Detection and Quantification of BCR-ABL1 Fusion Transcripts by Droplet Digital PCR

被引:94
作者
Jennings, Lawrence J. [1 ,2 ]
George, David [1 ]
Czech, Juliann [1 ]
Yu, Min [1 ]
Joseph, Loren [3 ]
机构
[1] Ann & Robert H Lurie Childrens Hosp Chicago, Dept Pathol & Lab Med, Chicago, IL 60614 USA
[2] Northwestern Univ, Dept Pathol & Lab Med, Feinberg Sch Med, Chicago, IL 60611 USA
[3] Univ Chicago, Dept Pathol, Chicago, IL 60637 USA
关键词
CHRONIC MYELOID-LEUKEMIA; MINIMAL RESIDUAL DISEASE; COMPLETE MOLECULAR RESPONSE; POLYMERASE-CHAIN-REACTION; HARMONIZING CURRENT METHODOLOGY; INTERNATIONAL REPORTING SCALE; COMPLETE CYTOGENETIC RESPONSE; TYROSINE KINASE INHIBITORS; TIME QUANTITATIVE PCR; BCR-ABL TRANSCRIPTS;
D O I
10.1016/j.jmoldx.2013.10.007
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Monitoring BCR-ABL1 fusion transcripts by real-time quantitative RT-PCR has become an important clinical test for the management of patients with chronic myeloid leukemia. However, it has some inherent Limitations with regard to its lower limit of detection and limit of quantification. Improvement in the Lower limit of detection could aid clinicians in selecting candidates for discontinuation of tyrosine kinase inhibitors without relapse. Improvement in the limit of quantification may also avoid unnecessary testing or changes in therapy. Here, we demonstrate the advantages of droplet digital RTPCR with regard to simplicity, lower Limit of detection, and Limit of quantification. We expect the advantages of droplet digital RT-PCR wilt make it the preferred method for quantification of BCR-ABL1 fusion transcripts.
引用
收藏
页码:174 / 179
页数:6
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