يعرض 51 - 60 نتائج من 5,368 نتيجة بحث عن '"controlled clinical trial"', وقت الاستعلام: 0.91s تنقيح النتائج
  1. 51
    دورية أكاديمية
  2. 52
    دورية أكاديمية
  3. 53
    دورية أكاديمية
  4. 54
    دورية أكاديمية
  5. 55
    دورية أكاديمية
  6. 56
    دورية أكاديمية
  7. 57
    دورية أكاديمية

    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

    العلاقة: https://www.surgonco.ru/jour/article/view/810/547Test; 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. J Clin Pharmacol. 2017; 57 (9): 1138–47. DOI:10.1002/jcph.917; Finn R. S., Ikeda M., Zhu A. X., Sung M. W., Baron A. D., Kudo M., et al. Phase Ib study of lenvatinib plus pembrolizumab in patients with unresectable hepatocellular carcinoma. J Clin Oncol. 2020; 38 (26): 2960–70. DOI:10.1200/JCO.20.00808; Pishvaian M. J., Lee M. S., Ryoo B.-Y., Stein S., Lee K-H., Verret W., et al. Updated safety and clinical activity results from a phase Ib study of atezolizumab + bevacizumab in hepatocellular carcinoma (HCC). Ann Oncol. 2018; 29 (Suppl.8): 718–9.; Finn R. S., Qin S., Ikeda M., Galle P. R., Ducreux M., Kim T. Y., et al. Atezolizumab plus bevacizumab in unresectable hepatocellular carcinoma. N Engl J Med. 2020; 382 (20): 1894–905. DOI:10.1056/NEJMoa1915745; Giannini E. G., Aglitti A., Borzio M., Gambato M., Guarino M., Iavarone M., et al. Overview of immune checkpoint inhibitors therapy for hepatocellular carcinoma, and The ITA.LI.CA Cohort derived estimate of amenability rate to immune checkpoint inhibitors in clinical practice. Cancers (Basel). 2019;11(11):1689. DOI:10.3390/cancers11111689; Gordan J. D., Kennedy E. B., Abou-Alfa G. K., Beg M. S., Brower S. T., Gade T. P., et al. Systemic therapy for advanced hepatocellular carcinoma: ASCO Guideline. J Clin Oncol. 2020; 38 (36): 4317–45. DOI:10.1200/JCO.20.02672; de Castro T., Jochheim L. S., Bathon M., Welland S., Scheiner B., Shmanko K., et al. Atezolizumab and bevacizumab in patients with advanced hepatocellular carcinoma with impaired liver function and prior systemic therapy: a real-world experience. Ther Adv Med Oncol. 2022; 14: 17588359221080298. DOI:10.1177/17588359221080298; Hatanaka T., Kakizaki S., Hiraoka A., Tada T., Hirooka M., Kariyama K., et al. Comparative efficacy and safety of atezolizumab and bevacizumab between hepatocellular carcinoma patients with viral and non-viral infection: A Japanese multicenter observational study. Cancer Med. 2023; 12 (5): 5293–303. DOI:10.1002/cam4.5337; Shimose S., Hiraoka A., Nakano M., Iwamoto H., Tanaka M., Tanaka T., et al. First-line sorafenib sequential therapy and liver disease etiology for unresectable hepatocellular carcinoma using inverse probability weighting: A multicenter retrospective study. Cancer Med. 2021; 10 (23): 8530–41. DOI:10.1002/cam4.4367; Hatanaka T., Kakizaki S., Nagashima T., Namikawa M., Ueno T., Tojima H., et al. Lenvatinib for hepatocellular carcinoma patients with nonviral infection who were unlikely to respond to immunotherapy: a retrospective, comparative study. Oncology. 2021; 99 (10): 641–51. DOI:10.1159/000517494; Tsuchiya K., Kurosaki M., Sakamoto A., Marusawa H., Kojima Y., Hasebe C., et al. The real-world data in japanese patients with unresectable hepatocellular carcinoma treated with lenvatinib from a nationwide multicenter study. Cancers (Basel). 2021; 13 (11): 2608. DOI:10.3390/cancers13112608; Hiraoka A., Kumada T., Tada T., Tani J., Kariyama K., Fukunishi S., et al. Efficacy of lenvatinib for unresectable hepatocellular carcinoma based on background liver disease etiology: multi-center retrospective study. Sci Rep. 2021; 11 (1): 16663. DOI:10.1038/s41598-021-96089-x; Tomonari T., Sato Y., Tanaka H., Mitsuhashi T., Hirao A., Tanaka T., et al. Th erapeutic efficacy of lenvatinib in nonviral unresectable hepatocellular carcinoma. JGH Open. 2021; 5 (11): 1275–83. DOI:10.1002/jgh3.12663; Pugh R. N., Murray-Lyon I. M., Dawson J. L., Pietroni M. C., Williams R. Transection of the oesophagus for bleeding oesophageal varices. Br J Surg. 1973; 60 (8): 646–9. DOI:10.1002/bjs.1800600817; Tada T., Kumada T., Hiraoka A., Hirooka M., Kariyama K., Tani J., et al. Safety and efficacy of atezolizumab plus bevacizumab in elderly patients with hepatocellular carcinoma: A multicenter analysis. Cancer Med. 2022; 11 (20): 3796–808. DOI:10.1002/cam4.4763; Singal A. G., Lampertico P., Nahon P. Epidemiology and surveillance for hepatocellular carcinoma: New trends. J Hepatol. 