Clinical Drug Experience Knowledgebase

Criteria

Inclusion Criteria:

Metastatic colorectal cancer expressing the wtKRAS status
No previous EGFR targeted therapy.
Must have failed a prior regimen containing irinotecan for metastatic disease and a prior regimen containing oxaliplatin for metastatic disease
Must have previously received a thymidylate synthase inhibitor (eg, fluorouracil, capecitabine, raltitrexed, or fluorouracil-uracil) at any point for treatment of colorectal cancer (CRC)
Life expectancy of at least 3 months.
Patient with ECOG ≤ 1
Patients aged ≥ 18.
Patient with measurable lesions according to RECIST criteria (version 1.1) with spiral CT scan and defined as ≥ 10 mm in longest diameter and 2X the slice thickness for extra nodal lesions and/or > 15 mm in short axis diameter for nodal lesions
Patient able to receive adequate oral nutrition of ≥ 1500 calories per day and free of significant nausea and vomiting

Patient with adequate organ function:

Absolute neutrophil count (ANC) ≥ 1.5 x 109/L
Haemoglobin ≥ 9 g/dL
Platelets (PTL) ≥ 100 x 109/L
AST/ALT ≤ 3 x ULN (≤ 5 x ULN in case of liver metastases)
GammaGT < 3 x ULN (< 5 x ULN in case of liver involvement)
Bilirubin ≤ 1.5 x ULN
Creatinine clearance ≥ 50 mL/min (Cockcroft and Gault formula)
Adequate contraception if applicable.
Ability to take oral medication in the opinion of the investigator
Patient able and willing to comply with study procedures as per protocol
Patient able to understand and willing to sign and date the written voluntary informed consent form at screening visit prior to any protocol-specific procedures
Patient affiliated to a social security regimen

Exclusion Criteria:

Previous EGFR targeted therapy.
Mutant KRAS status
Prior severe reaction to a monoclonal antibody
No heart failure or coronary heart disease symptoms Clinically relevant cardiovascular abnormalities, as judged by the investigator, such as, but not limited to, uncontrolled hypertension, congestive heart failure NYHA classification > III, unstable angina, myocardial infarction within six months prior to randomisation, or poorly controlled arrhythmia
Cardiac left ventricular dysfunction with resting ejection fraction of less than institutional lower limit of normal (if no lower limit of normal is defined in the institution, the lower limit is 50%)
Symptomatic brain metastases requiring treatment
Major surgery within 28 days or minor surgery within 14 days of the start of the study treatment
Radiotherapy less than two weeks prior to the start of the study treatment
Systemic chemotherapy, hormonal therapy, immunotherapy ≤ 21 days before study treatment
No major comorbidity that may preclude the delivery of treatment or active infection (HIV or chronic hepatitis B or C) or uncontrolled diabetes.
Concomitant occurrence of another cancer, or history of cancer within the past five years except in situ carcinoma of the cervix treated or basal cell carcinoma or squamous cell carcinoma.
Known pre-existing interstitial lung disease
Significant or recent acute gastrointestinal disorders with diarrhea as a major symptom e.g., Crohn's disease, malabsorption, or CTCAE grade >2 diarrhea of any etiology
Pregnant woman or lactating woman.
Persons deprived of liberty or under guardianship.
Psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule.
Previous history of keratitis, ulcerative keratitis or severe dry eye.