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1Academic Journal
Πηγή: ScienceRise: Medical Science; No. 2(63) (2025); 31-38
ScienceRise: Medical Science; № 2(63) (2025); 31-38Θεματικοί όροι: стимулятори еритропоезу, якість життя, перевантаження залізом, деферазирокс, алогенна трансплантація стовбурових клітин, хронічна мієлоїдна лейкемія, виживаність, феритин, магнітно-резонансна томографія печінки, еритропоетин
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Σύνδεσμος πρόσβασης: https://journals.uran.ua/sr_med/article/view/340317
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2Academic Journal
Συγγραφείς: N. A. Batmanova, T. T. Valiev, K. I. Kirgizov, S. R. Varfolomeeva, Н. А. Батманова, Т. Т. Валиев, К. И. Киргизов, С. Р. Варфоломеева
Πηγή: Russian Journal of Pediatric Hematology and Oncology; Том 7, № 3 (2020); 70-77 ; Российский журнал детской гематологии и онкологии (РЖДГиО); Том 7, № 3 (2020); 70-77 ; 2413-5496 ; 2311-1267 ; 10.21682/2311-1267-2020-7-3
Θεματικοί όροι: наследственные гемохроматозы, chelation therapy, deferasirox, myelodysplastic syndrome, hereditary hemochromatosis, хелаторная терапия, деферазирокс, миелодиспластический синдром
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Relation: https://journal.nodgo.org/jour/article/view/627/573; Slonim A.D., Joseph J., Turenne W., Sharangpani A., Luban N.L.C. Blood transfusions in children: a multi-institutional analysis of practices and complications. Transfusion 2008:48(1):73–80. doi:10.1111/j.1537-2995.2007.01484.; Bercovitz S., Josephson C. Transfusion considerations in pediatric hematology and oncology. Hematol Oncol Clin North America 2019;33(5):903–13. doi:10.1016/j.hoc.2019.05.011.; Gauvin F., Champagne M., Robillard P. Long-term survival rate of pediatric patients after blood transfusions. Transfusion 2008;48(5):801–8. doi:10.1111/j.1537-2995.2007.01614.; Jang J.H., Lee J.-H., Yoon S.-S., Jo D.-Y., Kim H.-J., Chung J., Lee J.W. Korean guidline for iron chelator therapy in transfusion-indused iron overload. J Korean Med Sci 2013;28:1563–72. doi:10.3346/jkms2013.28.11.1563.; Wrighting D., Andrews N. Iron homeostasis and erythropoiesis. Curr Top Dev Biol 2008;82:141–67. doi:10.1016/S0070-2153(07)00006-3.; Brissot E., Bernard D., Loreal O., Brissot P., Troadec M.-B. Too much iron: a mask foe for leukemias. Blood Rev 2020;39:100617. doi:10.1016/j.blre.2019.100617.; Som D., Jodie B.L. Overview of iron metabolism in health and disease. Hemodial Int 2017;21(Suppl 1):6–20. doi:10.1111/hdi.12542.; Савченко В.Г., Абдулкадыров К.М., Масчан А.А., Сметанина Н.С., Голенков А.К., Кохно А.В., Сысоева Е.П., Савинова М.Т., Шелехова Т.В., Финогенова Н.А., Зубаровская Л.С., Капланов К.Д., Кравченко Е.Г., Лопатина Е.Г. Открытое многоцентровое исследование деферазирокса в лечении посттрансфузионной перегрузки железом у больных миелодиспластическими синдромами, талассемией и другими формами анемий. Гематология и трансфузиология 2015;60(4):7–14.; List A.F. Iron overload in myelodysplastic syndromes. Diagnosis and management. Cancer control 2010;17 Suppl:2–8. doi:10.1177/107327481001701s01.; Siddique A., Kowdley K.V. Review article: the iron overload syndromes. Aliment Pharmacol Ther 2012;35(8):876–93. doi:10.1111/j.1365-2036.2012.05051.; Циммерман Я.