Phase II and Pharmacokinetic Study of CPT-11 and Trastuzumab (RhuMab HER2, Herceptin) in Advanced Colo-Rectal Cancer With p185 HER 2 Overexpression
trastuzumab
+ irinotecan hydrochloride
Colonic Diseases+10
+ Digestive System Diseases
+ Digestive System Neoplasms
Treatment Study
Summary
Study start date: September 1, 1999
Actual date on which the first participant was enrolled.OBJECTIVES: I. Determine the objective response rate of irinotecan and trastuzumab in patients with stage IV colorectal cancer and p185 HER2 overexpression. II. Evaluate the safety and toxic effects of this treatment regimen in these patients. III. Determine the overall survival and time to progression in these patients in response to this treatment regimen. IV. Determine the pharmacokinetics of trastuzumab in combination with irinotecan and antibodies to trastuzumab in these patients. V. Determine the expression of HER2/neu in these patients. OUTLINE: This is a multicenter study. Patients receive a loading dose of trastuzumab IV over 90 minutes on week 1, and over 30-90 minutes weekly thereafter. Patients receive irinotecan IV over 90 minutes following trastuzumab weekly for 4 weeks. Courses are repeated every 6 weeks in the absence of disease progression or unacceptable toxicity. Patients are followed every 3 months.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.32 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
DISEASE CHARACTERISTICS: Histologically confirmed stage IV colorectal cancer with p185 HER2 overexpression Bidimensionally measurable disease Indicator lesion must be outside of irradiated field No symptomatic CNS brain metastases PATIENT CHARACTERISTICS: Performance status: ECOG 0-2 Absolute granulocyte count at least 1,500/mm3 Platelet count at least 100,000/mm3 Bilirubin no greater than 1.5 times upper limit of normal (ULN) SGOT no greater than 3.0 times ULN Creatinine no greater than 2.0 mg/dL LVEF at least 45% by MUGA or ECHO No myocardial infarction within the past 6 months No congestive heart failure No unstable angina No clinically significant pericardial effusion or arrhythmia Not pregnant or nursing Negative pregnancy test Fertile patients must use effective contraception during and for 6 months after study No other prior malignancy within the past 5 years, except: Curatively treated basal or squamous cell skin cancer Curatively treated carcinoma in situ of the cervix No active serious infection or serious underlying medical condition that would prevent compliance No dementia or significantly altered mental status PRIOR CONCURRENT THERAPY: Concurrent filgrastim (G-CSF), sargramostim (GM-CSF), or epoetin alfa allowed No prior trastuzumab No more than 1 prior chemotherapy regimen for advanced disease (if progressed during or within 6 months of adjuvant therapy considered to have had 1 regimen for advanced disease) No prior irinotecan Concurrent contraception, estrogen replacement therapy, or megestrol acetate for anorexia allowed Greater than 3 weeks since prior radiotherapy and recovered Greater than 3 weeks since major surgery (except simple biopsy or venous access placement) and recovered At least 3 weeks since prior investigational nonneoplastic drugs
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 5 locations
Albert Einstein Comprehensive Cancer Center
The Bronx, United StatesOpen Albert Einstein Comprehensive Cancer Center in Google MapsUniversity of Pittsburgh Cancer Institute
Pittsburgh, United StatesLifespan: The Miriam Hospital
Providence, United StatesSarah Cannon-Minnie Pearl Cancer Center
Nashville, United States