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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">Cancer Urology</journal-id><journal-title-group><journal-title xml:lang="en">Cancer Urology</journal-title><trans-title-group xml:lang="ru"><trans-title>Онкоурология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-9776</issn><issn publication-format="electronic">1996-1812</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">974</article-id><article-id pub-id-type="doi">10.17650/1726-9776-2019-15-4-18-29</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>LECTURE</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ЛЕКЦИЯ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Basic characteristics and features of the molecular genetic test systems designed for non-invasive diagnostics and prognosis of prostate cancer and bladder cancer</article-title><trans-title-group xml:lang="ru"><trans-title>Основные характеристики и особенности молекулярно-генетических тест-систем, предназначенных для неинвазивной диагностики и оценки прогноза рака предстательной железы и рака мочевого пузыря</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9780-8708</contrib-id><name-alternatives><name xml:lang="en"><surname>Mikhaylenko</surname><given-names>D. S.</given-names></name><name xml:lang="ru"><surname>Михайленко</surname><given-names>Д. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>Build. 2, 8 Trubetskaya St., Moscow 119991, </italic></p><p><italic>513rd Parkovaya St., Moscow 105425, </italic></p><p><italic>1 Moskvorech'e St., Moscow 115522 </italic></p></bio><bio xml:lang="ru"><p><bold>Михайленко Дмитрий Сергеевич, </bold>кандидат медицинских наук, доцент, ведущий научный сотрудник отдела патологической анатомии с группой молекулярной генетики</p><p><italic>119991 Москва, ул. Трубецкая, 8, стр. 2, </italic></p><p><italic>105425 Москва, 3-я Парковая ул., 51, </italic></p><p><italic>115522 Москва, ул. Москворечье, 1 </italic></p><p> </p><p>SPIN-код: 2083-9060</p></bio><email>dimserg@mail.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Sergienko</surname><given-names>S. A.</given-names></name><name xml:lang="ru"><surname>Сергиенко</surname><given-names>С. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>513rd Parkovaya St., Moscow 105425</italic></p></bio><bio xml:lang="ru"><p><bold>Сергиенко Сергей Александрович, </bold>аспирант отдела онкоурологии</p><p><italic>105425 Москва, 3-я Парковая ул., 51</italic></p><p>SPIN-код: 4395-6905</p></bio><email>sergienko.s91@gmail.com</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3398-4128</contrib-id><name-alternatives><name xml:lang="en"><surname>Alekseev</surname><given-names>B. Ya.</given-names></name><name xml:lang="ru"><surname>Алексеев</surname><given-names>Б. Я.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>513rd Parkovaya St., Moscow 105425</italic></p></bio><bio xml:lang="ru"><p><bold>Алексеев Борис Яковлевич, </bold>заместитель генерального директора по науке</p><p><italic>105425 Москва, 3-я Парковая ул., 51</italic></p><p>SPIN-код: 4692-5705</p></bio><email>byalekseev@mail.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8784-8415</contrib-id><name-alternatives><name xml:lang="en"><surname>Kaprin</surname><given-names>A. D.</given-names></name><name xml:lang="ru"><surname>Каприн</surname><given-names>А. Д.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>513rd Parkovaya St., Moscow 105425</italic></p></bio><bio xml:lang="ru"><p><bold>Каприн Андрей Дмитриевич, </bold>генеральный директор</p><p><italic>105425 Москва, 3-я Парковая ул., 51</italic></p><p>SPIN-код: 1759-8101</p></bio><email>contact@nmicr.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2835-5992</contrib-id><name-alternatives><name xml:lang="en"><surname>Nemtsova</surname><given-names>M. V.