يعرض 1 - 20 نتائج من 54 نتيجة بحث عن '"O. Lipatov"', وقت الاستعلام: 0.50s تنقيح النتائج
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    Academic Journal

    المصدر: Meditsinskiy sovet = Medical Council; № 22 (2023); 130-138 ; Медицинский Совет; № 22 (2023); 130-138 ; 2658-5790 ; 2079-701X

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    Relation: https://www.med-sovet.pro/jour/article/view/7982/7069; Каприн АД, Старинский ВВ, Шахзадова АО (ред.). Состояние онкологической помощи населению России в 2021 г. М.: МНИОИ им. П.А. Герцена – филиал ФГБУ «НМИЦ радиологии» Минздрава России; 2022. 239 с. Режим доступа: https://oncology-association.ru/wp-content/uploads/2022/05/sostoyanie-onkologicheskoj-pomoshhi-naseleniyu-rossii-v-2021-godu.pdf.; Parise CA, Caggiano V. Breast Cancer Survival Defined by the ER/PR/HER2 Subtypes and a Surrogate Classification according to Tumor Grade and Immunohistochemical Biomarkers. J Cancer Epidemiol. 2014:469251. https://doi.org/10.1155/2014/469251.; Hart CD, Migliaccio I, Malorni L, Guarducci C, Biganzoli L, Di Leo A. Challenges in the management of advanced, ER-positive, HER2-negative breast cancer. Nat Rev Clin Oncol. 2015;12(9):541–552. https://doi.org/10.1038/nrclinonc.2015.99.; Flaum LE, Gradishar WJ. Advances in Endocrine Therapy for Postmenopausal Metastatic Breast Cancer. In: Gradishar W (ed.). Optimizing Breast Cancer Management. Cancer Treatment and Research. Vol. 173. Springer, Cham; 2018, pp. 141–154. https://doi.org/10.1007/978-3-319-70197-4_9.; Hoffmann J, Bohlmann R, Heinrich N, Hofmeister H, Kroll J, Künzer H et al. Characterization of new estrogen receptor destabilizing compounds: effects on estrogen-sensitive and tamoxifen-resistant breast cancer. J Natl Cancer Inst. 2004;96(3):210–218. https://doi.org/10.1093/jnci/djh022.; Clark AS, Karasic TB, DeMichele A, Vaughn DJ, O’Hara M, Perini R et al. Palbociclib (PD0332991) – a Selective and Potent Cyclin-Dependent Kinase Inhibitor: A Review of Pharmacodynamics and Clinical Development. JAMA Oncol. 2016;2(2):253–260. https://doi.org/10.1001/jamaoncol.2015.4701.; Hamilton E, Infante JR. Targeting CDK4/6 in patients with cancer. Cancer Treat Rev. 2016;45:129–138. https://doi.org/10.1016/j.ctrv.2016.03.002.; Corona SP, Generali D. Abemaciclib: a CDK4/6 inhibitor for the treatment of HR+/HER2-advanced breast cancer. Drug Des Devel Ther. 2018;12:321–330. https://doi.org/10.2147/DDDT.S137783.; Finn RS, Martin M, Rugo HS, Jones S, Im SA, Gelmon K et al. Palbociclib and Letrozole in Advanced Breast Cancer. N Engl J Med. 2016;375(20):1925–1936. https://doi.org/10.1056/NEJMoa1607303.; Hortobagyi GN, Stemmer SM, Burris HA, Yap YS, Sonke GS, Paluch-Shimon S et al. Ribociclib as First-Line Therapy for HR-Positive, Advanced Breast Cancer. N Engl J Med. 2016;375(18):1738–1748. https://doi.org/10.1056/NEJMoa1609709.; Goetz MP, Toi M, Campone M, Sohn J, Paluch-Shimon S, Huober J et al. MONARCH 3: Abemaciclib As Initial Therapy for Advanced Breast Cancer. J Clin Oncol. 2017;35(32):3638–3646. https://doi.org/10.1200/JCO.2017.75.6155.; Tripathy D, Im SA, Colleoni M, Franke F, Bardia A, Harbeck N et al. Ribociclib plus endocrine therapy for premenopausal women with hormone-receptor-positive, advanced breast cancer (MONALEESA-7): a randomised phase 3 trial. Lancet Oncol. 2018;19(7):904–915. https://doi.org/10.1016/S1470-2045(18)30292-4.; Sledge GW Jr, Toi M, Neven P, Sohn J, Inoue K, Pivot X et al. MONARCH 2: Abemaciclib in Combination With Fulvestrant in Women With HR+/HER2-Advanced Breast Cancer Who Had Progressed While Receiving Endocrine Therapy. J Clin Oncol. 2017;35(25):2875–2884. https://doi.org/10.1200/JCO.2017.73.7585.; Гольдина ТА, Колбин АС, Белоусов ДЮ, Боровская ВГ. Обзор исследований реальной клинической практики. Качественная клиническая практика. 2021;(1):56–63. https://doi.org/10.37489/2588-0519-2021-1-56-63.; Колядина ИВ. Рибоциклиб в лечении больных HR+ HER2-отрицательным распространенным раком молочной железы: обновленные результаты рандомизированных клинических исследований и их роль для клинической практики. Опухоли женской репродуктивной системы. 2021;17(2):58–67. https://doi.org/10.17650/1994-4098-2021-17-2-58-67.; Ганьшина ИП, Филоненко ДА, Гордеева ОО, Лубенникова ЕВ, Колядина ИВ, Мещеряков АА. Рибоциклиб в лечении гормонопозитивного HER2-негативного рака молочной железы. Медицинский совет. 2019;(10):72–80. https://doi.org/10.21518/2079-701X-2019-10-72-80.; Колядина ИВ. По следам SABCS 2022: TOP-12 исследований по распространенному раку молочной железы, которые могут изменить нашу клиническую практику. Современная онкология. 2023;25(1):46–54. https://doi.org/10.26442/18151434.2023.1.202102.; Da Silva SHK, de Oliveira LC, E Silva Lopes MSDM, Wiegert EVM, Motta RST, Ferreira Peres WA. The patient generated-subjective global assessment (PG-SGA) and ECOG performance status are associated with mortality in patients hospitalized with breast cancer. Clin Nutr ESPEN. 2023;53:87–92. https://doi.org/10.1016/j.clnesp.2022.11.019.; Llombart-Cussac A, Pérez-García JM, Bellet M, Dalenc F, Gil-Gil M, Ruíz- Borrego M et al. Fulvestrant-Palbociclib vs Letrozole-Palbociclib as Initial Therapy for Endocrine-Sensitive, Hormone Receptor-Positive, ERBB2-Negative Advanced Breast Cancer: A Randomized Clinical Trial. JAMA Oncol. 2021;7(12):1791–1799. https://doi.org/10.1001/jamaoncol.2021.4301.; Колядина ИВ, Поддубная ИВ. ESR1-мутация как потенциальный предсказательный маркер для выбора тактики лечения при гормонорезистентном HR+/HER2-негативном раке молочной железы. Медицинский алфавит. 2020;(29):68–73. https://doi.org/10.33667/2078-5631-2020-29-61-73.; Sanò MV, Martorana F, Lavenia G, Rossello R, Prestifilippo A, Sava S et al. Ribociclib efficacy in special populations and analysis of patient-reported out-comes in the MONALEESA trials. Expert Rev Anticancer Ther. 2022;22(4):343–351. https://doi.org/10.1080/14737140.2022.2052277.; Zhu K, Wu Y, He P, Fan Y, Zhong X, Zheng H, Luo T. PI3K/AKT/mTOR-Targeted Therapy for Breast Cancer. Cells. 2022;11(16):2508. https://doi.org/10.3390/cells11162508.; China Anti-cancer Association Tumor Drug Clinical Research Committee; Breast Cancer Expert Committee, National Tumor Quality Control Center; Tumor Pathology Committee of China Anti-cancer Association; Boao Institute of Oncology Innovation. Expert consensus on the clinical application of PI3K/AKT/mTOR inhibitors in the treatment of advanced breast cancer. Zhonghua Zhong Liu Za Zhi. 2022;44(7):673–692. (In Chinese) https://doi.org/10.3760/cma.j.cn112152-20220412-00251.; Reinhardt K, Stückrath K, Hartung C, Kaufhold S, Uleer C, Hanf V et al. PIK3CA-mutations in breast cancer. Breast Cancer Res Treat. 2022;196(3):483–493. https://doi.org/10.1007/s10549-022-06637-w.; Kim JH, Lee ST. Polyamine Oxidase Expression Is Downregulated by 17β-Estradiol via Estrogen Receptor 2 in Human MCF-7 Breast Cancer Cells. Int J Mol Sci. 2022;23(14):7521. https://doi.org/10.3390/ijms23147521.; Nemati Shafaee M, Goutsouliak K, Lin H, Bevers TB, Gutierrez-Barrera A, Bondy M, Arun B. Aromatase inhibitors and contralateral breast cancer in BRCA mutation carriers. Breast Cancer Res Treat. 2022;196(1):143–152. https://doi.org/10.1007/s10549-022-06688-z.; Dustin D, Gu G, Fuqua SAW. ESR1 mutations in breast cancer. Cancer. 2019;125(21):3714–3728. https://doi.org/10.1002/cncr.32345.; Zhu W, Xu B. Overcoming resistance to endocrine therapy in hormone receptor-positive human epidermal growth factor receptor 2-negative (HR+/HER2-) advanced breast cancer: a meta-analysis and systemic review of randomized clinical trials. Front Med. 2021;15(2):208–220. https://doi.org/10.1007/s11684-020-0795-4.; Radhi S. Molecular Changes During Breast Cancer and Mechanisms of Endocrine Therapy Resistance. Prog Mol Biol Transl Sci. 2016;144:539–562. https://doi.org/10.1016/bs.pmbts.2016.09.009.; https://www.med-sovet.pro/jour/article/view/7982

