Abstract
This study investigated the potential clinical utility of circulating free DNA (cfDNA) as a source of BRAF mutation detection in patients enrolled into a phase II study of AZD6244, a specific MEK1/2 inhibitor, in patients with advanced melanoma. BRAF mutations were detected using Amplification Refractory Mutation System allele-specific PCR. BRAF mutation status was assessed in serum-derived cfDNA from 126 patients enrolled into the study and from 94 matched tumour samples. Of 94 tumour samples, 45 (47.9%) were found to be BRAF mutation positive (BRAF+). Serum-derived cfDNA was BRAF+ in 33 of 126 (26.2%) samples, including in five samples for which tumour data were unavailable. Of BRAF+ tumours, 25 of 45 (55.6%) were BRAF+ in cfDNA. In three cases in which the tumour was negative, cfDNA was BRAF+. Progression-free survival (PFS) of patients with BRAF+ tumour and cfDNA was not significantly different compared with tumour BRAF+ but cfDNA BRAF-negative patients, indicating that cfDNA BRAF detection is not associated with poorer prognosis on PFS in stage III/IV advanced melanoma. These data demonstrate the feasibility of BRAF mutation detection in cfDNA of patients with advanced melanoma. Future studies should aim to incorporate BRAF mutation testing in cfDNA to further validate this biomarker for patient selection.
MeSH Terms
Antineoplastic Agents/pharmacology,therapeutic use
Benzimidazoles/therapeutic use
Cell Line, Tumor
DNA Mutational Analysis
DNA, Neoplasm/blood,genetics
Disease-Free Survival
HT29 Cells
Humans
Melanoma/blood,drug therapy,genetics,metabolism
Mutation
Prognosis
Proto-Oncogene Proteins B-raf/genetics,metabolism
Skin Neoplasms/blood,drug therapy,genetics,metabolism
Chemicals
AZD 6244
Antineoplastic Agents
Benzimidazoles
DNA, Neoplasm
BRAF protein, human
Proto-Oncogene Proteins B-raf
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Board R E
AstraZeneca Pharmaceuticals, Alderley Park, Cheshire SK10 4TG, UK.
Ellison G
Orr M C M
Kemsley K R
McWalter G
Blockley L Y
Dearden S P
Morris C
Ranson M
Cantarini M V
Dive C
Hughes A
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