Pharmacodiagnostic testing in breast cancer - Focus on HER2 and trastuzumab therapy

被引:22
作者
Bartlett, JMS [1 ]
机构
[1] Univ Glasgow, Glasgow Royal Infirm, Sect Surg & Translat Res, Div Canc Sci & Mol Pathol,Endocrine Canc Grp,Dept, Glasgow G31 2ER, Lanark, Scotland
关键词
D O I
10.2165/00129785-200505050-00003
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Pharmacogenomics is defined as research into inherited genetic variations that determine an individual's response to therapeutic agents. In oncology, pharmacogenomics based on somatic molecular alterations inherited by subsequent cancer cell generations forms the basis of molecular targeting of novel therapeutic agents. What has emerged from clinical experience with such agents is the need for appropriate pharmacodiagnostic approaches to ensure the drugs are correctly targeted. Given the broad range of pharmacogenomic agents currently under evaluation for cancer therapy, it appears that a rapid extension of pharmacodiagnostic profiling will be required in the next 5-10 years, if not sooner. If this is to be successfully achieved, lessons learned in the past, particularly during the development of HER2 (ERBB2) testing for directing trastuzumab therapy in breast cancer, may provide a valuable framework for the development of future pharmacodiagnostic assays system. This article reviews the biological and clinical rationale for targeting breast cancer with trastuzumab and the steps taken to validate and improve pharmacodiagnostic procedures for testing tumor HER2 protein expression and HER2 gene amplification. Attention is given to quality assurance and reproducibility of testing approaches and the optimal selection of patients for response to trastuzumab. This approach serves as a paradigm for the future development of pharmacodiagnostic tests in oncology.
引用
收藏
页码:303 / 315
页数:13
相关论文
共 143 条
[1]   An overview of targeted treatments in cancer [J].
Abou-Jawde, R ;
Choueiri, T ;
Alemany, C ;
Mekhail, T .
CLINICAL THERAPEUTICS, 2003, 25 (08) :2121-2137
[2]   Agreement between chromogenic in situ hybridisation (CISH) and FISH in the determination of HER2 status in breast cancer [J].
Arnould, L ;
Denoux, Y ;
MacGrogan, G ;
Penault-Llorca, F ;
Fiche, M ;
Treilleux, I ;
Mathieu, MC ;
Vincent-Salomon, A ;
Vilain, MO ;
Couturier, J .
BRITISH JOURNAL OF CANCER, 2003, 88 (10) :1587-1591
[3]   Immunohistochemical detection of EGFR in paraffin-embedded tumor tissues:: Variation in staining intensity due to choice of fixative and storage time of tissue sections [J].
Atkins, D ;
Reiffen, KA ;
Tegtmeier, CL ;
Winther, H ;
Bonato, MS ;
Störkel, S .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2004, 52 (07) :893-901
[4]   The clinical evaluation of HER-2 status: which test to use? [J].
Bartlett, J ;
Mallon, E ;
Cooke, T .
JOURNAL OF PATHOLOGY, 2003, 199 (04) :411-417
[5]   Type I receptor tyrosine kinases are associated with hormone escape in prostate cancer [J].
Bartlett, JMS ;
Brawley, D ;
Grigor, K ;
Munro, AF ;
Dunne, B ;
Edwards, J .
JOURNAL OF PATHOLOGY, 2005, 205 (04) :522-529
[6]   Is chromosome 9 loss a marker of disease recurrence in transitional cell carcinoma of the urinary bladder? [J].
Bartlett, JMS ;
Watters, AD ;
Ballantyne, SA ;
Going, JJ ;
Grigor, KM ;
Cooke, TG .
BRITISH JOURNAL OF CANCER, 1998, 77 (12) :2193-2198
[7]  
Bartlett JMS, 2001, BREAST CANCER RES TR, V69, P277
[8]   Evaluating HER2 amplification and overexpression in breast cancer [J].
Bartlett, JMS ;
Going, JJ ;
Mallon, EA ;
Watters, AD ;
Reeves, JR ;
Stanton, P ;
Richmond, J ;
Donald, B ;
Ferrier, R ;
Cooke, TG .
JOURNAL OF PATHOLOGY, 2001, 195 (04) :422-428
[9]  
BARTLETT JMS, 2003, CURR DIAGN PATHOL, V9, P48
[10]   Treating cancer's kinase 'addiction' [J].
Baselga, J ;
Arribas, J .
NATURE MEDICINE, 2004, 10 (08) :786-787