Jinawath Natini, Norris-Kirby Alexis, Smith B Douglas, Gocke Christopher D, Batista Denise A, Griffin Constance A, Murphy Kathleen M
Institute of Genetic Medicine, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA.
J Mol Diagn. 2009 Jul;11(4):359-63. doi: 10.2353/jmoldx.2009.090008. Epub 2009 Jun 4.
Patients with chronic myelogenous leukemia have a t(9;22)(q34;q11.2) or variant translocation that results in a BCR-ABL fusion gene. BCR-ABL detection by quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) is the standard practice for monitoring residual disease in patients with chronic myelogenous leukemia who receive tyrosine kinase inhibitor therapies. In this study, we describe a patient who tested positive for the BCR-ABL translocation by fluorescence in situ hybridization and cytogenetic analysis but tested negative by qRT-PCR molecular analysis at the time of diagnosis. Further PCR analysis and DNA sequencing with alternative primer sets demonstrated the presence of an e14a3 (also known as b3a3) BCR-ABL fusion. The e14a3 fusion is rare, but may be underreported as a result of many commercially available and laboratory-developed primer sets that fail to detect breakpoints in the ABL gene that are downstream of intron 1. For this patient, if the qRT-PCR assay had been used to monitor disease response/progression after treatment and not in conjunction with fluorescence in situ hybridization or cytogenetics at the time of diagnosis, the negative result would have been misinterpreted as molecular remission.
慢性粒细胞白血病患者存在t(9;22)(q34;q11.2)或变异易位,导致BCR-ABL融合基因。通过定量逆转录聚合酶链反应(RT-PCR)检测BCR-ABL是监测接受酪氨酸激酶抑制剂治疗的慢性粒细胞白血病患者残留疾病的标准做法。在本研究中,我们描述了一名患者,其在诊断时通过荧光原位杂交和细胞遗传学分析检测BCR-ABL易位呈阳性,但通过qRT-PCR分子分析检测呈阴性。进一步的PCR分析和使用替代引物组的DNA测序证明存在e14a3(也称为b3a3)BCR-ABL融合。e14a3融合很少见,但可能由于许多市售和实验室开发的引物组未能检测到ABL基因内含子1下游的断点而报告不足。对于该患者,如果在诊断时使用qRT-PCR检测来监测治疗后的疾病反应/进展,而不是与荧光原位杂交或细胞遗传学结合使用,阴性结果可能会被误解为分子缓解。