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1Academic Journal
المؤلفون: M. Mandrina O., V. Breder V., M. Ivanov V., A. Lebedeva A., V. Gorbatsevich V., K. Laktionov K., P. Kononets V., М. Мандрина О., В. Бредер В., М. Иванов В., А. Лебедева А., В. Горбацевич В., К. Лактионов К., П. Кононец В.
المصدر: Meditsinskiy sovet = Medical Council; № 9 (2021); 154-159 ; Медицинский Совет; № 9 (2021); 154-159 ; 2658-5790 ; 2079-701X
مصطلحات موضوعية: MET mutation, PD-L1, immunotherapy, NSCLC, crizotinib, мутация MET, иммунотерапия, немелкоклеточный рак легкого, кризотиниб
وصف الملف: application/pdf
Relation: https://www.med-sovet.pro/jour/article/view/6267/5681; König D., Savic Prince S., Rothschild S.I. Targeted Therapy in Advanced and Metastatic Non-Small Cell Lung Cancer. An Update on Treatment of the Most Important Actionable Oncogenic Driver Alterations. Cancers (Basel). 2021;13(4):804. https://doi.org/10.3390/cancers13040804.; Socinski M.A., Pennell N.A., Davies K.D. MET Exon 14 Skipping Mutations in Non-Small-Cell Lung Cancer: An Overview of Biology, Clinical Outcomes, and Testing Considerations. JCO Precis Oncol. 2021;5:653–663. https://doi.org/10.1200/PO.20.00516.; Sierra J.R., Tsao M.S. c-MET as a Potential Therapeutic Target and Biomarker in Cancer. Ther Adv Med Oncol. 2011;3(1 Suppl):S21–S35. https://doi.org/10.1177/1758834011422557.; Awad M.M., Oxnard G.R., Jackman D.M., Savukoski D.O, Hall D., Shivdasanietal P. et al. MET Exon 14 Mutations in Non-Small-Cell Lung Cancer Are Associated With Advanced Age and Stage-Dependent MET Genomic Amplification and c-Met Overexpression. J Clin Oncol. 2016;34(7):721–730. https://doi.org/10.1200/JCO.2015.63.4600.; Titmarsh H.F., O’Connor R., Dhaliwal K., Akram A.R. The Emerging Role of the c-MET-HGF Axis in Non-small Cell Lung Cancer Tumor Immunology and Immunotherapy. Front Oncol. 2020;10:54. https://doi.org/10.3389/fonc.2020.00054.; Sabari J.K., Montecalvo J., Chen R., Dienstag J.A., Mrad C., Bergagnini I. et al. PD-L1 Expression and Response to Immunotherapy in Patients with MET Exon 14-Altered Non-Small Cell Lung Cancers (NSCLC). J Clin Oncol. 2017;35(15_ suppl):8512–8512. https://doi.org/10.1200/JCO.2017.35.15_suppl.8512.; Xing X., Guo J., Ding G., Li B., Dong B., Feng Q. et al. Analysis of PD1, PDL1, PDL2 Expression and T Cells Infiltration in 1014 Gastric Cancer Patients. Oncoimmunology. 2017;7(3):e1356144. https://doi.org/10.1080/2162402x.2017.1356144.; Glodde N., Bald T., van den Boorn-Konijnenberg D., Nakamura K., O’Donnell J.S., Szczepanski S. et al. Reactive Neutrophil Responses Dependent on the Receptor Tyrosine Kinase c-MET Limit Cancer Immunotherapy. Immunity. 2017;47(4):789.e9–802.e9. https://doi.org/10.1016/j.immuni.2017.09.012.; Papaccio F., Della Corte C.M., Viscardi G., Di Liello R., Esposito G., Sparano F. et al. HGF/MET and the Immune System: Relevance for Cancer Immunotherapy. Int J Mol Sci. 2018;19(11):3595. https://doi.org/10.3390/ijms19113595.; Salgia R., Sattler M., Scheele J., Stroh C., Felip E. The Promise of Selective MET Inhibitors in Non-Small Cell Lung Cancer with MET Exon 14 Skipping. Cancer Treat Rev. 2020;87:102022. https://doi.org/10.1016/j.ctrv.2020.102022.; Liang H., Wang M. MET Oncogene in Non-Small Cell Lung Cancer: Mechanism of MET Dysregulation and Agents Targeting the HGF/c-Met Axis. Onco Targets Ther. 2020;13:2491–2510. https://doi.org/10.2147/OTT.S231257.; Garajová I., Giovannetti E., Biasco G., Peters G.J. c-Met as a Target for Personalized Therapy. Transl Oncogenomics. 