. В процессе терапии наблюдалось снижение уровня sEcad после третьего и шестого курсов ХТ до 2,8±0,3 нг/мл и 2,4±0,4 нг/мл. В подгруппах без рецидива (<italic>n</italic>=31) и с рецидивом лимфом (<italic>n</italic>=22) уровни sEcad до начала терапии, после трёх и шести курсов ХТ, составили 3,5±0,4, 2,4±0,3 и 1,5±0,2 нг/мл против 4,1±0,9, 3,4±0,5 и 3,5±0,7 нг/мл, <italic>р</italic>=0,5, <italic>р</italic>=0,1 и <italic>р</italic>=0,003 соответственно. Уровень sEcad у пациентов без рецидива достоверно снизился после 6-ти курсов ХТ по сравнению с моментом постановки диагноза (<italic>р</italic>=0,0001). Безрецидивная выживаемость (БРВ) в общей группе пациентов составила 50,3±8%, средний период наблюдения 43,9±5,2 мес. БРВ при уровне sEcad ≤1,0 нг/мл и &gt;1,0 нг/мл после шести курсов ХТ составила 58,3±16% против 43,3±11% при среднем сроке наблюдения 46,4±10,3 мес. против 28,2±4,1 мес. соответственно (<italic>р</italic>=0,045).</p> <p><bold>Заключение. </bold>Риск рецидива В-лимфомы ниже при уровне sEcad ≤1,0 нг/мл после шести курсов терапии, чем при более высоких значениях данного маркёра. Снижение этого маркёра во время лечения свидетельствует о хорошем ответе на терапию. Для дальнейших исследований нужно расширить группы наблюдения и стандартизировать методы определения уровня sEcad.</p></trans-abstract><kwd-group xml:lang="en"><kwd>serum soluble E-cadherin, intercellular interaction, B-cell lymphoma, relapse-free survival, prognosis factor.</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>сывороточный растворимый Е-кадгерин</kwd><kwd>межклеточное взаимодействие</kwd><kwd>В-клеточная лимфома</kwd><kwd>безрецидивная выживаемость</kwd><kwd>фактор прогноза.</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Sawalha Y. Relapsed/Refractory Diffuse Large B-Cell Lymphoma: A Look at the Approved and Emerging Therapies. J Pers Med. 2021;11(12):1345. doi: 10.3390/jpm11121345 EDN: OCUWEG</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Li J, Liu X, Yao Z, Zhang M. 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