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    المصدر: Malignant tumours; Том 13, № 4 (2023); 84-92 ; Злокачественные опухоли; Том 13, № 4 (2023); 84-92 ; 2587-6813 ; 2224-5057

    وصف الملف: application/pdf

    Relation: https://www.malignanttumors.org/jour/article/view/1142/798; https://www.malignanttumors.org/jour/article/view/1142/910; Lord, C. J.; Ashworth, A. The DNA damage response and cancer therapy. Nature 2012, 481, 287–294.; Valerie, K.; Povirk, L. F. Regulation and mechanisms of mammalian double-strand break repair. Oncogene 2003, 22, 5792–5812.; Jaco, I.; Muñoz, P.; Goytisolo, F.; Wesoly, J.; Bailey, S.; Taccioli, G.; Blasco, M. A. Role of mammalian Rad54 in telomere length maintenance. Mol. Cell Biol. 2003, 23, 5572–5580.; Salzano, A.; Kochiashvili, N.; Nergadze, S. G.; Khoriauli, L.; Smirnova, A.; Ruiz-Herrera, A.; Mondello, C.; Giulotto, E. Enhanced gene amplification in human cells knocked down for DNA-Kcs. DNA Repair 2009, 8, 19–28.; Khouriauli, L.; Giulotto, E. Gene amplification in human cells knocked down for RAD54. Genome Integr. 2011, 2, doi:10.1186/2041-9414-2-5.; Keeney, S.; Giroux, C. N.; Kleckner, N. Meiosis-specific DNA double-strand breaks are catalyzed by Spo11, a member of a widely conserved protein family. Cell 1997, 88, 375–384.; Roeder, G. S. Meiotic chromosomes : It takes two to tango. Genes Dev. 1997, 11, 2600–2621.; Moens, P. B.; Kolas, N. K.; Tarsounas, M.; Marcon, E.; Cohen, P. E.; Spyropoulos, B. The time course and chromosomal localization of recombination-related proteins at meiosis in the mouse are compatible with models that can resolve the early DNA-DNA interactions without reciprocal recombination. J. Cell Sci. 2002, 115, 1611–1622.; Baker, S. M.; Plug, A. W.; Prolla, T. A.; Bronner, C. E.; Harris, A. C.; Yao, X.; Christie, D. M.; Monell, C.; Arnheim, N.; Bradley, A.; et al. Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over. Nat. Genet. 1996, 13, 336–342.; Turner, J. M.; Aprelikova, O.; Xu, X.; Wang, R.; Kim, S.; Chandramouli, G. V.; Barrett, J. C.; Burgoyne, P. S.; Deng, C. X. BRCA1, histone H2AX phosphorylation, and male meiotic sex chromosome inactivation. Curr. Biol. 2004, 14, 2135–2142.; Wallace, W. H.; Thomson, A. B.; Kelsey, T. W. The radiosensitivity of the human oocyte. Hum. Reprod. 2003, 18, 117–121.; Saran, F.; Kelsey, T. W. Predicting age of ovarian failure after radiation to a field that includes the ovaries. Int. J. Radiat. Oncol. Biol. Phys. 2005, 62, 738–744.; Hodgson DC : Late effects in the era of modern therapy for Hodgkin lymphoma. Hematology Am Soc Hematol Educ Program 2011, 2011 : 323–329.; Ng AK : Review of the cardiac long-term effects of therapy for Hodgkin lymphoma. Br J Haematol 2011, 154 (1) : 23–31.; Elkin EB, Klem ML, Gonzales AM, et al : Characteristics and outcomes of breast cancer in women with and without a history of radiation for Hodgkin’s lymphoma : a multi-institutional, matched cohort study. J Clin Oncol 2011, 29 (18) : 2466–2473.; Baker, T. G. Comparative aspects of the effects of radiation during oogenesis. Mutat. Res. 1971, 11, 9±22.; Donin N, Filson C, Drakaski A, et al. Risk of second primary malignancies among cancer survivors in the United States, 1992 through 2008. Cancer 2016; 122 : 3075–3086.; Saletta F, Seng M and Lau L. Advances in pediatric cancer treatment. Transl Pediatr 3 (2) : 156–82. 4. Ward E, DeSantis C, Robbins A, et al. Childhood and adolescent cancer statistics, 2014. CA Cancer J Clin 2014; 64 : 83–103.; Institute NC. Childhood Cancer by site incidence, survival and mortality 2019, April, https://seer.cancer.gov/csr/1975_2016/results_merged/sect_28_childhood_cancer.pdf.; Armstrong GT, Liu Q, Yasui Y, et al. Late mortality among 5-year survivors of childhood cancer : a summary from the childhood cancer survivor study. J Clin Oncol 2009; 27 : 2328–2338.; Lee JS, Dubois SG, Coccia PF, et al. Increased risk of second malignant neoplasms in adolescents and young adults with cancer. Cancer 2016; 122 : 116–123.; Howlader N, Noone AM, Krapcho M, et al, eds. SEER Cancer Statistics Review, 1975–2012. Bethesda, MD : National Cancer Institute; 2015.; Travis LB, Gospodarowicz M, Curtis RE, et al. Lung cancer following chemotherapy and radiotherapy for Hodgkin’s disease. J Natl Cancer Inst. 2002; 94 : 182–192.; Travis LB, Curtis RE, Boice JD Jr, Hankey BF, Fraumeni JF Jr. Second cancers following non-Hodgkin’s lymphoma. Cancer. 