Post-remission measurable residual disease directs treatment choice and improves outcomes for patients with intermediate-risk acute myeloid leukemia in CR1.
Post-remission measurable residual disease directs treatment choice and improves outcomes for patients with intermediate-risk acute myeloid leukemia in CR1.
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DOI:
10.1007/s12185-022-03441-6
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发表时间:
2022-12
影响因子:
2.1
通讯作者:
Yu, Jifeng
中科院分区:
文献类型:
--
作者:
Han, Lijie;Li, Yilu;Wu, Jiaying;Peng, Jie;Han, Xiaolin;Zhao, Hongmian;He, Chen;Li, Yuanyuan;Wang, Weimin;Zhang, Mengmeng;Li, Yafei;Sun, Hui;Cao, Haixia;Sang, Li'na;Jiang, Zhongxing;Yu, Jifeng
关键词:
This study retrospectively investigated in which cycle measurable residual disease (MRD) is associated with prognosis in patients in first complete remission (CR1) of intermediate-risk acute myeloid leukemia (AML). The study enrolled 235 younger patients with intermediate-risk AML. MRD was evaluated by multiparameter flow cytometry after the 1st, 2nd, and 3rd chemotherapy cycles (MRD1–3, respectively). No significant association was detected after the 1st and 2nd cycles. However, the 5-year incidence of relapse was higher in the MRD3-positive group (n = 99) than in the negative group (n = 136) (48.7% vs. 13.7%, P = 0.005), while 5-year disease-free survival (DFS) and overall survival (OS) were lower in the MRD3-positive group than in the negative group (43.2% vs. 81.0% and 45.4% vs. 84.1%; P = 0.003 and 0.005, respectively). Allogeneic hematopoietic stem cell transplantation led to a lower 5-year relapse, and higher DFS and OS rates than chemotherapy in the MRD3-positive group (22.3% vs. 71.5%, 65.9% vs. 23.0%, and 67.1% vs. 23.9%; P < 0.001, 0.002, and 0.022, respectively), but did not affect the MRD-negative group. MRD3 could serve as an indicator for post-remission treatment choice and help improve outcomes for intermediate-risk AML in CR1. The online version contains supplementary material available at 10.1007/s12185-022-03441-6.
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影响因子:
10.1
作者:
Keating, Armand;DaSilva, Gisela;Weisdorf, Daniel J.
通讯作者:
Weisdorf, Daniel J.
影响因子:
6.2
作者:
Gorin, Norbert-Claude;Labopin, Myriam;Mohty, Mohamad
通讯作者:
Mohty, Mohamad
影响因子:
11.4
作者:
Burnett AK;Hills RK;Nielsen OJ;Freeman S;Ali A;Cahalin P;Hunter A;Thomas IF;Russell NH
通讯作者:
Russell NH
影响因子:
120.7
作者:
Koreth, John;Schlenk, Richard;Kopecky, Kenneth J.;Honda, Sumihisa;Sierra, Jorge;Djulbegovic, Benjamin J.;Wadleigh, Martha;DeAngelo, Daniel J.;Stone, Richard M.;Sakamaki, Hisashi;Appelbaum, Frederick R.;Doehner, Hartmut;Antin, Joseph H.;Soiffer, Robert J.;Cutler, Corey
通讯作者:
Cutler, Corey
影响因子:
11.4
作者:
Paiva, Bruno;Vidriales, Maria-Belen;Montesinos, Pau
通讯作者:
Montesinos, Pau