С. Первичный (наследственный) гемохроматоз. Клиническая медицина 2017;95(6);513–8. doi: 0.18821/0023-21492017-95-6-513-518.; Emy P.Y., Levin T.L., Sheth S.S., Ruzal-Shapiro C., Garvin J., Berdon W.E. Iron overload in reticuloendothelial systems of pediatric oncology patients who have undergone transfusions: MR observations. Am J Roentgenol 1997;168:1011–5. doi:10.2214/ajr.168.4.9124106.; Shan J., Kurtin E.S., Arnold L., Lindroos-Kolqvist P., Tinsley S. Management of transfusion-related iron overload in patients with myelodysplastic syndromes. Clin J Oncol Nursing 2012;16 Suppl:37–46. doi:10.1188/12.CJON.S1.37-46.; Gattermann N. Overview in guidelines on iron chelation therapy in patients with myelodysplastic syndromes and transfusional iron overload. Int J Hematol 2008;88:24–9. doi:10.1007/s12185-008-0118-z.; Kushner J.P., Porter J.P., Olivieri N.F. Secondary iron overload. Hematology Am Soc Hematol Educ Program 2001;47–61. doi:10.1182/asheducation-2001.1.47.; Coates T., Wood J. How we manage iron overload in sickle cell patients. Br J Haematol 2017;177(5):703–16. doi:10.1111/bjh.14575.; Brissot P., Troadec M.-B., Loreal O., Brissot E. Pathophysiology and classification of iron overload diseases. Transfus Clin Biol 2019;26(1):80–8. doi:10.1016/j.tracli.2018.08.006.; Trinder D., Fox C., Vautier G., Olynyk J.K. Molecular pathogenesis of iron overload. GUT 2002;51(2):290–5. doi:10.1136/gut.51.2.290.; Delea E.T., Edelsberg J., Sofrygin O., Thomas S.K., Baladi J.F., Phatak P.D., Coates T.D. Consequences and costs of noncompliance with iron chelation therapy in patients with transfusion-depending thalassemia: a literature review. Transfusion 2007;47(10):1919–29. doi:10.1111/j.1537-2995.2007.01416.x.; Baran E.J. Chelation therapies: a chemical and biochemical perspective. Curr Med Chem 2010;17(31):3658–72. doi:10.2174/092986710793213760.; Goldberg K.E., Neogi S., Lal A., Higa A., Fung E. Nutritional deficiencies are common in patients with transfusion-dependent thalassemia and associated with iron overload. J Food Nutr Research 2018;6(10):674–81. doi:10.12691/jfnr-6-10-9.; Bollig C., Schell L.K., Rucker G., Allert R., Motschall E., Niemeyer C.M., Bassler D., Meerpohl J.J. Deferazirox for managing irin overload in people with thalassemia. Cochrane Database Syst Rev 2017;2017(8):CD007476. doi:10.1002/14651858.CD007476.pub3.; Messa E., Ciloni D., Saglio G. Iron chelation therapy in myelodysplastic syndromes. Adv Hematol 2010;2010:756289. doi:10.1155/2010/756289.; Kontoghiorghe C.N., Kontoghiorghes G.J. Efficacy and safety of ironchelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with non-transfusion-dependent thalassemia syndromes. Drug Des Devel Therapy 2016;10:465–81. doi:10.2147/DDDT.S79458.; Leitch A.H., Gatterman N. Hematologic improvement with iron chelation therapy in myelodysplastic syndromes: Clinical data, potential mechanisms, and outstanding questions. Crit Rev Oncol Hematol 2019;141:54–72. doi:10.1016/j.critrevonc.2019.06.002.; https://journal.nodgo.org/jour/article/view/627
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3Academic Journal
Συγγραφείς: N. S. Smetanina, Наталия Сергеевна Сметанина
Πηγή: Russian Journal of Pediatric Hematology and Oncology; № 1 (2014); 51-61 ; Российский журнал детской гематологии и онкологии (РЖДГиО); № 1 (2014); 51-61 ; 2413-5496 ; 2311-1267 ; 10.17650/2311-1267-2014-0-1
Θεματικοί όροι: интенсивная хелаторная терапия, chelation therapy, deferoxamine, deferasirox, deferiprone, combined chelation therapy, intensive chelation therapy, хелаторная терапия, дефероксамин, деферазирокс, деферипрон, комбинированная хелаторная терапия
