search
Back to results

Comparative Study of Cetuximab and Radiation Vs Surgery Before or After Radiation in Patients With Colorectal Carcinoma

Primary Purpose

Colorectal Carcinoma

Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Cetuximab and Radiation Therapy
Surgery and Radiation Therapy
Sponsored by
American Scitech International
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colorectal Carcinoma focused on measuring Colorectal Cancer, Erbitux, Cetuximab, Surgery, Radiation

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with stage II- IV Colorectal Cancer
  • Patients must be 40 years and older
  • Patients may be of any race and either gender
  • Signed Informed Consent

Patient characteristics:

  • Age: 40 years and older
  • Sex: Both
  • Performance status: Not specified
  • Life expectancy: Not specified

Hematopoietic:

  • Granulocyte count ≥ 1,500/mm^3
  • Platelet count ≥ 100,000/mm^3
  • Hemoglobin ≥ 9.0 g/dL
  • No history of significant bleeding events within the past 6 months

Hepatic:

  • Bilirubin ≤ 1.5 mg/dL
  • Albumin ≥ 2.5 g/dL

Renal:

  • Creatinine ≤ 1.5 times upper limit of normal
  • Protein < 1+ by urinalysis
  • Protein < 1 g by 24-hour urine collection

Cardiovascular:

  • No conduction defect in heart
  • No congestive heart failure
  • No myocardial infarction within last 6 months
  • No cerebrovascular accident
  • No uncontrolled hypertension
  • No clinically significant peripheral artery disease

Pulmonary:

  • No pulmonary embolism
  • No interstitial pneumonia
  • No extensive or symptomatic interstitial fibrosis of the lung

Neurologic:

  • No uncontrolled seizure disorder
  • No active neurological disease

Other:

  • Not pregnant or nursing
  • Negative pregnancy test

Exclusion Criteria:

  • Age below 40 years
  • Brain or nervous system metastases
  • Any current mental illness
  • Hemoglobin is less than 9.0 g/dl
  • CBC results are below normal range
  • Patients with Hepatitis B or C or who are HIV positive
  • Pregnant or nursing patients are not eligible for entry into the study
  • Hepatic abnormality AST/ALT > 4 folds

Sites / Locations

  • Practicing Physician in New Jersey

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

1

2

Arm Description

Patients will receive a Cetuximab and Radiation Therapy.

Patients will undergo Surgery before or after Radiation Therapy.

Outcomes

Primary Outcome Measures

Objective tumor response rate

Secondary Outcome Measures

Tolerability
Progression free survival
Overall survival
Quality of life

Full Information

First Posted
July 28, 2008
Last Updated
July 19, 2011
Sponsor
American Scitech International
Collaborators
Eli Lilly and Company, Bristol-Myers Squibb
search

1. Study Identification

Unique Protocol Identification Number
NCT00725400
Brief Title
Comparative Study of Cetuximab and Radiation Vs Surgery Before or After Radiation in Patients With Colorectal Carcinoma
Official Title
Phase II Open Label Comparative Study of Cetuximab and Radiation Therapy Vs Surgery Before or After Radiation Therapy in Patients With Stage II to IV Colorectal Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
July 2011
Overall Recruitment Status
Withdrawn
Why Stopped
Study is withdrawn due to unavailability of eligible subject population. We will request the sponsors to extend the time for enrollment.
Study Start Date
February 2010 (undefined)
Primary Completion Date
February 2014 (Anticipated)
Study Completion Date
February 2014 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
American Scitech International
Collaborators
Eli Lilly and Company, Bristol-Myers Squibb

