Detection of RAS genes mutation using the Cobas ® method in a private laboratory of pathology: Medical and economical study in comparison to a public platform of molecular biology of cancer

被引:5
作者
Albertini, Anne-Flore [1 ]
Raoux, Delphine [1 ]
Neumann, Frederic [1 ]
Rossat, Stephane [1 ]
Tabet, Farid [1 ]
Pedeutour, Florence [2 ]
Duranton-Tanneur, Valerie [2 ]
Kubiniek, Valerie [2 ]
Vire, Olivier [1 ]
Weinbreck, Nicolas [1 ]
机构
[1] Lab Medipath, Pole Excellence Jean Louis, 263,Via Nova, F-83600 Frejus, France
[2] CHU Nice, Fac Med, Lab Genet Somat Tumeurs Solides, 22,Ave Valombrose, F-06107 Nice 02, France
关键词
Molecular pathology; RAS; Accreditation; METASTATIC COLORECTAL-CANCER; PARAFFIN-EMBEDDED TISSUES; COST-EFFECTIVENESS; PCR AMPLIFICATION; KRAS; CARCINOMA; CETUXIMAB; BRAF;
D O I
10.1016/j.bulcan.2017.05.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In France, determination of the mutation status of RAS genes for predictive response to anti-EGFR targeted treatments is carried out by public platforms of molecular biology of cancer created by the French National Cancer Institute. This study aims to demonstrate the feasibility of these analyses by a private pathology laboratory (MEDIPATH) as per the requirements of accreditation. We retrospectively studied the mutation status of KRAS and NRAS genes in 163 cases of colorectal metastatic cancer using the Cobas (R) technique. We compared our results to those prospectively obtained through pyrosequencing and allelic discrimination by the genetic laboratory of solid tumors at the Nice University Hospital (PACA-EST regional platform). The results of both series were identical: 98.7% positive correlation; negative correlation of 93.1%; overall correlation of 95.7% (Kappa = 0.92). This study demonstrates the feasibility of molecular analysis in a private pathology laboratory. As this practice requires a high level of guarantee, its accreditation, according to the NF-EN-ISO15189 quality compliance French standard, is essential. Conducting molecular analysis in this context avoids the steps of routing the sample and the result between the pathology laboratory and the platform, which reduces the overall time of rendering the result. In conclusion, the transfer of some analysis from these platforms to private pathology laboratories would allow the platforms to be discharged from a part of routine testing and therefore concentrate their efforts to the development of new analyses constantly required to access personalized medicine.
引用
收藏
页码:662 / 674
页数:13
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