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dc.contributor.authorAzevedo, A.P.-
dc.contributor.authorReichert, A.-
dc.contributor.authorAfonso, C.-
dc.contributor.authorAlberca, M.D.-
dc.contributor.authorTavares, P.-
dc.contributor.authorLima, F.-
dc.date.accessioned2018-01-09T11:31:41Z-
dc.date.available2018-01-09T11:31:41Z-
dc.date.issued2017-
dc.identifier.issn1179-5549-
dc.identifier.otherPURE: 3409376-
dc.identifier.otherPURE UUID: f17d9eee-10b8-4735-944e-b6cc0466eff3-
dc.identifier.otherRIS: urn:36A8B04607F1A98BEFB272DE462E7119-
dc.identifier.otherPubMed: 28469513-
dc.identifier.otherPubMedCentral: PMC5395261-
dc.identifier.otherScopus: 85034627995-
dc.identifier.otherWOS: 000399413600001-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85034627995&doi=10.1177%2f1179554917702870&partnerID=40&md5=2f9e733c9917a0a3235f85279d0de323-
dc.descriptionExport Date: 28 December 2017 Correspondence Address: Azevedo, A.P.; Department of Clinical Pathology, Hospital São Francisco Xavier, Centro Hospitalar Lisboa Ocidental, Estrada do Forte do Alto do Duque, Portugal; email: anpazevedo@gmail.com Chemicals/CAS: glycine, 56-40-6, 6000-43-7, 6000-44-8; hydroxyurea, 127-07-1; imatinib, 152459-95-5, 220127-57-1; nilotinib, 641571-10-0; valine, 7004-03-7, 72-18-4 References: Radich, J.P., Shah, N.P., Mauro, M.J., Integrating current treatment options for TKIresistant chronic myeloid leukemia (2014) Clin Adv Hematol Oncol, 12 (11), pp. 3-17; Savona, M.R., Molecular monitoring and minimal residual disease in the management of chronic myelogenous leukemia (2014) J Community Support Oncol, 12, pp. 171-178; Kantarjian, H.M., Cortes, J., La Rosée, P., Hochhaus, A., Optimizing therapy for patients with chronic myelogenous leukemia in chronic phase (2010) Cancer, 116, pp. 1419-1430; Weisberg, E., Manley, P.W., Cowan-Jacob, S.W., Hochhaus, A., Griffin, J.D., Second generation inhibitors of BCR-ABL for the treatment of imatinib-resistant chronic myeloid leukaemia (2007) Nat Rev Cancer, 7, pp. 345-356; Nicolini, F.E., Corm, S., Lê, Q.H., Mutation status and clinical outcome of 89 imatinib mesylate-resistant chronic myelogenous leukemia patients: A retrospective analysis from the French intergroup of CML (Fi(phi)-LMC GROUP) (2006) Leukemia, 20, pp. 1061-1066; Soverini, S., Colarossi, S., Gnani, A., Contribution of ABL kinase domain mutations to imatinib resistance in different subsets of Philadelphia-positive patients: By the GIMEMA Working Party on Chronic Myeloid Leukemia (2006) Clin Cancer Res, 12, pp. 7374-7379; Sokal, J.E., Cox, E.B., Baccarani, M., Prognostic discrimination in “good-risk” chronic granulocytic leukemia (1984) Blood, 63, pp. 789-799; Hasford, J., Pfirrmann, M., Hehlmann, R., A new prognostic score for survival of patients with chronic myeloid leukemia treated with interferon alfa. 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A Belgian study [published online ahead of print December 22, 2016] Clin Biochem; Vine, J., Cohen, S.B., Ruchlemer, R., Polymorphisms in the human organic cation transporter and the multidrug resistance gene: Correlation with imatinib levels and clinical course in patients with chronic myeloid leukemia (2014) Leuk Lymphoma, 55, pp. 2525-2531; Sundar, H., Radich, J., Optimizing patient care in chronic phase Chronic Myelogenous Leukemia: A multidisciplinary approach (2016) J Natl Compr Cancer Netw, 14, pp. s1-s6; McDougall, J., Ramsey, S.D., Radich, J., What happens when imatinib goes generic? (2016) J Natl Compr Canc Netw, 14, pp. 128-131; Hochhaus, A., Saglio, G., Hughes, T.P., Long-term benefits and risks of frontline nilotinib vs imatinib for chronic myeloid leukemia in chronic phase: 5-year update of the randomized ENESTnd trial (2016) Leukemia, 30, pp. 1044-1054; Cortes, J.E., Saglio, G., Kantarjian, H.M., Final 5-year study results of DASISION: The dasatinib versus imatinib study in treatment-naïve chronic myeloid leukemia patients trial (2016) J Clin Oncol, 34, pp. 2333-2340; Druker, B.J., Guilhot, F., O’Brien, S.G., Five-year follow-up of patients receiving imatinib for chronic myeloid leukemia (2006) N Engl J Med, 355, pp. 2408-2417; Soverini, S., De Benedittis, C., Mancini, M., Martinelli, G., Mutations in the BCRABL1 kinase domain and elsewhere in chronic myeloid leukemia (2015) Clin Lymphoma