Comparison of High-Resolution Melting Analysis, Sanger Sequencing and ARMS for KRAS Mutation Detection in Metastatic Colorectal Cancer

被引:5
作者
Zhang, Haiyan [1 ]
Zhang, Xiaoming [3 ,4 ]
Wang, Jie [1 ]
Xian, Jiang [1 ]
Chen, Xiaodong [2 ]
Zhang, Wei [2 ]
机构
[1] Guangzhou Mil Command, Gen Hosp, Dept Med Res, Guangzhou 510010, Guangdong, Peoples R China
[2] Guangzhou Mil Command, Gen Hosp, Dept Pathol, Guangzhou 510010, Guangdong, Peoples R China
[3] Guangzhou Mil Command, Gen Hosp, Dept Urol, Guangzhou 510010, Guangdong, Peoples R China
[4] Guangzhou Huabo Biopharmaceut Res Inst, Guangzhou, Guangdong, Peoples R China
关键词
KRAS; metastatic colorectal cancer; mutation detection; PANITUMUMAB; CETUXIMAB; EGFR; CARCINOMA;
D O I
10.7754/Clin.Lab.2014.140923
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Treatment of metastatic colon carcinoma with the anti-epidermal growth factor receptor antibody cetuximab/panitumumab is reported to be ineffective in KRAS-mutant tumors; therefore, it is necessary to perform KRAS mutation analysis before cetuximab or panitumumab treatment is initiated. Methods: This study was designed to compare and evaluate the efficacy of three different methodologies - high resolution melting (HRM), Sanger sequencing, and Amplification Refractory Mutation System (ARMS) - for KRAS mutation detection in a clinical setting. Results: In total, 55 samples from patients with metastatic colorectal cancer were analyzed. Compared to Sanger sequencing, good consistency was found between the results of the ARMS (Kappa = 0.839) and HRM (Kappa = 0.839). The sensitivities of the methods were compared after a consensus was reached: if two of the three methodologies showed a similar result, it was considered as the consensus result. The frequency of KRAS mutations in our population was 34.5%, and discordant findings were observed in five samples. No significant difference in sensitivity was found among the three methodologies. Conclusions: From the results, we can conclude that after careful in-laboratory validation, HRM is a good alternative to the ARMS and Sanger sequencing for KRAS mutation testing.
引用
收藏
页码:435 / 439
页数:5
相关论文
共 50 条
[21]   Characteristics and prevalence of KRAS, BRAF, and PIK3CA mutations in colorectal cancer by high-resolution melting analysis in Taiwanese population [J].
Hsieh, Li-Ling ;
Er, Tze-Kiong ;
Chen, Chih-Chieh ;
Hsieh, Jan-Sing ;
Chang, Jan-Gowth ;
Liu, Ta-Chih .
CLINICA CHIMICA ACTA, 2012, 413 (19-20) :1605-1611
[22]   KRAS Mutation Analysis Prior to EGFR-Directed Therapy for Metastatic Colorectal Cancer: A Review and Cost Analysis [J].
Deming, Dustin ;
Holen, Kyle .
CURRENT CANCER THERAPY REVIEWS, 2010, 6 (04) :256-261
[23]   Validation of targeted next-generation sequencing for RAS mutation detection in FFPE colorectal cancer tissues: comparison with Sanger sequencing and ARMS-Scorpion real-time PCR [J].
Gao, Jie ;
Wu, Huanwen ;
Wang, Li ;
Zhang, Hui ;
Duan, Huanli ;
Lu, Junliang ;
Liang, Zhiyong .
BMJ OPEN, 2016, 6 (01)
[24]   Biased Discordance of KRAS Mutation Detection in Archived Colorectal Cancer Specimens Between the ARMS-Scorpion Method and Direct Sequencing [J].
Bando, Hideaki ;
Tsuchihara, Katsuya ;
Yoshino, Takayuki ;
Kojima, Motohiro ;
Ogasawara, Naomi ;
Fukushima, Hiraku ;
Ochiai, Atsushi ;
Ohtsu, Atsushi ;
Esumi, Hiroyasu .
JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2011, 41 (02) :239-244
[25]   Locked nucleic acid probe enhances Sanger sequencing sensitivity and improves diagnostic accuracy of high-resolution melting-based KRAS mutational analysis [J].
Ishige, Takayuki ;
Itoga, Sakae ;
Matsushita, Kazuyuki ;
Nomura, Fumio .
CLINICA CHIMICA ACTA, 2016, 457 :75-80
[26]   Comparison of KRAS mutation analysis of colorectal cancer samples by standard testing and next-generation sequencing [J].
Kothari, Nishi ;
Schell, Michael J. ;
Teer, Jamie K. ;
Yeatman, Timothy ;
Shibata, David ;
Kim, Richard .
JOURNAL OF CLINICAL PATHOLOGY, 2014, 67 (09) :764-767
[27]   Impact of fixation artifacts and threshold selection on high resolution melting analysis for KRAS mutation screening [J].
Perez-Baez, Wendy ;
Garcia-Latorre, Ethel A. ;
Maldonado-Martinez, Hector Aquiles ;
Coronado-Martinez, Iris ;
Flores-Garcia, Leonardo ;
Taja-Chayeb, Lucia .
MOLECULAR AND CELLULAR PROBES, 2017, 35 :34-43
[28]   Observational study on conditions for access to the analysis of KRAS mutation in patients with metastatic colorectal cancer receiving panitumumab treatment [J].
Bibeau, Frederic ;
Louvet, Christophe ;
Afchain, Pauline ;
Mitry, Emmanuel ;
Artru, Pascal ;
Andre, Thierry .
BULLETIN DU CANCER, 2012, 99 (7-8) :743-751
[29]   High resolution melting analysis of KRAS, BRAF and PIK3CA in KRASexon 2 wild-type metastatic colorectal cancer [J].
Joana G Guedes ;
Isabel Veiga ;
Patrícia Rocha ;
Pedro Pinto ;
Carla Pinto ;
Manuela Pinheiro ;
Ana Peixoto ;
Maria Fragoso ;
Ana Raimundo ;
Paula Ferreira ;
Manuela Machado ;
Nuno Sousa ;
Paula Lopes ;
António Araújo ;
Joana Macedo ;
Fernando Alves ;
Camila Coutinho ;
Rui Henrique ;
Lúcio L Santos ;
Manuel R Teixeira .
BMC Cancer, 13
[30]   Comparative analysis of pyrosequencing and QMC-PCR in conjunction with high resolution melting for KRAS/BRAF mutation detection [J].
Ibrahem, Salih ;
Seth, Rashmi ;
O'Sullivan, Brendan ;
Fadhil, Wakkas ;
Taniere, Philippe ;
Ilyas, Mohammad .
INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, 2010, 91 (06) :500-505