يعرض 1 - 20 نتائج من 1,367 نتيجة بحث عن '"МЕТАСТАЗЫ"', وقت الاستعلام: 0.52s تنقيح النتائج
  1. 1
    Academic Journal
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    Academic Journal

    المصدر: Meditsinskiy sovet = Medical Council; № 22 (2023); 154-160 ; Медицинский Совет; № 22 (2023); 154-160 ; 2658-5790 ; 2079-701X

    وصف الملف: application/pdf

    Relation: https://www.med-sovet.pro/jour/article/view/8001/7090; Osterlund P, Salminen T, Soveri LM, Kallio R, Kellokumpu I, Lamminmäki A et al. Repeated centralized multidisciplinary team assessment of resectability, clinical behavior, and outcomes in 1086 Finnish metastatic colorectal cancer patients (RAXO): A nationwide prospective intervention study. Lancet Reg Health Eur. 2021;3:100049. https://doi.org/10.1016/j.lanepe.2021.100049.; Kunst N, Alarid-Escudero F, Aas E, Coupé VMH, Schrag D, Kuntz KM. Estimating Population-Based Recurrence Rates of Colorectal Cancer over Time in the United States. Cancer Epidemiol Biomarkers Prev. 2020;29(12):2710–2718. https://doi.org/10.1158/1055-9965.EPI-20-0490.; Duineveld LA, van Asselt KM, Bemelman WA, Smits AB, Tanis PJ, van Weert HC, Wind J. Symptomatic and Asymptomatic Colon Cancer Recurrence: A Multicenter Cohort Study. Ann Fam Med. 2016;14(3):215–220. https://doi.org/10.1370/afm.1919.; Haria PD, Baheti AD, Palsetia D, Ankathi SK, Choudhari A, Guha A et al. Follow-up of colorectal cancer and patterns of recurrence. Clin Radiol. 2021;76(12):908–915. https://doi.org/10.1016/j.crad.2021.07.016.; Nordlinger B, Sorbye H, Glimelius B, Poston GJ, Schlag PM, Rougier P et al. Perioperative FOLFOX4 chemotherapy and surgery versus surgery alone for resectable liver metastases from colorectal cancer (EORTC 40983): long-term results of a randomised, controlled, phase 3 trial. Lancet Oncol. 2013;14(12):1208–1215. https://doi.org/10.1016/S1470-2045(13)70447-9.; Araujo RL, Gönen M, Herman P. Chemotherapy for patients with colorectal liver metastases who underwent curative resection improves long-term outcomes: systematic review and meta-analysis. Ann Surg Oncol. 2015;22(9):3070–3078. https://doi.org/10.1245/s10434-014-4354-6.; Kobayashi S, Beppu T, Honda G, Yamamoto M, Takahashi K, Endo I et al. Survival Benefit of and Indications for Adjuvant Chemotherapy for Resected Colorectal Liver Metastases-a Japanese Nationwide Survey. J Gastrointest Surg. 2020;24(6):1244–1260. https://doi.org/10.1007/s11605-019-04250-9.; Wang ZM, Chen YY, Chen FF, Wang SY, Xiong B. Peri-operative chemotherapy for patients with resectable colorectal hepatic metastasis: A meta-analysis. Eur J Surg Oncol. 2015;41(9):1197–1203. https://doi.org/10.1016/j.ejso.2015.05.020.; Ciliberto D, Prati U, Roveda L, Barbieri V, Staropoli N, Abbruzzese A et al. Role of systemic chemotherapy in the management of resected or resectable colorectal liver metastases: a systematic review and meta-analysis of randomized controlled trials. Oncol Rep. 2012;27(6):1849–1856. https://doi.org/10.3892/or.2012.1740.; Mitry E, Fields AL, Bleiberg H, Labianca R, Portier G, Tu D et al. Adjuvant chemotherapy after potentially curative resection of metastases from colorectal cancer: a pooled analysis of two randomized trials. J Clin Oncol. 2008;26(30):4906–4911. https://doi.org/10.1200/JCO.2008.17.3781.; Portier G, Elias D, Bouche O, Rougier P, Bosset JF, Saric J et al. Multicenter randomized trial of adjuvant fluorouracil and folinic acid compared with surgery alone after resection of colorectal liver metastases: FFCD ACHBTH AURC 9002 trial. J Clin Oncol. 