1991; 67 : 2002–2009.; Curtis RE, Freedman DM, Ron E, et al. New Malignancies Among Cancer Survivors : SEER Cancer Registries, 1973–2000. Bethesda, MD : National Cancer Institute; 2006. NIH Pub. No. 05–5302.; Важенин А. В., Шаназаров Н. А., Шунько Е. Л. Некоторые закономерности развития радиоиндуцированных метахронных опухолей. Вестник рентгенологии и радиологии № 6, 2015. С 30–35.; Bertin F, Deluche E, Tricard J, Piccardo A, Denes E. First case of sternum replacement with a bioceramic prosthesis after radio-induced sarcoma. Curr Oncol. 2018 Aug; 25 (4) : e351-e353. doi:10.3747/co.25.4020. Epub 2018 Aug 14. PMID : 30111981; PMCID : PMC6092061.; Majdoubi A, Serji B, Harroudi TE. Angiosarcome mammaire radio-induit : à propos d’un cas [Radiation-induced breast angiosarcoma : about a case]. Pan Afr Med J. 2020 May 21; 36 : 29. French. doi:10.11604/pamj.2020.36.29.21599. PMID : 32774606; PMCID : PMC7388625.; Меньшиков К. В., Пушкарев А. В., Султанбаев А. В., Пушкарев В. А., Шарифгалиев И. А. Радиоиндуцированная ангиосаркома влагалища : клинический случай. Креативная хирургия и онкология. 2020; 10 (2) : 143–148. https://doi.org/10.24060/2076-3093-2020-10-2-143-148.; Dores GM, Metayer C, Curtis RE, et al. Second malignant neoplasms among long-term survivors of Hodgkin’s disease : a population-based evaluation over 25 years. J Clin Oncol. 2002; 20 : 3484–94. DOI:10.1200/JCO. 2002.09.038.; Огнерубов Н. А., Антипова Т. С. Радиационно-индуцированная саркома мягких тканей шеи после лучевой терапии лимфомы Ходжкина. Клиническое наблюдение. Современная Онкология. 2022; 24 (3) : 325–330. DOI:10.26442/18151434.2022.3.201904.; van Eggermond AM, Schaapveld M, Lugtenburg PJ. Risk of multiple primary malignancies following treatment of Hodgkin lymphoma. Blood. 2014; 124 (3) : 319–27. DOI:10.1182/blood-2013-10-532184.; Ng AK, Mauch PM. Late effects of Hodgkin’s disease and its treatment. Cancer J. 2009; 15 : 164–8. DOI:10.1097/PPO.0b013e31819e30d7.; Carde P, Burgers JM, Henry-Amar M, et al. Clinical stages I and II Hodgkin’s disease : a specifically tailored therapy according to prognostic factors. J Clin Oncol. 1988; 6 (2) : 239–252.; Eghbali H, Raemaekers J, Carde P; EORTC Lymphoma Group. The EORTC strategy in the treatment of Hodgkin’s lymphoma. Eur J Haematol Suppl. 2005; (66) : 135–140.; Raemaekers J, Kluin-Nelemans H, Teodorovic I, et al; European Organisation for Research and Treatment of Cancer. The achievements of the EORTC Lymphoma Group. Eur J Cancer. 2002; 38 (suppl 4) : S107-S113.; Somers R, Tubiana M, Henry-Amar M. EORTC Lymphoma Cooperative Group studies in clinical stage I–II Hodgkin’s disease 1963–1987. Recent Results Cancer Res. 1989; 117 : 175–181.; Tubiana M, Henry-Amar M, Carde P, et al. Toward comprehensive management tailored to prognostic factors of patients with clinical stages I and II in Hodgkin’s disease. The EORTC Lymphoma Group controlled clinical trials : 1964–1987. Blood. 1989; 73 (1) : 47–56.; van Eggermond AM, Schaapveld M, Lugtenburg PJ, Krol AD, de Boer JP, Zijlstra JM, Raemaekers JM, Kremer LC, Roesink JM, Louwman MW, Aleman BM, van Leeuwen FE. Risk of multiple primary malignancies following treatment of Hodgkin lymphoma. Blood. 2014 Jul 17; 124 (3) : 319–27; quiz 466. doi:10.1182/blood-2013-10-532184. Epub 2014 Apr 16. PMID : 24740811.; Cahan WG, Woodard HQ, Higinbotham NL, et al. Sarcoma in irradiated bone. Report of eleven cases. Cancer. 1948 : 3–29. DOI:10.1002/1097-0142(194805) 1 : 13.0. CO; 2–7.; Hall EJ, Wuu CS. Radiation-induced second cancers : the impact of 3D-CRT and IMRT. Int J Radiat Oncol Biol Phys. 2003; 56 : 83–8. DOI:10.1016/S0360–3016 (03) 00073–7.; https://www.malignanttumors.org/jour/article/view/1142

