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  3. 3
    Academic Journal

    Source: Surgery and Oncology; Том 10, № 1 (2020); 20-27 ; Хирургия и онкология; Том 10, № 1 (2020); 20-27 ; 2949-5857

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    Relation: https://www.onco-surgery.info/jour/article/view/462/331; Tudyka V., Blomqvist L., Beets-Tan R.G.H. et al. EURECCA consensus conference highlights about colon & rectal cancer multidisciplinary management: The radiology experts review. Ejso 2014;40(4):469–75. DOI:10.1016/j.ejso.2013.10.029.; Sauer R., Becker H., Hohenberger W. et al. Preoperative versus postoperative chemoradiotherapy for rectal cancer. New Engl J Med 2004;351(17):1731–40. DOI:10.1056/NEJMoa040694.; Kapiteijn E., Marijnen C.A.M., Nagtegaal I.D. et al. Dutch Colorectal Canc G. Preoperative radiotherapy combined with total mesorectal excision for resectable rectal cancer. New Engl J Med 2001;345(9):638–46. DOI:10.1056/NEJMoa010580.; Patel U.B., Taylor F., Blomqvist L. et al. Magnetic resonance imaging-detected tumor response for locally advanced rectal cancer predicts survival outcomes: MERCURY experience. J Clin Oncol 2011;29(28):3753–60. DOI:10.1200/JCO.2011.34.9068.; Lee E.S., Kim M.J., Park S.C. et al. Magnetic resonance imaging-detected extramural venous invasion in rectal cancer before and after preoperative chemoradiotherapy: diagnostic performance and prognostic significance. Eur Rad 2018;28(2):496–505. DOI:10.1007/s00330-017-4978-6.; Patel U.B., Brown G., Machado I. et al. MRI assessment and outcomes in patients receiving neoadjuvant chemotherapy only for primary rectal cancer: long-term results from the GEMCAD 0801 trial. Ann Oncol 2017;28(2):344–53. DOI:10.1093/annonc/mdw616.; Habr-Gama A., Gama-Rodrigues J., Juliao G.P.S. et al. Local recurrence after complete clinical response and watch and wait in rectal cancer after neoadjuvant chemoradiation: impact of salvage therapy on local disease control. Int J Rad Oncol Biol Phys 2014;88(4):822–8. DOI:10.1016/j.ijrobp.2013.12.012; Patel U.B., Brown G., Rutten H. et al. Comparison of magnetic resonance imaging and histopathological response to chemoradiotherapy in locally advanced rectal cancer. Ann Surg Oncol 2012;19(9):2842–52.; Xiao H., Tan Y.T., Li W.Y. et al. Tumor volume reduction rate is superior to RECIST for predicting the pathological response of rectal cancer treated with neoadjuvant chemoradiation: Results from a prospective study. Oncol Lett 2015;9(6):2680–6. DOI:10.1245/s10434-012-2309-3.; Yeo S.-G., Kim D.Y., Park J.W. et al. Tumor volume reduction rate after preoperative chemoradiotherapy as a prognostic factor in locally advanced rectal cancer. Int J Rad Oncol Biol Phys 2012;82(2):193–9. DOI:10.1016/j.ijrobp.2011.03.022.; Han Y.B., Oh S.N., Choi M.H. et al. Clinical impact of tumor volume reduction in rectal cancer following preoperative chemoradiation. Diagn Interv Imaging 2016;97(9):843–50.; Nougaret S., Rouanet P., Molinari N. et al. MR volumetric measurement of low rectal cancer helps predict tumor response and outcome after combined chemotherapy and radiation therapy. Radiology 2012;263(2):409–18. DOI:10.1148/radiol.12111263.; Yu S.K.T., Tait D., Chau I., Brown G. MRI predictive factors for tumor response in rectal cancer following neoadjuvant chemoradiation therapy – implications for induction chemotherapy? Int J Rad Oncol Biol Phys 2013;87(3):505–11. DOI:10.1016/j.ijrobp.2013.06.2052.; Kuo L.-J., Liu M.-C., Jian J.J.-M. et al. Is final TNM staging a predictor for survival in locally advanced rectal cancer after preoperative chemoradiation therapy? Ann Surg Oncol 2007;14(10):2766–72. DOI:10.1245/s10434-007-9471-z.; Siddiqui M.R.S., Bhoday J., Battersby N.J. et al. Defining response to radiotherapy in rectal cancer using magnetic resonance imaging and histopathological scales. World J Gastroenterol 2016;22(37):8414–34. DOI:10.3748/wjg.v22.i37.8414.; Sclafani F., Brown G., Cunningham D. et al. PAN-EX: a pooled analysis of two trials of neoadjuvant chemotherapy followed by chemoradiotherapy in MRI-defined, locally advanced rectal cancer. Ann Oncol 2016;27(8):1557–65. DOI:10.1093/annonc/mdw215.; Rullier E., Rouanet P., Tuech J.J. et al. Organ preservation for rectal cancer (GRECCAR 2): a prospective, randomised, open-label, multicentre, phase 3 trial. Lancet 2017;390(10093):469–79. DOI:10.1016/S0140-6736(17)31056-5.; Benson A.B., Venook A.P., Al-Hawary M.M. et al. Rectal Cancer, Version 2.2018, NCCN Clinical Practice Guidelines in Oncology. JNCCN 2018;16(7):874–901. DOI:10.6004/jnccn.2018.0061.

