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. 2012 Nov 30;7(11):e50925. doi: 10.1371/journal.pone.0050925

Table 1. Randomized controlled trials (OXA+anti-EGFR vs OXA alone).

Studies Intervention Patients (KRASwild typepopulation) Median follow-up(mo) Median OS and95%CI(mo) HR and 95%CI for OS Median PFSand 95%CI(mo) HR and 95%CI for PFS ORR KRAS test Jadadscore
COIN [13] FOLFOX/XELOX 367 21 17.9(no report) 1.04 [0.88, 1.22] 8.6(no report) 0.96 [0.82, 1.12] 57% Prospective 3
FOLFOX/XELOX+Cetuximab 362 23 17.0(no report) 8.6(no report) 64%
Nordic VII [14] FLOX 97 No report 22.0(17.9 to 26.1) 1.14 [0.80, 1.62] 8.7(7.4 to 9.9) 1.07 [0.79, 1.45] 47% Prospective 3
FLOX+Cetuximab 97 No report 20.1(14.5 to 25.7) 7.9(6.3 to 9.5) 46%
OPUS [11], [12] FOLFOX4 97 No report 18.5(no report) 0.85 [0.60, 1.22] 7.2(no report) 0.57 [0.38, 0.86] 37% Retrospective 3
FOLFOX4+Cetuximab 82 No report 22.8(no report) 8.3(no report) 59%
PRIME [15], [16] FOLFOX4 325 12.5 19.7(17.6 to 22.7) 0.88 [0.73, 1.06] 8.6(7.5 to 9.5) 0.80 [0.67, 0.95] 48% Prospective 3
FOLFOX4+Panitumumab 331 13.2 23.9(20.3 to 27.7) 10.0(9.3 to 11.4) 55%

FOLFOX in COIN study: oxaliplatin 85 mg/m2 on day 1, L-folinic acid 175 mg or D,L-folinic acid 350 mg on day 1, FU 400 mg/m2 bolus and FU 2400 mg/m2 infusion over 46 h. Every 2 weeks.

XELOX in COIN study: oxaliplatin 130 mg/m2 on day 1, capecitabine 850 mg/m2 twice a day on day 1 to 14. Every 3 weeks.

Cetuximab in COIN study: an initial dose of 400 mg/m2 and thereafter 250 mg/m2. Every week.

FLOX in NORDIC VII study: oxaliplatin 85 mg/m2 on day 1, FU 500 mg/m2 bolus +FA 60 mg/m2 bolus on days 1 and 2. Every 2 weeks.

Cetuximab in NORDIC VII study: an initial dose of 400 mg/m2 and thereafter 250 mg/m2. Every week.

FOLFOX4 in OPUS study: oxaliplatin 85 mg/m2 on day 1, leucovorin 200 mg/m2 followed by FU 400 mg/m2 bolus and 600 mg/m2 22-hour continuous infusion on days 1 and 2. Every 2 weeks.

Cetuximab in OPUS study: an initial dose of 400 mg/m2 and thereafter 250 mg/m2. Every week.

FOLFOX4 in PRIME study: oxaliplatin 85 mg/m2 on day 1, leucovorin 200 mg/m2 followed by FU 400 mg/m2 bolus and 600 mg/m2 22-hour continuous infusion on days 1 and 2. Every 2 weeks.

Panitumumab in PRIME study: 6 mg/kg. Every 2 weeks.