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
RATIONALE: Monoclonal antibodies, such as Cetuximab, can target tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells.This is an anti-cancer drug which has already been approved by the FDA for use in patients who have Colorectal Cancer. Cetuximab can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Radiation Therapy uses high-energy x-rays to kill tumor cells and cause less damage to normal tissue . Giving the drug Cetuximab together with Radiation Therapy may kill more tumor cells. Surgery is the most common treatment for Colorectal Cancer to remove the tumor, as well as a small margin of surrounding normal tissue and possibly nearby lymph nodes. Surgery is usually used in conjunction with other conventional treatments such as Radiation Therapy. Radiation Therapy before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. Radiation Therapy after surgery may kill any tumor cells that remain after surgery. Screening test such as Fecal Occult Blood Test (FOBT) and Colonoscopy has to be done. Tumor markers for Colorectal Carcinoma are Carcinoembryonic antigen (CAE) and CA 19-9 and to assess the response of tumor markers Carcinoembryonic antigen (CAE) and CA 19-9 will be used and periodically Colonoscopy has to be done. Colorectal Cancer Surgery are Colon resection (Colectomy), Rectum resection (Proctectomy), Colostomy, and Radiofrequency ablation. PURPOSE: Determine the tumor response rate treated with Cetuximab and Radiation Therapy Vs Surgery before or after Radiation Therapy in patients with Colorectal Cancer from stage II to IV
Detailed Description
OBJECTIVES: Primary: Determine the response rate in patients with Colorectal Cancer treated with Cetuximab and Radiation Therapy Vs Surgery before or after Radiation Therapy. Secondary: To determine the progression-free survival and overall survival of patients treated with these regimens. Compare the treatment compliance of patients treated with these regimens. Compare the safety of these regimens in these patients. OUTLINE: This is an Open-label, Controlled, Multicenter study. Patients will be assigned into two different Arms. Arm I: Patients will receive Cetuximab and Radiation Therapy. Patients will receive a dose of Cetuximab through Intravenous (IV). The initial dose is 400 mg/m2 administered as a 120-minute intravenous infusion (maximum infusion rate 10 mg/min) and weekly dose is 250 mg/m2 infused over 60 minutes (maximum infusion rate 10 mg/min) until disease progression or unacceptable toxicity. Radiation treatment for Colorectal Cancer are Intensity Modulated Radiation Therapy (IMRT). IMRT delivers radiation directly to the tumor and modulates the intensity of the radiation with laser accuracy. Arm II: Patients will undergo surgery before or after Radiation Therapy. Colorectal Cancer Surgery are Colon resection (Colectomy), Rectum resection (Proctectomy), Colostomy, and Radiofrequency ablation. Radiation treatment for Colorectal Cancer are Intensity Modulated Radiation Therapy (IMRT). IMRT delivers radiation directly to the tumor and modulates the intensity of the radiation with laser accuracy. PROJECTED ACCRUAL: Approximately 450 patients will be accrued for this study within 18 to 24 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Carcinoma
Keywords
Colorectal Cancer, Erbitux, Cetuximab, Surgery, Radiation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
450 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Patients will receive a Cetuximab and Radiation Therapy.
Arm Title
2
Arm Type
Active Comparator
Arm Description
Patients will undergo Surgery before or after Radiation Therapy.
Intervention Type
Other
Intervention Name(s)
Cetuximab and Radiation Therapy
Other Intervention Name(s)
Erbitux and Radiotherapy
Intervention Description
Patients will receive Cetuximab and Radiation Therapy. Patients will receive a dose of Cetuximab through Intravenous (IV). The initial dose is 400 mg/m2 administered as a 120-minute intravenous infusion (maximum infusion rate 10 mg/min) and weekly dose is 250 mg/m2 infused over 60 minutes (maximum infusion rate 10 mg/min) until disease progression or unacceptable toxicity. Radiation treatment for Colorectal Cancer are Intensity Modulated Radiation Therapy (IMRT). IMRT delivers radiation directly to the tumor and modulates the intensity of the radiation with laser accuracy.
Intervention Type
Procedure
Intervention Name(s)
Surgery and Radiation Therapy
Other Intervention Name(s)
Surgery and Radiotherapy
Intervention Description
Patients will undergo Surgery before or after Radiation Therapy. Colorectal Cancer Surgery are Colon resection (Colectomy), Rectum resection (Proctectomy), Colostomy, and Radiofrequency ablation. Radiation treatment for Colorectal Cancer are Intensity Modulated Radiation Therapy (IMRT). IMRT delivers radiation directly to the tumor and modulates the intensity of the radiation with laser accuracy.
Primary Outcome Measure Information:
Title
Objective tumor response rate
Time Frame
4 year
Secondary Outcome Measure Information:
Title
Tolerability
Time Frame
4 years
Title
Progression free survival
Time Frame
4 years
Title
Overall survival
Time Frame
4 Years
Title
Quality of life
Time Frame
4 Years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with stage II- IV Colorectal Cancer Patients must be 40 years and older Patients may be of any race and either gender Signed Informed Consent Patient characteristics: Age: 40 years and older Sex: Both Performance status: Not specified Life expectancy: Not specified Hematopoietic: Granulocyte count ≥ 1,500/mm^3 Platelet count ≥ 100,000/mm^3 Hemoglobin ≥ 9.0 g/dL No history of significant bleeding events within the past 6 months Hepatic: Bilirubin ≤ 1.5 mg/dL Albumin ≥ 2.5 g/dL Renal: Creatinine ≤ 1.5 times upper limit of normal Protein < 1+ by urinalysis Protein < 1 g by 24-hour urine collection Cardiovascular: No conduction defect in heart No congestive heart failure No myocardial infarction within last 6 months No cerebrovascular accident No uncontrolled hypertension No clinically significant peripheral artery disease Pulmonary: No pulmonary embolism No interstitial pneumonia No extensive or symptomatic interstitial fibrosis of the lung Neurologic: No uncontrolled seizure disorder No active neurological disease Other: Not pregnant or nursing Negative pregnancy test Exclusion Criteria: Age below 40 years Brain or nervous system metastases Any current mental illness Hemoglobin is less than 9.0 g/dl CBC results are below normal range Patients with Hepatitis B or C or who are HIV positive Pregnant or nursing patients are not eligible for entry into the study Hepatic abnormality AST/ALT > 4 folds
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ratna Grewal, MD
Organizational Affiliation
American Scitech International- eCRO
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Prem A Nandiwada, MD
Organizational Affiliation
Raritan Bay Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sarat Babu, MD
Organizational Affiliation
St. Peter's Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
S N Agrawal, MD
Organizational Affiliation
JLR Hospital in India
Official's Role
Principal Investigator
Facility Information:
Facility Name
Practicing Physician in New Jersey
City
Englishtown
State/Province
New Jersey
ZIP/Postal Code
07726
Country
United States

12. IPD Sharing Statement

Links:
URL
http://www.americanscitech.com
Description
Web based electronic data capture research center; Contract Research Organization
URL
http://www.imclone.com
Description
Related Info
URL
http://www.bristolmyers.com
Description
Related Info

Learn more about this trial

Comparative Study of Cetuximab and Radiation Vs Surgery Before or After Radiation in Patients With Colorectal Carcinoma

We'll reach out to this number within 24 hrs