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Cetuximab Combined With Irinotecan in First-Line Therapy for Metastatic Colorectal Cancer (CRYSTAL)
This study is ongoing, but not recruiting participants.
Sponsored by: Merck KGaA
Information provided by: EMD Pharmaceuticals
ClinicalTrials.gov Identifier: NCT00154102
  Purpose

Drugs used against cancer work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as cetuximab, can block tumor growth in different ways. Giving combination chemotherapy together with cetuximab as first treatment after diagnosis of a metastatic colorectal cancer ('1st-line' treatment) may improve the treatment efficacy. However, it is not yet known whether giving combination chemotherapy together with cetuximab is more effective than combination chemotherapy alone. This open-label trial investigates the effectiveness of cetuximab in combination with a standard and effective chemotherapy (5-Fluorouracil/Folinic acid plus irinotecan) for metastatic colorectal cancer in first-line setting, compared to the same chemotherapy alone on patient expressing the EGF receptor.

Patients expressing this EGF Receptor will be randomly assign in one of the 2 groups to either receive the combination chemotherapy alone or with cetuximab (open-label study) and will then be treated until progression of the disease or unacceptable toxicity occur. Regular efficacy assessments (every 8 weeks) based on imaging will be performed throughout the study together with regular safety assessments (e.g. safety labs). An independent Safety Board of experts will also monitor safety data.

After participant discontinuation from the trial, regular updates on further treatments and survival status will be requested from the investigator.

The entire study (from the first patient entering the study to the last collect of follow-up information) is 4-5 years long.


Condition Intervention Phase
EGFR-Expressing Metastatic Colorectal Cancer
Drug: Cetuximab, 5-Fluorouracil, Folinic acid, Irinotecan
Drug: 5-Fluorouracil, Folinic acid, Irinotecan
Phase III

MedlinePlus related topics: Cancer Colorectal Cancer Methamphetamine
Drug Information available for: Leucovorin Calcium Citrovorum factor Folinic acid calcium salt pentahydrate Leucovorin Irinotecan Irinotecan hydrochloride Fluorouracil Cetuximab Epidermal Growth Factor Amphetamine Methamphetamine
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title: Open, Randomized, Controlled, Multicenter Phase III Study Comparing 5FU/ FA Plus Irinotecan Plus Cetuximab Versus 5FU/FA Plus Irinotecan as First-Line Treatment for Epidermal Growth Factor Receptor-Expressing Metastatic Colorectal Cancer

Further study details as provided by EMD Pharmaceuticals:

Primary Outcome Measures:
  • Progression-free survival time under 5-FU/FA plus irinotecan with or without cetuximab [ Time Frame: various timepoints ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Overall Survival time [ Time Frame: every 3 months ] [ Designated as safety issue: No ]
  • Response Rate and Disease Control rate [ Time Frame: various timepoints ] [ Designated as safety issue: No ]
  • Duration or Response [ Time Frame: various timepoints ] [ Designated as safety issue: No ]
  • Quality of Life [ Time Frame: various timepoints ] [ Designated as safety issue: No ]
  • Safety [ Time Frame: various timepoints ] [ Designated as safety issue: Yes ]

Enrollment: 1221
Study Start Date: May 2004
Estimated Study Completion Date: December 2008
Primary Completion Date: July 2006 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental Drug: Cetuximab, 5-Fluorouracil, Folinic acid, Irinotecan
Cetuximab intravenous infusion of 400mg/m2 for the first infusion then weekly intravenous infusion of 250mg/m2. Bi-weekly Irinotecan infusion of 180mg/m2, Folinic Acid infusion of 400mg/m2 (racemic) or 200mg/m2 (L-form), 5-Fluorouracil bolus of 400mg/m2 followed by a 46-hour continuous infusion of 2400mg/m2 Number of Cycles: until progression or unacceptable toxicity develops
2: Active Comparator Drug: 5-Fluorouracil, Folinic acid, Irinotecan
Bi-weekly Irinotecan infusion of 180mg/m2, Folinic Acid infusion of 400mg/m2 (racemic) or 200mg/m2 (L-form), 5-Fluorouracil bolus of 400mg/m2 followed by a 46-hour continuous infusion of 2400mg/m2 Number of Cycles: until progression or unacceptable toxicity develops

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Diagnosis of histologically confirmed adenocarcinoma of the colon or rectum
  • Inoperable metastatic disease
  • Immunohistochemical evidence of epidermal growth factor receptor expression in tumor tissue
  • Presence of at least 1 bi-dimensionally measurable index lesion

Exclusion Criteria:

  • Previous irinotecan-based chemotherapy
  • Previous chemotherapy for colorectal cancer except adjuvant treatment if terminated more than 6 months before the start of study treatment
  • Radiotherapy, surgery (excluding prior diagnostic biopsy) or any investigational drug in the 30 days before the start of study treatment
  • Brain metastasis
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00154102

  Show 154 Study Locations
Sponsors and Collaborators
Merck KGaA
Investigators
Principal Investigator: Eric van Cutsem, Professor University Hospital Gasthuisberg, Department Internal Medicine, Leuven, Belgium
  More Information

Responsible Party: Merck KGaA ( Patrick Lebrun )
Study ID Numbers: EMR 62202-013
Study First Received: September 8, 2005
Last Updated: April 9, 2008
ClinicalTrials.gov Identifier: NCT00154102  
Health Authority: Belgium: Directorate general for the protection of Public health: Medicines

Keywords provided by EMD Pharmaceuticals:
Metastatic colorectal cancer
EGFR
Irinotecan
cetuximab
first-line treatment

Study placed in the following topic categories:
Digestive System Neoplasms
Gastrointestinal Diseases
Colonic Diseases
Irinotecan
Cetuximab
Leucovorin
Intestinal Diseases
Rectal Diseases
Intestinal Neoplasms
Methamphetamine
Digestive System Diseases
Fluorouracil
Gastrointestinal Neoplasms
Amphetamine
Colorectal Neoplasms

Additional relevant MeSH terms:
Antimetabolites
Antimetabolites, Antineoplastic
Vitamin B Complex
Molecular Mechanisms of Pharmacological Action
Immunologic Factors
Antineoplastic Agents
Growth Substances
Physiological Effects of Drugs
Enzyme Inhibitors
Immunosuppressive Agents
Pharmacologic Actions
Neoplasms
Neoplasms by Site
Therapeutic Uses
Vitamins
Micronutrients
Antineoplastic Agents, Phytogenic

ClinicalTrials.gov processed this record on January 16, 2009