2015;7(Suppl 1):13–31. https://doi.org/10.4137/TOG.S30534.; Baltschukat S., Engstler B.S., Huang A., Hao H.X., Tam A., Wang H.Q. et al. Capmatinib (INC280) Is Active Against Models of Non-Small Cell Lung Cancer and Other Cancer Types with Defined Mechanisms of MET Activation. Clin Cancer Res. 2019;25(10):3164–3175. https://doi.org/10.1158/1078-0432.ccr-18-2814.; Klempner S.J., Borghei A., Hakimian B., Ali S.M., Ou S.I. Intracranial Activity of Cabozantinib in MET Exon 14-Positive NSCLC with Brain Metastases. J Thorac Oncol. 2017;12(1):152–156. https://doi.org/10.1016/j.jtho.2016.09.127.; Wang S.X.Y., Zhang B.M., Wakelee H.A., Koontz M.Z., Pan M., Diehn M. et al. Case Series of MET Exon 14 Skipping Mutation-Positive Non-Small-Cell Lung Cancers with Response to Crizotinib and Cabozantinib. Anticancer Drugs. 2019;30(5):537–541. https://doi.org/10.1097/CAD.0000000000000765.; Waqar S.N., Morgensztern D., Sehn J. MET Mutation Associated with Responsiveness to Crizotinib. J Thorac Oncol. 2015;10(5):e29–e31. https://doi.org/10.1097/JTO.0000000000000478.; https://www.med-sovet.pro/jour/article/view/6267
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2Academic Journal
المؤلفون: N. Mitiushkina V., I. Stepanov A., D. Yurlov O., E. Filippova A., S. Odintsova V., A. Lozhkina M., S. Orlov V., A. Iyevleva G., Н. Митюшкина В., И. Степанов А., Д. Юрлов О., Е. Филиппова А., С. Одинцова В., А. Ложкина М., С. Орлов В., А. Иевлева Г.
المساهمون: This work was supported by the grant of the Russian Science Foundation № 19-15-00312., Работа поддержана грантом Российского научного фонда № 19-15-00312.
المصدر: Siberian journal of oncology; Том 19, № 4 (2020); 132-137 ; Сибирский онкологический журнал; Том 19, № 4 (2020); 132-137 ; 2312-3168 ; 1814-4861 ; 10.21294/1814-4861-2020-19-4
مصطلحات موضوعية: lung cancer, ALK translocation, crizotinib, ceritinib, alectinib, рак легкого, транслокации ALK, кризотиниб, церитиниб, алектиниб
وصف الملف: application/pdf
Relation: https://www.siboncoj.ru/jour/article/view/1539/777; Soda M., Choi Y.L., Enomoto M., Takada S., Yamashita Y., Ishikawa S., Fujiwara S,. Watanabe H., Kurashina K., Hatanaka H., Bando M., Ohno S., Ishikawa Y., Aburatani H., Niki T., Sohara Y., Sugiyama Y., Mano H. Identification of the transforming EML4-ALK fusion gene in non-smallcell lung cancer. Nature. 2007 Aug 2; 448(7153): 561–6. doi:10.1038/nature05945.; Rikova K., Guo A., Zeng Q., Possemato A., Yu J., Haack H., Nardone J., Lee K., Reeves C., Li Y., Hu Y., Tan Z., Stokes M., Sullivan L., Mitchell J., Wetzel R., Macneill J., Ren J.M., Yuan J., Bakalarski C.E., Villen J., Kornhauser J.M., Smith B., Li D., Zhou X., Gygi S.P., Gu T.L., Polakiewicz R.D., Rush J., Comb M.J. Global survey of phosphotyrosine signaling identifies oncogenic kinases in lung cancer. 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3Academic Journal
المؤلفون: E. Reutova V., L. Laktionova V., D. Marinov T., D. Peregudov A., T. Borisova N., Е. Реутова В., Л. Лактионова В., Д. Маринов Т., Д. Перегудов А., Т. Борисова Н.