2006;24(31):4976–4982. https://doi.org/10.1200/JCO.2006.06.8353.; Ychou M, Raoul JL, Douillard JY, Gourgou-Bourgade S, Bugat R, Mineur L et al. A phase III randomised trial of LV5FU2 + irinotecan versus LV5FU2 alone in adjuvant high-risk colon cancer (FNCLCC Accord02/FFCD9802). Ann Oncol. 2009;20(4):674–680. https://doi.org/10.1093/annonc/mdn680.; Engstrand J, Nilsson H, Strömberg C, Jonas E, Freedman J. Colorectal cancer liver metastases – a population-based study on incidence, management and survival. BMC Cancer. 2018;18(1):78. https://doi.org/10.1186/s12885-017-3925-x.; Li J, Yuan Y, Yang F, Wang Y, Zhu X, Wang Z et al. Expert consensus on multidisciplinary therapy of colorectal cancer with lung metastases (2019 edition). J Hematol Oncol. 2019;12(1):16. https://doi.org/10.1186/s13045-019-0702-0.; Lumachi F, Chiara GB, Tozzoli R, Del Conte A, Basso SM. Factors Affecting Survival in Patients with Lung Metastases from Colorectal Cancer. A Short Meta-analysis. Anticancer Res. 2016;36(1):13–19. https://ar.iiarjournals.org/content/36/1/13.long.; Penna C, Nordlinger B. Colorectal metastasis (liver and lung). Surg Clin North Am. 2002;82(5):1075–1090. https://doi.org/10.1016/s0039-6109(02)00051-8.; Liu LL, Sun JD, Xiang ZL. Survival nomograms for colorectal carcinoma patients with lung metastasis and lung-only metastasis, based on the SEER database and a single-center external validation cohort. BMC Gastroenterol. 2022;22(1):446. https://doi.org/10.1186/s12876-022-02547-9.; Rahbari NN, Reissfelder C, Schulze-Bergkamen H, Jäger D, Büchler MW, Weitz J, Koch M. Adjuvant therapy after resection of colorectal liver metastases: the predictive value of the MSKCC clinical risk score in the era of modern chemotherapy. BMC Cancer. 2014;14:174. https://doi.org/10.1186/1471-2407-14-174.; Федянин МЮ, Гладков ОА, Гордеев СС, Карачун АМ, Козлов НА, Мамедли ЗЗ и др. Практические рекомендации по лекарственному лечению рака ободочной кишки, ректосигмоидного соединения и прямой кишки. Злокачественные опухоли. 2022;12(3s2–1):401–454. https://doi.org/10.18027/2224-5057-2022-12-3s2-401-454.; Kanemitsu Y, Shimizu Y, Mizusawa J, Inaba Y, Hamaguchi T, Shida D et al. Hepatectomy Followed by mFOLFOX6 Versus Hepatectomy Alone for Liver-Only Metastatic Colorectal Cancer (JCOG0603): A Phase II or III Randomized Controlled Trial. J Clin Oncol. 2021;39(34):3789–3799. https://doi.org/10.1200/JCO.21.01032.; Mauri D, Zarkavelis G, Filis P, Tsali L, Zafeiri G, Papadaki A et al. Postoperative chemotherapy with single-agent fluoropyrimidines after resection of colorectal cancer liver metastases: a meta-analysis of randomised trials. ESMO Open. 2018;3(4):e000343. https://doi.org/10.1136/esmoopen-2018-000343.; Brandi G, De Lorenzo S, Nannini M, Curti S, Ottone M, Dall’Olio FG et al. Adjuvant chemotherapy for resected colorectal cancer metastases: Literature review and meta-analysis. World J Gastroenterol. 2016;22(2):519–533. https://doi.org/10.3748/wjg.v22.i2.519.; Park HS, Jung M, Shin SJ, Heo SJ, Kim CG, Lee MG et al. Benefit of Adjuvant Chemotherapy After Curative Resection of Lung Metastasis in Colorectal Cancer. Ann Surg Oncol. 2016;23(3):928–935. https://doi.org/10.1245/ s10434-015-4951-z.; Zhang C, Tan Y, Xu H. Does adjuvant chemotherapy improve the prognosis of patients after resection of pulmonary metastasis from colorectal cancer? A systematic review and meta-analysis. Int J Colorectal Dis. 2019;34(10):1661–1671. https://doi.org/10.1007/s00384-019-03362-7.; Imanishi M, Yamamoto Y, Hamano Y, Yamada T, Moriwaki T, Gosho M et al. Efficacy of adjuvant chemotherapy after resection of pulmonary metastasis from colorectal cancer: a propensity score-matched analysis. Eur J Cancer. 2019;106:69–77. https://doi.org/10.1016/j.ejca.2018.10.003.; https://www.med-sovet.pro/jour/article/view/8001