</given-names></name><name xml:lang="ru"><surname>Немцова</surname><given-names>М. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><italic>Build. 2, 8 Trubetskaya St., Moscow 119991, </italic></p><p><italic>1 Moskvorech'e St., Moscow 115522 </italic></p></bio><bio xml:lang="ru"><p><bold>Немцова Марина Вячеславовна, </bold>заведующая лабораторией</p><p> <italic>119991 Москва, ул. Трубецкая, 8, стр. 2, </italic></p><p><italic>115522 Москва, ул. Москворечье, 1 </italic></p><p>SPIN-код: 6906-2960</p></bio><email>nemtsova_m_v@mail.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff3"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">I.M. Sechenov First Moscow State Medical University (Sechenov University), Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГАОУ ВО Первый Московский государственный медицинский университет им. И.М. Сеченова Минздрава России (Сеченовский университет)</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">N.A. Lopatkin Research Institute of Urology and Interventional Radiology – branch of the National Medical Research Radiological Center, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">Научно-исследовательский институт урологии и интервенционной радиологии им. Н.А. Лопаткина – филиал ФГБУ «Национальный медицинский исследовательский центр радиологии» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">N.P. Bochkov Research Centre for Medical Genetics</institution></aff><aff><institution xml:lang="ru">ФГБНУ «Медико-генетический научный центр им. акад. Н.П. Бочкова»</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2019-12-30" publication-format="electronic"><day>30</day><month>12</month><year>2019</year></pub-date><volume>15</volume><issue>4</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>18</fpage><lpage>29</lpage><history><date date-type="received" iso-8601-date="2019-09-09"><day>09</day><month>09</month><year>2019</year></date><date date-type="accepted" iso-8601-date="2019-10-07"><day>07</day><month>10</month><year>2019</year></date></history><permissions><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://oncourology.abvpress.ru/oncur/article/view/974">https://oncourology.abvpress.ru/oncur/article/view/974</self-uri><abstract xml:lang="en"><p>Improving the laboratory diagnosis of prostate cancer and bladder cancer are still an actual problem in modern urologic oncology. Test systems for DNA or RNA alterations that occurred during carcinogenesis and associated with the malignant tumor and the prognosis of disease have been actively developed in recent years. Here we reviewed the data published mainly in the last 5 years about the molecular genetic kits for diagnosis (Progensa, SelectMDx, ExoDx Prostate Test, Prosta-Test, Confirm MDx) and assessment of prognosis (Prolaris, Decipher, Oncotype DX) in patients with prostate cancer, discussed their sensitivity and specificity. The characteristics of analogous kits and panels for bladder cancer (UroVysion, CertNDx Bladder Cancer Assay, UroSEEK, mutations in the FGFR3 and TERT genes, and the Cxbladder Monitor/Detect/Triage kit's line) were systematized. Particularly we focused on the description of the patient cohorts for whom kits mentioned above have greater diagnostic accuracy, described limitations of these test systems in consequence both a methodological and registration aspects, and their use in combination with other tumor markers. This review is aimed at oncologists, urologists, laboratory geneticists and specialists in related professions.