Previous Page  17 / 40 Next Page
Information
Show Menu
Previous Page 17 / 40 Next Page
Page Background

CAIRO5: NCT02162563 (Phase III)

1

Study sponsor: Dutch Colorectal Cancer Group (DCCG).

Liver-limited mCRC

Unresectable

(N ~ 640)

R

WT RAS/

BRAF and

left-sided

primary

MT RAS/

BRAF

and/or

right-sided

primary

R

Panitumumab 6 mg/kg

+ FOLFOX or FOLFIRI

Q2W

Bevacizumab 5 mg/kg

+ FOLFOX or FOLFIRI

Q2W

Bevacizumab

5 mg/kg

+ FOLFOX or FOLFIRI

Q2W

Bevacizumab 5 mg/kg

+ FOLFOXIRI

Q2W

Stratification factors include:

Resectability of liver metastases

(potentially resectable vs

permanently unresectable)

1. Huiskens J, et al. BMC Cancer 2015;15:365; ClinicalTrials.gov identifier: NCT02162563 (accessed 08-03-18)

2. ClinicalTrials.gov identifier: NCT02885753 (accessed 08-03-18)

OSCAR: NCT02885753 (Phase III)

2

Study sponsor: Federation Francophone de Cancerologie Digestive

Liver-limited mCRC

(N

~

268)

Panitumumab 6 mg/kg (WT RAS) or bevacizumab 5 mg/kg (MT RAS) +

oxaliplatin 85 mg/m

2

intra-arterial

+ LV5FU2

Q2W

R

Panitumumab 6 mg/kg (WT RAS) or bevacizumab 5 mg/kg (MT RAS) +

oxaliplatin 85 mg/m2 intravenous

+ LV5FU2† Q2W

Treatment until PD or toxicity

Baseline ctDNA

Early response (Day 28) evaluation by ctDNA