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Combination Chemotherapy With or Without Irinotecan in Treating Patients With Stage III Colon Cancer

This study is ongoing, but not recruiting participants.

Sponsors and Collaborators: Federation Nationale des Centres de Lutte Contre le Cancer
Federation Francophone de Cancerologie Digestive
Information provided by: National Cancer Institute (NCI)
ClinicalTrials.gov Identifier: NCT00005979
  Purpose

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. It is not yet known if combination chemotherapy is more effective with or without irinotecan in treating colon cancer.

PURPOSE: Randomized phase III trial to compare the effectiveness of combination chemotherapy with or without irinotecan in treating patients who have stage III colon cancer.


Condition Intervention Phase
Colorectal Cancer
Drug: fluorouracil
Drug: irinotecan hydrochloride
Drug: leucovorin calcium
Phase III

MedlinePlus related topics:   Cancer    Colorectal Cancer   

ChemIDplus related topics:   Leucovorin Calcium    Citrovorum factor    Folinic acid calcium salt pentahydrate    Leucovorin    Irinotecan    Irinotecan hydrochloride    Fluorouracil    Calcium gluconate   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized
Official Title:   Phase III Randomized Study of Intensive Adjuvant Chemotherapy for Resected Colon Cancer at High Risk of Recurrence

Further study details as provided by National Cancer Institute (NCI):

Study Start Date:   February 1998

Detailed Description:

OBJECTIVES:

  • Compare the effect of leucovorin calcium and fluorouracil with or without irinotecan on the 3 year survival rate and overall survival of patients with resected node positive colon cancer at high risk of recurrence.
  • Compare toxicities of these regimens in these patients.
  • Compare quality of life of these patients.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to center, disease type (occlusion vs perforation vs N2 only), delay between surgery and chemotherapy (28 days or less vs over 28 days), and age (under 65 vs 65 and over). Patients are randomized to one of two treatment arms.

  • Arm I: Patients receive leucovorin calcium IV over 2 hours and fluorouracil IV over 22 hours on days 1 and 2.
  • Arm II: Patients receive irinotecan IV over 90 minutes on day 1 followed by leucovorin calcium and fluorouracil as in arm I.

Treatment repeats every 14 days for up to 12 courses in the absence of disease progression or unacceptable toxicity.

Quality of life is assessed before treatment, after 6 and 12 courses, and then at 1 year.

Patients are followed every 3 months for 2 years, then every 6 months for 3 years.

PROJECTED ACCRUAL: A total of 400 patients (200 per arm) will be accrued for this study within 3 years.

  Eligibility
Ages Eligible for Study:   18 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

DISEASE CHARACTERISTICS:

  • Histologically proven stage III adenocarcinoma of the colon that has been curatively resected within past 42 days
  • No metastatic disease
  • Node positive

    • No more than 4 nodes affected (Tx, N2, M0) AND/OR
    • N1 or N2 with perforation and/or occlusion
  • No prior rectal cancer within 10 cm of anal margin or that was treated with preoperative radiotherapy
  • No prior inflammatory disease of the intestine

PATIENT CHARACTERISTICS:

Age:

  • 18 to 75

Performance status:

  • Not specified

Life expectancy:

  • Not specified

Hematopoietic:

  • Neutrophil count at least 2,000/mm3
  • Platelet count at least 100,000/mm3

Hepatic:

  • Bilirubin less than 1.25 times upper limit of normal (ULN)
  • SGOT and SGPT less than 3 times ULN
  • Alkaline phosphatase less than 3 times ULN

Renal:

  • Not specified

Cardiovascular:

  • No myocardial infarction within past 6 months
  • No insufficient cardiac function

Other:

  • No other serious medical illness
  • No active infection
  • No other malignancy except skin cancer or carcinoma in situ of the cervix
  • No psychological or social condition that would preclude study
  • Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • Not specified

Chemotherapy:

  • Not specified

Endocrine therapy:

  • Not specified

Radiotherapy:

  • See Disease Characteristics

Surgery:

  • See Disease Characteristics
  • No prior extensive intestinal resection
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00005979

Locations
France
Centre Alexis Vautrin    
      Vandoeuvre-les-Nancy, France, 54511
Centre Eugene Marquis    
      Rennes, France, 35064
Centre Hospitalier de Bourgoin - Jallieu    
      Bourgoin-Jallieu, France, 38300
Centre Hospitalier de Fleyriat    
      Bourg-En-Bresse, France, 01012
Centre Hospitalier de Tarbes    
      Tarbes, France, 65013
Centre Hospitalier General    
      Brive, France, 19101
Centre Hospitalier Maie Madeleine    
      Forbach, France, 57600
Centre Hospitalier P. Chubert    
      Vannes, France, 56260
Centre Hospitalier Regionale de Vichy    
      Vichy, France, 03201
Centre Hospitalier Universitaire Henri Mondor    
      Creteil, France, 94010
Centre Hospitalier Universitaire    
      Reims, France, 51092
Centre Hospitalier Valence    
      Valence, France, 26000
Centre Leon Berard    
      Lyon, France, 69008
Centre Paul Papin    
      Angers, France, 49036
Centre Regional de Lutte Contre le Cancer - Centre Val d'Aurelle    
      Montpellier, France, 34298
St Joseph's Medical Center    
      Reims, France, 51056
Centre Rene Huguenin    
      Saint Cloud, France, 92210
CHR D'Orleans - Hopital de la Source    
      Orleans, France, 45067
Clinique St. Etienne    
      Bayonne, France, 64100
CRLCC Nantes - Atlantique    
      Nantes-Saint Herblain, France, 44805
Faculte de Medecine    
      Dijon, France, 21033
Hopital Charles Nicolle    
      Rouen, France, 76031
Hopital Du Bocage    
      Dijon, France, 21034
Hopitaux Universitaire de Strasbourg    
      Strasbourg, France, 67091
Institut Bergonie    
      Bordeaux, France, 33076
Institut Claudius Regaud    
      Toulouse, France, 31052
Institut Gustave Roussy    
      Villejuif, France, F-94805
Institut J. Paoli and I. Calmettes    
      Marseille, France, 13273
Institut Jean Godinot    
      Reims, France, 51056
Centre Regional Francois Baclesse    
      Caen, France, 14076

Sponsors and Collaborators
Federation Nationale des Centres de Lutte Contre le Cancer
Federation Francophone de Cancerologie Digestive

Investigators
Study Chair:     Marc Ychou, MD, PhD     Centre Regional de Lutte Contre le Cancer - Centre Val d'Aurelle    
Study Chair:     Jean Faivre     Federation Francophone de Cancerologie Digestive    
  More Information


Clinical trial summary from the National Cancer Institute's PDQ® database  This link exits the ClinicalTrials.gov site
 

Publications of Results:

Study ID Numbers:   CDR0000067967, FRE-FNCLCC-ACCORD-2, FFCD-9802, EU-20014
First Received:   July 5, 2000
Last Updated:   July 23, 2008
ClinicalTrials.gov Identifier:   NCT00005979
Health Authority:   United States: Federal Government

Keywords provided by National Cancer Institute (NCI):
stage III colon cancer  
adenocarcinoma of the colon  

Study placed in the following topic categories:
Digestive System Neoplasms
Gastrointestinal Diseases
Irinotecan
Colonic Diseases
Leucovorin
Intestinal Diseases
Rectal Diseases
Camptothecin
Recurrence
Intestinal Neoplasms
Digestive System Diseases
Fluorouracil
Gastrointestinal Neoplasms
Adenocarcinoma
Colonic Neoplasms
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 October 10, 2008




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