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    المساهمون: This work is not funded, Данная работа не финансировалась

    المصدر: Creative surgery and oncology; Том 13, № 2 (2023); 131-142 ; Креативная хирургия и онкология; Том 13, № 2 (2023); 131-142 ; 2076-3093 ; 2307-0501

    وصف الملف: application/pdf

    Relation: https://www.surgonco.ru/jour/article/view/810/547; Villanueva A. Hepatocellular carcinoma. N Engl J Med. 2019; 380 (15): 1450–62. DOI:10.1056/NEJMra1713263; Ахметгареева К. Т., Липатов О. Н., Меньшиков К. В., Султанбаев А. В. Заболеваемость первичным раком печени в Республике Башкортостан. В кн.: Белые ночи 2020 : тезисы VI Петербургского международного онкологического форума. СПб; 2020. С. 22.; Xie Y. Hepatitis B virus-associated hepatocellular carcinoma. Adv Exp Med Biol. 2017; 1018: 11–21. DOI:10.1007/978-981-10-5765-6_2; Kanwal F., Kramer J. R., Mapakshi S., Natarajan Y., Chayanupatkul M., Richardson P. A., et al. Risk of hepatocellular cancer in patients with non-alcoholic fatty liver disease. Gastroenterology. 2018; 155 (6): 1828–37.e2. DOI:10.1053/j.gastro.2018.08.024; Меньшиков К. В., Султанбаев А. В., Мусин Ш. И., Рахматуллина И. Р., Меньшикова И. А., Абдеев Р. Р. и др. Гепатоцеллюлярная карцинома: этиологические факторы и механизмы развития. Обзор литературы. Креативная хирургия и онкология. 2022; 12 (2): 139–50. DOI:10.24060/2076-3093-2022-12-2-139-150; Llovet J. M., Villanueva A., Lachenmayer A., Finn R. S. Advances in targeted therapies for hepatocellular carcinoma in the genomic era. Nat Rev Clin Oncol. 2015; 12 (7): 408–24. DOI:10.1038/nrclinonc.2015.103; Cheng A. L., Kang Y. K., Chen Z., Tsao C. J., Qin S., Kim J. S., et al. Efficacy and safety of sorafenib in patients in the Asia-Pacific region with advanced hepatocellular carcinoma: a phase III randomised, doubleblind, placebo-controlled trial. Lancet Oncol. 2009; 10 (1): 25–34. DOI:10.1016/S1470-2045(08)70285-7; Llovet J. M., Ricci S., Mazzaferro V., Hilgard P., Gane E., Blanc J. F., et al. SHARP Investigators Study Group. Sorafenib in advanced hepatocellular carcinoma. N Engl J Med. 2008; 359 (4): 378–90. DOI:10.1056/NEJMoa0708857; Меньшиков К. В., Султанбаев А. В., Мусин Ш. И., Меньшикова И. A., Абдеев Р. Р., Султанбаева Н. И. и др. Иммунотерапия распространенной гепатоцеллюлярной карциномы : обзор литературы и клинический случай. Медицинский совет. 2022; 16 (9): 31–9. DOI:10.21518/2079-701X-2022-16-9-31-39; Kudo M., Finn R. S., Qin S., Han K. H., Ikeda K., Piscaglia F., et al. Lenvatinib versus sorafenib in first-line treatment of patients with unresectable hepatocellular carcinoma: a randomised phase 3 non-inferiority trial. Lancet. 2018; 391 (10126): 1163–73. DOI:10.1016/S0140-6736(18)30207-1; Bruix J., Qin S., Merle P., Granito A., Huang Y. H., Bodoky G., et al. Regorafenib for patients with hepatocellular carcinoma who progressed on sorafenib treatment (RESORCE): a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet. 2017; 389 (10064): 56–66. DOI:10.1016/S0140-6736(16)32453-9; Меньшиков К. В., Султанбаев А. В., Ахметгареева К. Т., Липатов Д. О. Лечение метастатического гепатоцеллюлярного рака ленватинибом. Клинический случай и обзор литературы. Современная онкология. 2021; 23 (1): 156–61. DOI:10.26442/18151434.2021.1.200785; European Association for the Study of the Liver. EASL Clinical Practice Guidelines: Management of hepatocellular carcinoma. J Hepatol. 2018; 69 (1): 182–236. DOI:10.1016/j.jhep.2018.03.019; Heimbach J. K., Kulik L. M., Finn R. S., Sirlin C. B., Abecassis M. M., Roberts L. R., et al. AASLD guidelines for the treatment of hepatocellular carcinoma. Hepatology. 2018; 67 (1): 358–80. DOI:10.1002/hep.29086; Matsui J., Yamamoto Y., Funahashi Y., Tsuruoka A., Watanabe T., Wakabayashi T., et al. E7080, a novel inhibitor that targets multiple kinases, has potent antitumor activities against stem cell factor producing human small cell lung cancer H146, based on angiogenesis inhibition. Int J Cancer. 2008; 122 (3): 664–71. DOI:10.1002/ijc.23131; Tamai T., Hayato S., Hojo S., Suzuki T., Okusaka T., Ikeda K., et al. Dose finding of lenvatinib in subjects with advanced hepatocellular carcinoma based on population pharmacokinetic and exposure-response analyses. 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    Academic Journal

    المصدر: Creative surgery and oncology; Том 12, № 4 (2022); 309-319 ; Креативная хирургия и онкология; Том 12, № 4 (2022); 309-319 ; 2076-3093 ; 2307-0501

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  10. 10
    Academic Journal

    المصدر: Creative surgery and oncology; Том 12, № 4 (2022); 267-274 ; Креативная хирургия и онкология; Том 12, № 4 (2022); 267-274 ; 2076-3093 ; 2307-0501

