Detection of BRAF mutations in the tumour and serum of patients enrolled in the AZD6244 (ARRY-142886) advanced melanoma phase II study

被引:76
作者
Board, R. E. [1 ,2 ]
Ellison, G. [1 ]
Orr, M. C. M. [1 ]
Kemsley, K. R. [1 ]
McWalter, G. [1 ]
Blockley, L. Y. [1 ]
Dearden, S. P. [1 ]
Morris, C. [1 ]
Ranson, M. [3 ]
Cantarini, M. V. [1 ]
Dive, C. [2 ]
Hughes, A. [1 ]
机构
[1] AstraZeneca, Macclesfield SK10 4TG, Cheshire, England
[2] Univ Manchester, Paterson Inst Canc Res, Clin & Expt Pharmacol Grp, Manchester M20 4BX, Lancs, England
[3] Christie Hosp NHS Trust, CRUK Dept Med Oncol, Manchester M20 4BX, Lancs, England
关键词
AZD6244; amplification refractory mutation system; BRAF; circulating free DNA; cutaneous melanoma; LUNG-CANCER; DNA; PREDICTOR; GEFITINIB; PLASMA; KINASE;
D O I
10.1038/sj.bjc.6605371
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: 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. METHODS: 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. RESULTS: 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. CONCLUSIONS: 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. British Journal of Cancer (2009) 101, 1724-1730. doi: 10.1038/sj.bjc.6605371 www.bjcancer.com Published online 27 October 2009 (C) 2009 Cancer Research UK
引用
收藏
页码:1724 / 1730
页数:7
相关论文
共 18 条
[1]  
Brose MS, 2002, CANCER RES, V62, P6997
[2]   Clinical significance of BRAF mutations in metastatic melanoma [J].
Chang D.Z. ;
Panageas K.S. ;
Osman I. ;
Polsky D. ;
Busam K. ;
Chapman P.B. .
Journal of Translational Medicine, 2 (1)
[3]  
Coombs N J, 1999, Nucleic Acids Res, V27, pe12, DOI 10.1093/nar/27.16.e12
[4]   Detection of mutated BRAFV600E variant in circulating DNA of stage III-IV melanoma patients [J].
Daniotti, Maria ;
Vallacchi, Viviana ;
Rivoltini, Licia ;
Patuzzo, Roberto ;
Santinami, Mario ;
Arienti, Flavio ;
Cutolo, Gianluca ;
Pierotti, Marco A. ;
Parmiani, Giorgio ;
Rodolfo, Monica .
INTERNATIONAL JOURNAL OF CANCER, 2007, 120 (11) :2439-2444
[5]   Mutations of the BRAF gene in human cancer [J].
Davies, H ;
Bignell, GR ;
Cox, C ;
Stephens, P ;
Edkins, S ;
Clegg, S ;
Teague, J ;
Woffendin, H ;
Garnett, MJ ;
Bottomley, W ;
Davis, N ;
Dicks, N ;
Ewing, R ;
Floyd, Y ;
Gray, K ;
Hall, S ;
Hawes, R ;
Hughes, J ;
Kosmidou, V ;
Menzies, A ;
Mould, C ;
Parker, A ;
Stevens, C ;
Watt, S ;
Hooper, S ;
Wilson, R ;
Jayatilake, H ;
Gusterson, BA ;
Cooper, C ;
Shipley, J ;
Hargrave, D ;
Pritchard-Jones, K ;
Maitland, N ;
Chenevix-Trench, G ;
Riggins, GJ ;
Bigner, DD ;
Palmieri, G ;
Cossu, A ;
Flanagan, A ;
Nicholson, A ;
Ho, JWC ;
Leung, SY ;
Yuen, ST ;
Weber, BL ;
Siegler, HF ;
Darrow, TL ;
Paterson, H ;
Marais, R ;
Marshall, CJ ;
Wooster, R .
NATURE, 2002, 417 (6892) :949-954
[6]   Circulating mutant DNA to assess tumor dynamics [J].
Diehl, Frank ;
Schmidt, Kerstin ;
Choti, Michael A. ;
Romans, Katharine ;
Goodman, Steven ;
Li, Meng ;
Thornton, Katherine ;
Agrawal, Nishant ;
Sokoll, Lori ;
Szabo, Steve A. ;
Kinzler, Kenneth W. ;
Vogelstein, Bert ;
Diaz, Luis A., Jr. .
NATURE MEDICINE, 2008, 14 (09) :985-990
[7]  
Dummer R., 2008, J CLIN ONCOL, V26
[8]   Evaluation of epidermal growth factor receptor mutation status in serum DNA as a predictor of response to gefitinib (IRESSA) [J].
Kimura, H. ;
Suminoe, M. ;
Kasahara, K. ;
Sone, T. ;
Araya, T. ;
Tamori, S. ;
Koizumi, F. ;
Nishio, K. ;
Miyamoto, K. ;
Fujimura, M. ;
Nakao, S. .
BRITISH JOURNAL OF CANCER, 2007, 97 (06) :778-784
[9]   Detection of epidermal growth factor receptor mutations in serum as a predictor of the response to gefitinib in patients with non-small-cell lung cancer [J].
Kimura, Hideharu ;
Kasahara, Kazuo ;
Kawaishi, Makoto ;
Kunitoh, Hideo ;
Tamura, Tomohide ;
Holloway, Brian ;
Nishio, Kazuto .
CLINICAL CANCER RESEARCH, 2006, 12 (13) :3915-3921
[10]   TRANSFORMATION OF MAMMALIAN-CELLS BY CONSTITUTIVELY ACTIVE MAP KINASE KINASE [J].
MANSOUR, SJ ;
MATTEN, WT ;
HERMANN, AS ;
CANDIA, JM ;
RONG, S ;
FUKASAWA, K ;
VANDEWOUDE, GF ;
AHN, NG .
SCIENCE, 1994, 265 (5174) :966-970