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. 2016 Mar 30;4(6):1017–1024. doi: 10.3892/mco.2016.836

Table I.

Baseline characteristics of patients in the trials included in the meta-analysis.

Authors, year Clinical trial Type of study Treatment regimen Subgroup analysis Refs.
Maughan et al, 2011 COIN Phase III Oxa+FU vs. Oxa+FU+cet KRAS BRAF (4)
Bokemeyer et al, 2011 OPUS Phase II FOLFOX-4+cet vs. FOLFOX-4 ITT KRAS BRAF (3)
Van Cutsem et al, 2011 CRYSTAL Phase III FOLFIRI vs. FOLFIRI+cet ITT KRAS BRAF (2)
Tveita et al, 2012 NORDIC-VII Phase III A; Nordic FLOX B: FLOX+cet C: intermittent FLOX +cet ITT KRAS (5)
Stintzing et al, 2012 AIO-0306 Phase III FOLFIRI+cet vs. FOLFIRI +bev ITTb (17)
Ye et al, 2013 Phase III CT+cet vs. CT ITTc (19)
Heinemann et al, 2014 FIRE-3 Phase III FOLFIRI +cet vs. FOLFORI +bev ITTc KRAS RAS (18)
Van Cutsem et al, 2015 CRYSTAL Phase III FOLFIRI vs. FOLFIRI+cet KRAS RAS (16)
Bokemeyer et al, 2015 OPUS Phase II FOLFOX-4+cet vs. FOLFOX-4 KRAS RAS (20)
a

Tveit 1: arms B vs. A; Tveit 2: arms C vs. arms A.

b

Among the whole population with data available on KRAS-mt status.

c

Among the whole population with data available about KRAS-wt status. cet, cetuximab; bev; bevacizumab; Oxa + FU, oxaliplatin + fluoropyrimidine; FOLFOX-4, 5-fluoropyrimidine + folinic acid + oxaliplatin; FOLFIRI, fluorouracil + leucovorin + irinotecan; Nordic FLOX, fluorouracil/folinic acid and oxaliplatin; FLOX, oxaliplatin + fluoropyrimidine; CT, FOLFIRI (fluorouracil + leucovorin + irinotecan) or mFOLFOX6 (modified fluorouracil + leucovorin + oxaliplatin); ITT, intention-to-treat.