The role of new agents in the treatment of colorectal cancer

被引:27
作者
Folprecht, G [1 ]
Köhne, CH [1 ]
机构
[1] Univ Hosp Carl Gustav Carus, Dept Med 1, DE-01307 Dresden, Germany
关键词
colorectal cancer; chemotherapy; irinotecan; oxaliplatin; capecitabine; UFT; cetuximab;
D O I
10.1159/000076329
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
New drugs improved efficacy or convenience of treatment in metastatic colorectal cancer. The oral fluoropyrimidines capecitabine and UFT are less toxic but equally efficacious relative to intravenous bolus 5- fluorouracil ( 5- FU)/ folinic acid ( FA). These agents might be beneficial for patients who unlikely benefit from the more intensive combination therapy with infusional 5- FU/ FA and irinotecan or oxaliplatin. First- line therapy with irinotecan or oxaliplatin and 5- FU/ FA induces an objective response in up to 50% of the patients and may allow neoadjuvant concepts in unresectable liver metastasis. The combination therapy increased progression- free survival and in the case of irinotecan/ 5- FU/ FA also overall survival when compared to 5- FU/ FA. Sequential treatment with infusional 5- FU/ FA plus oxaliplatin followed by 5- FU/ FA plus irinotecan or vice versa results in a median survival exceeding 20 months. Thus, patients in a good performance status and with favorable prognostic parameters should be offered first- line combination treatment of irinotecan or oxaliplatin with 5- FU/ FA, whereby 5- FU is preferably administered as an infusion for combination therapy. New targets in the treatment of colorectal cancer are the EGF and VEGF receptor. The monoclonal EGF receptor antibody cetuximab alone and in combination with irinotecan is active in second- line treatment. The VEGF antibody bevacizumab prolongs survival when given in combination with 5- FU/ FA and irinotecan. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:1 / 17
页数:17
相关论文
共 113 条
[1]   Phase I trial of weekly irinotecan combined with UFT as second-line treatment for advanced colorectal cancer [J].
Alonso, V ;
Escudero, P ;
Zorrilla, M ;
Isla, MD ;
Herrero, A ;
Mayordomo, JI ;
Martinez-Trufero, J ;
Sáenz, A ;
Tres, A ;
Antón, A .
EUROPEAN JOURNAL OF CANCER, 2001, 37 (18) :2385-2391
[2]   CPT-11 (irinotecan) addition to bimonthly, high-dose leucovorin and bolus and continuous-infusion 5-fluorouracil (FOLFIRI) for pretreated metastatic colorectal cancer [J].
André, T ;
Louvet, C ;
Maindrault-Goebel, F ;
Couteau, C ;
Mabro, M ;
Lotz, JP ;
Gilles-Amar, V ;
Krulik, M ;
Carola, E ;
Izrael, V ;
de Gramont, A .
EUROPEAN JOURNAL OF CANCER, 1999, 35 (09) :1343-1347
[3]  
[Anonymous], 2002, P ASCO
[4]  
[Anonymous], P AM SOC CLIN ONCOL
[5]  
Aschele C, 2002, P AN M AM SOC CLIN, V21, p132a
[6]   Randomized multicenter phase II study comparing a combination of fluorouracil and folinic acid and alternating irinotecan and oxaliplatin with oxaliplatin and irinotecan in fluorouracil-pretreated metastatic colorectal cancer patients [J].
Bécouarn, Y ;
Gamelin, E ;
Coudert, B ;
Négrier, S ;
Pierga, JY ;
Raoul, JL ;
Provençal, J ;
Rixe, O ;
Krisch, C ;
Germa, C ;
Bekradda, M ;
Mignard, D ;
Mousseau, M .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (22) :4195-4201
[7]  
BERGSLAND E, 2000, P AN M AM SOC CLIN, V19, pA242
[8]   Acute cardiotoxicity during capecitabine treatment:: A case report [J].
Bertolini, A ;
Fiumanò, M ;
Fusco, O ;
Muffatti, A ;
Scarinci, A ;
Pontiggia, G ;
Scopelliti, M .
TUMORI, 2001, 87 (03) :200-206
[9]  
BLANKE CD, 2002, P AN M AM SOC CLIN, V21, pA127
[10]   Phase II study of capecitabine and oxaliplatin in first- and second-line treatment of advanced or metastatic colorectal cancer [J].
Borner, MM ;
Dietrich, D ;
Stupp, R ;
Moran, R ;
Honegger, H ;
Wernli, M ;
Herrmann, R ;
Pestalozzi, BC ;
Saletti, P ;
Hanselmann, S ;
Müller, S ;
Brauchli, P ;
Castiglione-Gertsch, M ;
Goldhirsch, A ;
Roth, AD .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (07) :1759-1766