Are RAS mutations predictive markers of resistance to standard chemotherapy?

被引:64
作者
Loriot, Yohann [1 ]
Mordant, Pierre [2 ]
Deutsch, Eric [2 ]
Olaussen, Ken Andre [3 ]
Soria, Jean-Charles [1 ]
机构
[1] Univ Paris 11, Inst Gustave Roussy, SITEP, Dept Med, F-94805 Villejuif, France
[2] Univ Paris 11, Inst Gustave Roussy, UPRES 2710, F-94805 Villejuif, France
[3] Univ Paris 11, Inst Gustave Roussy, Translat Res Lab, F-94805 Villejuif, France
关键词
CELL LUNG-CANCER; HUMAN-COLON-CANCER; K-RAS; COLORECTAL-CANCER; MICROSATELLITE INSTABILITY; ADJUVANT CHEMOTHERAPY; RANDOMIZED-TRIAL; GENE-EXPRESSION; B-RAF; KRAS;
D O I
10.1038/nrclinonc.2009.106
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
KRAS mutations may be predictive of resistance to anti-EGFR monoclonal-based therapy in patients with colorectal cancer (CRC). Screening for KRAS mutations in patients with CRC and non-small-cell lung cancer (NSCLC) may provide additional information on optimizing treatment options with targeted therapies. Only limited studies, however, have assessed the predictive value of KRAS mutations in response to conventional chemotherapy. We reviewed all relevant papers investigating the association of KRAS mutations and conventional chemotherapy-related outcome in NSCLC, CRC, and other solid tumors, both in the adjuvant and advanced settings. Our Review strongly suggests that KRAS mutations have no value in response prediction to conventional chemotherapy in NSCLC, CRC and other solid tumors. Therefore, KRAS mutations should not be used as molecular predictors of response to conventional chemotherapy.
引用
收藏
页码:528 / 534
页数:7
相关论文
共 54 条
[51]   H-RAS TRANSFECTION IN MINK LUNG EPITHELIAL-CELLS MAY INDUCE ATYPICAL MULTIDRUG RESISTANCE [J].
WISHART, GC ;
PLUMB, JA ;
SPANDIDOS, DA ;
KERR, DJ .
EUROPEAN JOURNAL OF CANCER, 1991, 27 (05) :673-673
[52]   Gallbladder cancer: Lessons from a rare tumour [J].
Wistuba, II ;
Gazdar, AF .
NATURE REVIEWS CANCER, 2004, 4 (09) :695-706
[53]   Ability to acquire drug resistance arises early during the tumorigenesis process [J].
Yague, Ernesto ;
Arance, Ana ;
Kubitza, Loic ;
O'Hare, Michael ;
Jat, Parmjit ;
Ogilvie, Caroline M. ;
Hart, Ian R. ;
Higgins, Christopher F. ;
Raguz, Selina .
CANCER RESEARCH, 2007, 67 (03) :1130-1137
[54]  
ZALCMAN G, 2008, ASCO M, V26