المصدر: Meditsinskiy sovet = Medical Council; № 9 (2020); 176-181 ; Медицинский Совет; № 9 (2020); 176-181 ; 2658-5790 ; 2079-701X
مصطلحات موضوعية: ALK translocation, non-small cell lung cancer, targeted therapy, crizotinib, транслокация ALK, немелкоклеточный рак легкого, таргетная терапия, кризотинибтранслокация ALK, кризотиниб
وصف الملف: application/pdf
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Laktionov K.K., Artamonova E.V., Breder V.V., Gorbunova V.A., Moiseenko F.V., Reutova E.V. et al. Practical guidelines for the medicinal treatment of non-small cell cancer. Zlokachestvennye opukholi = Malignant Tumours. 2019;9(3s2):2–48. (In Russ.) Available at: https://rosoncoweb.ru/standarts/RUSSCO/2019/2019-01.pdf.; Demidova I., Grinevich V., Avdalian A., Imyanitov E., Gikalo М., Savelov et al. Detection of ALK rearrangements in 4002 Russian patients: The utility of different diagnostic approaches Lung Cancer. 2017;103:17–23. 10.1016/j.lungcan.2016.11.001.; Solomon B., Varella-Garcia M., Camidge D.R. ALK gene rearrangements: a new therapeutic target in a molecularly defined subset of non-small cell lung cancer. SOJ Thoracic Oncology. 2009;4(12):1450–1454. doi:10.1097/JTO.0b013e3181c4dedb.; Soda M., Choi Y.L., Enomoto M., Takada S., Yamashita Y., Ishikawa S. et al. Identification of the transforming EML4-ALK fusion gene in nonsmall-cell lung cancer. Nature. 2007;448(7153):561–566. doi:10.1038/nature05945.; Shaw A.T., Yeap B.Y., Mino-Kenudson M., Digumarthy S.R., Costa D.B., Heist R.S. et al. Clinical features and outcome of patients with non-small-cell lung cancer who harbor EML4-ALK. J Clin Oncol. 2009;27(26):4247–4253. doi:10.1200/JCO.2009.22.6993.; Демидова И.А., Цепенщикова Е.О., Баринов А.А., Гагарин И.М., Савелов Н.А., Гриневич В.Н., Тюляндин С.А. Определение перестроек гена ALK в селектированной популяции российских больных немелкоклеточным раком легкого. Злокачественные опухоли. 2013;3(7):3–9. doi:10.18027/2224-5057-2013-3-3-9. Demidova I.A., Tepenshchikova E.O., Barinov А.А., Gagarin I.M., Savelov N.A., Grinevich V.N., Tulyandin S.A. Determination of ALK gene rearrangements in a selected population of Russian patients with non-small cell lung cancer. Zlokachestvennye opukholi = Malignant Tumours. 2013;3(7):3–9. (In Russ.) doi:10.18027/2224-5057-2013-3-3-9.; Camidge D.R., Bang Y.J., Kwak E.L., Iafrate A.J., Varella-Garcia M., Fox S.B. et al. Activity and safety of crizotinib in patients with ALK-positive non-smallcell lung cancer: updated results from a phase 1 study. Lancet Oncol. 2012;13(10):1011–1019. doi:10.1016/S1470-2045(12)70344-3.; Blackhall F., Ross Camidge D., Shaw A.T., Soria J.C., Solomon B.J., Mok T. et al. Final results of the large-scale multinational trial PROFILE 1005: efficacy and safety of crizotinib in previously treated patients with advanced/metastatic ALK-positive non-small-cell lung cancer. ESMO Open. 2017;2(3):e000219. doi:10.1136/esmoopen-2017-000219.; Shaw A.T., Kim T.M., Crinò L., Gridelli C., Kiura K., Liu G. et al. Ceritinib versus chemotherapy in patients with ALK-rearranged non-small-cell lung cancer previously given chemotherapy and crizotinib (ASCEND-5): a randomised, controlled, open-label, phase 3 trial. Lancet Oncol. 2017;18(7):874–886. doi:10.1016/S1470-2045(17)30339-X.; Novello S., Mazières J., Oh I.J., de Castro J., Migliorino M. R., Helland Å. et al. Alectinib versus chemotherapy in crizotinib-pretreated anaplastic lymphoma kinase (ALK)-positive non-small-cell lung cancer: results from the phase III ALUR study. Ann Oncol. 