يعرض 1 - 16 نتائج من 16 نتيجة بحث عن '"T. I. Deshkina"', وقت الاستعلام: 0.46s تنقيح النتائج
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    المصدر: Meditsinskiy sovet = Medical Council; № 11 (2023); 172-177 ; Медицинский Совет; № 11 (2023); 172-177 ; 2658-5790 ; 2079-701X

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    Relation: https://www.med-sovet.pro/jour/article/view/7702/6834; 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):209–249. https://doi.org/10.3322/caac.21660.; Siegel R.L., Miller K.D., Fuchs H.E., Jemal A. Cancer Statistics, 2021. CA Cancer J Clin. 2021;71(1):7–33. https://doi.org/10.3322/caac.21654.; Sohal D.P., Mangu P.B., Khorana A.A., Shah M.A, Philip P.A., O’Reilly E.M. et al. Metastatic Pancreatic Cancer: American Society of Clinical Oncology Clinical Practice Guideline. J Clin Oncol. 2016;34(23):2784–2796. https://doi.org/10.1200/JCO.2016.67.1412.; Conroy T., Desseigne F., Ychou M., Bouché O., Guimbaud R., Bécouarn Y. et al. FOLFIRINOX versus gemcitabine for metastatic pancreatic cancer. N Engl J Med. 2011;364(19):1817–1825. https://doi.org/10.1056/NEJMoa1011923.; Von Hoff D.D., Ervin T., Arena F.P., Chiorean E.G., Infante J., Moore M. et al. Increased survival in pancreatic cancer with nab-paclitaxel plus gemcitabine. N Engl J Med. 2013;369(18):1691–1703. https://doi.org/10.1056/NEJMoa1304369.; Burris H.A. 3rd, Moore M.J., Andersen J., Green M.R., Rothenberg M.L., Modiano M.R. et al. Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: a randomized trial. J Clin Oncol. 1997;15(6):2403–2413. https://doi.org/10.1200/JCO.1997.15.6.2403.; Swayden M., Iovanna J., Soubeyran P. Pancreatic cancer chemo-resistance is driven by tumor phenotype rather than tumor genotype. Heliyon. 2018;4(12):e01055. https://doi.org/10.1016/j.heliyon.2018.e01055.; Klein A.P. Genetic susceptibility to pancreatic cancer. Mol Carcinog. 2012;51(1):14–24. https://doi.org/10.1002/mc.20855.; Klein A.P., Brune K.A., Petersen G.M., Goggins M., Tersmette A.C., Offerhaus G.J. et al. Prospective risk of pancreatic cancer in familial pancreatic cancer kindreds. Cancer Res. 2004;64(7):2634–2638. https://doi.org/10.1158/0008-5472.can-03-3823.; Hiripi E., Lorenzo Bermejo J., Li X., Sundquist J., Hemminki K. Familial association of pancreatic cancer with other malignancies in Swedish families. Br J Cancer. 2009;101(10):1792–1797. https://doi.org/10.1038/sj.bjc.6605363.; Schneider R., Slater E.P., Sina M., Habbe N., Fendrich V., Matthäi E. et al. German national case collection for familial pancreatic cancer (FaPaCa): ten years experience. Fam Cancer. 2011;10(2):323–330. https://doi.org/10.1007/s10689-010-9414-x.; Goggins M., Overbeek K.A., Brand R., Syngal S., Del Chiaro M., Bartsch D.K. et al. Management of patients with increased risk for familial pancreatic cancer: updated recommendations from the International Cancer of the Pancreas Screening (CAPS) Consortium. Gut. 2020;69(1):7–17. https://doi.org/10.1136/gutjnl-2019-319352.; Gardiner A., Kidd J., Elias M.C., Young K., Mabey B., Taherian N. et al. Pancreatic Ductal Carcinoma Risk Associated With Hereditary Cancer-Risk Genes. J Natl Cancer Inst. 2022;114(7):996–1002. https://doi.org/10.1093/jnci/djac069.; Vietri M.T., D’Elia G., Caliendo G., Albanese L., Signoriello G., Napoli C., Molinari A.M. Pancreatic Cancer with Mutation in BRCA1/2, MLH1, and APC Genes: Phenotype Correlation and Detection of a Novel Germline BRCA2 Mutation. Genes (Basel). 