  3. 3
    Academic Journal

    المصدر: Creative surgery and oncology; Том 14, № 3 (2024); 216-222 ; Креативная хирургия и онкология; Том 14, № 3 (2024); 216-222 ; 2076-3093 ; 2307-0501

    وصف الملف: application/pdf

    Relation: https://www.surgonco.ru/jour/article/view/982/612; Frost P. Unknown primary tumors: an example of accelerated (type 2) tumor progression. Basic Life Sci. 1991;57:233–7; discussion 237–40. DOI:10.1007/978-1-4684-5994-4_20; Varadhachary G. New strategies for carcinoma of unknown primary: the role of tissue-of-origin molecular profiling. Clin Cancer Res. 2013;19:4027–33. DOI:10.1158/1078-0432.CCR-12-3030; Куликов Е.П., Захаркина Т.В., Сашина Е.Л., Мануковская О.В., Редькин А.Н., Чевардов Н.И. и др. Поиск первичного очага при метастатическом поражении лимфоузлов шеи. Российский медико-биологический вестник им. академика И.П. Павлова. 2016;24(4):119–25. DOI:10.23888/PAVLOVJ20164119-125; Al Kadah B., Papaspyrou G., Linxweiler M., Schick B, Rübe C., Büchler B.S., et al. Cancer of unknown primary (CUP) of the head and neck: retrospective analysis of 81 patients. Eur Arch Otorhinolaryngol. 2017;274:2557–66. DOI:10.1007/s00405-017-4525-8; Рудык А.Н., Зинченко С.В., Хасанов Р.Ш., Хамидуллин Р.Г., Чернышева В.А. Определение локализации первичной опухоли у пациентов с метастазами в лимфатические узлы шеи без выявленного первичного очага. Онкохирургия. 2013;5(2):57–9.; Саприна О.А. Метастазы плоскоклеточного рака в лимфоузлы шеи без выявленного первичного очага. Опухоли головы и шеи. 2012;4:53–8. DOI:10.17650/2222-1468-2012-0-4-53-58; Farooq S., Khandavilli S., Dretzke J., Moore D., Nankivell P.C., Sharma N., et al. Transoral tongue base mucosectomy for the identification of the primary site in the work-up of cancers of unknown origin: Systematic review and meta-analysis. Oral Oncol. 2019;91:97–106. DOI:10.1016/j.oraloncology.2019.02.018; Mistry R., Walker A., Kim D., Ofo E. Transoral robotic surgery for the benefit of patients with head and neck cancer of unknown primary: our experience at St George’s University Hospital, London. Ann R Coll Surg Engl. 2020;102(6):442–50. DOI:10.1308/rc-sann.2020.0071; Al-Lami A., Gao C., Saddiq M., Al Zuhir N., Simo R., Arora A., et al. Reducing the unknowns: A systematic review & meta-analysis of the effectiveness of trans-oral surgical techniques in identifying head and neck primary cancer in carcinoma unknown primary. Oral Oncol. 2022;126:105–7. DOI:10.1016/j.oraloncology; Kubik M.W., Channir H.I., Rubek N., Kim S., Ferris R.L., von Buchwald C., et al. TORS Base-of-Tongue mucosectomy in human papilloma virus-negative carcinoma of unknown primary. Laryngoscope. 2021;131(1):78–81. DOI:10.1002/lary.28617; Liu X., Li D., Li N., Zhu X. Optimization of radiotherapy for neck carcinoma metastasis from unknown primary sites: a meta-analysis. Oncotarget. 2016;7(48):78736–46. DOI:10.18632/oncotarget.12852; Maghami E., Ismaila N., Alvarez A., Chernock R., Duvvuri U., Geiger J., et al. Diagnosis and management of squamous cell carcinoma of unknown primary in the head and neck: ASCO Guideline. J Clin Oncol. 2020;38(22):2570–96. DOI:10.1200/JCO.20.00275; Chen A.M., Farwell D.G., Lau D.H., Li B.Q., Luu Q., Donald P.J. Radiation therapy in the management of head-and-neck cancer of unknown primary origin: how does the addition of concurrent chemotherapy affect the therapeutic ratio? Int J Radiat Oncol Biol Phys. 2011;81(2):346–52. DOI:10.1016/j.ijrobp.2010.06.031; Ofo E., Spears H., Kim D., Duvvuri U. Transoral robotic surgery and unknown primary surgery. ORL J Otorhinolaryngol Relat Spec. 2018;80:148–55. DOI:10.1159/000490596; Civantos F.J., Vermorken J.B., Shah J.P., Rinaldo A., Suárez C., Kowalski L.P., et al. Metastatic squamous cell carcinoma to the cervical lymph nodes from an unknown primary cancer: management in the HPV era. Front Oncol. 2020;10:593164. DOI:10.3389/fonc.2020.593164; https://www.surgonco.ru/jour/article/view/982