2018;29(6):1409–1416. doi:10.1093/annonc/mdy121.; Huber R.M., Hansen K.H., Paz-Ares Rodriguez L., West H.L., Reckamp K.L., Leighl N.B. et al. Brigatinib in Crizotinib-Refractory ALK+ NSCLC: 2-Year Follow-up on Systemic and Intracranial Outcomes in the Phase 2 ALTA Trial. J Thorac Oncol. 2020;15(3):404–415. doi:10.1016/j.jtho.2019.11.004.; Solomon B.J., Besse B., Bauer T.M., Felip E., Soo R.A., Camidge D.R. et al. Lorlatinib in patients with ALK-positive non-small-cell lung cancer: results from a global phase 2 study. Lancet Oncol. 2018;19(12):1654– 1667. doi:10.1016/S1470-2045(18)30649-1.; Rangachari D., Le X., Shea M., Huberman M. S., Van der Laan P.A., Kobayashi S.S., Costa D.B. Cases of ALK-Rearranged Lung Cancer with 5-Year ProgressionFree Survival with Crizotinib as Initial Precision Therapy. J Thorac Oncol. 2017;12(11):e175-e177. doi:10.1016/j.jtho.2017.06.002.; Solomon B.J., Kim D.W., Wu Y.L., Nakagawa K., Mekhail T., Felip E. et al. Final Overall Survival Analysis From a Study Comparing First-Line Crizotinib Versus Chemotherapy in ALK-Mutation-Positive Non-Small-Cell Lung Cancer. J Clin Oncol. 2018;36(22):2251–2258. doi:10.1200/JCO.2017.77.4794.; Duruisseaux M., Besse B., Cadranel J., Pérol M., Mennecier B., Bigay-Game L. et al. Overall survival with crizotinib and next-generation ALK inhibitors in ALK-positive non-small-cell lung cancer (IFCT-1302 CLINALK): a French nationwide cohort retrospective study. Oncotarget. 2017;8(13):21903– 21917. doi:10.18632/oncotarget.15746.; Peters S., Camidge D.R., Shaw A.T., Gadgeel S., Ahn J.S., Kim D.W. et al. Alectinib versus crizotinib in untreated ALK-positive non-small-cell lung cancer. N Engl J Med. 2017;377:829–838. doi:10.1056/NEJMoa1704795.; Sakakibara-Konishi J., Kitai H., Ikezawa Y., Hatanaka Y., Sasaki T., Yoshida R. et al. Response to Crizotinib Re-administration After Progression on Lorlatinib in a Patient With ALK-rearranged Non-small-cell Lung Cancer. Clinical Lung Cancer. 2019;20(5):e555-e559. doi:10.1016/j.cllc.2019.06.021.; Shaw A.T., Friboulet L., Leshchiner I., Gainor J.F., Bergqvist S., Brooun A. et al. Resensitization to Crizotinib by the Lorlatinib ALK Resistance Mutation L1198F. N Engl J Med. 2016;374(1):54–61. doi:10.1056/NEJMoa1508887.; https://www.med-sovet.pro/jour/article/view/5721
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4Academic Journal
المؤلفون: S. Bagrova G., A. Kolomeytseva A., E. Trusilova V., V. Gorbunova A., С. Багрова Г., А. Коломейцева А., Е. Трусилова В., В. Горбунова А.
المصدر: Meditsinskiy sovet = Medical Council; № 19 (2019); 120-124 ; Медицинский Совет; № 19 (2019); 120-124 ; 2658-5790 ; 2079-701X ; 10.21518/2079-701X-2019-19
مصطلحات موضوعية: non-small cell lung cancer, ALK translocation, alectinib, crizotinib, немелкоклеточный рак легкого, транслокация ALK, кризотиниб, алектиниб
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Relation: https://www.med-sovet.pro/jour/article/view/5278/4808; Shaw A.T., Kim D.W., Nakagawa K., Seto T., Crinó L., Ahn M.J., De Pas T., Besse B., Solomon B.J., Blackhall F., et al. Crizotinib versus chemotherapy in advanced ALK-positive lung cancer. N Engl J Med. 2013;368(25):2385-2394. doi:10.1056/NEJMoa1214886.; Tsao A.S., Scagliotti G.V., Bunn P.A. Jr, Carbone D.P., Warren G.W., Bai C., et al. Scientific Advances in Lung Cancer 2015. J Thorac Oncol. 2016;11(5):613-638. DOI:10.1016/j.jtho.2016.03.012.; Novello S., Mazieres J., Oh I.J., de Castro J., Migliorino M.R., Helland A., et al. Primary Results from the Phase III ALUR Study of Alectinib versus Chemotherapy in Previously Treated ALK+Non-Small-Cell Lung Cancer (NSCLC). Annals of Oncology 2017;28(suppl_5):v605-v649. doi:10.1093/annonc/mdx440.058.; Kerr K.M., López-Ríos F. Precision medicine in NSCLC and pathology: how does ALK fit in the pathway? Ann Oncol. 