</p></abstract><trans-abstract xml:lang="ru"><p>Совершенствование лабораторной диагностики рака предстательной железы (РПЖ) и рака мочевого пузыря (РМП) остается актуальной проблемой современной онкоурологии. В последние годы активно разрабатываются тест-системы, где в качестве биомаркеров выступают изменения ДНК или РНК, которые происходят при канцерогенезе и могут отражать наличие опухоли и прогноз заболевания. В настоящей работе рассмотрены опубликованные, преимущественно, в последние 5 лет данные о молекулярно-генетических тест-системах для диагностики (Progensa, SelectMDx, ExoDxProstateTest, Проста-Тест, ConfirmMDx) и оценки прогноза РПЖ (Prolaris, Decipher, OncotypeDX) с обсуждением их чувствительности и специфичности. Систематизированы данные об аналогичных тест-системах для РМП (UroVysion, CertNDxBladderCancerAssay, UroSEEK, панели с мутациями генов <italic>FGFR3</italic> и <italic>TERT</italic>, пакет тестов CxbladderMonitor/Detect/Triage). Особое внимание акцентировано на характеристике тех групп пациентов, в отношении которых рассматриваемые тесты обладают большей диагностической точностью, описаны их основные ограничения как методического, так и регистрационного характера, применение в сочетании с другими онкомаркерами. Обзор ориентирован на онкологов, урологов, врачей – лабораторных генетиков и специалистов смежных профессий.</p></trans-abstract><kwd-group xml:lang="en"><kwd>test system</kwd><kwd>prostate cancer</kwd><kwd>somatic mutation</kwd><kwd>bladder cancer</kwd><kwd>DNA methylation</kwd><kwd>gene expression</kwd><kwd>polymerase chain reaction</kwd><kwd>prognostic classificator</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>тест-система</kwd><kwd>рак предстательной железы</kwd><kwd>соматическая мутация</kwd><kwd>рак мочевого пузыря</kwd><kwd>метилирование ДНК</kwd><kwd>экспрессия генов</kwd><kwd>полимеразная цепная реакция</kwd><kwd>прогностический классификатор</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">Axel E.M., Matveev V.B. Statistics of malignant tumors of urinary and male urogenital organs in Russia and the countries of the former USSR. Oncourologiya = Cancer Urology 2019;15(2):15-24. (in Russ.). DOI: 10.17650/1726-9776-2019-15-2-15-24.</mixed-citation><mixed-citation xml:lang="ru">Аксель Е.М., Матвеев В.Б. Статистика злокачественных новообразований мочевых и мужских половых органов в России и странах бывшего СССР. Онкоурология 2019;15(2):15-24. DOI: 10.17650/1726-9776-2019-15-2-15-24.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">Chissov V.I., Alekseev B.Y., Rusakov I.G. М.: Geotar-Media, 2012, 688 pp. ISBN: 978-5-9704-2181-9.</mixed-citation><mixed-citation xml:lang="ru">Чиссов В.И., Алексеев Б.Я., Русаков И.Г. Онкоурология. Национальное руководство. М.: ГЭОТАР-Медиа, 2012, 688 с. ISBN: 978-5-9704-2181-9.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">Mikhaylenko D.S., Efremov G.D., Alekseev B.Y. Molecular genetic methods in diagnostics of hereditary and sporadic urological tumors. Spravochnik zaveduyuschego KLD = Handbook of the head of clinical laboratory 2016;2:38-46. (in Russ.).</mixed-citation><mixed-citation xml:lang="ru">Михайленко Д.С., Ефремов Г.Д., Алексеев Б.Я. Молекулярно-генетические методы диагностики при наследственных и спорадических опухолях в урологии. Справочник заведующего КДЛ 2016;2:38-46.</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><mixed-citation>Wu D., Ni J., Beretov J. et al. Urinary biomarkers in prostate cancer detection and monitoring progression. Crit Rev Oncol Hematol 2017;118:15-26. PMID: 28917266. DOI: 10.1016/j.critrevonc.2017.08.002.</mixed-citation></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">Mikhailenko D.S., Kushlinskii N.E. The somatic mutations and aberrant methylation as potential genetic markers of urinary bladder cancer. Klinicheskaya laboratornaya diagnostica = Klin Lab Diagn 2016;61(2):78-83. (in Russ.). PMID: 27455559. DOI: 10.18821/0869-2084-2016-61-2-78-83.</mixed-citation><mixed-citation xml:lang="ru">Михайленко Д.С., Кушлинский Н.