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    Academic Journal

    المصدر: Сборник статей

    وصف الملف: application/pdf

    Relation: Актуальные вопросы современной медицинской науки и здравоохранения : Сборник статей IX Международной научно-практической конференции молодых ученых и студентов, 17-18 апреля 2024 г. Т. 1.; Бахолдина, Я. С. Карцинома шейки матки / Я. С. Бахолдина, Л. В. Тимеева, Т. П. Самойлова. - Текст: электронный // Актуальные вопросы современной медицинской науки и здравоохранения : Сборник статей IX Международной научно-практической конференции молодых ученых и студентов, 17-18 апреля 2024 г. Т. 1. - Екатеринбург, 2024. – C. 593-596.; http://elib.usma.ru/handle/usma/21308

  6. 6
    Academic Journal

    المصدر: Siberian journal of oncology; Том 23, № 2 (2024); 37-46 ; Сибирский онкологический журнал; Том 23, № 2 (2024); 37-46 ; 2312-3168 ; 1814-4861

    وصف الملف: application/pdf

    Relation: https://www.siboncoj.ru/jour/article/view/3037/1215; Hua K.C., Hu Y.C. Establishment of predictive model for patients with kidney cancer bone metastasis: a study based on SEER database. Transl Androl Urol. 2020; 9(2): 523–43. https://doi.org/10.21037/tau.2020.01.24.; Ged Y., Voss M.H. Novel emerging biomarkers to immunotherapy in kidney cancer. Ther Adv Med Oncol. 2021; 13. doi:10.1177/17588359211059367.; Chung C. From oxygen sensing to angiogenesis: Targeting the hypoxia signaling pathway in metastatic kidney cancer. Am J Health Syst Pharm. 2020; 77(24): 2064–73. doi:10.1093/ajhp/zxaa308.; Xue J., Chen W., Xu W., Xu Z., Li X., Qi F., Wang Z. Patterns of distant metastases in patients with clear cell renal cell carcinoma A population-based analysis. Cancer Med. 2021; 10(1): 173–87. doi:10.1002/cam4.3596.; Nishida J., Momoi Y., Miyakuni K., Tamura Y., Takahashi K., Koinuma D., Miyazono K., Ehata S. Epigenetic remodelling shapes inflammatory renal cancer and neutrophil-dependent metastasis. Nat Cell Biol. 2020; 22(4): 465–75. doi:10.1038/s41556-020-0491-2.; Zhang G., Zhang L., Sun S., Chen M. Identification of a Novel Defined Immune-Autophagy-Related Gene Signature Associated With Clinical and Prognostic Features of Kidney Renal Clear Cell Carcinoma. Front Mol Biosci. 2021; 8. doi:10.3389/fmolb.2021.790804.; Abdel-Rahman O. Clinical correlates and prognostic value of different metastatic sites in metastatic renal cell carcinoma. Future Oncol. 2017; 13(22): 1967–80. doi:10.2217/fon-2017-0175.; Lin S., Zheng Y., Qin Z., Hu X., Qi F., Yin R., Xu L., Li X. Surgical intervention in renal cell carcinoma patients with lung and bronchus metastasis is associated with longer survival time: a population-based analysis. Ann Transl Med. 2019; 7(14): 323. doi:10.21037/atm.2019.06.02.; Danno T., Iwata S., Niimi F., Honda S., Okada H., Azuma T. Nivolumab and Ipilimumab Combination Immunotherapy for Patients with Metastatic Collecting Duct Carcinoma. Case Rep Urol. 2021. doi:10.1155/2021/9936330.; Schulz S., Woerl A.C., Jungmann F., Glasner C., Stenzel P., Strobl S., Fernandez A., Wagner D.C., Haferkamp A., Mildenberger P., Roth W., Foersch S. Multimodal Deep Learning for Prognosis Prediction in Renal Cancer. Front Oncol. 2021; 11. doi:10.3389/fonc.2021.788740.; Xi W., Hou Y., Hu X., Xia Y., Jiang S., Wang H., Bai Q., Hou J., Guo J. Prognostic significance of pseudocapsule status in patients with metastatic renal cell carcinoma treated with tyrosine kinase inhibitors. Transl Androl Urol. 2021; 10(11): 4132–41. doi:10.21037/tau-21-429.; Xu C., Zhou Q., Liu W., Li W., Dong S., Li W., Xu X., Qiao X., Jiang Y., Chen J., Yin C. Dynamic Predictive Models with Visualized Machine Learning for Assessing the Risk of Lung Metastasis in Kidney Cancer Patients. J Oncol. 2022. doi:10.1155/2022/5798602.; Xiao R., Liu C., He W., Ma L. Prognostic Factors and a Nomogram Predicting Overall Survival and Cancer-Specific Survival for Patients with Collecting Duct Renal Cell Carcinoma. Biomed Res Int. 2021. doi:10.1155/2021/6736008.; Volpe A., Bollito E., Bozzola C., Di Domenico A., Bertolo R., Zegna L., Duregon E., Boldorini R., Porpiglia F., Terrone C. Classification of Histologic Patterns of Pseudocapsular Invasion in Organ-Confined Renal Cell Carcinoma. Clin Genitourin Cancer. 2016; 14(1): 69–75. doi:10.1016/j.clgc.2015.07.020.; Bridgeman V.L., Vermeulen P.B., Foo S., Bilecz A., Daley F., Kostaras E., Nathan M.R., Wan E., Frentzas S., Schweiger T., Hegedus B., Hoetzenecker K., Renyi-Vamos F., Kuczynski E.A., Vasudev N.S., Larkin J., Gore M., Dvorak H.F., Paku S., Kerbel R.S., Dome B., Reynolds A.R. Vessel co-option is common in human lung metastases and mediates resistance to anti-angiogenic therapy in preclinical lung metastasis models. J Pathol. 2017; 241(3): 362–74. doi:10.1002/path.4845.; Lu Z., Yang C., He W., Zhou J., Xiang R. Nomogram to predict risk and prognosis of synchronous lung metastasis in renal cell carcinoma: A large cohort analysis. Medicine (Baltimore). 2022; 101(27). doi:10.1097/MD.0000000000029764.; Petrozza V., Costantini M., Tito C., Giammusso L.M., Sorrentino V., Cacciotti J., Porta N., Iaiza A., Pastore A.L., Di Carlo A., Simone G., Carbone A., Gallucci M., Fazi F. Emerging role of secreted miR-210-3p as potential biomarker for clear cell Renal Cell Carcinoma metastasis. Cancer Biomark. 2020; 27(2): 181–8. doi:10.3233/CBM-190242.; https://www.siboncoj.ru/jour/article/view/3037