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    Relation: https://www.surgonco.ru/jour/article/view/730/516; Pytynia K.B., Dahlstrom K.R., Sturgis E.M. Epidemiology of HPVassociated oropharyngeal cancer. Oral Oncol. 2014;50(5):380–6. DOI:10.1016/j.oraloncology.2013.12.019; Timbang M.R., Sim M.W., Bewley A.F., Farwell D.G., Mantravadi A., Moore M.G. HPV-related oropharyngeal cancer: a review on burden of the disease and opportunities for prevention and early detection. Hum Vaccin Immunother. 2019;15(7–8):1920–8. DOI:10.1080/21645515.2019.1600985; Каприн А.Д., Старинский В.В., Шахзадава А.О. (ред.) Состояние онкологической помощи населению России в 2020 году. М.: МНИОИ им. П.А. Герцена филиал ФГБУ «НМИЦ радиологии» Минздрава России; 2021.; Мудунов А.М., Чойнзонов Е.Л., Решетов И.В. и др. Рак ротоглотки: Клинические рекомендации. М., 2020.; Machczyński P., Majchrzak E., Niewinski P., Marchlewska J., Golusiński W. A review of the 8th edition of the AJCC staging system for oropharyngeal cancer according to HPV status. Eur Arch Otorhinolaryngol. 2020;277(9):2407–12. DOI:10.1007/s00405-020-05979-9; Mehanna H., Beech T., Nicholson T., El-Hariry I., McConkey C., Paleri V., et al. Prevalence of human papillomavirus in oropharyngeal and nonoropharyngeal head and neck cancer--systematic review and metaanalysis of trends by time and region. Head Neck. 2013;35(5):747–55. DOI:10.1002/hed.22015; Карпенко А. В., Сибгатуллин Р. Р., Бойко А. А., Воробьев С.Л., Кораблина И.М., Николаева О.М. и др. Частота встречаемости и прогноз ВПЧ-позитивного рака ротоглотки. Онкология. Журнал им. П.А. Герцена. 2019;8(1):20–5. DOI:10.17116/onkolog2019801120; Стукань А.И., Чухрай О.Ю., Порханов В.А., Мурашко Р.А., Бодня В.Н., Элизбарян И.С. Клинико-морфологические и прогностические особенности плоскоклеточного рака органов головы и шеи, ассоциированного с вирусом папилломы человека. Онкология. Журнал им. П.А. Герцена. 2019;8(1):13–9. DOI:10.17116/onkolog2019801113; Пхешхова Б.Г., Мудунов А.М., Азизян Р.И., Пак М.Б., Ищенко К.Б. Оценка распространенности ВПЧ-положительного плоскоклеточного рака ротоглотки на примере отдельной выборки в Российской Федерации. Опухоли головы и шеи. 2022;12(1):72–8. DOI; 17650/2222-1468-2022-12-1-72-78 10 Nauta I.H., Riebergen M.M., van Bokhoven A.A.J.D., Bloemena E., Lissenberg-Witte B.I., Heideman D.A.M., et al. Evaluation of the eighth TNM classification on p16-positive oropharyngeal squamous cell carcinomas in the Netherlands and the importance of additional HPV DNA testing. Ann Oncol. 2018;29(5):1273–79. DOI:10.1093/annonc/mdy060. PMID: 29438466; Cancer Genome Atlas Network. Comprehensive genomic characterization of head and neck squamous cell carcinomas. Nature. 2015;517(7536):576–82. DOI:10.1038/nature14129; Yakin M., Seo B., Hussaini H., Rich A., Hunter K. Human papillomavirus and oral and oropharyngeal carcinoma: the essentials. Aust Dent J. 2019;64(1):11–8. DOI:10.1111/adj.12652; Machiels J.P., René Leemans C., Golusinski W., Grau C., Licitra L., Gregoire V. Squamous cell carcinoma of the oral cavity, larynx, oropharynx and hypopharynx: EHNS-ESMO-ESTRO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2020;31(11):1462–75. DOI:10.1016/j.annonc.2020.07.011; Tawk B., Debus J., Abdollahi A. Evolution of a paradigm switch in diagnosis and treatment of HPV-driven head and neck cancer-striking the balance between toxicity and cure. Front Pharmacol. 2022;12:753387. DOI:10.3389/fphar.2021.753387; Malm I.J., Fan C.J., Yin L.X., Li D.X., Koch W.M., Gourin C.G., et al. Evaluation of proposed staging systems for human papillomavirus-related oropharyngeal squamous cell carcinoma. Cancer. 2017;123(10):1768–77. DOI:10.1002/cncr.30512; Nichols A.C., Theurer J., Prisman E. Radiotherapy versus transoral robotic surgery and neck dissection for oropharyngeal squamous cell carcinoma (ORATOR): an open-label, phase 2, randomised trial. Lancet Oncol. 2019;20(10):1349–59. DOI:10.1016/S1470-2045 (19)30410-3; Tiedemann D., Jakobsen K.K., von Buchwald C., Grønhøj C. Systematic review on location and timing of distant progression in human papillomavirus-positive and human papillomavirus-negative oropharyngeal squamous cell carcinomas. Head Neck. 2019;41(3):793–8. DOI:10.1002/hed.25458; https://www.surgonco.ru/jour/article/view/730

  11. 11
    Academic Journal

    المصدر: Meditsinskiy sovet = Medical Council; № 9 (2022); 85-92 ; Медицинский Совет; № 9 (2022); 85-92 ; 2658-5790 ; 2079-701X

