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标准风险成人B系急性淋巴细胞白血病诱导/巩固治疗期间微小残留病的动力学

Kinetics of minimal residual disease during induction/consolidation therapy in standard-risk adult B-lineage acute lymphoblastic leukemia.

作者信息

Scholten C, Födinger M, Mitterbauer M, Laczika K, Mitterbauer G, Haas O A, Knöbl P, Schwarzinger I, Thalhammer R, Purtscher B

机构信息

Department of Clinical Chemistry and Laboratory Diagnostics, University of Vienna, Austria.

出版信息

Ann Hematol. 1995 Oct;71(4):155-60. doi: 10.1007/BF01910311.

Abstract

We have compared the kinetics of minimal residual disease (MRD) by simultaneous polymerase chain reaction (PCR) monitoring with oligonucleotides for the immunoglobulin heavy chain (IgH) complementarity-determining region 3 (CDR3) and the T-cell receptor gamma chain gene (TCR gamma), as well as clone-specific CDR3 sequences in adult patients (aged 17-51 years) with acute lymphoblastic leukemia (ALL) who entered a complete hematological remission (CR) after chemotherapy with the German multicenter ALL (GMALL) protocol. The sensitivities were one in 10(2-3) for the CDR3- and TCR gamma-PCR and one in 10(5-6) for a two-step, seminested CDR3/clone-specific PCR. At diagnosis, 7/7 patients were CDR3 positive and four were TCR gamma positive in their bone marrow (BM). At the end of induction therapy (after 2 months) 4/6 tested positive for CDR3, 2/6 for TCR gamma, and 5/6 for clone-specific rearrangements. At the end of consolidation treatment (after 7 months) only 1/7 remained positive for CDR3, 2/7 for TCR gamma, and 5/7 for clone-specific rearrangements. After an observation period of 18-36 months, 4/7 patients were still in CR and all were PCR negative by the clone-specific method during or after maintenance therapy. Two patients died in leukemic relapse; one patient relapsed but is still alive. All three of these patients remained PCR positive throughout the course of their disease. Clonal evolution in the IgH locus was found in one of these patients. We conclude that the molecular response to chemotherapy in adult B-lineage ALL is slow, even in patients without risk factors other than age. As in childhood ALL, most patients with long-term CR convert to PCR negativity approximately 18 months after the start of chemotherapy. The data also suggest the existence of early clone-specific PCR negativity in a small proportion of long-term survivors. The predictive value of this observation will now have to be confirmed in a larger study.

摘要

我们通过同时使用针对免疫球蛋白重链(IgH)互补决定区3(CDR3)和T细胞受体γ链基因(TCRγ)的寡核苷酸进行聚合酶链反应(PCR)监测,以及对采用德国多中心急性淋巴细胞白血病(ALL)方案(GMALL方案)化疗后达到完全血液学缓解(CR)的成年患者(年龄17 - 51岁)的克隆特异性CDR3序列,比较了微小残留病(MRD)的动力学。CDR3 - 和TCRγ - PCR的灵敏度为1/10²⁻³,两步半巢式CDR3/克隆特异性PCR的灵敏度为1/10⁵⁻⁶。诊断时,7/7例患者骨髓(BM)中CDR3呈阳性,4例TCRγ呈阳性。诱导治疗结束时(2个月后),4/6例CDR3检测呈阳性,2/6例TCRγ呈阳性,5/6例克隆特异性重排呈阳性。巩固治疗结束时(7个月后),只有1/7例CDR3仍呈阳性,2/7例TCRγ呈阳性,5/7例克隆特异性重排呈阳性。经过18 - 36个月的观察期,4/7例患者仍处于CR状态,并且在维持治疗期间或之后通过克隆特异性方法检测均为PCR阴性。2例患者死于白血病复发;1例患者复发但仍存活。这3例患者在疾病过程中PCR始终呈阳性。在其中1例患者中发现了IgH基因座的克隆进化。我们得出结论,即使在除年龄外无其他危险因素的成年B系ALL患者中,对化疗的分子反应也较慢。与儿童ALL一样,大多数长期CR的患者在化疗开始后约18个月转为PCR阴性。数据还表明,一小部分长期存活者中存在早期克隆特异性PCR阴性。这一观察结果的预测价值现在必须在更大规模的研究中得到证实。

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