PRIME: Panitumumab Randomized Trial In Combination With Chemotherapy for Metastatic Colorectal Cancer to Determine Efficacy

Last updated: November 3, 2022
Sponsor: Amgen
Overall Status: Completed

Phase

3

Condition

Metastatic Cancer

Colorectal Cancer

Treatment

N/A

Clinical Study ID

NCT00364013
20050203
  • Ages > 18
  • All Genders

Study Summary

The purpose of this study is to determine the treatment effect of panitumumab in combination with FOLFOX compared to FOLFOX alone as first line therapy for metastatic colorectal cancer

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Man or woman at least 18 years old
  • Diagnosis of metastatic colorectal cancer
  • At least 1 uni-dimensionally measurable lesion of at least 20 mm per modified RECIST
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2
  • Paraffin-embedded tumor tissue from the primary tumor or metastasis available for

Exclusion

central analyse Exclusion Criteria:

  • History or known presence of central nervous system (CNS) metastases
  • History of another primary cancer, except: Curatively treated in situ cervical cancer,or Curatively resected non-melanoma skin cancer, or Other primary solid tumorcuratively treated with no known active disease present and no treatment administeredfor ≥ 5 years before randomization
  • Prior chemotherapy or systemic therapy for the treatment of metastatic colorectalcarcinoma except: adjuvant fluoropyrimidine-based chemotherapy or priorfluoropyrimidine therapy administered solely for the purpose of radiosensitization
  • Prior oxaliplatin therapy
  • Prior anti-epidermal growth factor receptor (EGFr) antibody therapy (eg, cetuximab) ortreatment with small molecule EGFr inhibitors (eg, erlotinib)
  • Clinically significant cardiovascular disease (including myocardial infarction,unstable angina, symptomatic congestive heart failure, serious uncontrolled cardiacarrhythmia) 1 year prior to randomization History of interstitial lung disease (eg,pneumonitis or pulmonary fibrosis) or evidence of interstitial lung disease onbaseline chest computed tomography (CT) scan
  • Active inflammatory bowel disease or other bowel disease causing chronic diarrhea (defined as > Common terminology criteria (CTC) grade 2 [CTCAE version 3.0])
  • Peripheral sensory neuropathy with functional impairment

Study Design

Total Participants: 1183
Study Start date:
August 01, 2006
Estimated Completion Date:
March 22, 2013