2022;13(2):321. https://doi.org/10.3390/genes13020321.; Murphy K.M., Brune K.A., Griffin C., Sollenberger J.E., Petersen G.M., Bansal R. et al. Evaluation of candidate genes MAP2K4, MADH4, ACVR1B, and BRCA2 in familial pancreatic cancer: deleterious BRCA2 mutations in 17%. Cancer Res. 2002;62(13):3789–3793. https://pubmed.ncbi.nlm.nih.gov/12097290/; George A., Kaye S., Banerjee S. Delivering widespread BRCA testing and PARP inhibition to patients with ovarian cancer. Nat Rev Clin Oncol. 2017;14(5):284–296. https://doi.org/10.1038/nrclinonc.2016.191.; Li S., Silvestri V., Leslie G., Rebbeck T.R., Neuhausen S.L., Hopper J.L. et al. Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants. J Clin Oncol. 2022;40(14):1529–1541. https://doi.org/10.1200/JCO.21.02112; Farmer H., McCabe N., Lord C.J., Tutt A.N., Johnson D.A., Richardson T.B. et al. Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy. Nature. 2005;434(7035):917–921. https://doi.org/10.1038/nature03445.; Kindler H.L., Hammel P., Reni M., Van Cutsem E., Macarulla T., Hall M.J. et al. Overall Survival Results From the POLO Trial: A Phase III Study of Active Maintenance Olaparib Versus Placebo for Germline BRCA-Mutated Metastatic Pancreatic Cancer. J Clin Oncol. 2022;40(34):3929–3939. https://doi.org/10.1200/JCO.21.01604.; Axilbund J.E., Argani P., Kamiyama M., Palmisano E., Raben M., Borges M. et al. Absence of germline BRCA1 mutations in familial pancreatic cancer patients. Cancer Biol Ther. 2009;8(2):131–135. https://doi.org/10.4161/cbt.8.2.7136.; Hahn S.A., Greenhalf B., Ellis I., Sina-Frey M., Rieder H., Korte B. et al. BRCA2 germline mutations in familial pancreatic carcinoma. J Natl Cancer Inst. 2003;95(3):214–221. https://doi.org/10.1093/jnci/95.3.214.; Couch F.J., Johnson M.R., Rabe K.G., Brune K., de Andrade M., Goggins M. et al. The prevalence of BRCA2 mutations in familial pancreatic cancer. Cancer Epidemiol Biomarkers Prev. 2007;16(2):342–346. https://doi.org/10.1158/1055-9965.EPI-06-0783.; https://www.med-sovet.pro/jour/article/view/7702

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    المصدر: Malignant tumours; Том 13, № 3 (2023); 29-36 ; Злокачественные опухоли; Том 13, № 3 (2023); 29-36 ; 2587-6813 ; 2224-5057

    وصف الملف: application/pdf

    Relation: https://www.malignanttumors.org/jour/article/view/1166/809; Состояние онкологической помощи населению России в 2021 г, под редакцией А. Д. Каприна, В. В. Старинского, А. О. Шахзадовой. Москва 2022 г, с. 23–25.; Cronin KA, Harlan LC, Dodd KW, Abrams JS, Ballard-Barbash R. Population-based estimate of the prevalence of HER-2 positive breast cancer tumors for early stage patients in the US. Cancer Invest. 2010 Nov; 28 (9) : 963–8. doi:10.3109/07357907.2010.496759. PMID: 20690807; PMCID: PMC5094051.; Slamon, D. J.; Clark, G. M.; Wong, S. G.; Levin, W. J.; Ullrich, A.; McGuire, W. L. Human breast cancer : Correlation of relapse and survival with amplification of the HER-2/neu oncogene. Science 1987, 235, 177–182.; Leyland-Jones, B.; Shak, S.; Fuchs, H.; Paton, V.; Bajamonde, A.; Fleming, T.; Eiermann, W.; Wolter, J.; Pegram, M.; et al. Use of Chemotherapy plus a Monoclonal Antibody against HER2 for Metastatic Breast Cancer That Overexpresses HER2. New Engl. J. Med. 2001, 344, 783–792.; Клинические рекомендации «Рак молочной железы» Общероссийский национальный союз «Ассоциация онкологов России» • Общероссийская общественная организация «Российское общество клинической онкологии» • Общероссийская общественная организация «Российское общество онкомаммологов», 2021 г.; Тюляндин С. А., Жукова Л. Г., Королева И. А., Пароконная А. А., Семиглазова Т. Ю., Стенина М. Б. и соавт. Практические рекомендации по лекарственному лечению рака молочной железы. Злокачественные опухоли : Практические рекомендации RUSSCO #3s2, 2021 (том 11). 