    وصف الملف: application/pdf

    Relation: https://www.med-sovet.pro/jour/article/view/6921/6218; Abrams T.J., Lee L.B., Murray L.J., Pryer N.K., Cherrington J.M. SU11248 inhibits KIT and platelet-derived growth factor receptor beta in preclinical models of human small cell lung cancer. Mol Cancer Ther. 2003;2(5):471-478. Available at: https://pubmed.ncbi.nlm.nih.gov/12748309/.; Mendel D.B., Laird A.D., Xin X., Louie S.G., Christensen J.G., Li G. et al. In vivo antitumor activity of SU11248, a novel tyrosine kinase inhibitor targeting vascular endothelial growth factor and platelet-derived growth factor receptors: determination of a pharmacokinetic/pharmacodynamic relationship. Clin Cancer Res. 2003;9(1):327-337. Available at: https://pubmed.ncbi.nlm.nih.gov/12538485/.; O'Farrell A.M., Abrams T.J., Yuen H.A., Ngai T.J., Louie S.G., Yee K.W. et al. SU11248 is a novel FLT3 tyrosine kinase inhibitor with potent activity in vitro and in vivo. Blood. 2003;101(9):3597-3605. https://doi.org/10.1182/blood-2002-07-2307.; Motzer R.J., Michaelson M.D., Redman B.G., Hudes G.R., Wilding G., Figlin R.A. et al. Activity of SU11248, a multitargeted inhibitor of vascular endothelial growth factor receptor and platelet-derived growth factor receptor, in patients with metastatic renal cell carcinoma. J Clin Oncol. 2006;24(1):16-24. https://doi.org/10.1200/JCO.2005.02.2574.; Motzer R.J., Rini B.I., Bukowski R.M., Curti B.D., George D.J., Hudes G.R. et al. Sunitinib in patients with metastatic renal cell carcinoma. JAMA. 2006;295(21):2516-2524. https://doi.org/10.1001/jama.295.21.2516.; Калпинский А.С., Алексеев Б.Я. Эффективность Сунитиниба в таргетной терапии метастатического рака почки. Онкоурология. 2009;(3):63-67. Режим доступа: https://oncourology.abvpress.ru/oncur/article/view/272.; Najjar Y.G., Mittal K., Elson P., Wood L., Garcia J.A., Dreicer R., Rini B.I. A 2 weeks on and 1 week off schedule of sunitinib is associated with decreased toxicity in metastatic renal cell carcinoma. Eur J Cancer. 2014;50(6):1084-1089. https://doi.org/10.1016/j.ejca.2014.01.025.; Jonasch E., Slack R.S., Geynisman D.M., Hasanov E., Milowsky M.I., Rathmell W.K. et al. Phase II Study of Two Weeks on, One Week off Sunitinib Scheduling in Patients With Metastatic Renal Cell Carcinoma. J Clin Oncol. 2018;36(16):1588-1593. https://doi.org/10.1200/JCO.2017.77.1485.; Bjarnason G.A., Knox J.J., Kollmannsberger C.K., Soulieres D., Ernst D.S., Zalewski P. et al. The efficacy and safety of sunitinib given on an individualised schedule as first-line therapy for metastatic renal cell carcinoma: A phase 2 clinical trial. J Clin Oncol. 2019;108:69-77. https://doi.org/10.1016/j.ejca.2018.12.006.; Lee J.L., Kim M.K., Park I., Ahn J.-H., Lee D.H., Ryoo H.M. et al. Randomized phase II trial of Sunitinib four weeks on and two weeks off versus Two weeks on and One week off in metastatic clear-cell type REnal cell carcinoma: RESTORE trial. Ann Oncol. 2015;26(11):2300-2305. https://doi.org/10.1093/annonc/mdv357.; Bracarda S., Iacovelli R., Boni L., Rizzo M., Derosa L., Rossi M. et al. Sunitinib administered on 2/1 schedule in patients with metastatic renal cell carcinoma: the RAINBOW analysis. Ann Oncol. 2015;26(10):2107-2713. https://doi.org/10.1093/annonc/mdv315.; Kalra S., Rini B.I., Jonasch E. Alternate sunitinib schedules in patients with metastatic renal cell carcinoma. Ann Oncol. 2015;26(7):1300-1304. https://doi.org/10.1093/annonc/mdv030.; Kondo T., Takagi T., Kobayashi H., Iizuka J., Nozaki T., Hashimoto Y. et al. Superior tolerability of altered dosing schedule of sunitinib with 2-weeks-on and 1-week-off in patients with metastatic renal cell carcinoma - comparison to standard dosing schedule of 4-weeks-on and 2-weeks-off. Jpn J Clin Oncol. 2014;44(3):270-277. https://doi.org/10.1093/jjco/hyt232.; Atkinson B.J., Kalra S., Wang X., Bathala T., Corn P., Tannir N.M., Jonasch E. Clinical outcomes for patients with metastatic renal cell carcinoma treated with alternative sunitinib schedules. J Urol. 2014;191(3):611-618. https://doi.org/10.1016/j.juro.2013.08.090.; Neri B., Vannini A., Brugia M., Muto A., Rangan S., Rediti M. et al. Biweekly sunitinib regimen reduces toxicity and retains efficacy in metastatic renal cell carcinoma: a single-center experience with 31 patients. Int J Urol. 2013;20(5):478-483. https://doi.org/10.1111/j.1442-2042.2012.03204.x.; Bjarnason G.A., Khalil B., Hudson J.M., Williams R., Milot L.M., Atri M. et al. Outcomes in patients with metastatic renal cell cancer treated with individ-ualized sunitinib therapy: correlation with dynamic microbubble ultrasound data and review of the literature. Urol Oncol. 2014;32(4):480-487. https//doi.org/10.1016/j.urolonc.2013.10.004.; Bracarda S., Sisani M., Marrocolo F., Hamzaj A., del Buono S., De Simone V. GOAL: an inverse toxicity-related algorithm for daily clinical practice decision making in advanced kidney cancer. Crit Rev Oncol Hematol. 2014;89(3):386-393. https://doi.org/10.1016Zj.critrevonc.2013.09.002.; Ravaud A. Treatment-associated adverse event management in the advanced renal cell carcinoma patient treated with targeted therapies. Oncologist. 2011;16(Suppl. 2):32-44. https://doi.org/10.1634/theoncologist.2011-S2-32.; Mouillet G., Paillard M.-J., Maurina T., Vernerey D., Hon T.N.T., Almotlak H. et. al. Open-label, randomized multicentre phase II study to assess the efficacy and tolerability of sunitinib by dose administration regimen (dose modification or dose interruptions) in patients with advanced or metastatic renal cell carcinoma: study protocol of the SURF trial. Trials. 2018;19(1):221. https://doi.org/10.1186/s13063-018-2613-8.; Волкова М.И., Калинин С.А. Осталось ли место сунитинибу в современных рекомендациях по системному лечению распространенного почечноклеточного рака? Медицинский совет. 2021;(9):89-94. https//doi.org/10.21518/2079-701X-2021-9-89-94.; Ravaud A., Motzer R.J., Pandha H.S., George D.J., Pantuck A.J., Patel A. et al. Adjuvant sunitinib in high-risk renal-cell carcinoma after nephrectomy. N Engl J Med. 2016;375(23):2246-2254. https://doi.org/10.1056/NEJMoa1611406.; Mejean A., Ravaud A., Thezenas S., Colas S., Beauval J.-B., Bensalah K. et al. Sunitinib Alone or after Nephrectomy in Metastatic Renal-Cell Carcinoma. N Engl J Med. 2018;379(5):417-427. https://doi.org/10.1056/NEJMoa1803675.; Матвеев В.Б., Маркова А.С. Рак почки: что нового в 2018 году. Онкоурология. 2018;14(4):48-52. https//doi.org/10.17650/1726-9776-2018-14-4-48-52.; Ljungberg B., Albiges L., Abu-Ghanem Y., Bensalah K., Dabestani S., Fernandez-Pello S. et al. European Association of Urology Guidelines on Renal Cell Carcinoma: The 2019 Update. Eur Urol. 2019;75(5):799-810. https://doi.org/10.1016/j.eururo.2019.02.011.; Antonelli A., Minervini A., Sandri M., Bertini R., Bertolo R., Carini M. et al. Below Safety Limits, Every Unit of Glomerular Filtration Rate Counts: Assessing the Relationship Between Renal Function and Cancer-specific Mortality in Renal Cell Carcinoma. Eur Urol. 2018;74(5):661-667. https//doi.org/10.1016/j.eururo.2018.07.029.; Меньшиков К.В., Измайлов А.А., Султанбаев А.В., Мусин Ш.И., Чалов В.С., Меньшикова И.А. и др. Метастатический почечно-клеточный рак, возможности таргетной терапии. Медицинский совет. 2021;(20):138-144. https://doi.org/10.21518/2079-701X-2021-20-138-144.; Bracarda S., Negrier S., Casper J., Porta C., Schmidinger M., Larkin J. et al. How clinical practice is changing the rules: the sunitinib 2/1 schedule in metastatic renal cell carcinoma. Expert Rev Anticancer Ther. 2017;17(3):227-233. https://doi.org/10.1080/14737140.2017.1276830.; https://www.med-sovet.pro/jour/article/view/6921

