Molecularly targeted therapies for colorectal cancer: Strategies for implementing translational research in clinical trials

被引:0
|
作者
Zwierzina, Heinz [1 ]
Bardelli, Alberto [2 ]
Ciardiello, Fortunato [3 ]
Gariboldi, Manuela [4 ]
Hakansson, Leif [5 ,6 ]
Lambrechts, Diether [7 ]
Lind, Guro E. [8 ]
Loeffler-Ragg, Judith [1 ]
Schmoll, Hans [9 ]
Siena, Salvatore [10 ]
Tabernero, Josep [11 ]
Van Cutsem, Eric [12 ]
机构
[1] Med Univ Klin, A-6020 Innsbruck, Austria
[2] Inst Canc Res & Treatment, I-10060 Turin, Italy
[3] Univ Naples 2, Dipartimento Med Chirurg Internist Clin & Sperime, I-80131 Naples, Italy
[4] IRCCS Ist Nazl Tumori, Dept Expt Oncol & Mol Med, Fdn Milan, I-20133 Milan, Italy
[5] Linkoping Univ Hosp, Div Clin Tumorimmunol, SE-58183 Linkoping, Sweden
[6] Linkoping Univ Hosp, Dept Oncol, SE-58183 Linkoping, Sweden
[7] VRC, B-3000 Louvain, Belgium
[8] Norwegian Radium Hosp, Rikshosp, Univ Hosp, Dept Canc Prevent, N-0379 Oslo, Norway
[9] Univ Clin Halle, Univ Halle Wittenberg, DE-06120 Halle, Germany
[10] Osped Niguarda Ca Granda, Dipartimento Oncol, Div Oncol Falck, I-20162 Milan, Italy
[11] P Vall Hebron Univ Hosp, Dept Med Oncol, Barcelona 08035, Spain
[12] Univ Hosp Gasthuisberg, Digest Oncol Unit, B-3000 Louvain, Belgium
关键词
Biomarker; colorectal cancer; drug development; EGFR; Fc gamma receptor; immunotherapy; translational research; VEGF; ENDOTHELIAL GROWTH-FACTOR; PATIENT-REPORTED OUTCOMES; PROGRESSION-FREE SURVIVAL; METASTATIC BREAST-CANCER; GENE COPY NUMBER; FACTOR RECEPTOR; MONOCLONAL-ANTIBODY; KRAS STATUS; PHASE-II; CETUXIMAB;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Few breakthroughs in preclinical research have translated into meaningful benefits, either in clinical terms or quality of life, for patients with advanced colorectal cancer, despite important preclinical discoveries regarding aberrant biological pathways associated with disease development and progression. The many reasons for the slow progress are diverse, ranging from the failure to codevelop biomarkers and targeted therapies, the regulatory burdens imposed on academic investigators, and the failure to collect serial tumor biopsies during clinical trials. This review discusses promising translational research that could help reduce the disparity between preclinical discovery and patient benefit, and advocate the concentration of efforts and resources on the most promising therapeutic targets in colorectal cancer, such as EGFR, VEGF and Fc gamma receptor.
引用
收藏
页码:703 / 711
页数:9
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