Overview

This trial is active, not recruiting.

Condition colorectal carcinoma
Treatments su011248, irinotecan, cetuximab
Phase phase 1/phase 2
Targets EGFR, VEGF, FLT-3, KIT, PDGF
Sponsor Massachusetts General Hospital
Collaborator Beth Israel Deaconess Medical Center
Start date July 2006
End date December 2007
Trial size 44 participants
Trial identifier NCT00361244, 05-439

Summary

The purpose of this study is to determine the safety of SU011248 and the highest dose of this drug that can be given safely in combination with the chemotherapy drugs irinotecan and cetuximab. Laboratory studies have shown that SU011248 may block the growth of blood vessels in tumors, which may prevent tumors from growing any further. Other studies have demonstrated the possibility that SU011248 may enhance the anti-tumor activity of other chemotherapy drugs such as irinotecan and cetuximab.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation non-randomized
Endpoint classification safety/efficacy study
Intervention model single group assignment
Masking open label
Primary purpose treatment

Primary Outcomes

Measure
To determine the maximum tolerated dose of SU011248 when given in combination with irinotecan and cetuximab in patients with previously treated locally advanced, locally recurrent, or metastatic colorectal adenocarcinoma
time frame: 1 year
To determine the response rate of SU011248 when given in combination with irinotecan and cetuximab in this patient population.
time frame: TBD

Secondary Outcomes

Measure
To evaluate the toxicities of this combination of drugs in this patient population
time frame: 1 year
to assess overall survival, progression-free survival, time to progression and duration of response.
time frame: TBD

Eligibility Criteria

Male or female participants at least 18 years old.

Inclusion Criteria: - Histologic proof of adenocarcinoma of the colon or rectum with evidence of metastatic disease. The site of the primary lesion must be or have been confirmed endoscopically, radiologically, or surgically to be or have been in the large bowel - Patients must have received one (and only one) prior chemotherapy regimen for metastatic disease using 5-FU/LV or Xeloda in combination with oxaliplatin and Avastin. - > 4 weeks must have elapsed from the time of major surgery - > 2 weeks must have elapsed from the time of minor surgery - > 4 weeks must have elapsed from the time of major radiotherapy - Normal organ and marrow function - Measurable disease be RECIST criteria - Older than 18 years of age - ECOG performance status of 0-1 - Life expectancy > 12 weeks Exclusion Criteria: - Previous treatment with irinotecan, cetuximab or SU011248 - Any of the following within the 12 months prior to study drug administration: severe/unstable angina; myocardial infarction; symptomatic congestive heart failure; cerebrovascular accident; or transient ischemic attack. - Known brain metastases or carcinomatous meningitis - Uncontrolled serious medical or psychiatric illness - NCI CTCAE grade 3 or greater hemorrhage within 4 weeks of starting study treatment - Uncontrolled hypertension - Diagnosis of any secondary malignancies with the last 5 years, except for adequately treated basal cell carcinoma, squamous cell skin cancer, localized prostate cancer with a normal PSA within the past 3 months, in situ bladder cancer, or in situ cervical cancer - Pregnant or breastfeeding - Concurrent treatment on another clinical trial

Additional Information

Official title A Phase I/II Study of SU011248 (Sutent) in Combination With Irinotecan and Cetuximab as a Second Line Regimen for Patients With Stage IV Colorectal Cancer
Principal investigator Andrew X. Zhu, MD
Description - Participants will be given a supply of SU011248 capsules to take at home in the morning for two weeks. After taking the capsules for two weeks, there will be a one-week rest period. - Irinotecan will be administered on days 1 and 8 of every 21-day cycle as an intravenous infusion over 90 minutes. Cetuximab will be administered intravenously on days 1, 8 and 15 of every 21-day cycle. The first treatment of cetuximab is a larger dose. Beginning with the second treatment, the participant will receive a smaller dose of cetuximab. - Blood work will be repeated at every clinic visit on days 1 and 8. During cycle 1, blood will also be drawn on day 15. - Tumor assessments will be repeated after 6 weeks, 12 weeks, and every 9 weeks thereafter, and will be assessed by both a CT scan of the abdomen, pelvis, and a chest x-ray. MUGA scans will be repeated every 4 cycles (12 weeks). - Participants may continue to receive cycles of study treatment as long as their disease does not progress and they do not experience any serious side effects.
Trial information was received from ClinicalTrials.gov and was last updated in December 2007.
Information provided to ClinicalTrials.gov by Massachusetts General Hospital.