  12. 12
    Academic Journal

    المصدر: Malignant tumours; Том 12, № 2 (2022); 45-51 ; Злокачественные опухоли; Том 12, № 2 (2022); 45-51 ; 2587-6813 ; 2224-5057

    وصف الملف: application/pdf

    Relation: https://www.malignanttumors.org/jour/article/view/962/682; Bray F, Ferlay J, Soerjomataram I, et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018;68 (6):394–424. doi:10.3322/caac.21492. Epub 2018 Sep 12.; Измайлов А. А., Аюпов Р. Т., Сулатнбаев А. В., Мусин Ш. И., Меньшиков К. В., Забелин М. В. Организация работы онкологической службы в Республике Башкортостан в условиях пандемии COVID-19. Современные проблемы здравоохранения и медицинской статистики 2020 г., № 3. C. 195-208. DOI:10.24411/2312-2935-2020-00067.; Состояние онкологической помощи населению России в 2021 году. Под редакцией Каприна А. Д., Старинского В. В., Шахазадовой А. О.: МНИОИ им. П. А. Герцена – филиал ФГБУ «НМИЦ радиологии» Минздрава России, 2021. 239 с. ISBN 978-5-85502-262-9.; Choueiri TK, Motzer RJ. Systemic therapy for metastatic renal-cell carcinoma. N Engl J Med 2017;376:354-66.; McKay RR, Bosse D, Choueiri TK. Evolving systemic treatment landscape for patients with advanced renal cell carcinoma. J Clin Oncol 2018 October 29 (Epub ahead of print).; Heidegger I, Pircher A, Pichler R. Targeting the tumor microenvironment in renal cell cancer biology and therapy. Front Oncol 2019;9:490.; Apolo AB, Nadal R, Girardi DM, et al. Phase I study of cabozantinib and nivolumab alone or with ipilimumab for advanced or metastatic urothelial carcinoma and other genitourinary tumors. J Clin Oncol 2020;38:3672-84.; Amin A, Plimack ER, Ernstoff MS, et al. Safety and efficacy of nivolumab in combination with sunitinib or pazopanib in advanced or metastatic renal cell carcinoma: the CheckMate 016 study. J Immunother Cancer 2018;6:109.; Rini BI, Plimack ER, Stus V, et al. Pembrolizumab plus axitinib versus sunitinib for advanced renal-cell carcinoma. N Engl J Med 2019;380:1116-27.; Motzer RJ, Penkov K, Haanen J, et al. Avelumab plus axitinib versus sunitinib for advanced renal-cell carcinoma. N Engl J Med 2019;380:1103-15.; Agarwal N, Vaishampayan U, Green M, et al. Phase Ib study (COSMIC-021) of cabozantinib in combination with atezolizumab: results of the dose escalation stage in patients (pts) with treatmentnaive advanced renal cell carcinoma (RCC). J Clin Oncol 2020;29: Suppl 8:872P. abstract.; Pal S, Tsao C-K, Suarez C, et al. Cabozantinib (C) in combination with atezolizumab (A) as first-line therapy for advanced clear cell renal cell carcinoma (ccRCC): Results from the COSMIC-021 study. Ann Oncol 2020;31: Suppl 4: S554. abstract.; Меньшиков К. В., Султанбаев А. В., Мусин Ш. И., Измайлов А. А., Меньшикова И. А., Хамматова Л. А., Попова Е. В., Султанбаева Н. И., Липатов Д. О. Вторая линия терапии метастатического почечноклеточного рака. Обзор литературы. Поволжский онкологический вестник. Том 12, № 4. 2021 С. 39-52.; Меньшиков К. В., Измайлов А. А., Султанбаев А. В., Мусин Ш. И., Чалов В. С., Меньшикова И. А., Султанбаева Н. И., Липатов Д. О. Метастатический почечно-клеточный рак, возможности таргетной терапии. Медицинский Совет. 2021; (20):138-144. https://doi.org/10.21518/2079-701X-2021-20-138-144.; Меньшиков К. В., Султанбаев А. В., Мусин Ш. И., Рахматуллина И. Р., Меньшикова И. А., Хамматова Л. А., Попова Е. В., Султанбаева Н. И., Липатов Д. О. Возможности комбинированной иммунотаргетной терапии метастатического почечно-клеточного рака. Обзор литературы. Поволжский онкологический вестник. Том 13, № 1. 2022. С. 46-61.; Motzer RJ, Escudier B, McDermott DF, et al. Nivolumab versus everolimus in advanced renal-cell carcinoma. N Engl J Med 2015;373:1803-13.; Schmidt E, Lister J, Neumann M, et al. Cabozantinib versus standard-of-care comparators in the treatment of advanced/ metastatic renal cell carcinoma in treatment-naive patients: a systematic review and network meta-analysis. Target Oncol 2018;13:205-16.; Choueiri TK, Halabi S, Sanford BL, et al. Cabozantinib versus sunitinib as initial targeted therapy for patients with metastatic renal cell carcinoma of poor or intermediate risk: the Alliance A031203 CABOSUN trial. J Clin Oncol 2017;35:591-7.; Choueiri TK, Escudier B, Powles T, et al. Cabozantinib versus everolimus in advanced renal cell carcinoma (METEOR): final results from a randomised, openlabel, phase 3 trial. Lancet Oncol 2016;17: 917-27.; Меньшиков К. В., Султанбаев А. В., Мусин Ш. И., Измай лов А. A., Мугинов Р. Р., Меньшикова И. А., Шарифгалеев И. А., Липатов Д. О., Султанбаева Н. И. Почечно-клеточный рак с метастазами в наружных половых органах. Обзор литературы и клинический случай. Онкоурология. 2021;17 (2):174-181. https://doi.org/10.17650/1726-9776-2021-17-2-174-181.; Saeed A, Phadnis M, Park R, et al. Cabozantinib (cabo) combined with durvalumab (durva) in gastroesophageal (GE) cancer and other gastrointestinal (GI) malignancies: Preliminary phase Ib CAMILLA study results. J Clin Oncol 2020; 38: Suppl:4563. abstract.; Bergerot P, Lamb P, Wang E, Pal SK. Cabozantinib in combination with immunotherapy for advanced renal cell carcinoma and urothelial carcinoma: rationale and clinical evidence. Mol Cancer Ther 2019;18:2185-93.; Lu X, Horner JW, Paul E, et al. Effective combinatorial immunotherapy for castration-resistant prostate cancer. Nature 2017;543:728-32.; Apolo AB, Nadal R, Tomita Y, et al. Cabozantinib in patients with platinumrefractory metastatic urothelial carcinoma: an open-label, single-centre, phase 2 trial. Lancet Oncol 2020;21:1099-109.; Heng DY, Xie W, Regan MM, et al. Prognostic factors for overall survival in patients with metastatic renal cell carcinoma treated with vascular endothelial growth factor-targeted agents: results from a large, multicenter study. J Clin Oncol 2009;27:5794-9.; Heng DYC, Xie W, Regan MM, et al. External validation and comparison with other models of the International Metastatic Renal-Cell Carcinoma Database Consortium prognostic model: a populationbased study. Lancet Oncol 2013;14:141-8.; Choueiri TK, Powles T, Burotto M, Escudier B, Bourlon MT, Zurawski B, Oyervides Juarez VM, Hsieh JJ, Basso U, Shah AY, Suarez C, Hamzaj A, Goh JC, Barrios C, Richardet M, Porta C, Kowalyszyn R, Feregrino JP, Zolnierek J, Pook D, Kessler ER, Tomita Y, Mizuno R, Bedke J, Zhang J, Maurer MA, Simsek B, Ejzykowicz F, Schwab GM, Apolo AB, Motzer RJ; CheckMate 9ER Investigators. Nivolumab plus Cabozantinib versus Sunitinib for Advanced Renal-Cell Carcinoma. N Engl J Med. 2021 Mar 4;384 (9):829-841. doi:10.1056/NEJMoa2026982. PMID: 33657295; PMCID: PMC8436591.; Носов Д. А., Б. Я. Алексеев, Гладков О. А., Волкова М. И., Попов А. М., Харкевич Г. Ю. Практические рекомендации по лекарственному лечению почечноклеточного рака. Злокачественные опухоли: Практические рекомендации RUSSCO #3s2, 2021 (том 11). 31. 10.18027/2224-5057-2021-11-3s2-31.; Aeppli S, Schmaus M, Eisen T, Escudier B, Grunwald V, Larkin J, McDermott D, Oldenburg J, Porta C, Rini BI, Schmidinger M, Sternberg CN, Rothermundt C, Putora PM. First-line treatment of metastatic clear cell renal cell carcinoma: a decision-making analysis among experts. ESMO Open. 2021 Feb;6 (1):100030. doi:10.1016/j.esmoop.2020.100030. Epub 2021 Jan 15. PMID: 33460963; PMCID: PMC7815472.; McKay RR, Lin X, Perkins JJ, Heng DY, Simantov R, Choueiri TK. Prognostic significance of bone metastases and bisphosphonate therapy in patients with renal cell carcinoma. Eur Urol 2014;66 (3):502e9.; Hanna N, Sun M, Meyer CP, Nguyen PL, Pal SK, Chang SL, et al. Survival analyses of patients with metastatic renal cancer treated with targeted therapy with or without cytoreductive nephrectomy: a national cancer data base study. J Clin Oncol 2016; 34 (27):3267e75; https://www.malignanttumors.org/jour/article/view/962

