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通过定量Southern印迹分析监测的α-干扰素治疗的慢性粒细胞白血病(CML)患者的分子反应。德国慢性粒细胞白血病(CML)研究组

Molecular response of CML patients treated with interferon-alpha monitored by quantitative Southern blot analysis. German chronic myeloid leukaemia (CML) Study Group.

作者信息

Reiter A, Skladny H, Hochhaus A, Seifarth W, Heimpel H, Bartram C R, Cross N C, Hehlmann R

机构信息

III. Medizinische Klinik, Klinikum Mannheim der Universität Heidelberg, Germany.

出版信息

Br J Haematol. 1997 Apr;97(1):86-93. doi: 10.1046/j.1365-2141.1997.32645.x.

Abstract

We analysed 459 samples from 206 chronic myeloid leukaemia (CML) patients at diagnosis and during or after treatment with interferon-alpha (IFN-alpha) by quantitative Southern blot analysis for BCR rearrangement. In a minority (2%) of Ph-positive patients, no BCR rearrangement was detectable due to breakpoints outside the major breakpoint cluster region (M-bcr) or possibly due to M-bcr deletions. Results from 235 samples were compared with the proportion of Ph-positive metaphases found in contemporaneous bone marrow specimens analysed by conventional cytogenetics. The rank correlation between both methods was 0.82 (P < 0.001). The proportion of CML cells in samples determined by Southern blot analysis (BCR ratio) was significantly different between cytogenetically-defined minor, partial, and complete response groups (P < 0.001). Empirically-derived cut-off points in the BCR ratio were introduced in order to define molecular response groups for comparison to standard cytogenetic response groups: a BCR ratio of 0% was defined as complete molecular response and ratios of 1-24%, 25-50%, and > 50% were defined as partial, minor, and no molecular response, respectively. Using these cut-off points the concordance between both methods was 67% (P < 0.0001), a major cytogenetic response could be predicted or excluded in more than 90% of cases (P < 0.0001). Our findings demonstrated that quantitative Southern blot was as sensitive as cytogenetics and as peripheral blood samples are suitable for this technique it should be considered as the method of choice for routine monitoring IFN-alpha therapy in CML patients.

摘要

我们通过定量Southern印迹分析BCR重排,对206例慢性髓性白血病(CML)患者在诊断时以及使用α-干扰素(IFN-α)治疗期间或治疗后采集的459份样本进行了分析。在少数(2%)Ph阳性患者中,由于断点位于主要断点簇区域(M-bcr)之外,或者可能是由于M-bcr缺失,未检测到BCR重排。将235份样本的结果与通过传统细胞遗传学分析的同期骨髓标本中Ph阳性中期细胞的比例进行了比较。两种方法的等级相关性为0.82(P < 0.001)。通过Southern印迹分析确定的样本中CML细胞比例(BCR比率)在细胞遗传学定义的微小、部分和完全缓解组之间存在显著差异(P < 0.001)。引入了根据经验得出的BCR比率临界值,以定义分子反应组,以便与标准细胞遗传学反应组进行比较:BCR比率为0%被定义为完全分子反应,比率为1 - 24%、25 - 50%和> 50%分别被定义为部分、微小和无分子反应。使用这些临界值,两种方法之间的一致性为67%(P < 0.0001),在超过90%的病例中可以预测或排除主要细胞遗传学反应(P < 0.0001)。我们的研究结果表明,定量Southern印迹与细胞遗传学一样敏感,并且由于外周血样本适用于该技术,它应被视为CML患者IFN-α治疗常规监测的首选方法。

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