09.; Cortazar P, Zhang L, Untch M, et al. Pathological complete response and long-term clinical benefit in breast cancer : the CTNeoBC pooled analysis [published correction appears in Lancet. 2019 Mar 9; 393 (10175) : 986]. Lancet. 2014; 384 (9938) : 164–172. doi:10.1016/S0140-6736(13)62422-8.; von Minckwitz G, Untch M, Blohmer JU, et al. Definition and impact of pathologic complete response on prognosis after neoadjuvant chemotherapy in various intrinsic breast cancer subtypes. J Clin Oncol. 2012; 30 (15) : 1796–1804. doi:10.1200/JCO. 2011.38.8595.; Untch M, Fasching PA, Konecny GE, et al. Pathologic complete response after neoadjuvant chemotherapy plus trastuzumab predicts favorable survival in human epidermal growth factor receptor 2-overexpressing breast cancer : results from the TECHNO trial of the AGO and GBG study groups. J Clin Oncol. 2011; 29 (25) : 3351–3357. doi:10.1200/ JCO.2010.31.4930.; Broglio KR, Quintana M, Foster M, et al. Association of Pathologic Complete Response to Neoadjuvant Therapy in HER2-Positive Breast Cancer With Long-Term Outcomes : A Meta-Analysis. JAMA Oncol. 2016; 2 (6) : 751–760. doi:10.1001/jamaoncol. 2015.6113.; von Minckwitz G, Huang CS, Mano MS, et al. Trastuzumab Emtansine for Residual Invasive HER2-Positive Breast Cancer. N Engl J Med. 2019; 380 (7) : 617–628. doi:10.1056/NEJMoa1814017.; Gianni L, Eiermann W, Semiglazov V, et al. Neoadjuvant and adjuvant trastuzumab in patients with HER2-positive locally advanced breast cancer (NOAH) : follow-up of a randomised controlled superiority trial with a parallel HER2-negative cohort [published correction appears in Lancet Oncol. 2018 Dec; 19 (12) : e667]. Lancet Oncol. 2014; 15 (6) : 640–647. doi:10.1016/S1470-2045(14)70080-4.; Gianni L, Pienkowski T, Im YH, et al. Efficacy and safety of neoadjuvant pertuzumab and trastuzumab in women with locally advanced, inflammatory, or early HER2-positive breast cancer (NeoSphere) : a randomised multicentre, open-label, phase 2 trial. Lancet Oncol. 2012; 13 (1) : 25–32. doi:10.1016/S1470-2045(11)70336-9.; Untch M, Jackisch C, Schneeweiss A, et al. NAB-Paclitaxel Improves Disease-Free Survival in Early Breast Cancer : GBG 69-GeparSepto. J Clin Oncol. 2019; 37 (25) : 2226–2234. doi:10.1200/JCO. 18.01842.; Schneeweiss A, Chia S, Hickish T, et al. Pertuzumab plus trastuzumab in combination with standard neoadjuvant anthracycline-containing and anthracycline-free chemotherapy regimens in patients with HER2-positive early breast cancer : a randomized phase II cardiac safety study (TRYPHAENA). Ann Oncol. 2013; 24 (9) : 2278–2284. doi:10.1093/ annonc/mdt182.; van Ramshorst MS, van der Voort A, van Werkhoven ED, et al. Neoadjuvant chemotherapy with or without anthracyclines in the presence of dual HER2 blockade for HER2-positive breast cancer (TRAIN-2) : a multicentre, open-label, randomised, phase 3 trial. Lancet Oncol. 2018; 19 (12) : 1630–1640. doi:10.1016/S1470-2045(18)30570-9.; Rimawi MF, Mayer IA, Forero A, et al. Multicenter phase II study of neoadjuvant lapatinib and trastuzumab with hormonal therapy and without chemotherapy in patients with human epidermal growth factor receptor 2-overexpressing breast cancer : TBCRC 006. J Clin Oncol. 