  13. 13
  14. 14
    Academic Journal

    المساهمون: Исследование не имело спонсорской поддержки.

    المصدر: Malignant tumours; Том 10, № 4 (2020); 38-46 ; Злокачественные опухоли; Том 10, № 4 (2020); 38-46 ; 2587-6813 ; 2224-5057

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    Relation: https://www.malignanttumors.org/jour/article/view/816/571; Насретдинов А. Ф., Султанбаева Н. И., Мусин Ш. И. и др. Терапия ингибиторами циклинзависимых киназ CDK4/6 при разных спектрах соматических мутаций гена PIK3CA у больных раком молочной железы. Медицинский совет. 2020; (20):40-46. doi: 10.21 518/2079-701X-2020-20-40-46.; Sultanbaev, A. & Minniakhmetov, I. & Sultanbaeva, N. & Menshikov, K. & Nasretdinov, A. & Musin, S. (2020). 25P Identification of gene mutations in patients with breast cancer in a region located in the southeast of the European part of Russia. Annals of Oncology. 31. S1250. https://doi.org/10.1016/j. annonc. 2020.10.045.; Состояние онкологической помощи населению России в 2019 году. Под. ред. А. Д. Каприна, В. В. Старинского, А. О. Шахазадовой. М.: МНИОИ им. П. А. Герцена. 2020; 239 с. [Sostoyanie onkologicheskoy pomoshchi naseleniyu Rossiiv 2019 godu. (The status of cancer care for the population of Russia in 2019.) A. D. Kaprin, V. V. 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    المصدر: Meditsinskiy sovet = Medical Council; № 20 (2020); 40-46 ; Медицинский Совет; № 20 (2020); 40-46 ; 2658-5790 ; 2079-701X

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    المصدر: Creative surgery and oncology; Том 10, № 4 (2020); 330-338 ; Креативная хирургия и онкология; Том 10, № 4 (2020); 330-338 ; 2076-3093 ; 2307-0501

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    Academic Journal

    المصدر: Creative surgery and oncology; Том 10, № 3 (2020); 183-189 ; Креативная хирургия и онкология; Том 10, № 3 (2020); 183-189 ; 2076-3093 ; 2307-0501

    وصف الملف: application/pdf

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