| Literature DB >> 30758645 |
Ho-Jin Shin1, Woo-Sung Min2, Yoo Hong Min3, June-Won Cheong3, Je-Hwan Lee4, In-Ho Kim5, Dae Sik Hong6, Jae-Sook Ahn7, Hyeoung-Joon Kim7, Won-Sik Lee8, Chul Won Jung9, Jun-Ho Jang9, Young Park10, Hee-Je Kim11.
Abstract
Core-binding factor acute myeloid leukemia (CBF-AML) data in Asian countries has been rarely reported. We analyzed 392 patients with CBF-AML [281 with t(8;21), 111 with inv.(16)/t(16;16)] among data from 3041 patients with AML from the Korean AML Registry. Interestingly, del(9q) was less frequently detected in Korean than in German patients with t(8;21) (7.5% vs. 17%), and del(7q) was more frequently detected in Korean patients with inv(16). Overall survival (OS) was similar between patients in the first complete remission (CR) who received allogeneic (alloSCT) and autologous stem cell transplantation (ASCT) for CBF-AML. OS of t(8;21) patients was poor when undergoing alloSCT in second/third CR, while OS of inv(16) patients in second/third CR was similar to that in first CR. Patients with > 3-log reduction of RUNX1/RUNX1T1 qPCR had improved 3-year event-free survival (EFS) than those without (73.2% vs. 50.3%). Patients with t(8;21) AML with D816 mutation of the c-Kit gene showed inferior EFS and OS. These poor outcomes might be overcome by alloSCT. Multivariate analysis for OS in patients with t(8;21) revealed older age, > 1 course of induction chemotherapy to achieve CR, loss of sex chromosome, del(7q), and second/third CR or not in CR before SCT as independent prognostic variables. Especially, del(7q) is the most powerful prediction factor of poor outcomes, especially in patients with t(8;21) (hazard ratio, 27.23; P < 0.001). Further study is needed to clarify the clinical effect of cytogenetics and gene mutation in patients with CBF-AML, between Asian and Western countries.Entities:
Keywords: Acute myeloid leukemia; Core-binding factor; Cytogenetics; D816 mutation; RUNX1/RUNX1T1; Stem cell transplantation
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Year: 2019 PMID: 30758645 DOI: 10.1007/s00277-019-03624-y
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673