Е. Соматические мутации и аберрантное метилирование – потенциальные генетические маркеры рака мочевого пузыря. Клиническая лабораторная диагностика 2016;61(2):78-83. PMID: 27455559. DOI: 10.18821/0869-2084-2016-61-2-78-83.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><mixed-citation>Ploussard G., de la Taille A. The role of prostate cancer antigen 3 (PCA3) in prostate cancer detection. Expert Rev Anticancer Ther 2018;18(10):1013-20. PMID: 30016891. DOI: 10.1080/14737140.2018.1502086.</mixed-citation></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">Hologic. Progensa PCA3 Assay 502083 rev. 003. User Guide, USA, 47 pp. URL: https://www.hologic.com/sites/default/files/2019-05/502083-IFU-PI_003_01.pdf.</mixed-citation><mixed-citation xml:lang="ru">Hologic. Progensa PCA3 Assay 502083 rev. 003. User Guide, USA, 47 pp. Доступно по: https://www.hologic.com/sites/default/files/2019-05/502083-IFU-PI_003_01.pdf.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">Mikhailenko D.S., Perepechin D.V., Apolikhin O.I. et al. Markers for non-invasive molecular genetic diagnosis of oncourological diseases. Urologiia 2014;5:116-20. (in Russ.). PMID: 25807773.</mixed-citation><mixed-citation xml:lang="ru">Михайленко Д.С., Перепечин Д.В., Аполихин О.И. и др. Маркеры для неинвазивной молекулярно-генетической диагностики онкоурологических заболеваний. Урология 2014;5:116-20. PMID: 25807773.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><mixed-citation>de la Taille A., Irani J., Graefen M. et al. Clinical evaluation of the PCA3 assay in guiding initial biopsy decisions. J Urol 2011;185(6):2119-25. PMID: 21496856. DOI: 10.1016/j.juro.2011.01.075.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Crawford E.D., Rove K.O., Trabulsi E.J. et al. Diagnostic performance of PCA3 to detect prostate cancer in men with increased prostate specific antigen: a prospective study of 1,962 cases. J Urol 2012;188:1726-31. PMID: 22998901. DOI: 10.1016/j.juro.2012.07.023.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Filella X., Foj L. Novel biomarkers for prostate cancer detection and prognosis. Adv Exp Med Biol 2018;1095:15-39. PMID: 30229547. DOI: 10.1007/978-3-319-95693-0_2.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Chevli K.K., Duff M., Walter P. et al. Urinary PCA3 as a predictor of prostate cancer in a cohort of 3,073 men undergoing initial prostate biopsy. J Urol 2014;191(6) 1743-48. PMID: 24333241. DOI: 10.1016/j.juro.2013.12.005.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Osses D.F., Roobol M.J., Schoots I.G. Prediction medicine: biomarkers, risk calculators and magnetic resonance imaging as risk stratification tools in prostate cancer diagnosis. Int J Mol Sci 2019;20(7):pii: E1637. PMID: 30986955. DOI: 10.3390/ijms20071637.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Rodon N., Trias I., Verdu M. et al. Correlation of mRNA-PCA3 urine levels with the new grading system in prostate cancer. Rev Esp Patol 2019;52(1):20-26. PMID: 30583827. DOI: 10.1016/j.patol.2018.04.003.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Alshalalfa M., Verhaegh G.W., Gibb E.A. et al. Low PCA3 expression is a marker of poor differentiation in localized prostate tumors: exploratory analysis from 12,076 patients. Oncotarget 2017;8(31):50804-13. PMID: 28881605. DOI: 10.18632/oncotarget.15133.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Hegde J.V., Veruttipong D., Said J.W. et al. Prostate cancer antigen 3 score does not predict for adverse pathologic features at radical prostatectomy or for progression-free survival in clinically localized, intermediate- and high-risk prostate cancer. Urology 2017;107:171-7. PMID: 28552819. DOI: 10.1016/j.urology.2017.05.028.