Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/47256
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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorLAGE, Luis Alberto de Padua Covas-
dc.contributor.authorBRITO, Claudio Vinicius-
dc.contributor.authorLEVY, Debora-
dc.contributor.authorCULLER, Hebert Fabricio-
dc.contributor.authorCOUTO, Samuel Campanelli Freitas-
dc.contributor.authorOLIVEIRA, Lucas Bassolli Alves de-
dc.contributor.authorZERBINI, Maria Claudia Nogueira-
dc.contributor.authorROCHA, Vanderson-
dc.contributor.authorPEREIRA, Juliana-
dc.date.accessioned2022-06-20T15:32:05Z-
dc.date.available2022-06-20T15:32:05Z-
dc.date.issued2022-
dc.identifier.citationLEUKEMIA RESEARCH, v.114, article ID 106794, 9p, 2022-
dc.identifier.issn0145-2126-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/47256-
dc.description.abstractBackground: Nodal peripheral T-cell lymphomas (nPTCL) encompass a heterogeneous group of mature and aggressive lymphoid malignancies, including peripheral T-cell lymphoma, not otherwise specified (PTCL, NOS), angioimmunoblastic T-cell lymphoma (AITL) and anaplastic large cell lymphoma (ALCL) ALK-positive and ALKnegative. Their differential diagnosis and prognosis are an issue in clinical practice. Accurate biomarkers to define the different subtypes of nPTCL and to stratify their prognosis are essential to improve their treatment approach. The aim of this study was to test the prognostic impact of GATA-3 gene expression, and its capability to discriminate the different subtypes of nPTCL. Patients and methods: We retrospectively assessed GATA-3 gene expression by quantitative real time PCR (qRTPCR) from neoplastic biopsies in Formalin-Fixed Paraffin-Embedded samples (FFPE) of 80 patients with nPTCL that were admitted in a single cancer treatment center from 2000 to 2017. Results: Median age was 49 years-old (IqR 34-59), 43/80 (53.7%) were male. Median follow-up was 1.72 years, 36.3% were classified as PTCL, NOS, 31.2% as ALK-negative ALCL, 21.2% as ALK-positive ALCL and 11.3% as AITL. The majority of cases had advanced stage cancer (III/IV). Two-year estimated overall survival (OS) and progression-free survival (PFS) were 52.2% and 39.5%, respectively. The median GATA-3 gene expression leveleng
dc.description.sponsorshipFAPESP [2012/50495-3]-
dc.language.isoeng-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTDeng
dc.relation.ispartofLeukemia Research-
dc.rightsrestrictedAccesseng
dc.subjectNodal peripheral T-cell lymphomaseng
dc.subjectAngioimmunoblastic T-cell lymphoma (AITL)eng
dc.subjectDiagnosiseng
dc.subjectPrognosiseng
dc.subjectGATA-3 gene expressioneng
dc.subjectPeripheral T-cell lymphomaeng
dc.subjectnot otherwise specified (PTCLeng
dc.subjectNOS)eng
dc.subjectALK-negative anaplastic large-cell lymphoma (ALK-negative ALCL)eng
dc.subject.othergata-3eng
dc.subject.otherdiseaseeng
dc.subject.othermarkereng
dc.subject.otheradultseng
dc.titleDiagnostic and prognostic implications of tumor expression of the GATA-3 gene in nodal peripheral T-cell lymphoma (nPTCL): Retrospective data from a Latin American cohorteng
dc.typearticleeng
dc.rights.holderCopyright PERGAMON-ELSEVIER SCIENCE LTDeng
dc.identifier.doi10.1016/j.leukres.2022.106794-
dc.identifier.pmid35131666-
dc.subject.wosPeripheral Vascular Diseaseeng
dc.type.categoryoriginal articleeng
dc.type.versionpublishedVersioneng
hcfmusp.author.externalBRITO, Claudio Vinicius:Sao Paulo Univ FMUSP, Fac Med, Dept Hematol Hemotherapy & Cell Therapy, Sao Paulo, Brazil-
hcfmusp.description.articlenumber106794-
hcfmusp.description.volume114-
hcfmusp.origemWOS-
