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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" article-type="research-article" dtd-version="1.1d1" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher">Problems of Social Hygiene, Public Health and History of Medicine</journal-id><journal-title-group><journal-title>Problems of Social Hygiene, Public Health and History of Medicine</journal-title></journal-title-group><issn publication-format="print">0869-866X</issn><issn publication-format="electronic">2412-2106</issn><publisher><publisher-name>Joint-Stock Company Chicot</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">2782</article-id><article-id pub-id-type="doi">10.32687/0869-866X-2026-34-4-911-916</article-id><article-categories><subj-group subj-group-type="heading"><subject>Original Article</subject></subj-group></article-categories><title-group><article-title>IMPLEMENTATION OF A DYNAMIC SURVEILLANCE PROGRAM FOR EARLY CANCER DETECTION IN HEALTHY INDIVIDUALS CARRYING PATHOGENIC VARIANTS</article-title></title-group><contrib-group><contrib contrib-type="author"><name name-style="western"><surname>Bodunova</surname><given-names>N. A.</given-names></name><email></email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author"><name name-style="western"><surname>Naigovzina</surname><given-names>N. B.</given-names></name><email></email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author"><name name-style="western"><surname>Khatkov</surname><given-names>I. E.</given-names></name><email></email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author"><name name-style="western"><surname>Mineeva</surname><given-names>D. T.</given-names></name><email></email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author"><name name-style="western"><surname>Patrushev</surname><given-names>M. A.</given-names></name><email></email><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author"><name name-style="western"><surname>Bilyalov</surname><given-names>A. I.</given-names></name><email></email><xref ref-type="aff" rid="aff-1"/><xref ref-type="aff" rid="aff-4"/></contrib><contrib contrib-type="author"><name name-style="western"><surname>Danishevich</surname><given-names>A. M.</given-names></name><email></email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff id="aff-1">A. S. Loginov Moscow Clinical Scientific and Practical Center of the Moscow City Health Department, Moscow, Russian Federation, 111123</aff><aff id="aff-2">Russian University of Medicine, Moscow, Russian Federation, 127006</aff><aff id="aff-3">HSE University, Moscow, Russian Federation, 101000</aff><aff id="aff-4">LIFT — Research Center for Fundamental and Applied Biomedical Studies, Moscow, Russian Federation, 121205</aff><pub-date date-type="epub" iso-8601-date="2026-08-31" publication-format="electronic"><day>31</day><month>08</month><year>2026</year></pub-date><volume>34</volume><issue>4</issue><fpage>911</fpage><lpage>916</lpage><history><pub-date date-type="received" iso-8601-date="2026-09-01"><day>01</day><month>09</month><year>2026</year></pub-date></history><permissions><copyright-statement>Copyright © 2026,</copyright-statement><copyright-year>2026</copyright-year></permissions><abstract>The aim of the study was to develop and evaluate a multidisciplinary clinical routing model for healthy carriers of pathogenic germline variants for early cancer detection. An organizational study was conducted involving the creation of a registry of pathogenic variant carriers and implementation of a surveillance program including genetic counseling, specialist consultations, and instrumental screening. The registry included 986 carriers of pathogenic variants, including 551 clinically healthy individuals. During follow-up, 57 malignancies were detected, predominantly breast cancer; all cases were diagnosed at stages I—II. The study demonstrated that the clinical value of genetic testing is realized only within an organized system of patient routing and dynamic surveillance. The proposed model may serve as an organizational prototype for monitoring individuals at high hereditary cancer risk.</abstract><kwd-group xml:lang="en"><kwd>BRCA1</kwd><kwd>BRCA2</kwd><kwd>hereditary cancer syndromes, BRCA1, BRCA2, genetic testing, patient routing, surveillance, early diagnosis, multidisciplinary approach.</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>наследственные опухолевые синдромы</kwd><kwd>генетическое тестирование</kwd><kwd>маршрутизация пациентов</kwd><kwd>диспансерное наблюдение</kwd><kwd>ранняя диагностика</kwd><kwd>междисциплинарный подход.</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Cerretelli G, Ager A, Arends MJ, Frayling IM. Molecular pathology of Lynch syndrome. J Pathol. 2020;250(5):518—31. Doi: 10.1002/path.5422</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Daly MB, Pal T, Maxwell KN, Churpek J, Kohlmann W, AlHilli Z, и др. 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