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


ABSTRACT: 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 × 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.

SUBMITTER: Yao Q 

PROVIDER: S-EPMC7878533 | biostudies-literature | 2020

REPOSITORIES: biostudies-literature

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

Yao Qiumei Q   Bai Yinlei Y   Kumar Shaji S   Au Elaine E   Orfao Alberto A   Chim Chor Sang CS  

Frontiers in oncology 20210129


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<sup>-5</sup> was confirmed in 28/29 (96%) by NGS while sensitivity of RQ-PCR was 10<sup>-5</sup> in 7 (24%), 5 × 10<sup>-5</sup> in 15 (52%), and 10<sup>-4</sup>  ...[more]

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