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荧光原位杂交技术在检测常规骨髓标本间期细胞中bcr/abl基因融合的价值

Value of fluorescence in situ hybridization for detecting the bcr/abl gene fusion in interphase cells of routine bone marrow specimens.

作者信息

Werner M, Ewig M, Nasarek A, Wilkens L, von Wasielewski R, Tchinda J, Nolte M

机构信息

Institute of Pathology, Technische Universität München, Germany.

出版信息

Diagn Mol Pathol. 1997 Oct;6(5):282-7. doi: 10.1097/00019606-199710000-00006.

Abstract

Fluorescence in situ hybridization (FISH) is a new technique that allows demonstrating of the bcr/abl gene fusion in bone marrow cells of patients with Philadelphia translocation (Ph)-positive chronic myeloid leukemia (CML). In this study, bone marrow samples of 150 patients were investigated routinely by interphase FISH, cytogenetics, and bone marrow histopathology. In 20 patients with reactive hyperplasia of the granulopoiesis and normal karyotypes, FISH revealed nonspecific bcr/abl fusion signals at a mean frequency of 2.7% of the cells examined. The cutoff level for specific fusion signals was set at three times the standard deviation (9.0%). None of the 29 cytogenetically Ph-negative patients with myeloproliferative disease other than CML had fusion signals exceeding 9%. The mean frequency of specific fusion signals in nontreated patients with CML (n = 59) was 92.7%, and 49.3% in patients with CML who received therapy (n = 42). For diagnosing Ph-positive CML, interphase FISH has been faster, more reliable, and more sensitive than cytogenetics, which was successful in 54 of 59 patients investigated at first diagnosis but only in 27 of 42 patients receiving therapy, and it failed to detect Ph-positive cells in three patients with CML. However, small percentages of less than 9.0% of cells with bcr/abl fusion signals were below the threshold of interphase FISH, thereby limiting its use for detecting minimal residual disease.

摘要

荧光原位杂交(FISH)是一项新技术,可用于显示费城染色体易位(Ph)阳性慢性髓性白血病(CML)患者骨髓细胞中的bcr/abl基因融合。在本研究中,对150例患者的骨髓样本进行了间期FISH、细胞遗传学和骨髓组织病理学常规检查。在20例粒细胞生成反应性增生且核型正常的患者中,FISH显示非特异性bcr/abl融合信号,平均频率为所检查细胞的2.7%。特异性融合信号的临界值设定为标准差的三倍(9.0%)。29例除CML外的细胞遗传学Ph阴性骨髓增殖性疾病患者中,无一例融合信号超过9%。未治疗的CML患者(n = 59)中特异性融合信号的平均频率为92.7%,接受治疗的CML患者(n = 42)中为49.3%。对于诊断Ph阳性CML,间期FISH比细胞遗传学更快、更可靠、更敏感。细胞遗传学在初诊时检查的59例患者中有54例成功,但在接受治疗的42例患者中仅27例成功,且有3例CML患者未能检测到Ph阳性细胞。然而,小于9.0%的带有bcr/abl融合信号的细胞比例低于间期FISH的阈值,从而限制了其用于检测微小残留病的应用。

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