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    Academic Journal

    Source: Medical Visualization; № 3 (2019); 82-106 ; Медицинская визуализация; № 3 (2019); 82-106 ; 2408-9516 ; 1607-0763

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    Relation: https://medvis.vidar.ru/jour/article/view/797/565; GLOBOCAN 2018. Estimated cancer incidence, mortality and prevalence worldwide in 2012. [cited12 Sept 2018]. URL: http://gco.iarc.fr; Каприн А.Д., Старинский В.В., Петрова Г.В. Состояние онкологической помощи населению России в 2017 году М.: МНИОИ им. П.А. Герцена – филиал ФГБУ “НМИЦ радиологии” Минздрава России, 2018. 236 с.; In situ cervical carcinoma incidence statistics URL: https://www.cancerresearchuk.org/health-professional/cancerstatistics/statistics-by-cancer-type/cervical-cancer/incidence-in-situ?_ga=2.135120753.116604086.1551041700-535305463.1543059799; Barchuk A., Bespalov A., Huhtalac H., Chimedd T., Laricheva I., Belyaev A., Brayd F., Anttila A., Auvinen A. Breast and cervical cancer incidence and mortality trends in Russia 1980–2013. Cancer Epidemiol. 2018; 55: 73–80. https://doi.org/10.1016/j.canep.2018.05.008.; International Collaboration of Epidemiological Studies of Cervical Cancer. Comparison of risk factors for invasive squamous cell carcinoma and adenocarcinoma of the cervix: collaborative reanalysis of individual data on 8,097 women with squamous cell carcinoma and 1,374 women with adenocarcinoma from 12 epidemiological studies. Int. J. Cancer. 2007; 120 (4): 885.; Downey K., Riches S.F., Morgan A.V., Giles S., Attygalle A.D., Ind T.E.J., Barton D., Shepherd J.H , Desouza N.M. Relationship between imaging biomarkers of stage I cervical cancer and poor prognosis histologic features: quantitative histogram analysis of diffusion-weighted MR images. Am. J. Roentgenol. 2013; 200 (2): 314–320. https://doi.org/10.2214/AJR.12.9545.; Follen M., Levenback C.F., Iyer R.B., Grigsby P.W., Boss E.A., Delpassand E.S., Fornage B.D., Fishman E.K. Imaging in cervical cancer. Cancer. 2003; 98 (9): 2028–2038.; Bourgioti C., Chatoupis K., Moulopoulos L.A. Current imaging strategies for the evaluation of uterine cervical cancer. Wld J. 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Tomogr. 2010; 34 (6): 855–864. https://doi.org/10.1097/RCT.0b013e3181ed3090.; Sala E., Wakely S., Senior E., Lomas D. MRI of malignant neoplasms of the uterine corpus and cervix. Am. J. Roentgenol. 2007; 188: 1577–1587. https://doi.org/10.2214/AJR.06.1196.; Nicolate V., Carignan L., Bourdon F., Prosmanne O. MR imaging of cervical carcinoma: A practical staging approach. RadioGraphics. 2000; 20: 1539–1549. https://doi.org/10.1148/radiographics.20.6.g00nv111539.; Sala E., Rockall A.G., Freeman S.J., Mitchell D.G., Reinhold C. The added role of MR imaging in treatment stratification of patients with gynecologic malignancies: what the radiologist needs to know. Radiology. 