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The dynamics of RUNX1-RUNX1T1 transcript levels after allogeneic hematopoietic stem cell transplantation predict relapse in patients with t(8;21) acute myeloid leukemia

The optimal monitoring schedules and cutoff minimal residual disease (MRD) levels for the accurate prediction of relapse at all time points after allogeneic hematopoietic stem cell transplantation (allo-HSCT) remain unclear in patients with t(8;21) acute myeloid leukemia (AML). RUNX1-RUNX1T1 transcr...

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Published in:Journal of hematology and oncology 2017-02, Vol.10 (1), p.44-44, Article 44
Main Authors: Qin, Ya-Zhen, Wang, Yu, Xu, Lan-Ping, Zhang, Xiao-Hui, Chen, Huan, Han, Wei, Chen, Yu-Hong, Wang, Feng-Rong, Wang, Jing-Zhi, Chen, Yao, Mo, Xiao-Dong, Zhao, Xiao-Su, Chang, Ying-Jun, Liu, Kai-Yan, Huang, Xiao-Jun
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Language:English
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Summary:The optimal monitoring schedules and cutoff minimal residual disease (MRD) levels for the accurate prediction of relapse at all time points after allogeneic hematopoietic stem cell transplantation (allo-HSCT) remain unclear in patients with t(8;21) acute myeloid leukemia (AML). RUNX1-RUNX1T1 transcript levels were measured in bone marrow samples collected from 208 patients at scheduled time points after transplantation (1530 samples in total). A total of 92.3% of the requested samples were collected, and 74.0% of patients had complete sample collection. The 1-, 3-, and 6-month RUNX1-RUNX1T1 transcript levels could significantly discriminate between continuous complete remission and a hematologic relapse at 1.5-3, 4-6, and 7-12 months but not at >3, >6, and >12 months, respectively. Over 90% of the 175 patients who were in continuous complete remission had a ≥3-log reduction in RUNX1-RUNX1T1 transcript levels from the time of diagnosis at each time point after transplantation and a ≥4-log reduction at ≥12 months. A
ISSN:1756-8722
1756-8722
DOI:10.1186/s13045-017-0414-2