2013; 31 (14) : 1726–1731. doi:10.1200/JCO. 2012.44.8027.; Rimawi MF, Niravath P, Wang T, Rexer BN, Forero A, et al.; Translational Breast Cancer Research Consortium. TBCRC023 : A Randomized Phase II Neoadjuvant Trial of Lapatinib Plus Trastuzumab Without Chemotherapy for 12 versus 24 Weeks in Patients with HER2-Positive Breast Cancer. Clin Cancer Res. 2020 Feb 15; 26 (4) : 821–827. doi:10.1158/1078-0432.CCR-19-0851. Epub 2019 Oct 29. PMID: 31662331.; Llombart-Cussac A, Cortés J, Paré L, Galván P, Bermejo B, Martínez N, Vidal M, Pernas S, López R, Muñoz M, Nuciforo P, Morales S, Oliveira M, de la Peña L, Peláez A, Prat A. HER2-enriched subtype as a predictor of pathological complete response following trastuzumab and lapatinib without chemotherapy in early-stage HER2-positive breast cancer (PAMELA) : an open-label, single-group, multicentre, phase 2 trial. Lancet Oncol. 2017 Apr; 18 (4) : 545–554. doi:10.1016/S1470-2045(17)30021-9. Epub 2017 Feb 24. PMID: 28238593.; Guarneri V, Dieci MV, Bisagni G, et al. De-escalated therapy for HR + / HER2 + breast cancer patients with Ki67 response after 2-week letrozole : results of the PerELISA neoadjuvant study. Ann Oncol. 2019; 30 (6) : 921–926. doi:10.1093/annonc/mdz055.; Gianni L, Bisagni G, Colleoni M, Del Mastro L, Zamagni C, Mansutti M, Zambetti M, Frassoldati A, De Fato R, Valagussa P, Viale G. Neoadjuvant treatment with trastuzumab and pertuzumab plus palbociclib and fulvestrant in HER2-positive, ER-positive breast cancer (NA-PHER2) : an exploratory, open-label, phase 2 study. Lancet Oncol. 2018 Feb; 19 (2) : 249–256. doi:10.1016/S1470-2045(18)30001-9. Epub 2018 Jan 8. PMID: 29326029.; Hurvitz SA, Martin M, Symmans WF, et al. Neoadjuvant trastuzumab, pertuzumab, and chemotherapy versus trastuzumab emtansine plus pertuzumab in patients with HER2-positive breast cancer (KRISTINE) : a randomised, open-label, multicentre, phase 3 trial. Lancet Oncol. 2018; 19 (1) : 115–126. doi:10.1016/S1470-2045(17) 30716–7.; Hurvitz SA, Martin M, Jung KH, et al. Neoadjuvant Trastuzumab Emtansine and Pertuzumab in Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer : Three-Year Outcomes From the Phase III KRISTINE Study. J Clin Oncol. 2019; 37 (25) : 2206–2216. doi:10.1200/JCO. 19.00882.; Nitz UA, Gluz O, Christgen M, et al. De-escalation strategies in HER2-positive early breast cancer (EBC) : final analysis of the WSG-ADAPT HER2 +/HR- phase II trial : efficacy, safety, and predictive markers for 12 weeks of neoadjuvant dual blockade with trastuzumab and pertuzumab ± weekly paclitaxel [published correction appears in Ann Oncol. 2022 Mar; 33 (3) : 355]. Ann Oncol. 2017; 28 (11) : 2768–2772. doi:10.1093/annonc/mdx494.; Nitz U, Gluz O, Graeser M, et al. De-escalated neoadjuvant pertuzumab plus trastuzumab therapy with or without weekly paclitaxel in HER2-positive, hormone receptor-negative, early breast cancer (WSG-ADAPT-HER2 + / HR-) : survival outcomes from a multicentre, open-label, randomised, phase 2 trial. Lancet Oncol. 2022; 23 (5) : 625–635. doi:10.1016/S1470-2045(22)00159-0.; Pérez-García JM, Gebhart G, Ruiz Borrego M, et al. Chemotherapy de-escalation using an 18F-FDG-PET-based pathological response-adapted strategy in patients with HER2-positive early breast cancer (PHERGain) : a multicentre, randomised, open-label, non-comparative, phase 2 trial. Lancet Oncol. 2021; 22 (6) : 858–871. doi:10.1016/S1470- 2045 (21) 00122-4.; https://www.malignanttumors.org/jour/article/view/1166

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