
DROPLET DIGITAL PCR AS A MOLECULAR TOOL FOR THE DETECTION OF THE EGFR T790M MUTATION IN NSCLC PATIENTS WITH THE EGFR ACTIVATING MUTATIONS Durgut S, Salihefendić L, Pećar D, Čeko I, Mulahuseinović N, Izmirlija M, Konjhodžić R *Corresponding Author: Selma Durgut, MD, ALEA Genetic Center, Olovska 67, 71000 Sarajevo, Bosnia and Herzegovina; Mob.: +38761904549, Email: selma.durgut@agc.ba page: 21
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CONCLUSION
Monitoring the T790M mutation has an important
role in the examination of the effects of the prescribed
TKI therapy. This approach implies multiple tissue biopsy
sampling, which, as an invasive sampling method, has
its limitations and risks. Our results showed that ddPCR
technology has made it possible to use liquid biopsy as an
adequate minimally invasive alternative for the detection
of rare allele variants. Plasma ddPCR-based genotyping
can be significant in the detection of specific mutations and
patient monitoring. Using plasma as a sample for the detec-
tion of EGFR mutations by highly sensitive methods such
as ddPCR can enable early detection of the T790M muta-
tion, but also other inhibiting and activating mutations.
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