Mode
Text Size
Log in / Sign up
Phase 2 N=154 Treatment

Panitumumab Plus FOLFIRI in First-line Treatment of Metastatic Colorectal Cancer

Metastatic Colorectal Cancer

Enrolled (actual)
154
Serious AEs
54.6%
Results posted
Jan 2016
Primary outcome: Primary: Objective Response Rate — 56.47; 37.93 percentage of participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Panitumumab (Drug); FOLFIRI (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Amgen
Primary completion
Jun 2009

Outcome Measures

OutcomeResultp-value
PRIMARY
Objective Response Rate
56.47; 37.93
SECONDARY
Objective Response by 17 Weeks
49.41; 34.48
SECONDARY
Disease Control Rate
90.59; 89.66
SECONDARY
Duration of Response
13.0; 7.4
SECONDARY
Time to Initial Objective Response
3.8; NA
SECONDARY
Progression-free Survival
8.9; 7.2
SECONDARY
Time to Disease Progression
11.2; 7.3
SECONDARY
Duration of Stable Disease
5.9; 6.1
SECONDARY
Time to Treatment Failure
6.9; 5.8
SECONDARY
Time to Disease Relapse Following Surgical Intervention
NA; NA
SECONDARY
Resection Rate
15.12; 6.78

Summary

To estimate the effect of KRAS mutation status (Wild-type versus Mutant) on objective response rate and other measures of efficacy for patients treated with panitumumab in combination with a chemotherapy regimen of irinotecan, 5-fluorouracil, and leucovorin (FOLFIRI) as first-line therapy for metastatic colorectal cancer (mCRC).

Eligibility Criteria

Inclusion Criteria

  • Diagnosed with histologically- or cytologically-confirmed metastatic adenocarcinoma of the colon and/or rectum.
  • Measurable disease according to modified RECIST guidelines.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1 or 2.
  • Paraffin-embedded tissue or unstained tumour slides from primary or metastatic tumour available for central lab analysis.
  • Adequate haematologic, renal, hepatic and metabolic function.

Exclusion Criteria

  • Central nervous system metastases.
  • Prior systemic therapy for the treatment of metastatic colorectal carcinoma with the exception of adjuvant fluoropyrimidine-based chemotherapy given at least six months prior to initiating study treatment.
  • Prior anti-epidermal growth factor receptor (EGFr) antibody therapy (e.g. cetuximab) or treatment with small molecule EGFr tyrosine kinase inhibitors (e.g. erlotinib).
  • Prior radiotherapy within 14 days prior to screening, and for which all signs of early radiological toxicity have not abated.
  • Significant cardiovascular disease including unstable angina or myocardial infarction within six months before initiating study treatment or a history of ventricular arrhythmia.
  • History of interstitial pneumonitis or pulmonary fibrosis or evidence of interstitial pneumonitis or pulmonary fibrosis on baseline chest computed tomography (CT scan.
  • Active inflammatory bowel disease or other bowel disease causing chronic diarrhoea (defined as > 4 loose stools per day).
  • History of Gilbert's syndrome or dihydropyrimidine deficiency.
  • Known positive test for human immunodeficiency virus infection, hepatitis C virus, chronic active hepatitis B infection.
  • Any investigational agent within 30 days before initiation of study treatment.
  • Must not have had a major surgical procedure within 28 days prior to initiation of study treatment.
  • Subject who is pregnant or breast-feeding.
  • Woman or man of childbearing potential not consenting to use adequate contraceptive precautions during the course of the study and for six months after the last study drug administration for women, and one month for men.
  • Other protocol specified criteria and specific details may apply.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00508404). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search