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Fradet V., Toren P., Nguile-Makao M. et al. Prognostic value of urinary prostate cancer antigen 3 (PCA3) during active surveillance of patients with low-risk prostate cancer receiving 5α-reductase inhibitors. BJU Int 2018;121(3):399-404. PMID: 28972698. DOI: 10.1111/bju.14041.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Tosoian J.J., Patel H.D., Mamawala M. et al. Longitudinal assessment of urinary PCA3 for predicting prostate cancer grade reclassification in favorable-risk men during active surveillance. Prostate Cancer Prostatic Dis 2017;20(3):339-42. PMID: 28417979. DOI: 10.1038/pcan.2017.16.</mixed-citation></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">Zhou Y., Li Y., Li X.3, Jiang M. Urinary biomarker panel to improve accuracy in predicting prostate biopsy result in Chinese men with PSA 4-10 ng/mL. Biomed Res Int 2017:2512536. PMID: 28293631. DOI: 10.1155/2017/2512536.</mixed-citation><mixed-citation xml:lang="ru">Zhou Y., Li Y., Li X.3, Jiang M. Urinary biomarker panel to improve accuracy in predicting prostate biopsy result in Chinese men with PSA 4-10 ng/mL. Biomed Res Int 2017:2512536. PMID: 28293631. DOI: 10.1155/2017/2512536.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><mixed-citation>Mao Z., Ji A., Yang K. et al. Diagnostic performance of PCA3 and hK2 in combination with serum PSA for prostate cancer. Medicine (Baltimore) 2018;97(42):e12806. PMID: 30334974. DOI: 10.1097/MD.0000000000012806.</mixed-citation></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">Mikhaylenko D.S., Perepechin D.V., Grigoryeva M.V. et al. PCA3 and TMPRSS2:ERG genes expression in biopsies of benign prostate hyperplasia, intraepithelial neoplasia, and prostate cancer. Urologiia 2015;(5):46-50 (in Russ.). PMID: 26859937.</mixed-citation><mixed-citation xml:lang="ru">Михайленко Д.С., Перепечин Д.В., Григорьева М.В., и др. Экспрессия генов РСА3 и TMPRSS2:ERG в биоптатах при доброкачественной гиперплазии, интраэпителиальной неоплазии и раке предстательной железы. Урология 2015;5:46-50. PMID: 26859937.</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">Apolikhin O.I., Sivkov A.V., Efremov G.D. et al. The first Russian experience of using PCA3 and TMPRSS2-ERG for prostate cancer diagnosis. Klinicheskaya i experimentalnaya urologiya = Clinical and experimental urology 2015;2:30-6 (in Russ.).</mixed-citation><mixed-citation xml:lang="ru">Аполихин О.И., Сивков А.В., Ефремов Г.Д. и др. PCA3 и TMPRSS2-ERG в диагностике рака предстательной железы: первый опыт применения комбинации маркеров в России. Экспериментальная и клиническая урология 2015;2:30-6.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><mixed-citation>Li M., Zhou D., Zhang W. et al. Urine PCA3 mRNA level in diagnostic of prostate cancer. J Cancer Res Ther 2018;14(4):864-6. PMID: 29970667. DOI: 10.4103/jcrt.JCRT_734_17.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Wang T., Qu X., Jiang J. et al. Diagnostic significance of urinary long non-coding PCA3 RNA in prostate cancer. Oncotarget 2017;8(35):58577-86. PMID: 28938580. DOI: 10.18632/oncotarget.17272.</mixed-citation></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">Pavlov K.A., Shkoporov A.N., Khokhlova E.V. et al. Development of a diagnostic test system for early non-invasive detection of prostate cancer based on PCA3 mRNA levels in urine sediment using quantitative reverse tanscription polymerase chain reaction (qRT-PCR). Vestn Ross Akad Med Nauk 2013;(5):45-51 (in Russ.). PMID: 24000667.</mixed-citation><mixed-citation xml:lang="ru">Павлов К.А., Шкопоров А.Н., Хохлова Е.В. и др. Разработка диагностической тест-системы для ранней неинвазивной диагностики рака простаты, основанной на количественной детекции мРНК гена PCA3 в осадке мочи методом ОТ-ПЦР в режиме реального времени. Вестник РАМН 2013;5:45-51. PMID: 24000667.