Cetuximab plus FOLFOX6 or FOLFIRI in metastatic colorectal cancer: CECOG trial

被引:92
作者
Ocvirk, Janja [2 ]
Brodowicz, Thomas [1 ]
Wrba, Fritz [3 ]
Ciuleanu, Tudor E. [4 ]
Kurteva, Galina [5 ]
Beslija, Semir [6 ]
Koza, Ivan [7 ]
Zsuzsanna Papai [8 ]
Messinger, Diethelm [9 ]
Yilmaz, Ugur [10 ]
Zsolt Faluhelyi [11 ]
Yalcin, Suayib [12 ]
Papamichael, Demetris [13 ]
Miklos Wenczl [14 ]
Mrsic-Krmpotic, Zrinka [15 ]
Shacham-Shmueli, Einat [16 ]
Vrbanec, Damir [17 ]
Esser, Regina [18 ]
Scheithauer, Werner [1 ]
Zielinski, Christoph C. [1 ]
机构
[1] Med Univ Vienna, Dept Med 1, Clin Div Oncol, A-1090 Vienna, Austria
[2] Inst Oncol, Ljubljana 1000, Slovenia
[3] Med Univ Vienna, Clin Inst Pathol, A-1090 Vienna, Austria
[4] Inst Oncol Cluj, Cluj Napoca 400015, Romania
[5] Natl Specialized Hosp Act Treatment Oncol, Dept Oncol, Sofia 1754, Bulgaria
[6] Univ Sarajevo, Ctr Clin, Inst Oncol, Sarajevo 71000, Bosnia & Herceg
[7] Natl Canc Inst, Dept Oncol, Bratislava 83310, Slovakia
[8] AEK Onkol Osztaly, H-1122 Budapest, Hungary
[9] IST GmbH, Biometr, D-68219 Mannheim, Germany
[10] 9 Eylul Univ, Fac Med, Dept Gastroenterol, TR-35340 Izmir, Turkey
[11] Veszprem Cty Hosp, Dept Oncol, H-8200 Veszprem, Hungary
[12] Ankara Hacettepe Univ, Inst Oncol, TR-06100 Ankara, Turkey
[13] Bank Cyprus Oncol Ctr, Dept Med Oncol, CY-2006 Nicosia, Cyprus
[14] Markusovszky Teaching Hosp, Dept Oncoradiol, H-9700 Szombathely, Hungary
[15] Univ Zagreb, Univ Hosp Tumors, Dept Med Oncol, Zagreb 10000, Croatia
[16] Tel Aviv Sourasky Med Ctr, Div Oncol, IL-64239 Tel Aviv, Israel
[17] KBC Rebro, Dept Oncol, Zagreb 10000, Croatia
[18] Merck KGaA, D-64293 Darmstadt, Germany
关键词
Cetuximab; 5-fluorouracil folinic acid and oxaliplatin; 5-fluorouracil folinic acid and irinotecan; KRAS; Metastatic colorectal cancer; GROWTH-FACTOR RECEPTOR; MULTICENTER RANDOMIZED-TRIAL; K-RAS MUTATIONS; 1ST-LINE TREATMENT; FLUOROURACIL; LEUCOVORIN; KRAS; OXALIPLATIN; IRINOTECAN; CARCINOMA;
D O I
10.3748/wjg.v16.i25.3133
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate efficacy and safety of cetuximab combined with two chemotherapy regimens in patients with unresectable metastatic colorectal cancer (mCRC). METHODS: Randomized patients received cetuximab with 5-fluorouracil (5-FU), folinic acid (FA) and oxaliplatin (FOLFOX) 6 (arm A, n = 74) or 5-FU, FA and irinotecan (FOLFIRI) (arm B, n = 77). KRAS mutation status was determined retrospectively in a subset of tumors (n = 117). RESULTS: No significant difference was found between treatment arms A and B in the progression-free survival (PFS) rate at 9 mo, 45% vs 34%; median PFS, 8.6 mo vs 8.3 mo [hazard ratio (HR) = 1.06]; overall response rate (ORR) 43% vs 45% [odds ratio (OR) = 0.93] and median overall survival (OS), 17.4 mo vs 18.9 mo (HR = 0.98). Patients with KRA5 wild-type tumors demonstrated improved PFS (HR = 0.55, P = 0.0051), OS, (HR = 0.62, P = 0.0296) and ORR (53% vs 36%) and in arm A, improved PFS (HR = 0.49, P = 0.0196), OS (HR = 0.48, P = 0.0201) and ORR (56% vs 30%), compared with patients with KRAS mutated tumors. In arm B no significant differences were found in efficacy by KRAS mutation status. Treatment in arms A and B was generally well tolerated. CONCLUSION: This study confirms that combinations of cetuximab with FOLFOX6 or FOLFIRI are effective and significantly improve clinical outcome in KRAS wild-type compared with KRAS mutated mCRC. (C) 2010 Baishideng. All rights reserved.
引用
收藏
页码:3133 / 3143
页数:11
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