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    Academic Journal

    المساهمون: The study was supported by the Russian Science Foundation grant No. 22-15-00212 dated May 13, 2022 “Transcriptomic and proteomic markers for the prognosis and effectiveness of therapy for metastatic colon cancer.”, Работа поддержана грантом РНФ № 22-15-00212 от 13.05.2022 «Транскриптомные и протеомные маркеры прогноза и эффективности терапии метастатического рака толстой кишки».

    المصدر: Siberian journal of oncology; Том 23, № 1 (2024); 162-169 ; Сибирский онкологический журнал; Том 23, № 1 (2024); 162-169 ; 2312-3168 ; 1814-4861

    وصف الملف: application/pdf

    Relation: https://www.siboncoj.ru/jour/article/view/2969/1207; Sung H., Ferlay J., Siegel R.L., Laversanne M., Soerjomataram I., Jemal A., Bray F. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin. 2021; 71(3): 209–49. doi:10.3322/caac.21660.; Engstrand J., Strömberg C., Nilsson H., Freedman J., Jonas E. Synchronous and metachronous liver metastases in patients with colorectal cancer-towards a clinically relevant definition. World J Surg Oncol. 2019; 17(1): 228. doi:10.1186/s12957-019-1771-9.; Calderon Novoa F., Ardiles V., de Santibañes E., Pekolj J., Goransky J., Mazza O., Sánchez Claria R., de Santibañes M. Pushing the Limits of Surgical Resection in Colorectal Liver Metastasis: How Far Can We Go? Cancers (Basel). 2023; 15(7): 2113. doi:10.3390/cancers15072113.; Mohamad I., Barry A., Dawson L., Hosni A. Stereotactic body radiation therapy for colorectal liver metastases. Int J Hyperthermia. 2022; 39(1): 611–9. doi:10.1080/02656736.2021.1923836.; Афанасьев С.Г., Тузиков С.А. Нерезектабельные опухоли печени (обзор литературы). Сибирский онкологический журнал. 2006; 1: 49–54.; de Jong M.C., Pulitano C., Ribero D., Strub J., Mentha G., Schulick R.D., Choti M.A., Aldrighetti L., Capussotti L., Pawlik T.M. Rates and patterns of recurrence following curative intent surgery for colorectal liver metastasis: an international multi-institutional analysis of 1669 patients. Ann Surg. 2009; 250(3): 440–8. doi:10.1097/SLA.0b013e3181b4539b.; Tournigand C., André T., Achille E., Lledo G., Flesh M., Mery-Mignard D., Quinaux E., Couteau C., Buyse M., Ganem G., Landi B., Colin P., Louvet C., de Gramont A. FOLFIRI followed by FOLFOX6 or the reverse sequence in advanced colorectal cancer: a randomized GERCOR study. J Clin Oncol. 2004; 22(2): 229–37. doi:10.1200/JCO.2004.05.113. Corrected and republished in: J Clin Oncol. 2023; 41(19): 3469–77.; Benoist S., Brouquet A., Penna C., Julié C., El Hajjam M., Chagnon S., Mitry E., Rougier P., Nordlinger B. Complete response of colorectal liver metastases after chemotherapy: does it mean cure? J Clin Oncol. 2006; 24(24): 3939–45. doi:10.1200/JCO.2006.05.8727.; Добродеев А.Ю., Костромицкий Д.Н., Тарасова А.С., Афанасьев С.Г., Бабышкина Н.Н., Пономарева А.А., Ермоленко Р.В., Фролова И.Г., Черемисина О.В. Непосредственные результаты неоадъювантной химиотерапии у больных метастатическим колоректальным раком с изолированным поражением печени. Сибирский онкологический журнал. 2022; 21(6): 17–24. doi.:10.21294/1814-4861-2022-21-6-17-24.; Chow F.C., Chok K.S. Colorectal liver metastases: An update on multidisciplinary approach. World J Hepatol. 2019; 11(2): 150–72. doi:10.4254/wjh.v11.i2.150.; Ardito F., Panettieri E., Vellone M., Ferrucci M., Coppola A., Silvestrini N., Arena V., Adducci E., Capelli G., Vecchio F.M., Giovannini I., Nuzzo G., Giuliante F. The impact of R1 resection for colorectal liver metastases on local recurrence and overall survival in the era of modern chemotherapy: An analysis of 1,428 resection areas. Surgery. 2019; 165(4): 712–20. doi:10.1016/j.surg.2018.09.005.; Falcone A., Ricci S., Brunetti I., Pfanner E., Allegrini G., Barbara C., Crinò L., Benedetti G., Evangelista W., Fanchini L., Cortesi E., Picone V., Vitello S., Chiara S., Granetto C., Porcile G., Fioretto L., Orlandini C., Andreuccetti M., Masi G.; Gruppo Oncologico Nord Ovest. Phase III trial of infusional fluorouracil, leucovorin, oxaliplatin, and irinotecan (FOLFOXIRI) compared with infusional fluorouracil, leucovorin, and irinotecan (FOLFIRI) as first-line treatment for metastatic colorectal cancer: the Gruppo Oncologico Nord Ovest. J Clin Oncol. 2007; 25(13): 1670–6. doi:10.1200/JCO.2006.09.0928.; Martin J., Petrillo A., Smyth E.C., Shaida N., Khwaja S., Cheow H.K., Duckworth A., Heister P., Praseedom R., Jah A., Balakrishnan A., Harper S., Liau S., Kosmoliaptsis V., Huguet E. Colorectal liver metastases: Current management and future perspectives. World J Clin Oncol. 2020; 11(10): 761–808. doi:10.5306/wjco.v11.i10.761.; Araujo R.L.C., Milani J.M., Armentano D.P., Moreira R.B., Pinto G.S.F., de Castro L.A., Lucchesi F.R. Disappearing colorectal liver metastases: Strategies for the management of patients achieving a radiographic complete response after systemic chemotherapy. J Surg Oncol. 2020; 121(5): 848–56. doi:10.1002/jso.25784.; Xu D., Yan X.L., Liu J.M., Li J., Xing B.C. The characteristics and long-term survival of patients with colorectal liver metastases with pathological complete response after chemotherapy. J Cancer. 2020; 11(21): 6256–63. doi:10.7150/jca.47911.; Adam R., Wicherts D.A., de Haas R.J., Aloia T., Lévi F., Paule B., Guettier C., Kunstlinger F., Delvart V., Azoulay D., Castaing D. Complete pathologic response after preoperative chemotherapy for colorectal liver metastases: myth or reality? J Clin Oncol. 2008; 26(10): 1635–41. doi:10.1200/JCO.2007.13.7471.; Barimani D., Kauppila J.H., Sturesson C., Sparrelid E. Imaging in disappearing colorectal liver metastases and their accuracy: a systematic review. World J Surg Onc. 2020; 18. doi:10.1186/s12957-020-02037-w.; https://www.siboncoj.ru/jour/article/view/2969

  8. 8
    Academic Journal

    المصدر: Siberian journal of oncology; Том 23, № 1 (2024); 155-161 ; Сибирский онкологический журнал; Том 23, № 1 (2024); 155-161 ; 2312-3168 ; 1814-4861

