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Droplet Digital PCR Is a Robust Tool for Monitoring Minimal Residual Disease in Adult Philadelphia-Positive Acute Lymphoblastic Leukemia

Authors :
Coccaro, Nicoletta
Anelli, Luisa
Zagaria, Antonella
Casieri, Paola
Tota, Giuseppina
Orsini, Paola
Impera, Luciana
Minervini, Angela
Minervini, Crescenzio F.
Cumbo, Cosimo
Parciante, Elisa
Carluccio, Paola
Brunetti, Claudia
Specchia, Giorgina
Albano, Francesco
Source :
The Journal of Molecular Diagnostics; July 2018, Vol. 20 Issue: 4 p474-482, 9p
Publication Year :
2018

Abstract

The breakpoint cluster region–abelson 1 p190 fusion transcript is the most frequent variant observed in Philadelphia-positive (Ph+) acute lymphoblastic leukemia (ALL). Qualitative-PCR and real-time quantitative PCR are the currently used methods to monitor minimal residual disease (MRD) in Ph+ ALL patients; for the latter, full standardization and an international quality validation are lacking. Here, we developed a droplet digital PCR (ddPCR) assay for MRD monitoring in p190+ ALL cases. The analytical performance was assessed by the limit-of-detection determination, showing a reliability, sensitivity, and precision of the assay of up to 0.001%. Comparison of results obtained with qualitative PCR and ddPCR in 117 follow-up samples from 16 of 26 Ph+ ALL patients showed discordant results in 27% of cases (32 of 117). Real-time quantitative PCR analysis of 19 ddPCR-positive samples with a low tumor burden failed to provide quantitative results in 63% of cases (12 of 19). These results highlight that in p190+ ALL the ddPCR method has a sufficient analytical performance for very low MRD monitoring and for predicting molecular relapse several months before hematologic relapse. In conclusion, MRD monitoring by ddPCR may better stratify Ph+ ALL patients at risk of disease progression.

Details

Language :
English
ISSN :
15251578
Volume :
20
Issue :
4
Database :
Supplemental Index
Journal :
The Journal of Molecular Diagnostics
Publication Type :
Periodical
Accession number :
ejs45449597
Full Text :
https://doi.org/10.1016/j.jmoldx.2018.03.002