2013; 266: 717–740. https://doi.org/10.1148/radiol.12120315.; Sakuragi N., Satoh C., Takeda N., Hareyama H., Takeda M., Yamamoto R., Fujimoto T., Oikawa M., Fujino T., Fujimoto S. Incidence and distribution pattern of pelvic and paraaortic lymph node metastasis in patients with stages IB, IIA, and IIB cervical carcinoma treated with radical hysterectomy. Cancer. 1999; 85: 1547–1554.; Eisenhauera E.A., Therasseb P., Bogaertsc J., Schwartzd L.H., Sargente D., Fordf R., Danceyg J., Arbuckh S., Gwytheri S., Mooneyg M., Rubinsteing L., Shankarg L., Doddg L.,Kaplanj R., Lacombec D., Verweij J. New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1). Eur. J. Cancer. 2009; 45: 228–247. https://doi.org/10.1016/j.ejca.2008.10.026.; Hong K.S., Ju W., Choi H.J., Kim J.K., Kim M.H., Cho K.S. Differential diagnostic performance of magnetic resonance imaging in the detection of lymph node metastases according to the tumor size in early-stage cervical cancer patients. Int. J. Gynecol. Cancer. 2010; 20: 841–846. https://doi.org/10.1111/IGC.0b013e3181db5140.; Shen G., Zhou H., Jia Z., Deng H. Diagnostic performance of diffusion-weighted MRI for detection of pelvic metastatic lymph nodes in patients with cervical cancer: a systematic review and meta-analysis. Br. J. Radiol. 2015; 88 (1052): 20150063. https://doi.org/10.1259/bjr.20150063.; Drieskens O., Stroobants S., Gysen M., Vandenbosch G., Mortelmans L., Vergote I. Positron emission tomography with FDG in the detection of peritoneal and retroperitoneal metastases of ovarian cancer. Gynecol. Obstet. Invest. 2003; 55: 130–134. https://doi.org/10.1159/000071525.; Singh N., Arif S. Histopathologic parameters of prognosis in cervical cancer – a review. Int. J. Gynecol. Cancer. 2004; 14: 741–750. https://doi.org/10.1111/j.1048-891X.2004.014504.x.; Reagan J.W., Fu Y.S. Histologic types and prognosis of cancers of the uterine cervix. Int. J. Radiat. Oncol. Biol. Phys. 1979; 5: 1015–1020.; Crissman J.D., Budhraja M., Aron B.S. et al. Histopathologic prognostic factors in stage II and III squamous cell carcinoma of the uterine cervix. Int. J. Gynecol. Pathol. 1987; 6: 97–103.; Cohen J.G., Kapp D.S., Shin J.Y. et al. Small cell carcinoma of the cervix: treatment and survival outcomes of 188 patients. Am. J. Obstet Gynecol. 2010; 203 (347): 341–346. https://doi.org/10.1016/j.ajog.2010.04.019.; Mangler M., Lanowska M., Kohler C., Vercellino F., Schneider A., Speiser D. Pattern of cancer recurrence in 320 patients after radical vaginal trachelectomy. Int. J. Gynecol Cancer. 2014; 24: 130–134. https://doi.org/10.1097/IGC.0000000000000012.; Park J.Y., Lee J.W., Park B.K., Lee Y.Y., Choi C.H., Kim T.J., Bae D.S., Kim B.G., Park J.J., Park S.Y., Kim C.K. Postoperative outcomes of MR-invisible stage IB1 cervical cancer. Am. J. Obstet. Gynecol. 2014; 211: 168. 