    وصف الملف: application/pdf

    Relation: https://www.siboncoj.ru/jour/article/view/2968/1206; Поликарпов А.А., Таразов П.Г., Гранов Д.А., Полысалов В.Н. Рентгенэндоваскулярные процедуры в лечении больных с нерезектабельными метастазами колоректального рака в печени. Российский онкологический журнал. 2014; 19(4): 40–1.; Adam R., Kitano Y. Multidisciplinary approach of liver metastases from colorectal cancer. Ann Gastroenterol Surg. 2019; 3(1): 50–6. doi:10.1002/ags3.12227.; Tzeng C., Aloia T. Colorectal Liver Metastases. J Gastrointest Surg. 2012; 17: 195–201. doi:10.1007/s11605-012-2022-3.; Gruber-Rouh T., Naguib N., Eichler K., Ackermann H., Zangos S., Trojan J., Beeres M., Harth M., Schulz B., Nour-Eldin A., Vogl T.J. Transarterial chemoembolization of unresectable systemic chemotherapy-refractory liver metastases from colorectal cancer: Long-term results over a 10-year period. Int J Cancer. 2013; 134: 1225–31. doi:10.1002/ijc.28443.; Alexander H.R., Bartlett D.L., Libutti S.K., Pingpank J.F., Fraker D.L., Royal R., Steinberg S.M., Helsabeck C.B., Beresneva T.H. Analysis of factors associated with outcome in patients undergoing isolated hepatic perfusion for unresectable liver metastases from colorectal center. Ann Surg Oncol. 2009; 16(7): 1852–9. doi:10.1245/s10434-009-0482-9.; Ben-Shabat I., Hansson C.,Eilard M., Cahlin C., Rizell M., Lindnér P., Mattsson J., Bagge R. Isolated hepatic perfusion as a treatment for liver metastases of uveal melanoma. J Vis Exp. 2015; (95): 52490. doi:10.3791/52490.; van Iersel L.B.J., Koopman M., van de Velde C.J.H., Mol L., van Persijn van Meerten E.L., Hartgrink H.H., Kuppen P.J.K., Vahrmeijer A.L., Nortier J.W.R., Tollenaar R.A.E.M., Punt C., Gelderblom H. Management of isolated nonresectable liver metastases in colorectal cancer patients: a case-control study of isolated hepatic perfusion with melphalan versus systemic chemotherapy. Ann Oncol. 2010; 21(8): 1662–7. doi:10.1093/annonc/mdp589.; Hafström L.R., Holmberg S.B., Naredi P.L., Lindnér P.G., Bengtsson A., Tidebrant G., Scherstén T.S. Isolated hyperthermic liver perfusion with chemotherapy for liver malignancy. Surg Oncol. 1994; 3(2): 103–8. doi:10.1016/0960-7404(94)90005-1.; Huibers A., DePalo D.K., Perez M.C., Zager J.S., Olofsson Bagge R. Isolated hyperthermic perfusions for cutaneous melanoma in-transit metastasis of the limb and uveal melanoma metastasis to the liver. Clin Exp Metastasis. 2023. doi:10.1007/s10585-023-10234-6.; Olofsson Bagge R., Nelson A., Shafazand A., All-Eriksson C., Cahlin C., Elander N., Helgadottir H., Kiilgaard J.F., Kinhult S., Ljuslinder I., Mattsson J., Rizell M., Sternby Eilard M., Ullenhag G.J., Nilsson J.A., Ny L., Lindnér P. Isolated Hepatic Perfusion With Melphalan for Patients With Isolated Uveal Melanoma Liver Metastases: A Multicenter, Randomized, Open-Label, Phase III Trial (the SCANDIUM Trial). J Clin Oncol. 2023; 41(16): 3042–50. doi:10.1200/JCO.22.01705.; Bethlehem M.S., Katsarelias D., Olofsson Bagge R. Meta-Analysis of Isolated Hepatic Perfusion and Percutaneous Hepatic Perfusion as a Treatment for Uveal Melanoma Liver Metastases. Cancers (Basel). 2021; 13(18): 4726. doi:10.3390/cancers13184726.; Eggermont A.M., van IJken M.G., van Etten B., van der Sijp J.R., ten Hagen T.L., Wiggers T., Oudkerk M., de Boeck G., de Bruijn E.A. Isolated hypoxic hepatic perfusion (IHHP) using balloon catheter techniques: from laboratory to the clinic towards a percutaneous procedure. Hepatogastroenterology. 2000; 47(33): 776–81.; Dewald C.L.A., Becker L.S., Maschke S.K., Meine T.C., Alten T.A., Kirstein M.M., Vogel A., Wacker F.K., Meyer B.C., Hinrichs J.B. Percutaneous isolated hepatic perfusion (chemosaturation) with melphalan following right hemihepatectomy in patients with cholangiocarcinoma and metastatic uveal melanoma: peri- and post-interventional adverse events and therapy response compared to a matched group without prior liver surgery. Clin Exp Metastasis. 2020; 37(6): 683–92. doi:10.1007/s10585-020-10057-9.; Vogel A., Ochsenreither S., Zager J.S., Wacker F., Saborowski A. Chemosaturation for primary and secondary liver malignancies: A comprehensive update of current evidence. Cancer Treat Rev. 2023; 113: 102501. doi:10.1016/j.ctrv.2022.102501.; Rowcroft A., Loveday B.P.T., Thomson B.N.J., Banting S., Knowles B. Systematic review of liver directed therapy for uveal melanoma hepatic metastases. HPB (Oxford). 2020; 22(4): 497–505. doi:10.1016/j.hpb.2019.11.002.; https://www.siboncoj.ru/jour/article/view/2968

  9. 9
    Academic Journal

    المساهمون: The study was funded within the framework of the state task (no. AAAAA-A18-118030790008-7) of the Ministry of Health of the Russian Federation., Исследование профинансировано в рамках государственного задания (№ АААА-А18-118030790008-7) Министерства здравоохранения Российской Федерации.

    المصدر: Siberian journal of oncology; Том 22, № 6 (2023); 92-102 ; Сибирский онкологический журнал; Том 22, № 6 (2023); 92-102 ; 2312-3168 ; 1814-4861 ; 10.21294/1814-4861-2017-0-31-36