hcfmusp.origem.idWOS:000788077600008-
hcfmusp.origem.id2-s2.0-85123988600-
hcfmusp.publisher.cityOXFORDeng
hcfmusp.publisher.countryENGLANDeng
hcfmusp.relation.referenceAgarwal H, 2019, INDIAN J PATHOL MICR, V62, P244, DOI 10.4103/IJPM.IJPM_228_18eng
hcfmusp.relation.referenceCampo E, 2011, BLOOD, V117, P5019, DOI 10.1182/blood-2011-01-293050eng
hcfmusp.relation.referenceCastellar ERP, 2014, BLOOD, V124, P1473, DOI 10.1182/blood-2014-04-571091eng
hcfmusp.relation.referenceCheng Y, 2009, INT IMMUNOPHARMACOL, V9, P894, DOI 10.1016/j.intimp.2009.03.014eng
hcfmusp.relation.referenceCheson BD, 2014, J CLIN ONCOL, V32, P3059, DOI 10.1200/JCO.2013.54.8800eng
hcfmusp.relation.referenced'Amore F, 2012, J CLIN ONCOL, V30, P3093, DOI 10.1200/JCO.2011.40.2719eng
hcfmusp.relation.referenceDavis DG, 2016, HUM PATHOL, V47, P26, DOI 10.1016/j.humpath.2015.09.015eng
hcfmusp.relation.referencede Padua Covas Lage Luis Alberto, 2019, Oncotarget, V10, P5136, DOI 10.18632/oncotarget.27098eng
hcfmusp.relation.referenceDorfman DM, 2017, HUM PATHOL, V65, P166, DOI 10.1016/j.humpath.2017.05.009eng
hcfmusp.relation.referenceFalini B, 1999, BLOOD, V93, P2697eng
hcfmusp.relation.referenceFrelin C, 2013, NAT IMMUNOL, V14, P1037, DOI 10.1038/ni.2692eng
hcfmusp.relation.referenceHeavican TB, 2019, BLOOD, V133, P1664, DOI 10.1182/blood-2018-09-872549eng
hcfmusp.relation.referenceIqbal J, 2014, BLOOD, V123, P2915, DOI 10.1182/blood-2013-11-536359eng
hcfmusp.relation.referenceKansara R, 2014, LEUKEMIA LYMPHOMA, V55, P727, DOI 10.3109/10428194.2013.858154eng
hcfmusp.relation.referenceLage Luis Alberto de Pádua Covas, 2015, Rev. Bras. Hematol. Hemoter., V37, P277, DOI 10.1016/j.bjhh.2015.03.017eng
hcfmusp.relation.referenceLivak KJ, 2001, METHODS, V25, P402, DOI 10.1006/meth.2001.1262eng
hcfmusp.relation.referenceMa H, 2017, INT J CLIN ONCOL, V22, P18, DOI 10.1007/s10147-016-1045-2eng
hcfmusp.relation.referenceMete O, 2019, MODERN PATHOL, V32, P484, DOI 10.1038/s41379-018-0167-7eng
hcfmusp.relation.referenceOrtiz-Rey JA, 2017, ACTAS UROL ESP, V41, P577, DOI 10.1016/j.acuro.2017.03.004eng
hcfmusp.relation.referencePerez-Andreu V, 2013, NAT GENET, V45, P1494, DOI 10.1038/ng.2803eng
hcfmusp.relation.referencePetrich AM, 2015, BRIT J HAEMATOL, V168, P708, DOI 10.1111/bjh.13202eng
hcfmusp.relation.referencePro B, 2017, BLOOD, V130, P2709, DOI 10.1182/blood-2017-05-780049eng
hcfmusp.relation.referenceRonaghy A, 2018, INT J GYNECOL PATHOL, V37, P284, DOI 10.1097/PGP.0000000000000403eng
hcfmusp.relation.referenceSachsida-Colombo Elisabetta, 2016, Rev. Bras. Hematol. Hemoter., V38, P82, DOI 10.1016/j.bjhh.2015.11.002eng
hcfmusp.relation.referenceSibon D, 2019, HAEMATOLOGICA, V104, pE562, DOI 10.3324/haematol.2018.213512eng
hcfmusp.relation.referenceSibon D, 2012, J CLIN ONCOL, V30, P3939, DOI 10.1200/JCO.2012.42.2345eng
hcfmusp.relation.referenceSuzuki R, 2000, BLOOD, V96, P2993eng
hcfmusp.relation.referenceSwerdlow SH, 2016, BLOOD, V127, P2375, DOI 10.1182/blood-2016-01-643569eng
hcfmusp.relation.referenceTozbikian GH, 2019, HUM PATHOL, V85, P221, DOI 10.1016/j.humpath.2018.11.005eng
hcfmusp.relation.referenceVose JM, 2008, J CLIN ONCOL, V26, P4124, DOI 10.1200/JCO.2008.16.4558eng
hcfmusp.relation.referenceWang YQ, 2013, NAT IMMUNOL, V14, P714, DOI 10.1038/ni.2623eng
hcfmusp.relation.referenceXing HL, 2014, BMC PLANT BIOL, V14, DOI 10.1186/s12870-014-0327-yeng
hcfmusp.relation.referenceZhang W, 2016, ONCOTARGET, V7, P65284, DOI 10.18632/oncotarget.11673eng
dc.description.indexMEDLINEeng
dc.identifier.eissn1873-5835-
hcfmusp.citation.scopus3-
hcfmusp.scopus.lastupdate2024-04-12-
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