2016;27(Suppl 3):iii16-iii24. doi:10.1093/annonc/mdw302.; Solomon B.J., Mok T., Kim D.W., Wu Y.L., Nakagawa K., Mekhail T., Felip E., Cappuzzo F., Paolini J., Usari T., et al. First-line crizotinib versus chemotherapy in ALK-positive lung cancer. N Engl J Med. 2014;371(23):2167-2177. doi:10.1056/NEJMoa1408440.; Duruisseaux M., Besse B., Cadranel J., Pérol M., Mennecier B., Bigay-Game L., Descourt R., Dansin E., Audigier-Valette C., Moreau L., et al. Overall survival with crizotinib and next-generation ALK inhibitors in ALK-positive nonsmall-cell lung cancer (IFCT-1302 CLINALK): a French nationwide cohort retrospective study. Oncotarget. 2017;8(13):21903-21917. doi:10.18632/oncotarget.15746.; Peters S., Camidge D.R., Shaw A.T., Gadgeel S., Ahn J.S., Kim D.W. et al. Alectinib versus Crizotinib in Untreated ALK-Positive Non-SmallCell Lung Cancer. N Engl J Med. 2017;377(9):829-838. doi:10.1056/NEJMoa1704795.; Shaw A.T., Gandhi L., Gadgeel S., Riely G. et al. Alectinib in ALK-positive, crizotinib-resistant, non-small-cell lung cancer: a single-group, multicentre, phase 2 trial. Lancet Oncol. 2016;17(2):234-242. doi:10.1016/S1470-2045(15)00488-X.; Ou S.H., Ahn J.S., De Petris L., Govindan R., Yang J.C., Hughes B., Lena H., Moro-Sibilot D., Bearz A., Ramirez S.V., et al. Alectinib in crizotinib-refractory ALK- rearranged non-small-cell lung cancer: a phase II global study. J Clin Oncol. 2016;34(7):661-668. doi:10.1200/JCO.2015.63.9443.; Gadgeel S.M., Ganghi L., Riely G.J., Chiappori A.A., West H.L., Azada M.C. et al. Safety and activity of alectenib against systemic disease and brain metastases in patients with crizotinib-resistant ALK-rearranged non-small-cell lung cancer: results from the dose-finding portion of a phase 1/2 study. Lancet Oncol. 2014;15(10):1119-1128. doi:10.1016/S1470-2045(14)70362-6.; Реутова Е.В., Лактионов К.К. Новые возможности в лечении больных ALK-позитивным немелкоклеточным раком легкого. Онкология. Журнал им. П.А. Герцена. 2019;8(3):226-230. doi:10.17116/onkolog2019803115226.; Mok T.S.K., Shaw A.T., Camidge R.D., Gadgeel S.M., Rosell R., Dziadziuszko R., et al. Final PFS, updated OS and safety data from the randomised, phase III ALEX study of alectinib (ALC) versus crizotinib (CRZ) in untreated advanced ALK+ NSCLC. Annals of Oncology. 2019;30(Suppl_5):mdz260.006. doi:10.1093/annonc/mdz260.006.; https://www.med-sovet.pro/jour/article/view/5278
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5Academic Journal
المؤلفون: Бредер, В., Лактионов, К., Юдин, Денис, Хамрина, Н.
مصطلحات موضوعية: НЕМЕЛКОКЛЕТОЧНЫЙ РАК ЛЕГКОГО, ТРАНСЛОКАЦИЯ ГЕНА ALK, ALK-ПОЗИТИВНЫЙ РАК ЛЕГКОГО, КРИЗОТИНИБ, ЦЕРИТИНИБ, АЛЕКТИНИБ, РЕЗИСТЕНТНОСТЬ
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6
المؤلفون: Ovsiannikova, D.I.
المصدر: Practical oncology; Том 2, № 4 (2019); 50-56
Практическая онкология-Praktična onkologìâ; Том 2, № 4 (2019); 50-56
Практична онкологія-Praktična onkologìâ; Том 2, № 4 (2019); 50-56مصطلحات موضوعية: ALK-положительный немелкоклеточный рак легкого, ингибитор тирозинкиназы, ALK-ингибиторы, таргетные препараты, алектиниб, кризотиниб, ALK-позитивний недрібноклітинний рак легені, інгібітор тирозинкінази, ALK-інгібітори, таргетні препарати, алектиніб, кризотиніб, ALK-positive non-small-cell lung cancer, Tyr-kinase inhibitors, ALK inhibitors, target agents, alectinib, crizotinib
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7
المصدر: Российский онкологический журнал.
مصطلحات موضوعية: НЕМЕЛКОКЛЕТОЧНЫЙ РАК ЛЕГКОГО, ТРАНСЛОКАЦИЯ ГЕНА ALK, ALK-ПОЗИТИВНЫЙ РАК ЛЕГКОГО, КРИЗОТИНИБ, ЦЕРИТИНИБ, АЛЕКТИНИБ, РЕЗИСТЕНТНОСТЬ
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