Capecitabine in Treating Women With Advanced or Metastatic Breast Cancer

Breast Cancer Clinical Trial

Official title:

A Pilot Trial Of Two Different Doses Of Capecitabine (XELODA) In Patients With Advanced And/Or Metastatic Breast Cancer

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT00026442
• Other study ID #: CDR0000069030
• Secondary ID: PHARMATECH-XEL-1
• Status: Active, not recruiting
• Phase: Phase 2
• First received: November 9, 2001
• Last updated: December 17, 2013
• Start date: November 2001

Study information

• Verified date: April 2004
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die.

PURPOSE: Randomized phase II trial to compare the effectiveness of two different doses of capecitabine in treating women who have advanced or metastatic breast cancer.

Description:

OBJECTIVES:

• Compare the objective response rate in women with advanced or metastatic breast cancer treated with two dose levels of capecitabine.

• Compare the duration of response, time to progression, time to treatment failure, survival, incidence of adverse events, and time to onset of the adverse experience in patients treated with this drug.

• Compare the quality of life of patients treated with this drug.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to Karnofsky performance status (70-80% vs 90-100%) and presence of hepatic metastases (yes vs no). Patients are randomized to one of two treatment arms.

• Arm I: Patients receive lower-dose oral capecitabine twice daily on days 1-14.

• Arm II: Patients receive higher-dose oral capecitabine twice daily on days 1-14.

In both arms, courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

Quality of life is assessed at baseline, at the end of the third and sixth courses, and at completion of therapy.

PROJECTED ACCRUAL: A total of 120 patients (60 per treatment arm) will be accrued for this study within 9 months.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 0
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• Histologically and/or cytologically confirmed breast cancer

• Advanced and/or metastatic disease

• At least 1 measurable lesion

• At least 20 mm by conventional techniques OR at least 10 mm by spiral CT scan

• No CNS metastases

• Hormone receptor status:

• Not specified

PATIENT CHARACTERISTICS:

Age:

• 18 and over

Sex:

• Female

Menopausal status:

• Not specified

Performance status:

• Karnofsky 70-100%

Life expectancy:

• At least 12 weeks

Hematopoietic:

• Neutrophil count at least 1,500/mm^3

• Platelet count at least 100,000/mm^3

Hepatic:

• Bilirubin no greater than 1.25 times upper limit of normal (ULN)

• AST/ALT no greater than 2.5 times ULN (5 times ULN if liver metastases present)

• