神经母细胞瘤RAS病毒癌基因同源物
医学
免疫组织化学
黑色素瘤
转移性黑色素瘤
肿瘤科
突变
癌症研究
内科学
病理
癌症
生物
基因
生物化学
结直肠癌
克拉斯
作者
Marius Ilié,Elodie Long‐Mira,Elisa Funck‐Brentano,Sandra Lassalle,Catherine Butori,Virginie Lespinet-Fabre,Olivier Bordone,Ashley Gay,Katia Zahaf,Gilles Dolivet,J.‐P. Lacour,Philippe Bahadoran,Robert Ballotti,Audrey Gros,Caroline Dutriaux,Philippe Saïag,Jean‐Philippe Merlio,B. Vergier,Jean‐François Emile,Véronique Hofman,Paul Hofman
标识
DOI:10.1016/j.jaad.2015.01.012
摘要
It can be useful to assess the NRAS mutation status in patients with metastatic melanoma because NRAS-activating mutations confer resistance to RAF inhibitors, and NRAS-mutated patients appear to be sensitive to mitogen-activated protein kinase (MEK) inhibitors.We aimed to assess the diagnostic accuracy of an immunohistochemistry (IHC) approach using a novel anti-NRAS (Q61R) monoclonal antibody on formalin-fixed paraffin-embedded tissue samples from patients with metastatic melanoma.We conducted a retrospective multicenter cohort study on 170 patients with metastatic melanoma. The automated IHC assay was performed using the SP174 clone, and compared with results of the molecular testing.Evaluation of a test cohort with knowledge of the mutation status established a specific IHC pattern for the mutation. In the independent blinded analysis of the remaining cases, the anti-NRAS (Q61R) antibody accurately identified all NRAS Q61R-mutated tumors, and demonstrated 100% sensitivity and specificity.Limitations include retrospective design and lack of multicenter interobserver reproducibility.The NRAS (Q61R) IHC assay is reliable and specific for the evaluation of the Q61R mutation status in metastatic melanoma and may be an alternative to molecular biology in evaluation of metastatic melanoma in routine practice.
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