| Literature DB >> 33246263 |
Gioia Colafigli1, Emilia Scalzulli1, Alessio Di Prima1, Sara Pepe1, Maria Giovanna Loglisci1, Daniela Diverio1, Maurizio Martelli1, Robin Foà1, Massimo Breccia2.
Abstract
Tyrosine kinase inhibitors (TKIs) have drastically changed the outcome of chronic myeloid leukemia (CML) patients. A sustained and deep molecular response achieved over time paves the way to therapy discontinuation, and is a pre-requisite to attempt treatment-free remission. Monitoring of the molecular response during treatment discontinuation is routinely carried out by RQ-PCR, but it may not be the optimal tool to monitor minimal residual disease at the time of stopping treatment and during treatment discontinuation. Different digital PCR platforms (such as droplet dPCR) are available, a method based on water-emulsion droplet technology in which the sample is partitioned into 20,000 droplets and PCR amplification of the template subsequently occurs in each individual droplet. The consequent high sensitivity and precision with a very reliable quantification without the need of a calibration curve and the exquisite reproducibility makes this procedure as an ideal alternative method for the detection of very low levels of disease. Aim of this review is to describe and discuss the recent use of dPCR/ddPCR in CML, focusing in particular on its role in TKI treatment discontinuation strategies.Entities:
Keywords: CML; Deep molecular response; Digital PCR; Droplet digital PCR; TKIs; Treatment free remission
Year: 2020 PMID: 33246263 DOI: 10.1016/j.critrevonc.2020.103163
Source DB: PubMed Journal: Crit Rev Oncol Hematol ISSN: 1040-8428 Impact factor: 6.312