</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">Toropovsky A.N., Nikitin A.G., Gordiev M.G. et al. Results of validation of the Prosta-Test kit designed for mRNA PCA3 detection using two-steps RT – real time PCR in clinical diagnostics of prostate cancer. Vestnik medicinskogo instituta REAVIZ = Journal of the REAVIZ medical institution 2018;1:126-36 (in Russ.).</mixed-citation><mixed-citation xml:lang="ru">Тороповский А.Н., Никитин А.Г., Гордиев М.Г. и др. Результаты испытания набора реагентов для выявления мРНК гена РСА3 и определения уровня его экспрессии методом двустадийной ОТ-ПЦР-РВ (Проста-Тест) для диагностики рака предстательной железы in vitro в клинической практике. Вестник медицинского института «РЕАВИЗ» 2018;1:126-36.</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><mixed-citation>Fenstermaker M., Mendhiratta N., Bjurlin M.A. et al. Risk stratification by urinary prostate cancer gene 3 testing before magnetic resonance imaging-ultrasound fusion-targeted prostate biopsy among men with no history of biopsy. Urology 2017;99:174-9. PMID: 27562202. DOI: 10.1016/j.urology.2016.08.022.</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Cao L., Lee C.H., Ning J. et al. Combination of prostate cancer antigen 3 and prostate-specific antigen improves diagnostic accuracy in men at risk of prostate cancer. Arch Pathol Lab Med 2018;142(9):1106-12. PMID: 29547000. DOI: 10.5858/arpa.2017-0185-OA.</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Yang Z., Yu L., Wang Z. PCA3 and TMPRSS2-ERG gene fusions as diagnostic biomarkers for prostate cancer. Chin J Cancer Res 2016;28(1):65-71. PMID: 27041928. DOI: 10.3978/j.issn.1000-9604.2016.01.05.</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Ankerst D.P., Goros M., Tomlins S.A. et al. Incorporation of urinary prostate cancer antigen 3 and TMPRSS2:ERG into prostate cancer prevention trial risk calculator. Eur Urol Focus 2019;5(1):54-61. PMID: 29422418. DOI: 10.1016/j.euf.2018.01.010.</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Newcomb L.F., Zheng Y., Faino A.V. et al. Performance of PCA3 and TMPRSS2:ERG urinary biomarkers in prediction of biopsy outcome in the Canary Prostate Active Surveillance Study (PASS). Prostate Cancer Prostatic Dis 2019;22(3):438-45. PMID: 30664734. DOI: 10.1038/s41391-018-0124-z.</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Kornberg Z., Cooperberg M.R., Spratt D.E., Feng F.Y. Genomic biomarkers in prostate cancer. Transl Androl Urol 2018;7(3):459-71. PMID: 30050804. DOI: 10.21037/tau.2018.06.02.</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Govers T.M., Caba L., Resnick M.J. Cost-effectiveness of urinary biomarker panel in prostate cancer risk assessment. J Urol 2018;200(6):1221-6. PMID: 30012363. DOI: 10.1016/j.juro.2018.07.034.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Haese A., Trooskens G., Steyaert S. et al. Multicenter optimization and validation of a 2-gene mRNA urine test for detection of clinically significant prostate cancer before initial prostate biopsy. J Urol 2019;202(2):256-63. PMID: 31026217. DOI: 10.1097/JU.0000000000000293.</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Fujita K., Nonomura N. Urinary biomarkers of prostate cancer. Int J Urol 2018;25(9):770-9. PMID: 30129068. DOI: 10.1111/iju.13734.</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Arriaga-Canon C., Rosa-Velazquez I.A., Gonzalez-Barrios R. et al. The use of long non-coding RNAs as prognostic biomarkers and therapeutic targets in prostate cancer. Oncotarget 2018;9(29):20872-90. PMID: 29755696. DOI: 10.18632/oncotarget.25038.</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Loeb S. Biomarkers for prostate biopsy and risk stratification of newly diagnosed prostate cancer patients. Urol Pract 2017;4(4):315-21. PMID: 29104903. DOI: 10.1016/j.urpr.2016.08.001.