EpCAM an immunotherapeutic target for gastrointestinal malignancy: current experience and future challenges

被引:77
作者
Chaudry, M. A.
Sales, K.
Ruf, P.
Lindhofer, H.
Winslet, M. C.
机构
[1] UCL Royal Free & UCL Med Sch, Univ Dept, London NW3 2XA, England
[2] Trion Res GmbH, D-82152 Martinsried, Germany
[3] Trion Pharma GmbH, D-80807 Munich, Germany
关键词
EpCam; immunotherapy; trifunctional antibodies;
D O I
10.1038/sj.bjc.6603505
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite advances in surgery and adjuvant regimes, gastrointestinal malignancy remains a major cause of neoplastic mortality. Immunotherapy is an emerging and now successful treatment modality for numerous cancers that relies on the manipulation of the immune system and its effector functions to eradicate tumour cells. The discovery that the pan-epithelial homotypic cell adhesion molecule EpCAM is differentially expressed on gastrointestinal tumours has made this a viable target for immunotherapy. Clinical trials using naked anti EpCAM antibody, immunoconjugates, anti-idiotypic and dendritic cell vaccines have met variable success. The murine IgG2a Edrecolomab was shown to reduce mortality and morbidity at a level slightly lower than treatment with 5FU and Levamisole when administered to patients with advanced colorectal carcinoma in a large randomised controlled trial. Fully human and trifunctional antibodies that specifically recruit CD3-positive lymphocytes are now being tested clinically in the treatment of minimal residual disease and ascites. Although clinical trials are in their infancy, the future may bring forth an EpCAM mediated approach for the effective activation and harnessing of the immune system to destroy a pathological aberrance that has otherwise largely escaped its attention.
引用
收藏
页码:1013 / 1019
页数:7
相关论文
共 30 条
[1]   Inhibitory Fc receptors modulate in vivo cytoxicity against tumor targets [J].
Clynes, RA ;
Towers, TL ;
Presta, LG ;
Ravetch, JV .
NATURE MEDICINE, 2000, 6 (04) :443-446
[2]   MUC1 in carcinoma-host interactions [J].
Denda-Nagai, K ;
Irimura, T .
GLYCOCONJUGATE JOURNAL, 2000, 17 (7-9) :649-658
[3]   Monoclonal antibodies targeting cancer: 'magic bullets' or just the trigger? [J].
Eccles, SA .
BREAST CANCER RESEARCH, 2001, 3 (02) :86-90
[4]  
FAGERBERG J, 1995, CANCER RES, V55, P1824
[5]   Ep-CAM overexpression in breast cancer as a predictor of survival [J].
Gastl, G ;
Spizzo, G ;
Obrist, P ;
Dünser, M ;
Mikuz, G .
LANCET, 2000, 356 (9246) :1981-1982
[6]   Trastuzumab, a recombinant DNA-derived humanized monoclonal antibody, a novel agent for the treatment of metastatic breast cancer [J].
Goldenberg, MM .
CLINICAL THERAPEUTICS, 1999, 21 (02) :309-318
[7]  
Hainsworth JD, 2000, SEMIN ONCOL, V27, P25
[8]   Immunotherapy of malignant ascites with trifunctional antibodies [J].
Heiss, MM ;
Ströhlein, MA ;
Jäger, M ;
Kimmig, R ;
Burges, A ;
Schoberth, A ;
Jauch, KW ;
Schildberg, FW ;
Lindhofer, H .
INTERNATIONAL JOURNAL OF CANCER, 2005, 117 (03) :435-443
[9]  
HERLYN D, 1994, CELL BIOPHYS, V24-5, P143, DOI 10.1007/BF02789225
[10]   IMMUNOMODULATORY ACTIVITY OF MONOCLONAL ANTIIDIOTYPIC ANTIBODY TO ANTI-COLORECTAL CARCINOMA ANTIBODY-CO17-1A IN ANIMALS AND PATIENTS [J].
HERLYN, D ;
HARRIS, D ;
ZALOUDIK, J ;
SPERLAGH, M ;
MARUYAMA, H ;
JACOB, L ;
KIENY, MP ;
SCHECK, S ;
SOMASUNDARAM, R ;
HART, E ;
ERTL, H ;
MASTRANGELO, M .
JOURNAL OF IMMUNOTHERAPY, 1994, 15 (04) :303-311