    وصف الملف: application/pdf

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Vaccines (Basel). 2022; 10(1): 78. doi:10.3390/vaccines10010078.; Yu-Ling L., Hua Z., Xiu-Bao R. Relationship of VEGF/VEGFR with immune and cancer cells: staggering or forward? Cancer Biol Med. 2016; 13(2): 206–14. doi:10.20892/j.issn.2095-3941.2015.0070.; Sun Y., Ai X., Shen S., Gu L., Lu S. Detection and correlation analysis of serum cytokines in non-small-cell lung cancer patients with bone and non-bone metastases. Patient Prefer Adherence. 2015; 9: 1165–9. doi:10.2147/PPA.S86605.; Chen W., Qin T., Liu S. Cytokines, breast cancer stem cells (BCSCs) and chemoresistance. Clin Trans Med. 2018; 7(1): 27. doi:10.1186/s40169-018-0205-6.; Jabeen S., Espinoza J.A., Torland L.A., Zucknick M., Kumar S., Haakensen V.D., Lüders T., Engebraaten O., Børresen-Dale A., Kyte J.A., Gromov P., Naume B., Kristensen V., Gromova I., Tekpli X. Noninvasive profiling of serum cytokines in breast cancer patients and clinicopathological characteristics. OncoImmunology. 2018; 8(2). doi:10.1080/2162402X.2018.1537691.; Kawaguchi K., Sakurai M., Yamamoto Y., Suzuki E., Tsuda M., Kataoka T.R., Hirata M., Nishie M., Nojiri T., Kumazoe M., Saito K., Toi M. Alteration of specifc cytokine expression patterns in patients with breast cancer. Sci Rep. 2019; 9(1): 2924. doi:10.1038/s41598-019-39476-9.; Engel J., Eckel R., Halfter K., Schubert-Fritschle G., Hölzel D. Breast cancer: emerging principles of metastasis, adjuvant and neoadjuvant treatment from cancer registry data. J Cancer Res and Clin Oncol. 2023; 149(2): 721–35. doi:10.1007/s00432-022-04369-4.; Gong G., Kwon M. J., Han J., Lee H.J., Lee S.K., Lee J.E., Lee S.H., Park S., Choi J.S., Cho S.Y., Ahn S.H., Lee J.W., Cho S.R., Moon Y., Nam B.H., Nam S.J., Choi Y.L., Shin Y.K. A new molecular prognostic score for predicting the risk of istant metastasis in patients with HR+/HER2- early breast cancer. Scientifc Reports. 2017; 7. doi:10.1038/srep45554.; Zhang K., Luo Z., Zhang Y., Song X., Zhang L., Wu L., Liu J. Long non-coding RNAs as novel biomarkers for breast cancer invasion and metastasis. Oncology Lett. 2017; 14(2): 1895–904. doi:10.3892/ol.2017.6462.; Lee K.K., Chng W.J., Jha S. Prognostic biomarkers for breast cancer metastasis. Cancer Metastasis. 2018: 96–113. doi:10.5772/intechopen.80576.; Wu X., Baig A., Kasymjanova G., Kaf K., Holcroft C., Mekouar H., Carbonneau A., Bahoric B., Sultanem K., Muanza T. Pattern of local recurrence and distant metastasis in breast cancer by molecular subtype. Cureus. 2016; 8(12). doi:10.7759/cureus.924.; Ahmed A.A., Hassen A., Osman N., Elroufaie H. Immunohistochemical expression of angiogenic marker CD34 in invasive carcinoma of the breast. Eur Acad Res. 2015; 3(9): 9592–600.; Chen Z., Xu S., Xu W., Huang J., Zhang G.U., Lei L., Shao X., Wang X. Expression of cluster of diferentiation 34 and vascular endothelial growth factor in breast cancer, and their prognostic signifcance. Oncol Lett. 2015; 10(2): 723–9. doi:10.3892/ol.2015.3348.; Khan A.A., Alam K., Harris H. A Clinicopathological study of CD34 antigen expression in benign and malignant breast lesions. J Clin Exp Pathol. 2017; 7(4): 321. doi:10.4172/2161-0681.1000321.; Mehdi Hassanpour M., Salybekov A., Kobayashi S., Asahara T. CD34 positive cells as endothelial progenitor cells in biology and medicine. Front Cell Dev Biol. 2023; 17: 11: 1128134. doi:10.3389/fcell.2023.1128134.; Chen M., Sun H., Zhao Y., Fu W., Yang L., Gao S., Li L., Jiang H., Jin W. Comparison of patterns and prognosis among distant metastatic breast cancer patients by age groups: A SEER population-based analysis. Sci Rep. 2017; 7(1). doi:10.1038/s41598-017-10166-8.; Cai S., Zuo W., Lu X., Gou Z., Zhou Y., Liu P., Pan Y., Chen S. The prognostic impact of age at diagnosis upon breast cancer of diferent immunohistochemical subtypes: a surveillance, epidemiology, and end results (SEER) population-based analysis. Front Oncol. 2020; 10: 1729. doi:10.3389/fonc.2020.01729.; Kondov B., Milenkovikj Z., Kondov G., Petrushevska G., Basheska N., Bogdanovska-Todorovska M., Tolevska N., Ivkovski L. Presentation of the molecular subtypes of breast cancer detected by immunohistochemistry in surgically treated patients. J Med Sci. 2018; 6(6): 961–7. doi:10.3889/oamjms.2018.231.; Autenshlyus A., Arkhipov S., Kunts T., Marinkin I., Mikhailova E., Karpukhina X., Varaksin N. Cytokine profles of tumor supernatants in invasive ductal cancer and fbroadenoma of the breast and its relationship with VEGF-A expression in the tumors. Int J Immunopathol Pharmacol. 2017; 30(1): 83–8. doi:10.1177/0394632016681306.; Agilent [Internet]. ER/PR PharmDx Interpretation Manual. 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  10. 10
    Academic Journal

    المساهمون: The study was supported by the Russian Science Foundation (grant No. 21-15-00140 “Prediction of sites of breast cancer hematogenous metastases”)., Исследование было поддержано Российским научным фондом (грант № 21-15-00140 «Прогнозирование локализации гематогенных метастазов при раке молочной железы»).

    المصدر: Siberian journal of oncology; Том 22, № 6 (2023); 103-110 ; Сибирский онкологический журнал; Том 22, № 6 (2023); 103-110 ; 2312-3168 ; 1814-4861 ; 10.21294/1814-4861-2017-0-31-36