1–7. https://doi.org/10.1016/j.ajog.2014.02.032.; Kamimori T., Sakamoto K., Fujiwara K., Umayahara K., Sugiyama Y., Utsugi K., Takeshima N., Tanaka H., Gomi N., Takizawa K. Parametrial involvement in FIGO stage IB1 cervical carcinoma diagnostic impact of tumor diameter in preoperative magnetic resonance imaging. Int. J. Gynecol. Cancer. 2011; 21: 349–354.; Bourgioti C., Chatoupis K., Rodolakis A., Antoniou A., Tzavara C., Koutoulidis V., Moulopoulos L.A. Incremental prognostic value of MRI in the staging of early cervical cancer: a prospective study and review of the literature. Clin. Imaging. 2016; 40 (1): 72–78. https://doi.org/10.1016/j.clinimag.2015.09.012.; Kim S.H., Lee H.J., Kim Y.W. Correlation between tumor size and surveillance of lymph node metastasis for IB and IIA cervical cancer by magnetic resonance images. Eur. J. Radiol. 2012; 81: 1945–1950. https://doi.org/10.1016/j.ejrad.2011.04.053.; Kang S., Kim Y.S., Choi H.J., Kim M.H., Cho K.S. Additional value of combined evaluation of tumor size with lymph node size in the detection of lymph node metastases in early-stage cervical cancer patients. J. Comput. Assist. Tomogr. 2013; 37: 572–576. https://doi.org/10.1097/RCT.0b013e31828ba718.; Perez C.A., Camel H.M., Askin F., Breaux S. Endometrial extension of carcinoma of the uterine cervix: a prognostic factor that may modify staging. Cancer. 1981; 48: 170–180.; Kim H., Kim W., Lee M., Song E., Loh J.J.K. Tumor volume and uterine body invasion assessed by mri for prediction of outcome in cervical carcinoma treated with concurrent chemotherapy and radiotherapy. Jpn J. Clin. Oncol. 2007; 37 (11): 858–866. https://doi.org/10.1093/jjco/hym109.; Finan M.A., DeCesare S., Fiorica J.V., Chambers R., Hoffman M.S., Kline R.C., Roberts W.S., Cavanagh D. Radical hysterectomy for stage IB1 vs IB2 carcinoma of the cervix: dose the new staging system predict morbidity and survival? Gynecol. 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  5. 5
    Academic Journal

    Source: Medical Visualization; № 2 (2019); 7-26 ; Медицинская визуализация; № 2 (2019); 7-26 ; 2408-9516 ; 1607-0763

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    Relation: https://medvis.vidar.ru/jour/article/view/766/543; Glynne-Jones R., Wyrwicz L., Tiret E., Brown G., Rodel C., Cervantes A., Arnold D., ESMO Guidelines Committee. Rectal cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 2017; 28 (Suppl. 4): 22–40. http://doi.org/10.1093/annonc/mdx224.; American Cancer Society. Cancer Facts & Figures. 2017. Available at: https://www.cancer.org/content/dam/ cancer-org/research/cancer-facts-and-statistics/ annual-cancer-facts-and-figures/2017/cancer-factsand-figures-2017.pdf (accessed August 12, 2018).; Давыдов М.И., Аксель Е.М. Статистика злокачественных новообразований в России и странах СНГ в 2009 г. Вестник РОНЦ им. Н.Н. Блохина РАМН. 2011; 22 (3, Прил. 1) (85): 1–170.; Каприн А.Д., Старинский В.В., Петрова Г.В. Состояние онкологической помощи населению России в 2017 году. М.: МНИОИ им. П.А. 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