Myeloma Leuk, 15, pp. S120-S128; O’Brien, S., Radich, J.P., Abboud, C.N., Chronic myelogenous leukemia, version 1.2015 (2014) J Natl Compr Canc Netw, 12, pp. 1590-1610; Baccarani, M., Deininger, M.W., Rosti, G., European LeukemiaNet recommendations for the management of chronic myeloid leukemia: 2013 (2013) Blood, 122, pp. 872-884; Deininger, M.W., Molecular monitoring in CML and the prospects for treatmentfree remissions (2015) Hematology am Soc Hematol Educ Program, 2015, pp. 257-263; Soverini, S., Hochhaus, A., Nicolini, F.E., BCR-ABL kinase domain mutation analysis in chronic myeloid leukemia patients treated with tyrosine kinase inhibitors: Recommendations from an expert panel on behalf of European LeukemiaNet (2011) Blood, 118, pp. 1208-1215; Soverini, S., Branford, S., Nicolini, F.E., Implications of BCR-ABL1 kinase domain- mediated resistance in chronic myeloid leukemia (2014) Leuk Res, 38, pp. 10-20; Machova Polakova, K., Kulvait, V., Benesova, A., Next-generation deep sequencing improves detection of BCR-ABL1 kinase domain mutations emerging under tyrosine kinase inhibitor treatment of chronic myeloid leukemia patients in chronic phase (2015) J Cancer Res Clin Oncol, 141, pp. 887-899; Jabbour, E., Saglio, G., Hughes, T.P., Kantarjian, H., Suboptimal responses in chronic myeloid leukemia: Implications and management strategies (2012) Cancer, 118, pp. 1181-1191; Gruber, T.A., Chang, M.S., Sposto, R., Müschen, M., Activation-induced cytidine deaminase accelerates clonal evolution in BCR-ABL1-driven B-cell lineage acute lymphoblastic leukemia (2010) Cancer Res, 70, pp. 7411-7420-
dc.description.abstractIntroduction: The identification of BCR-ABL expression as the defining leukemogenic event in chronic myeloid leukemia (CML) and the introduction of BCR-ABL tyrosine kinase inhibitors in 2001 have revolutionized disease management, leading to a reduction in mortality rates and accordingly an increase in the estimated prevalence of CML. Case report: Based on medical records and clinical follow-up, the authors present the case of a Philadelphia chromosome–positive CML patient who developed resistance to imatinib. Quantitative reverse transcription-polymerase chain reaction testing revealed a V280G BCR-ABL mutation. Discussion and conclusions: This is the first report describing a new BCR-ABL kinase domain mutation—V280G—that might be associated with resistance to imatinib. Approximately 15% to 30% of patients treated with imatinib discontinue treatment due to resistance or intolerance. More than 90 BCR-ABL mutations were detected so far, conferring variable degrees of drug resistance, with consequent clinical, therapeutic, and prognostic impact. © The Author(s) 2017.en
dc.language.isoeng-
dc.rightsopenAccess-
dc.subjectBCR-ABL-
dc.subjectCML-
dc.subjectImatinib-
dc.subjectMutation-
dc.subjectNilotinib-
dc.subjectalpha interferon-
dc.subjectBCR ABL protein-
dc.subjectglycine-
dc.subjecthydroxyurea-
dc.subjectimatinib-
dc.subjectnilotinib-
dc.subjectvaline-
dc.subjectaged-
dc.subjectamino acid substitution-
dc.subjectArticle-
dc.subjectBCR ABL gene-
dc.subjectcase report-
dc.subjectchromosome 22-
dc.subjectchromosome 9-
dc.subjectchronic myeloid leukemia-
dc.subjectclinical article-
dc.subjectdisease course-
dc.subjectdrug dose escalation-
dc.subjectdrug withdrawal-
dc.subjectEUTOS score-
dc.subjectfemale-
dc.subjectgene-
dc.subjectgene mutation-
dc.subjectgene sequence-
dc.subjectHasford score-
dc.subjecthuman-
dc.subjectleukoderma-
dc.subjectreverse transcription polymerase chain reaction-
dc.subjectSokal score-
dc.subjectsplenomegaly-
dc.subjectSDG 3 - Good Health and Well-being-
dc.titleBCR-ABL V280G mutation, potential role in imatinib resistance: First case report-
dc.typearticle-
degois.publication.titleClinical Medicine Insights: Oncology-
degois.publication.volume11-
dc.peerreviewedyes-
dc.identifier.doihttps://doi.org/10.1177/1179554917702870-
dc.description.versionpublishersversion-
dc.description.versionpublished-
dc.contributor.institutionNOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)-
dc.contributor.institutionCentre for Toxicogenomics and Human Health (ToxOmics)-
Aparece nas colecções:NMS: ToxOmics - Artigos em revista internacional com arbitragem científica

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