KRAS MUTATION TESTING IN COLORECTAL CANCER AS AN EXAMPLE OF THE PATHOLOGIST'S ROLE IN PERSONALIZED TARGETED THERAPY: A PRACTICAL APPROACH

被引:31
|
作者
Domagala, Pawel [1 ]
Hybiak, Jolanta [1 ]
Sulzyc-Bielicka, Violetta [2 ]
Cybulski, Cezary [3 ]
Rys, Janusz [4 ]
Domagala, Wenancjusz [1 ]
机构
[1] Pomeranian Med Univ, Dept Pathol, PL-71252 Szczecin, Poland
[2] Pomeranian Med Univ, Dept Clin Oncol, PL-71252 Szczecin, Poland
[3] Pomeranian Med Univ, Dept Genet & Pathol, PL-71252 Szczecin, Poland
[4] Maria Sklodowska Curie Mem Inst Oncol, Ctr Oncol, Krakow Branch, Dept Tumour Pathol, Krakow, Poland
关键词
KRAS; EGFR; colorectal cancer; molecular pathology; targeted therapy; K-RAS MUTATIONS; FACTOR RECEPTOR INHIBITORS; PARAFFIN-EMBEDDED TISSUES; NUCLEIC-ACIDS EXTRACTION; LUNG-CANCER; MOLECULAR PATHOLOGY; 1ST-LINE TREATMENT; GENETIC-HETEROGENEITY; EXPRESSION PATTERNS; SENSITIVE DETECTION;
D O I
10.5114/PJP.2012.31499
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Identifying targets for personalized targeted therapy is the pathologist's domain and a treasure. For decades, pathologists have had to learn, understand, adopt and implement many new laboratory techniques as they arrived on the scene. Pathologists successfully integrate the results of those tests into final pathology reports that were, and still are, the basis of clinical therapeutic decisions. The molecular methods are different but no more difficult to comprehend in the era of "kit procedures". In recent years, the development of targeted therapies has influenced routine practices in pathology laboratories because the use of molecular techniques is required to include clinically useful predictive information in the pathology report. Pathologists have the knowledge and expertise to identify particular gene mutations using the appropriate molecular tests currently available. This review focuses on the most important recent developments in KRAs mutation testing in metastatic colorectal cancer (CRC), and shows that a pathologist is involved in 10 stages of this procedure. Recent studies have shown that highly sensitive, simple, reliable and rapid assays may significantly improve the identification of CRC patients resistant to anti-EGER therapy. Thus, direct sequencing does not seem to be an optimal procedure of KRAS testing for clinical purposes. Twelve currently available high-sensitivity diagnostic assays (with the CE-IVD mark) for KRAS mutation testing are briefly described and compared. The suggested pathology report content for somatic mutation tests is described. In conclusion, evidence is presented that sending away paraffin blocks with tumor tissue for KRAS mutation testing may not be in the best interest of patients. Instead, an evidence-based approach indicates that KRAS mutation testing should be performed in pathology departments, only with the use of CE-IVD/FDA-approved KRAS tests, and with the obligatory, periodic participation in the KRAS EQA scheme organized by the European Society of Pathology as an independent international body.
引用
收藏
页码:145 / 164
页数:20
相关论文
共 50 条
  • [31] AWARENESS AND PENETRATION OF KRAS MUTATION TESTING IN THE TREATMENT OF PATIENTS WITH METASTATIC COLORECTAL CANCER
    Ciardiello, F.
    Wohlschlegel, B.
    Teague, T.
    Mercadante, D.
    ANNALS OF ONCOLOGY, 2010, 21 : 20 - 20
  • [32] Comparison of three methods for "KRAS" mutation testing in patients with metastatic colorectal cancer
    Vasikova, A.
    Dvorakova, D.
    Ostrizkova, L.
    Brancikova, D.
    Pavlovsky, Z.
    Kyclova, J.
    Mayer, J.
    VIRCHOWS ARCHIV, 2010, 457 (02) : 228 - 228
  • [33] Awareness and penetration of KRAS mutation testing in the treatment of patients with metastatic colorectal cancer
    Ciardiello, F.
    Wohlschlegel, B.
    Teague, T.
    Mercadante, D.
    JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (15)
  • [34] Cetuximab as a Key Partner in Personalized Targeted Therapy for Metastatic Colorectal Cancer
    Gonzalez, Nadia Saoudi
    Ros, Javier
    Baraibar, Iosune
    Salva, Francesc
    Rodriguez-Castells, Marta
    Alcaraz, Adriana
    Garcia, Ariadna
    Tabernero, Josep
    Elez, Elena
    CANCERS, 2024, 16 (02)
  • [35] Biomarker testing for treatment of metastatic colorectal cancer: role of the pathologist in community practice
    Rodriguez, Rafael
    JOURNAL OF COMMUNITY AND SUPPORTIVE ONCOLOGY, 2014, 12 (01): : 27 - 32
  • [36] Optimization of routine KRAS mutation PCR-based testing procedure for rational individualized first-line-targeted therapy selection in metastatic colorectal cancer
    Chretien, Anne-Sophie
    Harle, Alexandre
    Meyer-Lefebvre, Magali
    Rouyer, Marie
    Husson, Marie
    Ramacci, Carole
    Harter, Valentin
    Genin, Pascal
    Leroux, Agnes
    Merlin, Jean-Louis
    CANCER MEDICINE, 2013, 2 (01): : 11 - 20
  • [37] PREDICTING RESPONSE TO ANTI-EGFR THERAPY FOR COLORECTAL CARCINOMA BY KRAS MUTATION TESTING
    Dubus, Pierre
    Berhouet, Sabine
    Carrere, Nathalie
    Merlio, Jean Philippe
    CYTOMETRY PART B-CLINICAL CYTOMETRY, 2009, 76B (06) : 420 - 421
  • [38] Personalized approach to the selection of standard and targeted therapies in metastatic colorectal cancer
    Engel, R.
    Boka, H.
    Archer, S.
    Nguyen, S.
    Nickless, D.
    Niap, A.
    Plazzer, J. P.
    Georges, C.
    Fennell, L.
    Skinner, L.
    Mcmurrick, P.
    Abud, H.
    JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2023, 38 : 32 - 33
  • [39] Anti-KRAS siRNA nanoparticles for targeted colorectal cancer therapy.
    Krasnick, Bradley
    Strand, Matthew S.
    Bi, Ye
    Goedegebuure, Peter S.
    Fleming, Timothy
    Wickline, Samuel A.
    Pan, Hua
    Fields, Ryan C.
    JOURNAL OF CLINICAL ONCOLOGY, 2017, 35 (04)
  • [40] Correlation of KRAS Mutation and Villous Adenoma in Colorectal Adenocarcinoma Guides Pretreatment Screening and Targeted Therapy
    Chen, H.
    Lefferts, J. A.
    Tsongalis, G. J.
    Suriawinata, A.
    MODERN PATHOLOGY, 2010, 23 : 140A - 140A