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Relation: https://journal.nodgo.org/jour/article/view/14/10; Porter J. B. Concepts and goals in the management of transfusional iron overload. Am J Hematol 2007;82(S12):1136–9.; Tanno T., Bhanu N. V., Oneal P. A. et al. High levels of GDF15 in thalassemia suppress expression of the iron regulatory protein hepcidin. Nat Med 2007;13(9):1096–1101.; Borgna-Pignatti C., Rugolotto S., De Stefano P. et al. Survival and complications in patients with thalassemia major treated with transfusion and deferoxamine. Haematologica 2004;89:1187–93.; Andrews N. C. Disorders of iron metabolism. N Engl J Med 1999;341:1986–95.; Porter J. B. Practical management of iron overload. Br J Haematol 2001;115:239–52.; Olivieri N. F., Nathan D. G., MacMillan J.H. et al. Survival in medically treated patients with homozygous beta-thalassemia. N Engl J Med 1994;331(9):574–8.; Gabutti V., Piga A. Results of long-term iron-chelating therapy. Acta Haematol 1996;95(1):26–36.; Angelucci E., Brittenham G. M., McLaren C.E. et al. Hepatic iron concentration and total body iron stores in thalassemia major. N Engl J Med 2000;343(5):327–31.; Telfer P. T., Prestcott E., Holden S. et al. Hepatic iron concentration combined with long-term monitoring of serum ferritin to predict complications of iron overload in thalassaemia major. Br J Haematol 2000;110(4):971–7.; Angelucci E., Baronciani D., Lucarelli G. et al. Needle liver biopsy in thalassaemia: analyses of diagnostic accuracy and safety in 1184 consecutive biopsies. Br J Haematol 1995;89(4):757–61.; Jensen P. D., Jensen F. T., Christensen T. et al. Relationship between hepatocellular injury and transfusional iron overload prior to and during iron chelation with desferrioxamine: a study in adult patients with acquired anemias. Blood 2003;101(1):91–6.; Villeneuve J. P., Bilodeau M., Lepage R. et al. Variability in hepatic iron concentration measurement from needle-biopsy specimens. J Hepatol 1996;25(2):172–7.; Wood J. C., Enriquez C., Ghugre N. et al. MRI R2 and R2* mapping accurately estimates hepatic iron concentration in transfusion-dependent thalassemia and sickle cell disease patients. Blood 2005;106(4):1460–5.; Hankins J. S., McCarville M.B., Loeffler R. B. et al. R2* magnetic resonance imaging of the liver in patients with iron overload. Blood 2009;113:4853–5.; Kirk P., He T., Anderson L. J. et al. International reproducibility of single breathhold T2* MR for cardiac and liver iron assessment among five thalassemia centers. J Magn Reson Imaging 2010;32(2):315–9.; Carpenter J. P., He T., Kirk P. et al. On T2* magnetic resonance and cardiac iron. Circulation 2011;123(14):1519–28.; Anderson L. J., Holden S., Davis B. et al. Cardiovascular T2‑star (T2*) magnetic resonance for the early diagnosis of myocardial iron overload. Eur Heart J 2001;22(23):2171–9.; Westwood M. A., Anderson L. J., Maceira A. M. et al. Normalized left ventricular volumes and function in thalassemia major patients with normal myocardial iron. J Magn Reson Imaging 2007;25(6):1147–51.; Alpendurada F., Carpenter J. P., Deac M. et al. Relation of myocardial T2* to right ventricular function in thalassaemia major. Eur Heart J 2010;31(13):1648–54.; Wood J. C., Tyszka J. M., Carson S. et al. Myocardial iron loading in transfusion-dependent thalassemia and sickle cell disease. Blood 2004;103(5):1934–6.; Davis B. A., O’Sullivan C., Jarritt P. H. et al. Value of sequential monitoring of left ventricular ejection fraction in the management of thalassemia major. Blood 2004;104(1):263–9.; Wood J. C. Cardiac iron