</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Shore N., Concepcion R., Saltzstein D. et al. Clinical utility of a biopsy-based cell cycle gene expression assay in localized prostate cancer. Curr Med Res Opin 2014;30(4):547-53. PMID: 24320750. DOI: 10.1185/03007995.2013.873398.</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Crawford E.D., Scholz M.C., Kar A.J. et al. Cell cycle progression score and treatment decisions in prostate cancer: results from an ongoing registry. Curr Med Res Opin 2014;30(6):1025-31. PMID: 24576172. DOI: 10.1185/03007995.2014.899208.</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Cuzick J., Stone S., Fisher G. et al. Validation of an RNA cell cycle progression score for predicting death from prostate cancer in a conservatively managed needle biopsy cohort. Br J Cancer 2015;113:382-9. PMID: 26103570. DOI: 10.1038/bjc.2015.223.</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Cuzick J., Berney D.M., Fisher G. et al. Prognostic value of a cell cycle progression signature for prostate cancer death in a conservatively managed needle biopsy cohort. Br J Cancer 2012;106:1095-9. PMID: 22361632. DOI: 10.1038/bjc.2012.39.</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Alford A.V., Brito J.M., Yadav K.K. et al. The use of biomarkers in prostate cancer screening and treatment. Rev Urol 2017;19(4):221-34. PMID: 29472826. DOI: 10.3909/riu0772.</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Klein E.A., Haddad Z., Yousefi K. et al. Decipher genomic classifier measured on prostate biopsy predicts metastasis risk. Urology 2016;90:148-52. PMID: 26809071. DOI: 10.1016/j.urology.2016.01.012.</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Marrone M., Potosky A.L., Penson D., Freedman A.N. A 22 gene-expression assay, Decipher® (GenomeDx Biosciences) to predict five-year risk of metastatic prostate cancer in men treated with radical prostatectomy. PLoS Curr 2015;7. PMID: 26664778. DOI: 10.1371/currents.eogt.761b81608129ed61b0b48d42c04f92a4.</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Carneiro A., Priante Kayano P., Gomes Barbosa A.R. et al. Are localized prostate cancer biomarkers useful in the clinical practice? Tumour Biol 2018;40(9). PMID: 30204063. DOI: 10.1177/1010428318799255.</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Knezevic D., Goddard A.D., Natraj N. et al. Analytical validation of the Oncotype DX prostate cancer assay – a clinical RT-PCR assay optimized for prostate needle biopsies. BMC Genomics 2013;14:690. PMID: 24103217. DOI: 10.1186/1471-2164-14-690.</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Cullen J., Rosner I.L., Brand T.C. et al. A biopsy-based 17-gene genomic prostate score predicts recurrence after radical prostatectomy and adverse surgical pathology in a racially diverse population of men with clinically low- and intermediate-risk prostate cancer. Eur Urol 2015;68(1):123-31. PMID: 25465337. DOI: 10.1016/j.eururo.2014.11.030.</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Kornberg Z., Cowan J.E., Westphalen A.C. et al. Genomic prostate score, PI-RADS™ version 2 and progression in men with prostate cancer on active surveillance. J Urol 2019;201(2):300-7. PMID: 30179620. DOI: 10.1016/j.juro.2018.08.047.</mixed-citation></ref><ref id="B49"><label>49.</label><citation-alternatives><mixed-citation xml:lang="en">UroVysion Bladder Cancer Kit. URL: https://www.molecular.abbott/sal/en-us/staticAssets/UroVysion-package-insert-R6---watermark.pdf.</mixed-citation><mixed-citation xml:lang="ru">UroVysion Bladder Cancer Kit. Доступно по: https://www.molecular.abbott/sal/en-us/staticAssets/UroVysion-package-insert-R6---watermark.pdf.