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Feasibility of monitoring advanced melanoma patients using cell-free DNA from plasma.

Authors :
Gangadhar TC
Savitch SL
Yee SS
Xu W
Huang AC
Harmon S
Lieberman DB
Soucier D
Fan R
Black TA
Morrissette JJD
Salathia N
Waters J
Zhang S
Toung J
van Hummelen P
Fan JB
Xu X
Amaravadi RK
Schuchter LM
Karakousis GC
Hwang WT
Carpenter EL
Source :
Pigment cell & melanoma research [Pigment Cell Melanoma Res] 2018 Jan; Vol. 31 (1), pp. 73-81. Date of Electronic Publication: 2017 Oct 23.
Publication Year :
2018

Abstract

To determine the feasibility of liquid biopsy for monitoring of patients with advanced melanoma, cell-free DNA was extracted from plasma for 25 Stage III/IV patients, most (84.0%) having received previous therapy. DNA concentrations ranged from 0.6 to 390.0 ng/ml (median = 7.8 ng/ml) and were positively correlated with tumor burden as measured by imaging (Spearman rho = 0.5435, p = .0363). Using ultra-deep sequencing for a 61-gene panel, one or more mutations were detected in 12 of 25 samples (48.0%), and this proportion did not vary significantly for patients on or off therapy at the time of blood draw (52.9% and 37.5% respectively; p = .673). Sixteen mutations were detected in eight different genes, with the most frequent mutations detected in BRAF, NRAS, and KIT. Allele fractions ranged from 1.1% to 63.2% (median = 29.1%). Among patients with tissue next-generation sequencing, nine of 11 plasma mutations were also detected in matched tissue, for a concordance of 81.8%.<br /> (© 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1755-148X
Volume :
31
Issue :
1
Database :
MEDLINE
Journal :
Pigment cell & melanoma research
Publication Type :
Academic Journal
Accession number :
28786531
Full Text :
https://doi.org/10.1111/pcmr.12623