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. 2017 Feb 14;38(2):118-123.
doi: 10.3760/cma.j.issn.0253-2727.2017.02.007.

[Effect of minimal residual disease monitoring by multiparameter flow cytometry pre-conditioning on prognosis of acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation]

[Article in Chinese]
Affiliations

[Effect of minimal residual disease monitoring by multiparameter flow cytometry pre-conditioning on prognosis of acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation]

[Article in Chinese]
Y Lu et al. Zhonghua Xue Ye Xue Za Zhi. .

Abstract

Objective: To investigate the effect of minimal residual disease (MRD) monitoring by multiparameter flow cytometry (MFC) pre-conditioning on prognosis of acute myeloid leukemia in first complete remission (CR(1)-AML) after allogeneic hematopoietic stem cell transplantation (allo-HSCT) , and to explore the value of MRD monitoring by MFC in the prognosis evaluation on allo-HSCT in CR(1)-AML. Methods: Between April 2012 and March 2015, consecutive 186 patients with CR(1)-AML who underwent allo-HSCT were analyzed retrospectively. MRD in BM before conditioning was detected by eight-color MFC. Any level of residual disease was considered to be MRD positive. Results: ①Of 186 patients, MRD was negative in 151 patients, positive in 35 patients (<1% in 25 patients and 1% to 3% in 10 patients) . ② With the median follow up of 18 (5-41) months, two-year DFS was 80.0% (95%CI 68.5%-92.3%) . Univariate analysis showed that MRD positive patients had lower DFS[62.9% (95%CI 50.6%-75.2%) vs 88.9% (95%CI 76.6%-100.0%) , P<0.001], higher relapse[11.4% (95%CI 4.1%-29.0%) vs 3.3% (95% CI 0.6%-20.9%) , P=0.003] and higher NRM [25.7% (95% CI 8.1%-43.3%) vs 7.9% (95% CI 1.3%-26.5%) , P=0.001] after HSCT compared with that of MRD negative patients. Secondary AML showed lower DFS than primary AML [60.0% (95% CI 42.4%-76.6%) vs 86.0% (95% CI 68.4%-100.0%) , P=0.004]. ③Multivariate analysis indicated that MRD positive pre-HSCT was the independent risk factor on DFS [HR=4.565 (95%CI 2.918-9.482) , P<0.001], relapse [HR=5.854 (95%CI 1.538-22.288) , P=0.010] and NRM [HR=3.379 (95%CI 1.361-8.391) , P=0.009] after allo-HSCT in CR(1)-AML. Conclusion: MRD positive pre-conditioning was the only negative impact factor for patients with CR(1)-AML after allo-HSCT. MRD by MFC can be used to assess the prognosis of CR(1)-AML after allo-HSCT.

目的:分析预处理前多参数流式细胞术(MFC)监测的骨髓微小残留病(MRD)对急性髓系白血病(AML)异基因造血干细胞移植(allo-HSCT)预后的影响,探讨MFC监测MRD在AML allo-HSCT预后评估中的价值。 方法:回顾性分析2012年4月至2015年3月行allo-HSCT的186例AML患者,预处理前骨髓细胞形态学均达第1次完全缓解(CR(1))。采用8色MFC对预处理前骨髓进行MRD检测,任何水平异常均定义为MRD阳性。 结果: ①186例AML患者中151例MRD阴性;35例MRD阳性,其中25例MRD<1%,10例MRD为1%~3%。②2年总体无病生存(DFS)率为80.0%(95% CI 68.5%~92.3%)。与MRD阴性组比较,MRD阳性组DFS率低[62.9%(95% CI 50.6%~75.2%)对88.9%(95%CI 76.6%~100.0%),P<0.001]、复发率高[11.4%(95%CI 4.1%~29.0%)对3.3%(95%CI 0.6%~20.9%),P=0.003]、非复发死亡率(NRM)高[25.7%(95%CI 8.1%~43.3%)对7.9%(95%CI 1.3%~26.5%),P=0.001]。继发性AML组DFS率低(P=0.004),NRM高(P=0.003)。③多因素分析结果显示预处理前MFC检测的MRD阳性是DFS[HR=4.565(95%CI 2.918~9.482),P<0.001]、复发[HR=5.854(95% CI 1.538~22.288),P=0.010]及非复发死亡[HR=3.379(95%CI 1.361~8.391),P=0.009]的独立危险因素。 结论:预处理前MFC监测的MRD阳性是影响allo-HSCT治疗CR(1)-AML独立危险因素,MFC监测MRD可用于AML allo-HSCT的预后评估。.

Keywords: Flow cytometry; Hematopoietic stem cell transplantation; Leukemia, myeloid, acute; Neoplasm, residual.

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