ABCG2 and CD200 define patients at high risk of relapse in ELN favorable subgroup of AML

التفاصيل البيبلوغرافية
العنوان: ABCG2 and CD200 define patients at high risk of relapse in ELN favorable subgroup of AML
المؤلفون: Mario Tiribelli, Antonella Geromin, Renato Fanin, Erica Simeone, Margherita Cavallin, Daniela Damiani, Sara Di Giusto
المصدر: European Journal of Haematology. 99:269-274
بيانات النشر: Wiley, 2017.
سنة النشر: 2017
مصطلحات موضوعية: Adult, Male, Oncology, medicine.medical_specialty, NPM1, Adolescent, Abcg2, ABCG2, Gene Expression, favorable risk, acute myeloid leukemia, Biology, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Molecular classification, Antigens, CD, Recurrence, Internal medicine, medicine, Overall survival, ATP Binding Cassette Transporter, Subfamily G, Member 2, Humans, In patient, Relapse risk, Aged, CD200, prognosis, Hematology, Complete remission, Myeloid leukemia, General Medicine, Middle Aged, Survival Analysis, Neoplasm Proteins, Leukemia, Myeloid, Acute, fms-Like Tyrosine Kinase 3, 030220 oncology & carcinogenesis, Cytogenetic Analysis, Mutation, embryonic structures, Cancer research, biology.protein, Female, sense organs, Nucleophosmin, Biomarkers, 030215 immunology
الوصف: Objective overexpression of ABCG2 and CD200 have been independently associated with poor outcome in acute myeloid leukemia (AML). However, no data are available on the role of these two factors in patients with core binding factor (CBF) positive or FLT3-negative / NPM1-mutated cytogenetically normal (CN) AML. Methods we analyzed 65 adult AML patients with CBF+ (n=16) or FLT3-/NPM1+ CN (n=49), evaluating clinical and biological factors associated with complete remission attainment, leukemia-free survival (LFS) and overall survival (OS). Results ABCG2 was expressed in 36 (55%) cases, and CD200 was positive in 33 (51%) cases, 6 at high levels. Both ABCG2 or CD200 positivity have a negative impact on relapse risk: 3-year LFS was 51% vs 82% in ABCG2+ cases (RR 3.3), 49% vs 82% in CD200+ patients (RR = 4.4) and 25% in CD200-high cases (RR = 17.1). ABCG2 and CD200 affected also OS with 3-year OS of 39% in ABCG2+ (compared to 71% in ABCG2-; RR = 2.6) and CD200+ (compared to 68% in CD200-; RR = 2.5) patients. Conclusion our data confirm a negative impact of ABCG2 and CD200 overexpression also in AML patients considered at favorable risk according to ELN cytogenetic/molecular classification. This article is protected by copyright. All rights reserved.
تدمد: 0902-4441
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63d0b6128cfd20f2c7ac66a65603a159Test
https://doi.org/10.1111/ejh.12915Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....63d0b6128cfd20f2c7ac66a65603a159
قاعدة البيانات: OpenAIRE