Study of Xeloda and Gleevec in Patients With Advanced Solid Tumors

NCT00183833 | Completed Phase 1

• 1 other identifier: 3C-02-1
• Study Type: interventional
• Target: 40
• Locations: 1 country
• Sites: 1

Brief Summary

This study is for people with solid tumors cancer for which the standard chemotherapy drugs have not worked. The purpose of this research is to evaluate the side effects of Xeloda (also called capecitabine) in combination with a new anticancer agent called Gleevec (also called imatinib mesylate). Xeloda is an anticancer drug, and can be taken by mouth. The active ingredient is a well-studied cancer drug called 5-FU. Xeloda is approved by the FDA for the treatment of colon cancer. Gleevec is approved in the US for the treatment of patients with a leukemia called CML (increase of white blood cells) after failure of standard therapy. It is also approved by the FDA for patients with Gastrointestinal Stromal Tumors (a rare tumor in the digestive tract). This study will test how much Gleevec we can safely give with Xeloda. Xeloda will be given at the recommended dose for colorectal cancer and Gleevec will be given in increasing amounts.

Conditions

Colon Cancer; Colorectal Cancer

Keywords

phase 1; phase I; phase one; colon cancer; colorectal cancer

Outcome Measures

Primary Outcomes (1)

• To determine the dose limiting toxicity (DLT) and maximum tolerated dose (MTD) of Gleevec in combination with a fixed dose of Xeloda po bid daily in patients with colon cancer.

  4 weeks

Secondary Outcomes (3)

• To determine the time to progression, survival and response rate.

  Until Patient goes off study

• To obtain preliminary data on molecular correlates to determine clinical efficacy

  Until Patient Goes off study

• Toxicity.

  30 days after patient receives last drug dose

Study Arms (1)

A

EXPERIMENTAL

Xeloda plus gleevec

Drug: capecitabine, imatinib mesylate

Interventions

capecitabine, imatinib mesylate DRUG

Capecitabine and imatinib mesylate will both be taken by mouth twice a day

A

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Histologically or cytologically confirmed metastatic or unresectable solid tumor for which standard curative or palliative measures do not exist or are no longer effective.
• SWOG performance status 0-2.
• ANC greater than 1500, platelets greater than 100,000.
• Total bilirubin less than 2 x upper limit of normal, or less than 3 x upper limit of normal in patients with liver metastasis. Transaminase (AST and/or ALT) less than 2 x upper limit of normal or less than 3 x upper limit of normal in patients with liver metastasis.
• Serum creatinine less than 1.25 x institutional upper limit of normal.
• Female patients of childbearing potential must have negative pregnancy test within 7 days before initiation of study drug dosing.

You may not qualify if:

• Patient has received any other investigational agent- within 28 days of first day of study drug dosing.
• Patient with another primary malignancy except if the other primary malignancy is neither currently clinically significant nor requiring active intervention.
• Patient has another severe and/or life-threatening medical disease.
• Patient has an acute or known chronic liver disease (e.g., chronic active hepatitis, cirrhosis).
• Patient has a known diagnosis of human immunodeficiency virus (HIV) infection.
• Patient has received chemotherapy within 4 weeks (6 weeks for nitrosourea, mitomycin-C or any antibody therapy) prior to study entry unless urgent enrollment needed and approved by Novartis.
• Patient had a major surgery within 2 weeks prior to study entry.
• Patients with symptomatic brain metastasis.
• Patient with Grade III/IV cardiac problems as defined by the New York Heart Association Criteria (e.g. congestive heart failure, myocardial infarction within 6 months of study)
• Medical, social or psychological factors interfering with compliance.
• Patients under therapeutic coumadin therapy.
• Patients under routine systemic corticosteroid therapy.

Sponsors & Collaborators

• University of Southern California: lead
• Novartis: collaborator

Study Sites (1)

USC/Norris Cancer Center

Los Angeles, California, 90033, United States

Location

MeSH Terms

Conditions

Colonic Neoplasms; Colorectal Neoplasms

Interventions

Capecitabine; Imatinib Mesylate

Condition Hierarchy (Ancestors)

Intestinal Neoplasms; Gastrointestinal Neoplasms; Digestive System Neoplasms; Neoplasms by Site; Neoplasms; Digestive System Diseases; Gastrointestinal Diseases; Colonic Diseases; Intestinal Diseases; Rectal Diseases

Intervention Hierarchy (Ancestors)

Deoxycytidine; Cytidine; Pyrimidine Nucleosides; Pyrimidines; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds; Fluorouracil; Uracil; Pyrimidinones; Deoxyribonucleosides; Nucleosides; Nucleic Acids, Nucleotides, and Nucleosides; Benzamides; Amides; Organic Chemicals; Benzoates; Acids, Carbocyclic; Carboxylic Acids; Benzene Derivatives; Hydrocarbons, Aromatic; Hydrocarbons, Cyclic; Hydrocarbons; Piperazines

Study Officials

• Heinz-Josef Lenz, M.D.

  U.S.C./Norris Cancer Center

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 9, 2005
• First Posted: September 16, 2005
• Study Start: December 1, 2002
• Primary Completion: July 1, 2009
• Study Completion: August 1, 2010
• Last Updated: May 22, 2014

Record last verified: 2014-05

Locations

US (1)