RÁČIL, Zdeněk, Eva KORIŤÁKOVÁ, Tomasz SACHA, Hana KLAMOVA, Petra BELOHLAVKOVA, Edgar FABER, Delphine REA, Ludmila MALASKOVA, Jiřina PROCHÁZKOVÁ, Daniela ŽÁČKOVÁ, Jaroslava VOGLOVA, Joanna WACLAW, Petr CETKOVSKY, Pavel ZAK and Jiří MAYER. Insulin resistance is an underlying mechanism of impaired glucose metabolism during nilotinib therapy. American Journal of Hematology. Hoboken: John Wiley & Sons, 2018, vol. 93, No 10, p. "E342"-"E345", 4 pp. ISSN 0361-8609. Available from: https://dx.doi.org/10.1002/ajh.25232.
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Basic information
Original name Insulin resistance is an underlying mechanism of impaired glucose metabolism during nilotinib therapy
Authors RÁČIL, Zdeněk (203 Czech Republic, guarantor, belonging to the institution), Eva KORIŤÁKOVÁ (203 Czech Republic, belonging to the institution), Tomasz SACHA (616 Poland), Hana KLAMOVA (203 Czech Republic), Petra BELOHLAVKOVA (203 Czech Republic), Edgar FABER (203 Czech Republic), Delphine REA (250 France), Ludmila MALASKOVA (203 Czech Republic), Jiřina PROCHÁZKOVÁ (203 Czech Republic), Daniela ŽÁČKOVÁ (203 Czech Republic, belonging to the institution), Jaroslava VOGLOVA (203 Czech Republic), Joanna WACLAW (616 Poland), Petr CETKOVSKY (203 Czech Republic), Pavel ZAK (203 Czech Republic) and Jiří MAYER (203 Czech Republic, belonging to the institution).
Edition American Journal of Hematology, Hoboken, John Wiley & Sons, 2018, 0361-8609.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30205 Hematology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 6.137
RIV identification code RIV/00216224:14110/18:00104917
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1002/ajh.25232
UT WoS 000447533300007
Keywords in English nilotinib therapy
Tags 14110212, 14119612, rivok
Tags International impact, Reviewed
Changed by Changed by: Soňa Böhmová, učo 232884. Changed: 2/5/2019 14:30.
Abstract
Impaired glucose metabolism (IGM) with hyperglycemia represents one of the most frequently observed adverse events (AE) during nilotinib therapy of chronic myeloid leukemia (CML). The exact mechanism of IGM remains controversial. Although a case report has shown a decrease in insulin secretion1 , our previous pilot data suggested development of insulin resistance as a possible mechanism.2 In this prospective study we aimed to confirm results from our pilot study using a larger cohort of CML patients treated with nilotinib and to compare results with data obtained on control groups receiving imatinib and dasatinib.
Links
NV17-30397A, research and development projectName: Mutační analýza primitivních buněčných populací u chronické myeloidní leukémie: za hranicí BCR-ABL1
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