Minimal Residual Disease Detection by Next-Generation Sequencing in Multiple Myeloma: A Comparison With Real-Time Quantitative PCR

被引:2
|
作者
Yao, Qiumei [1 ]
Bai, Yinlei [2 ,3 ]
Kumar, Shaji [4 ]
Au, Elaine [5 ]
Orfao, Alberto [6 ,7 ,8 ]
Chim, Chor Sang [1 ]
机构
[1] Univ Hong Kong, Dept Med, Pokfulam, Queen Mary Hosp, Hong Kong, Peoples R China
[2] Tsinghua Univ, Inst Immunol, Beijing, Peoples R China
[3] Tsinghua Univ, Sch Med, Beijing, Peoples R China
[4] Mayo Clin, Div Hematol, Rochester, MN USA
[5] Univ Hong Kong, Dept Pathol, Pokfulam, Queen Mary Hosp, Hong Kong, Peoples R China
[6] Univ Salamanca USAL, Dept Med, Salamanca, Spain
[7] Univ Salamanca USAL, Cytometry Serv Nucleus, Canc Res Ctr IBMCC, USAL CSIC, Salamanca, Spain
[8] Univ Salamanca USAL, CIBERONC, Inst Biomed Res Salamanca IBSAL, Salamanca, Spain
来源
FRONTIERS IN ONCOLOGY | 2021年 / 10卷
基金
中国国家自然科学基金;
关键词
minimal residual disease; multiple myeloma; next-generation sequencing; allele-specific oligonucleotide real-time quantitative-PCR; sensitivity;
D O I
10.3389/fonc.2020.611021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Here we compared clonotype identification by allele-specific oligonucleotide real-time quantitative-PCR (ASO RQ-PCR) and next-generation sequencing (NGS) in 80 multiple myeloma patients. ASO RQ-PCR was applicable in 49/55 (89%) and NGS in 62/78 (80%). Clonotypes identified by both methods were identical in 33/35 (94%). Sensitivity of 10(-5) was confirmed in 28/29 (96%) by NGS while sensitivity of RQ-PCR was 10(-5) in 7 (24%), 5 x 10(-5) in 15 (52%), and 10(-4) in 7 (24%). Among 14 samples quantifiable by ASO RQ-PCR, NGS yielded comparable results in 12 (86%). Applicability of NGS can be improved if immunoglobulin heavy-chain incomplete DJ primers are included.
引用
收藏
页数:5
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