出 处:《中华检验医学杂志》2023年第12期1298-1304,共7页Chinese Journal of Laboratory Medicine
摘 要:目的探讨CD7^(+)复发难治急性髓系白血病(r/r AML)患者的临床及分子学特征以及异基因造血干细胞移植术(allo-HSCT)的预后。方法回顾性分析2017年1月1日到2020年12月31日入航天中心医院血液科行allo-HSCT的172例r/r AML患者,根据初发免疫表型是否表达CD7分为CD7^(+)组75例,CD7-组97例。采用Mann-Whitney U和卡方检验对比两组患者的临床资料、分子学及细胞遗传学特征,Kaplan-Meier分析两组患者的中位无进展生存时间(PFS)和中位总生存时间(OS),Cox回归筛选影响患者预后因素。结果中位随访19个月,CD7-组复发率23.71%,CD7^(+)组复发率50.67%(χ^(2)=13.428,P<0.001)。复发患者中CD7-组86.96%不表达CD7,CD7^(+)组86.84%表达CD7。CD7-组和CD7^(+)组的中位无进展生存时间(PFS)分别为25个月和5个月,差异有统计学意义(χ^(2)=13.428,P=0.003);中位总生存时间(OS)分别为34个月和15个月,差异有统计学意义(χ^(2)=2.579,P=0.108)。单因素分析显示,CD7^(+)组患者移植前获得形态学缓解率较低(χ^(2)=10.014,P=0.002),获得分子学缓解率较低(χ^(2)=22.809,P<0.001),男性患者较多(χ^(2)=5.281,P=0.022),CEBPA双位点突变发生率高于CD7-组(23.4%比8.2%,χ^(2)=8.180,P=0.004),RUNX1::RUNX1T1融合基因发生率低于CD7-组(4.0%比18.6%,χ^(2)=8.362,P=0.004)。多因素分析显示,移植前肿瘤负荷是影响r/r AML患者PFS和OS的唯一预后因素,PFS(HR 1.600,95%CI 1.203~2.127,P=0.001);OS(HR 1.737,95%CI 1.273~2.369,P<0.001)。结论CD7阳性可作为r/r AML患者不良预后的危险因素,且复发后CD7表达稳定,可以作为免疫靶向治疗的靶点。Objective To investigate the clinical and molecular features of patients with CD7^(+)relapsed or refractory acute myeloid leukemia(r/rAML)and the prognosis of allogeneic hematopoietic stem cell transplantation(allo-HSCT).Methods 172 r/rAML patients who underwent allo-HSCT in department of hematology,Aerospace Center Hospital between January 1st 2017 and December 31st 2020 were retrospectively analyzed The patients were were divided into CD7^(+)group(n=75)and CD7-group(n=97)according to the expression CD7 in the initial immunophenotype.Mann-Whitney U and Chi-square test were used to compare the clinical data,molecular and cytogenetic characteristics of the two groups of patients.Kaplan-Meier method was used to analyze the median progression-free survival(PFS)and median overall survival(OS)of the two groups of patients,and Cox regression screenthe prognostic factors of the patients.Results The median follow-up time was 19 months.The recurrence rates were 23.71%and 50.67%,respectively in CD7-and CD7^(+)group(χ^(2)=13.428 P<0.001).In relapsed patients,86.96 percentage of CD7-group did not express CD7 while 86.84 percentage of CD7^(+)group expressed CD7.The median PFS was 25 and 5 months in CD7-and CD7^(+)group(χ^(2)=8.695,P=0.003),and the medianOS was 34 and 15 months in CD7-and CD7^(+)group(χ^(2)=2.579,P=0.108).Univariate analysis showed that the CD7^(+)group,had the lower rates of morphological remission(χ^(2)=10.014,P=0.002),molecular remission(χ^(2)=22.809,P<0.001),and more male patients(χ^(2)=5.281,P=0.022).The incidence of CEBPA double-site mutation was higher(23.4%vs 8.2%,χ^(2)=8.180,P=0.004)and the rearrangement of RUNX1::RUNX1T1 was lower(4.0%vs18.6%,χ^(2)=8.362,P=0.004)in CD7^(+)group than in CD7-group.Multivariate analysis showed that pre-transplant tumor load was the only prognostic factor for PFS(HR,1.600;95%CI,1.203 to 2.127;P=0.001)and OS(HR,1.737;95%CI,1.273 to 2.369;P<0.001)in r/r AML patients.Conclusion CD7 expression is a risk factor for poor prognosis in r/r AML patients,and CD7 expression
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