across different transfusion-dependent diseases. Blood Rev 2008;22 Suppl 2:S14–S21.; Hoffbrand A. V., Taher A., Cappelini M. D. How I treat transfusional iron overload, Blood 2012;120 (18):3657–68.; Noetzli L. J., Carson S. M., Nord A. S. et al. Longitudinal analysis of heart and liver iron in thalassemia major. Blood 2008;112(7):2973–8.; Anderson L. J., Westwood M. A., Prescott E. et al. Development of thalassaemic iron overload cardiomyopathy despite low liver iron levels and meticulous compliance to desferrioxamine. Acta Haematol 2006;115(1):106–8. 26. Inati A., Khoriaty E., Musallam K. M. et al. Iron chelation therapy for patients with sickle cell disease and iron overload. Am J Hematol 2010;85(10):782–6.; Kwiatkowski J. L., Kim H. Y., Thompson A. A. et al. Chelation use and iron burden in North America and British thalassemia patients: a report from the thalassemia longitudinal cohort. Blood 2012;119(12):2746–53.; Rachmilewitz E. A., Giardina P. J. How I treat thalassemia. Blood 2011;118(13):3479–88.; Cappellini M. D., Cohen A.,Eleftheriou A. et al. Guidelines for the Clinical Management of Thalassemia. Nicosia, Cyprus: Thalassaemia International Federation, 2009.; Rees D.C., Williams T.N., Gladwin M.T. Sickle-cell disease. Lancet 2010;376 (9757):2018–31.; Marsh J. C.W., Ball S. E., Cavenagh J. et al. Guidelines for the diagnosis anв management of aplastic anaemia. Br J Haematol 2009;147(1):43–70.; Gattermann N., Jarisch A., Schlag R. et al. Deferasirox treatment of iron-overloaded chelation-naive and prechelated patients with myelodysplastic syndromes in medical practice: results from the observational studies eXtend and eXjange. Eur J Haematol 2012;88(3):260–8.; Ladis V., Berdousi H., Gotsis E. et al. Deferasirox administration for the treatment of non-transfusional iron overload in patients with thalassaemia intermedia. Br J Haematol 2010;151(5):504–8.; Porter J. B., Lin K. H., Beris P. et al. Response of iron overload to deferasirox in rare transfusion-dependent anaemias: equivalent effects on serum ferritin and labile plasma iron for haemolytic or production anaemias. Eur J Haematol 2011;87(4):338–48.; Vichinsky E. P., Ohene-Frempong K., Thein S. L. et al. Transfusion and chelation practices in sickle cell disease: a regional perspective. Pediatr Hematol Oncol 2011;28(2):124–33.; Takatoku M., Uchiyama T., Okamoto S.et al. Retrospective nationwide survey of Japanese patients with transfusion-dependent MDS and aplastic anemia highlights the negative impact of iron overload on morbidity / mortality. Eur J Haematol 2007;78(6):487–94.; Alessandrino E. P., Porta M. G.D., Bacigalupo A. et al. Prognostic impact of pre-transplantation transfusion history and secondary iron overload in patients with myelodysplastic syndrome undergoing allogeneic stem cell ransplantation: a GITMO study. Haematologica 2010;95(3):476–84.; Jabbour E., Garcia-Manero G., Taher A. et al. Managing iron overload in patients with myelodysplastic syndromes with oral deferasirox therapy. Oncologist 2009;14(5):489–96.; Pullarkat V. Objectives of iron chelation therapy in myelodysplastic syndromes: more than meets the eye? Blood 2009;114(26):5251–5.; Leitch H. A. Controversies surrounding iron chelation therapy for MDS. Blood Rev 2011;25(1):17–31.; Neukarchen J., Fox F., Kündgen A. et al. Improved survival in MDS patients receiving iron chelation therapy: a matched pair analysis of 188 patients from the Düsseldorf MDS registry. Leuk Res 2012;36(8):1067–70.; Messa E., Cilloni