2020; 72 (2): 250–61. DOI:10.1016/j.jhep.2019.08.025; Global Burden of Disease Liver Cancer Collaboration; Akinyemiju T., Abera S., Ahmed M., Alam N., Alemayohu M. A., Allen C., et al. The burden of primary liver cancer and underlying etiologies from 1990 to 2015 at the global, regional, and national level: results from the global burden of disease study 2015. JAMA Oncol. 2017; 3 (12): 1683–91. DOI:10.1001/jamaoncol.2017.3055; Kumada T., Toyoda H., Tada T., Yasuda S., Tanaka J. Changes in background liver function in patients with hepatocellular carcinoma over 30 years: comparison of child-pugh classification and albumin bilirubin grade. Liver Cancer. 2020; 9 (5): 518–28. DOI:10.1159/000507933; Johnson P. J., Berhane S., Kagebayashi C., Satomura S., Teng M., Reeves H. L., et al. Assessment of liver function in patients with hepatocellular carcinoma: a new evidence-based approach-the ALBI grade. J Clin Oncol. 2015; 33 (6): 550–8. DOI:10.1200/JCO.2014.57.9151; Iwamoto H., Shimose S., Noda Y., Shirono T., Niizeki T., Nakano M., et al. Initial experience of atezolizumab plus bevacizumab for unresectable hepatocellular carcinoma in real-world clinical practice. Cancers (Basel). 2021; 13 (11): 2786. DOI:10.3390/cancers13112786; Finn R. S., Ryoo B. Y., Merle P., Kudo M., Bouattour M., Lim H. Y., et al. Pembrolizumab as second-line therapy in patients with advanced hepatocellular carcinoma in KEYNOTE-240: a randomized, double-blind, phase III trial. J Clin Oncol. 2020; 38 (3): 193–202. DOI:10.1200/JCO.19.01307; Yau T., Park J. W., Finn R. S., Cheng A. L., Mathurin P., Edeline J., et al. Nivolumab versus sorafenib in advanced hepatocellular carcinoma (CheckMate 459): a randomised, multicentre, open-label, phase 3 trial. Lancet Oncol. 2022; 23 (1): 77–90. DOI:10.1016/S1470-2045(21)00604-5; Cheng A. L., Qin S., Ikeda M., Galle P. R., Ducreux M., Kim T. Y., et al. Updated efficacy and safety data from IMbrave150: Atezolizumab plus bevacizumab vs. sorafenib for unresectable hepatocellular carcinoma. J Hepatol. 2022; 76 (4): 862–73. DOI:10.1016/j.jhep.2021.11.030; Finn R. S., Qin S., Ikeda M., Galle P. R., Ducreux M., Kim T.-Y., et al. IMbrave150: Updated Overall Survival (OS) Data from a Global, Randomized, Open-Label Phase III Study of Atezolizumab (Atezo) + Bevacizumab (Bev) versus Sorafenib (Sor) in Patients (Pts) with Unresectable Hepatocellular Carcinoma (HCC). J Clin Oncol. 2021; 39 (3S): 267. DOI:10.1200/JCO.2021.39.3_suppl.267; Galle P. R., Finn R. S., Qin S., Ikeda M., Zhu A. X., Kim T. Y., et al. Patient-reported outcomes with atezolizumab plus bevacizumab versus sorafenib in patients with unresectable hepatocellular carcinoma (IMbrave150): an open-label, randomised, phase 3 trial. Lancet Oncol. 2021; 22 (7): 991–1001. DOI:10.1016/S1470-2045(21)00151-0; Eisenhauer E. A., Therasse P., Bogaerts J., Schwartz L. H., Sargent D., Ford R., et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer. 2009; 45 (2): 228–47. DOI:10.1016/j.ejca.2008.10.026; Lencioni R., Llovet J. M. Modifi ed RECIST (mRECIST) assessment for hepatocellular carcinoma. Semin Liver Dis. 2010; 30 (1): 52–60. DOI:10.1055/s-0030-1247132; Common Terminology Criteria for Adverse Events v4.0 (CTCAE). Bethesda; 2009.; Common Terminology Criteria for Adverse Events (CTCAE). v.5.0; Cancer Therapy Evaluation Program (CTEP). Rockville; 2017.; Himmelsbach V., Pinter M., Scheiner B., Venerito M., Sinner F., Zimpel C., et al. Efficacy and safety of atezolizumab and bevacizumab in the real-world treatment of advanced hepatocellular carcinoma: experience from four tertiary centers. Cancers (Basel). 2022; 14 (7): 1722. DOI:10.3390/cancers14071722; Qin S., Ren Z., Feng Y. H., Yau T., Wang B., Zhao H., et al. Atezolizumab plus bevacizumab versus sorafenib in the chinese subpopulation with unresectable hepatocellular carcinoma: phase 3 randomized, open-label IMbrave150 study. Liver Cancer. 2021; 10 (4): 296–308. DOI:10.1159/000513486; Pfister D., Núñez N. G., Pinyol R., Govaere O., Pinter M., Szydlowska M., et al. NASH limits anti-tumour surveillance in immunotherapy-treated HCC. Nature. 2021; 592 (7854): 450–6. DOI:10.1038/s41586-021-03362-0; Inada Y., Mizukoshi E., Seike T., Tamai T., Iida N., Kitahara M., et al. Characteristics of immune response to tumor-associated antigens and immune cell profile in patients with hepatocellular carcinoma. Hepatology. 2019; 69 (2): 653–65. DOI:10.1002/hep.30212; https://www.surgonco.ru/jour/article/view/810Test

  8. 58
  9. 59
    دورية أكاديمية
  10. 60
    دورية أكاديمية