Anderson A E, Schneider N R, Allen G J, Ranganathan R, Burns J, Jhanwar S C, Klein E A, Cunningham I, O'Reilly R J, Chaganti R S
Laboratory of Cancer Genetics and Cytogenetics, Sloan-Kettering Institute, New York, New York.
Cancer Genet Cytogenet. 1989 Nov;43(1):67-71. doi: 10.1016/0165-4608(89)90128-3.
Until recently, cytogenetic detection of the Philadelphia chromosome (Ph) was the only reliable test to diagnose chronic myelogenous leukemia (CML) and detect minimal disease or early relapse following treatment. However, the recently developed ability to detect the Ph chromosome as a rearrangement in the bcr gene of chromosome 22 permits identification of the leukemic clone comprising as little as 5% of the cell population. We present results of simultaneous cytogenetic and DNA rearrangement studies in 28 CML patients considered for or treated with bone marrow transplantation. Our results show that the molecular method is significantly more sensitive than the cytogenetic method in the detection of minimal disease Ph-positive clones.
直到最近,费城染色体(Ph)的细胞遗传学检测仍是诊断慢性粒细胞白血病(CML)以及检测治疗后微小疾病或早期复发的唯一可靠检测方法。然而,最近发展起来的将Ph染色体检测为22号染色体bcr基因重排的能力,使得能够识别出仅占细胞群体5%的白血病克隆。我们展示了对28例考虑进行或已接受骨髓移植的CML患者同时进行细胞遗传学和DNA重排研究的结果。我们的结果表明,在检测微小疾病Ph阳性克隆方面,分子方法比细胞遗传学方法显著更敏感。