G., Messa F. et al. Deferasirox treatment improved the hemoglobin level and decreased transfusion requirements in four patients with the myelodysplastic syndrome and primary myelofibrosis. Acta Haematol 2008;120(2):70–4.; Gattermann N., Finelli C., DellaPorta M. et al. Hematological responses with deferasirox therapy in transfusion-dependent myelodysplastic syndrome patients. Haematologica 2012;97(9):1364–71.; List A. F., Baer M. R., Steensma D. P. et al. Deferasirox reduces serum ferritin and labile plasma iron in RBC transfusion-dependent patients with myelodysplastic syndrome. J Clin Oncol 2012;30(17):2134–9.; Koreth J., Antin J. H. Iron overload in hematologic malignancies and outcome of allogenei, hematopoietic stem cell transplantation. Haematologica 2010;95(3):364–6.; Taher A., Hershko C., Cappellini M. D. et al. Iron overload in thalassemia intermedia: reassessment of iron chelation strategies. Br J Haematol 2009;147(5):634–40.; Taher A., Porter J., Viprakasit V. et al. Deferasirox significantly reduces iron overload in non-transfusion-dependent thalassaemia: 1‑year results from a prospective, randomized, double-blind, placebo-controlled study. Blood 2012;120(5):970–7.; Evans P., Kayyali R., Hider R. C. et al. Mechanisms for the shuttling of plasma; non-trasferrin bound iron (NTBI) onto deferoxamine by deferiprone. Transl Res 2010;156(2):55–67.; Devanur L. D., Evans R. W., Evans P. J. et al. Chelator-facilitated removal of iron from transferrin: relevance to combined chelation therapy. Biochem J 2008;409(2):439–47.; Otto-Duessel M., Brewer C., Gonzalez I. et al. Safety and efficacy of combined chelatio, therapy with deferasirox and deferoxamine in a gerbil model of iron overload. Acta Haematol 2008;120(2):123–8.; Gomber S., Saxena R., Madan N. Comparative afficacy of Deferrioxamine, Deferiprone and in combination on iron chelation in thalassemic children. Indian; Pediatr 2004; 41(1): 21–7.; Galanello R., Agus A., Campus S. et al. Combined iron chelation therapy. Ann NY Acad Sci 2010;1202:79–86.; Jetsrisuparb A., Komvilaisak P., Wiangnon S. et al. Retrospective study on the combination of desferrioxamine and deferasirox for treatment of iron-overloaded thalassemic patients: first evidence of more than 2 years. J Pediatr Hematol Oncol 2010;32(5):400–3.; Dubourg L., Laurain C., Ranchin B. et al. Deferasirox-induced renal impairment in children: an increasing concern for pediatricians. Pediatr Nephrol; 27(11): 2115–22.; https://journal.nodgo.org/jour/article/view/14
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4Academic Journal
Συγγραφείς: Грицаев, С., Абдулкадыров, К.
Θεματικοί όροι: МИЕЛОДИСПЛАСТИЧЕСКИЙ СИНДРОМ, ДЕФЕРАЗИРОКС
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5Academic Journal
Συγγραφείς: Ягудина, Р., Куликов, А., Крысанов, И.
Θεματικοί όροι: ФАРМАКОЭКОНОМИКА, ДЕФЕРАЗИРОКС, АНАЛИЗ «ЗАТРАТЫ ЭФФЕКТИВНОСТЬ», АНАЛИЗ СТОИМОСТИ БОЛЕЗНИ, МОДЕЛЬ МАРКОВА
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6Academic Journal
Πηγή: Клиническая онкогематология. Фундаментальные исследования и клиническая практика.
Θεματικοί όροι: МИЕЛОДИСПЛАСТИЧЕСКИЙ СИНДРОМ, ДЕФЕРАЗИРОКС, 3. Good health
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7Academic Journal
Πηγή: Фармакоэкономика. Современная фармакоэкономика и фармакоэпидемиология.
Θεματικοί όροι: ФАРМАКОЭКОНОМИКА, ДЕФЕРАЗИРОКС, АНАЛИЗ «ЗАТРАТЫ ЭФФЕКТИВНОСТЬ», АНАЛИЗ СТОИМОСТИ БОЛЕЗНИ, МОДЕЛЬ МАРКОВА, 3. Good health
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