Clinical significance of monitoring E2A- PBX1 fusion gene expression in patients with allogeneic hematopoietic stem cell transplantation.
- VernacularTitle:急性淋巴细胞白血病患者造血干细胞移植后监测E2A-PBX1融合基因的意义初探
- Author:
Xiaosu ZHAO
1
;
Yazhen QIN
1
;
Yanling ZHANG
1
;
Yongyan XU
1
;
Yu WANG
1
;
Huan CHEN
1
;
Fengrong WANG
1
;
Jingzhi WANG
1
;
Xiaojun HUANG
1
Author Information
- Publication Type:Journal Article
- MeSH: Flow Cytometry; Hematopoietic Stem Cell Transplantation; Homeodomain Proteins; metabolism; Humans; Neoplasm, Residual; Oncogene Proteins, Fusion; metabolism; Precursor Cell Lymphoblastic Leukemia-Lymphoma; genetics; therapy; Real-Time Polymerase Chain Reaction; Recurrence; Retrospective Studies
- From: Chinese Journal of Hematology 2015;36(12):989-993
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the clinical characteristics of E2A-PBX1(immunoglobulin enhancer binding factor-pre-B leukemia)fusion gene in patients with acute lymphoblastic leukemia(ALL) after allogeneic stem cell transplantation(allo-HSCT).
METHODSClinical data of 10 patients received allo- HSCT in Peking University Institute of Hematology from December 2010 to January 2015 were retrospectively collected. The E2A-PBX1 gene was examined by real-time quantitative polymerase chain reaction(RQ- PCR). The correlation between its expression level and the disease status was analyzed.
RESULTSAmong 10 cases of enrolled ALL, the E2A-PBX1 expression of six patients converted to positive after transplant at a median time of 90 days(range, 75-180 days). The expression level of the first positive sample was 25.200%(range, 0.022%-353.600%). The duration from E2A-PBX1 positive to hematological relapse was 30 days(range, 0-74 days). Finally, 4 patients underwent relapse at a median time of 164 days (range, 75- 240 days) after allo- HSCT. The expression of E2A- PBX1 and minimal residual disease (MRD)level examined by flow cytometry were positive correlated(Spearman r=0.743, P=0.002). Once E2A-PBX1 expression converted to positive after transplant, MRD would increase rapidly. Patients with this type of ALL would have little response to the current intervention towards relapse.
CONCLUSIONMonitoring E2A-PBX1 by RQ-PCR could be used to evaluate MRD status after allo-HSCT. Patients with positive E2A-PBX1 at early stage of transplant will have a poor prognosis.
