Epidermal growth factor receptor-targeted therapy for pancreatic cancer

被引:24
作者
Papageorgio, Chris [1 ]
Perry, Michael C. [1 ]
机构
[1] Univ Missouri, Ellis Fischel Canc Ctr, Columbia, MO 65203 USA
关键词
targeted therapy; epidermal growth factor; tyrosine kinase; angiogenesis;
D O I
10.1080/07357900701522653
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Clinical and experimental work supports the view that the epidermal growth factor receptor (EGFR) is a relevant target for cancer therapy. Expression of EGFR is exaggerated in pancreatic adenocarcinoma and activation of EGFR appears to have an important role in the growth and differentiation of this and other types of cancers. EGFR-targeted therapeutic approaches have shown clinical activity in advanced human cancers for which chemotherapy over the last 30 years has sustained a mere palliative role at best. Therefore, the need remains for novel anticancer therapies that effectively and specifically target epithelial tumor cells while minimizing the toxic side-effects commonly associated with cytotoxic conventional therapies. Agents capable of inhibiting EGFR activity with resultant inhibition of cell proliferation and angiogenesis have significant potential as chemotherapeutic agents for the treatment of pancreatic adenocarcinomas as well as multiple other malignancies.
引用
收藏
页码:647 / 657
页数:11
相关论文
共 155 条
[31]   Is the therapeutic index better with gemcitabine-based chemoradiation than with 5-fluorouracil-based chemoradiation in locally advanced pancreatic cancer? [J].
Crane, CH ;
Abbruzzese, JL ;
Evans, DB ;
Wolff, RA ;
Ballo, MT ;
Delclos, M ;
Milas, L ;
Mason, K ;
Charnsangavej, C ;
Pisters, PWT ;
Lee, JE ;
Lenzi, R ;
Vauthey, JN ;
Wong, ABS ;
Phan, T ;
Nguyen, Q ;
Janjan, NA .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2002, 52 (05) :1293-1302
[32]   Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer [J].
Cunningham, D ;
Humblet, Y ;
Siena, S ;
Khayat, D ;
Bleiberg, H ;
Santoro, A ;
Bets, D ;
Mueser, M ;
Harstrick, A ;
Verslype, C ;
Chau, I ;
Van Cutsem, E .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (04) :337-345
[33]   Epidermal growth factor receptor dimerization and activation require ligand-induced conformational changes in the dimer interface [J].
Dawson, JP ;
Berger, MB ;
Lin, CC ;
Schlessinger, J ;
Lemmon, MA ;
Ferguson, KM .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (17) :7734-7742
[34]   Epidermal growth factor receptor: Is a novel therapeutic target for pancreatic cancer? [J].
Dhar, A ;
Mehta, S ;
Banerjee, S ;
Dhar, K ;
Dhar, G ;
Sengupta, K ;
Ray, G ;
Banerjee, SK ;
Campbell, DR .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2005, 10 :1763-1767
[35]   EGFR mutations and molecularly targeted therapy:: a new era in the treatment of lung cancer [J].
Dowell, JE ;
Minna, JD .
NATURE CLINICAL PRACTICE ONCOLOGY, 2006, 3 (04) :170-171
[36]  
Erickson BA, 1998, J SURG ONCOL, V67, P203, DOI 10.1002/(SICI)1096-9098(199803)67:3<203::AID-JSO12>3.0.CO
[37]  
2-2
[38]  
Erlichman C, 2001, CANCER RES, V61, P739
[39]  
FAN Z, 1993, CANCER RES, V53, P4637
[40]   Cetuximab and irinotecan/5-fluorouracil/folinic acid is a safe combination for the first-line treatment of patients with epidermal growth factor receptor expressing metastatic colorectal carcinoma [J].
Folprecht, G ;
Lutz, MP ;
Schöffski, P ;
Seufferlein, T ;
Nolting, A ;
Pollert, P ;
Köhne, CH .
ANNALS OF ONCOLOGY, 2006, 17 (03) :450-456