All about KRAS for clinical oncology practice: Gene profile, clinical implications and laboratory recommendations for somatic mutational testing in colorectal cancer

被引:42
作者
Linardou, Helena [3 ]
Briasoulis, Evangelos [5 ]
Dahabreh, Issa J. [6 ]
Mountzios, Giannis [7 ]
Papadimitriou, Christos [8 ]
Papadopoulos, Savvas [9 ]
Bafaloukos, Dimitrios [3 ]
Kosmidis, Paris [4 ]
Murray, Samuel [1 ,2 ]
机构
[1] BioMarker Solut, London, England
[2] GeneKOR, Dept Mol Oncol, Athens, Greece
[3] Metropolitan Hosp, Dept Med Oncol 1, Athens, Greece
[4] Hygeia Hosp, Dept Med Oncol 2, Athens, Greece
[5] Univ Ioannina, Sch Med, GR-45110 Ioannina, Greece
[6] Tufts Med Ctr, Inst Clin Res & Hlth Policy Studies, Ctr Clin Evidence Synth, Boston, MA USA
[7] 251 Airforce Gen Hosp, Dept Med Oncol & Translat Res, Athens, Greece
[8] Univ Athens, Sch Med, Dept Clin Therapeut, Alexandra Hosp, GR-11527 Athens, Greece
[9] Hygeia Hosp, Dept Pathol, Athens, Greece
关键词
KRAS; Candidate; Biomarker; Predictive; Prognostic; Metastatic colorectal cancer; Cetuximab; Panitumumab; K-RAS MUTATIONS; GROWTH-FACTOR-RECEPTOR; CELL LUNG-CANCER; TYROSINE KINASE INHIBITORS; CETUXIMAB PLUS IRINOTECAN; PLASMA-MEMBRANE LOCALIZATION; GTPASE-ACTIVATING PROTEINS; PROGRESSION-FREE-SURVIVAL; PREDICT DISEASE-CONTROL; MELTING CURVE ANALYSIS;
D O I
10.1016/j.ctrv.2010.07.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The KRAS oncogene has been extensively studied for more than three decades, however, it is only recently that it attained a central role in the clinical decision-making process for the practicing oncologist. Recently, based on retrospective analyses of large randomized clinical trials, the use of anti-epidermal growth factor (EGFR) monoclonal antibodies, cetuximab and panitumumab, was restricted to patients with metastatic colorectal cancer that carry the "wild-type" KRAS genotype. Challenges remain in the laboratory implementation of KRAS mutational testing and the clinical application of the test for treatment planning. This review attempts to offer a global view of KRAS biology, its functional role in cell signaling, mechanisms of resistance to anti-EGFR agents and its predictive potential in metastatic colorectal cancer. We also survey the growing list of candidate biomarkers that may shortly supplement KRAS in routine clinical patient stratification. Finally, we discuss practical aspects of KRAS testing that may be useful for those involved in mutational screening in their centers. This general overview of KRAS for clinical oncology practice aims to assist in data interpretation and offer insight into potential pitfalls of mutational testing. KRAS is a prime example of how translational research can fulfill the promises of personalized medicine for tailoring treatment to match the underlying tumor biology. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:221 / 233
页数:13
相关论文
共 118 条
[1]   Small molecules with EGFR-TK inhibitor activity [J].
Albanell, J ;
Gascón, P .
CURRENT DRUG TARGETS, 2005, 6 (03) :259-274
[2]   American Society of Clinical Oncology Provisional Clinical Opinion: Testing for KRAS Gene Mutations in Patients With Metastatic Colorectal Carcinoma to Predict Response to Anti-Epidermal Growth Factor Receptor Monoclonal Antibody Therapy [J].
Allegra, Carmen J. ;
Jessup, J. Milburn ;
Somerfield, Mark R. ;
Hamilton, Stanley R. ;
Hammond, Elizabeth H. ;
Hayes, Daniel F. ;
McAllister, Pamela K. ;
Morton, Roscoe F. ;
Schilsky, Richard L. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (12) :2091-2096
[3]   Wild-type KRAS is required for panitumumab efficacy in patients with metastatic colorectal cancer [J].