</mixed-citation></citation-alternatives></ref><ref id="B50"><label>50.</label><citation-alternatives><mixed-citation xml:lang="en">Karnes R.J., Fernandez C.A., Shuber A.P. A noninvasive multianalyte urine-based diagnostic assay for urothelial cancer o f the bladder in the evaluation of hematuria. Mayo Clin Proc 2012;87(9):835-42. PMID: 22883743. DOI: 10.1016/j.mayocp.2012.04.013.</mixed-citation><mixed-citation xml:lang="ru">Karnes R.J., Fernandez C.A., Shuber A.P. A noninvasive multianalyte urine-based diagnostic assay for urothelial cancer of the bladder in the evaluation of hematuria. Mayo Clin Proc 2012;87(9):835-42. PMID: 22883743. DOI: 10.1016/j.mayocp.2012.04.013.</mixed-citation></citation-alternatives></ref><ref id="B51"><label>51.</label><mixed-citation>Roperch J.P., Grandchamp B., Desgrandchamps F. et al. Promoter hypermethylation of HS3ST2, SEPTIN9 and SLIT2 combined with FGFR3 mutations as a sensitive/specific urinary assay for diagnosis and surveillance in patients with low or high-risk non-muscle-invasive bladder cancer. BMC Cancer 2016;16:704. PMID: 27586786. DOI: 10.1186/s12885-016-2748-5.</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Zhu F., Zhang Y., Shi L. et al. Gene mutation detection of urinary sediment cells for NMIBC early diagnose and prediction of NMIBC relapse after surgery. Medicine (Baltimore) 2019;98(32):e16451. PMID: 31393349. DOI: 10.1097/MD.0000000000016451.</mixed-citation></ref><ref id="B53"><label>53.</label><citation-alternatives><mixed-citation xml:lang="en">Mikhailenko D.S., Nemtsova M.V. Point somatic mutations in bladder cancer: key carcinogenesis events, diagnostic markers and therapeutic targets. Urologiia. 2016;1:100-5. (in Russ.). PMID: 28247712.</mixed-citation><mixed-citation xml:lang="ru">Михайленко Д.С., Немцова М.В. Точковые соматические мутации в развитии рака мочевого пузыря: ключевые события канцерогенеза, диагностические маркеры и мишени для терапии. Урология 2016;1:100-5. PMID: 28247712.</mixed-citation></citation-alternatives></ref><ref id="B54"><label>54.</label><mixed-citation>Descotes F., Kara N., Decaussin-Petrucci M. et al. Non-invasive prediction of recurrence in bladder cancer by detecting somatic TERT promoter mutations in urine. Br J Cancer 2017;117(4):583-7. PMID: 28683471. DOI: 10.1038/bjc.2017.210.</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Rodriguez Pena M.D., Springer S.U., Taheri D. et al. Performance of novel non-invasive urine assay UroSEEK in cohorts of equivocal urine cytology. Virchows Arch 2019 [Epub ahead of print]. PMID: 31482302. DOI: 10.1007/s00428-019-02654-1.</mixed-citation></ref><ref id="B56"><label>56.</label><citation-alternatives><mixed-citation xml:lang="en">Cxbladder Kits. URL: https://www.cxbladder.com/.</mixed-citation><mixed-citation xml:lang="ru">Cxbladder Kits. Доступно по: https://www.cxbladder.com/.</mixed-citation></citation-alternatives></ref><ref id="B57"><label>57.</label><mixed-citation>Kavalieris L., Sullivan P., Frampton C. et al. Performance characteristics of a multigene urine biomarker test for monitoring for recurrent urothelial carcinoma in a multicenter study. J Urol 2017;197(6):1419-26. PMID: 27986532. DOI: 10.1016/j.juro.2016.12.010.</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Davidson P.J., McGeoch G., Shand B. Inclusion of a molecular marker of bladder cancer in a clinical pathway for investigation of haematuria may reduce the need for cystoscopy. N Z Med J 2019;132(1497):55-64. PMID: 31220066.</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Konety B., Shore N., Kader A.K. et al. Evaluation of Cxbladder and adjudication of atypical cytology and equivocal cystoscopy. Eur Urol 2019;76(2):238-43. PMID: 31103391. DOI: 10.1016/j.eururo.2019.04.035.</mixed-citation></ref></ref-list></back></article>