    وصف الملف: application/pdf

    Relation: https://www.siboncoj.ru/jour/article/view/2840/1185; Злокачественные новообразования в России в 2020 году (заболеваемость и смертность). Под ред. А.Д. Каприна, В.В. Старинского, А.О. Шахзадовой. М., 2021. 252 с.; Su C.Y., Li J.Q., Zhang L.L., Wang H., Wang F.H., Tao Y.W., Wang Y.Q., Guo Q.R., Li J.J., Liu Y., Yan Y.Y., Zhang J.Y. The Biological Functions and Clinical Applications of Integrins in Cancers. Front Pharmacol. 2020; 11. doi:10.3389/fphar.2020.579068.; Bagati A., Kumar S., Jiang P., Pyrdol J., Zou A.E., Godicelj A., Mathewson N.D., Cartwright A.N.R., Cejas P., Brown M., Giobbie-Hurder A., Dillon D., Agudo J., Mittendorf E.A., Liu X.S., Wucherpfennig K.W. Integrin αvβ6-TGFβ-SOX4 Pathway Drives Immune Evasion in Triple-Negative Breast Cancer. Cancer Cell. 2021; 39(1): 54–67. doi:10.1016/j.ccell.2020.12.001.; Sökeland G., Schumacher U. The functional role of integrins during intra- and extravasation within the metastatic cascade. Mol Cancer. 2019; 18(1): 12. doi:10.1186/s12943-018-0937-3.; Kechagia J.Z., Ivaska J., Roca-Cusachs P. Integrins as biomechanical sensors of the microenvironment. Nat Rev Mol Cell Biol. 2019; 20(8): 457–73. doi:10.1038/s41580-019-0134-2.; Lokuhetty D., White, V.A., Watanabe R., Cree I.A. WHO Classifcation of Tumours. Breast tumours. Lyon (France): International Agency for Pesearch on Cancer, 2019.; Bertero L., Massa F., Metovic J., Zanetti R., Castellano I., Ricardi U., Papotti M., Cassoni P. Eighth Edition of the UICC Classifcation of Malignant Tumours: an overview of the changes in the pathological TNM classifcation criteria-What has changed and why? Virchows Arch. 2018; 472(4): 519–31. doi:10.1007/s00428-017-2276-y.; Стенина М.Б., Жукова Л.Г., Королева И.А., Пароконная А.А., Семиглазова Т.Ю., Тюляндин С.А., Фролова М.А. Практические рекомендации по лекарственному лечению рака молочной железы. Злокачественные опухоли: Практические рекомендации по лекарственному лечению рака молочной железы. Злокачественные опухоли. 2020; 10(3s2-1): 145–82. doi:10.18027/2224-5057-2020-10-3s2-09.; Truong H.H., Xiong J., Ghotra V.P., Nirmala E., Haazen L., Le Dévédec S.E., Balcioğlu H.E., He S., Snaar-Jagalska B.E., Vreugdenhil E., Meerman J.H., van de Water B., Danen E.H. β1 integrin inhibition elicits a prometastatic switch through the TGFβ-miR-200-ZEB network in E-cadherin-positive triplenegative breast cancer. Sci Signal. 2014; 7(312). doi:10.1126/scisignal.2004751.; Seguin L., Kato S., Franovic A., Camargo M.F., Lesperance J., Elliott K.C., Yebra M., Mielgo A., Lowy A.M., Husain H., Cascone T., Diao L., Wang J., Wistuba I.I., Heymach J.V., Lippman S.M., Desgrosellier J.S., Anand S., Weis S.M., Cheresh D.A. An integrin β₃-KRAS-RalB complex drives tumour stemness and resistance to EGFR inhibition. Nat Cell Biol. 2014; 16(5): 457–68. doi:10.1038/ncb2953.; Xiong J., Yan L., Zou C., Wang K., Chen M., Xu B., Zhou Z., Zhang D. Integrins regulate stemness in solid tumor: an emerging therapeutic target. J Hematol Oncol. 2021; 14(1): 177. doi:10.1186/s13045-021-01192-1.; Cooper J., Giancotti F.G. Integrin Signaling in Can- cer: Mechanotransduction, Stemness, Epithelial Plasticity, and Therapeutic Resistance. Cancer Cell. 2019; 35(3): 347–67. doi:10.1016/j.ccell.2019.01.007.; Böger C., Warneke V.S., Behrens H.M., Kalthoff H., Good- man S.L., Becker T., Röcken C. Integrins αvβ3 and αvβ5 as prognostic, diagnostic, and therapeutic targets in gastric cancer. Gastric Cancer. 2015; 18(4): 784–95. doi:10.1007/s10120-014-0435-2.; Berghoff A.S., Kovanda A.K., Melchardt T., Bartsch R., Hainfellner J.A., Sipos B., Schittenhelm J., Zielinski C.C., Widhalm G., Dieckmann K., Weller M., Goodman S.L., Birner P., Preusser M. αvβ3, αvβ5 and αvβ6 integrins in brain metastases of lung cancer. Clin Exp Metastasis. 2014; 31(7): 841–51. doi:10.1007/s10585-014-9675-0.; Hoshino A., Costa-Silva B., Shen T.L., Rodrigues G., Hashimoto A., Tesic Mark M., Molina H., Kohsaka S., Di Giannatale A., Ceder S., Singh S., Williams C., Soplop N., Uryu K., Pharmer L., King T., Bojmar L., Davies A.E., Ararso Y., Zhang T., Zhang H., Hernandez J., Weiss J.M., Dumont-Cole V.D., Kramer K., Wexler L.H., Narendran A., Schwartz G.K., Healey J.H., Sandstrom P., Labori K.J., Kure E.H., Grandgenett P.M., Hollingsworth M.A., de Sousa M., Kaur S., Jain M., Mallya K., Batra S.K., Jarnagin W.R., Brady M.S., Fodstad O., Muller V., Pantel K., Minn A.J., Bissell M.J., Garcia B.A., Kang Y., Rajasekhar V.K., Ghajar C.M., Matei I., Peinado H., Bromberg J., Lyden D. Tumour exosome integrins determine organotropic metastasis. Nature. 2015; 527(7578): 329–35. doi:10.1038/nature15756.; https://www.siboncoj.ru/jour/article/view/2840

  11. 11
    Academic Journal

    المساهمون: The work was performed without external funding, Работа выполнена без спонсорской поддержки

    المصدر: Head and Neck Tumors (HNT); Том 13, № 4 (2023); 116-123 ; Опухоли головы и шеи; Том 13, № 4 (2023); 116-123 ; 2411-4634 ; 2222-1468 ; 10.17650/2222-1468-2023-13-4

    وصف الملف: application/pdf

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    المصدر: Head and Neck Tumors (HNT); Том 14, № 1 (2024); 56-62 ; Опухоли головы и шеи; Том 14, № 1 (2024); 56-62 ; 2411-4634 ; 2222-1468 ; 10.17650/2222-1468-2024-14-1

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    المصدر: Meditsinskiy sovet = Medical Council; № 10 (2024); 46-53 ; Медицинский Совет; № 10 (2024); 46-53 ; 2658-5790 ; 2079-701X

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    المصدر: Meditsinskiy sovet = Medical Council; № 10 (2024); 60-65 ; Медицинский Совет; № 10 (2024); 60-65 ; 2658-5790 ; 2079-701X

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    المصدر: Meditsinskiy sovet = Medical Council; № 22 (2023); 181-187 ; Медицинский Совет; № 22 (2023); 181-187 ; 2658-5790 ; 2079-701X

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    Academic Journal

    المصدر: Malignant tumours; Принято в печать ; Злокачественные опухоли; Принято в печать ; 2587-6813 ; 2224-5057

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  17. 17
    Academic Journal

    المصدر: Malignant tumours; Том 14, № 1 (2024); 83-91 ; Злокачественные опухоли; Том 14, № 1 (2024); 83-91 ; 2587-6813 ; 2224-5057

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