A Phase II Trial of Lapatinib and Capectiabine for Patients With Refractory Advanced Colorectal Adenocarcinoma (LAP109859)

University of Wisconsin, Madison1 site in 1 country29 target enrollmentSeptember 2007

ConditionsMetastatic Colorectal Cancer

Interventionslapatinib Capecitabine

Drugslapatinib Capecitabine

Overview

Phase: Phase 2
Intervention: lapatinib
Conditions: Metastatic Colorectal Cancer
Sponsor: University of Wisconsin, Madison
Enrollment: 29
Locations: 1
Primary Endpoint: Response Rate of Lapatinib/Capecitabine.
Status: Completed
Last Updated: 6 years ago

Overview Investigators Eligibility Criteria Arms & Interventions Outcomes Sites Similar Trials

Overview

Brief Summary

The purpose of this study is to find out how effective this combination is as a second line treatment for colorectal cancer that has spread from one part of the body to another (metastasized) or has not metastasized but is considered inoperable (unable to be removed by surgery). The side effects and survival experienced by subjects receiving these drugs will also be evaluated. This is a phase II research study.

Detailed Description

1. To evaluate the response rate of lapatinib and capecitabine combination in patients with metastatic colon or rectal cancer. 2. To evaluate the toxicity and tolerability of lapatinib and capecitabine in this population. 3. To determine overall survival and disease free survival of lapatinib and capecitabine.

Registry

clinicaltrials.gov

Start Date

September 2007

End Date

August 2009

Last Updated

6 years ago

Study Type

Interventional

Study Design

Single Group

Sex

All

Investigators

Sponsor

University of Wisconsin, Madison

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•Age \> 18 years
•Pathologically confirmed, locally advanced or metastatic adenocarcinoma of the colon or rectum
•Patients must have had progression of disease on prior therapy with an oxaliplatin-containing or irinotecan containing regimen
•Proper radiographic documentation of measurable disease using RECIST criteria
•ECOG performance status (PS) of 0 or 1
•Laboratory parameters:
•Hgb: ≥ 9.0 g/dl ANC ≥ 1500/ul Platelet ≥ 100,000/ul Creatinine ≤ 2x ULN OR Creatinine clearance ≥ 30 mg/ml Bilirubin ≤ 2x ULN AST ≤ 2x ULN or 5X ULN if liver metastases are present
•Patient has signed informed consent
•Toxicities from prior therapy (except alopecia and neuropathy) must have resolved to grade 1 or better prior to enrollment

Exclusion Criteria

•Administration of more than one prior systemic chemotherapy for metastatic disease
•Pregnant or breast-feeding women: female patients must agree to use effective contraception, must be surgically sterile, or must be postmenopausal. Male patients must agree to use effective contraception or be surgically sterile. The definition of effective contraception will be based on the judgment of the principal investigator or a designated associate. All at-risk female patients must have a negative serum pregnancy test within 7 days prior to randomization.
•Active inflammatory bowel disease, significant bowel obstruction, or chronic diarrhea (grade 2).
•Known human immunodeficiency virus (HIV) positivity or acquired-immunodeficiency-syndrome (AIDS)-related illness.
•No previous or concurrent malignancy is allowed except for adequately treated basal cell or squamous cell skin cancer, in-situ cervical cancer, or other cancer for which the patient has been disease-free for 3 years.
•Known CNS metastases
•Prior therapy which specifically and directly targets the EGFR pathway
•Significant history of uncontrolled cardiovascular disease, defined as:
•History of uncontrolled or symptomatic angina
•History of arrhythmias requiring medications, or clinically significant, with the exception of asymptomatic atrial fibrillation requiring anticoagulation