Amado, Rafael G. ;
Wolf, Michael ;
Peeters, Marc ;
Van Cutsem, Eric ;
Siena, Salvatore ;
Freeman, Daniel J. ;
Juan, Todd ;
Sikorski, Robert ;
Suggs, Sid ;
Radinsky, Robert ;
Patterson, Scott D. ;
Chang, David D. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (10) :1626-1634
[4]   Kirsten ras mutations in patients with colorectal cancer:: the 'RASCAL II' study [J].
Andreyev, HJN ;
Norman, AR ;
Cunningham, D ;
Oates, J ;
Dix, BR ;
Iacopetta, BJ ;
Young, J ;
Walsh, T ;
Ward, R ;
Hawkins, N ;
Beranek, M ;
Jandik, P ;
Benamouzig, R ;
Jullian, E ;
Laurent-Puig, P ;
Olschwang, S ;
Muller, O ;
Hoffmann, I ;
Rabes, HM ;
Zietz, C ;
Troungos, C ;
Valavanis, C ;
Yuen, ST ;
Ho, JWC ;
Croke, CT ;
O'Donoghue, DP ;
Giaretti, W ;
Rapallo, A ;
Russo, A ;
Bazan, V ;
Tanaka, M ;
Omura, K ;
Azuma, T ;
Ohkusa, T ;
Fujimori, T ;
Ono, Y ;
Pauly, M ;
Faber, C ;
Glaesener, R ;
de Goeij, AFPM ;
Arends, JW ;
Andersen, SN ;
Lövig, T ;
Breivik, J ;
Gaudernack, G ;
Clausen, OPF ;
De Angelis, P ;
Meling, GI ;
Rognum, TO ;
Smith, R .
BRITISH JOURNAL OF CANCER, 2001, 85 (05) :692-696
[5]   Kirsten ras mutations in patients with colorectal cancer: the multicenter "RASCAL" study [J].
Andreyev, HJN ;
Norman, AR ;
Cunningham, D ;
Oates, JR ;
Clarke, PA .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (09) :675-684
[6]  
[Anonymous], MED ONCOL
[7]   Mind the GAP, Rho, Rab and GDI [J].
Antonarakis, SE ;
Van Aelst, L .
NATURE GENETICS, 1998, 19 (02) :106-108
[8]   Usefulness of Peptide Nucleic Acid (PNA)-Clamp Smart Amplification Process Version 2 (SmartAmp2) for Clinical Diagnosis of KRAS Codon 12 Mutations in Lung Adenocarcinoma Comparison of PNA-Clamp SmartAmp2 and PCR-Related Methods [J].
Araki, Takuya ;
Shimizu, Kimihiro ;
Nakamura, Katsunori ;
Nakamura, Tomonori ;
Mitani, Yasumasa ;
Obayashi, Kyoko ;
Fujita, Yukiyoshi ;
Kakegawa, Seiichi ;
Miyamae, Yohei ;
Kaira, Kyoichi ;
Ishidao, Takefumi ;
Lezhava, Alexander ;
Hayashizaki, Yoshihide ;
Takeyoshi, Izumi ;
Yamamoto, Koujirou .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2010, 12 (01) :118-124
[9]   Novel agents in the era of targeted therapy: what have we learned and how has our practice changed? [J].
Baselga, J. .
ANNALS OF ONCOLOGY, 2008, 19 :281-288
[10]   Impact of FcγRIIa-FcγRIIIa Polymorphisms and KRAS Mutations on the Clinical Outcome of Patients With Metastatic Colorectal Cancer Treated With Cetuximab Plus Irinotecan [J].
Bibeau, Frederic ;
Lopez-Crapez, Evelyne ;
Di Fiore, Frederic ;
Thezenas, Simon ;
Ychou, Marc ;
Blanchard, France ;
Lamy, Aude ;
Penault-Llorca, Frederique ;
Frebourg, Thierry ;
Michel, Pierre ;
Sabourin, Jean-Christophe ;
Boissiere-Michot, Florence .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (07) :1122-1129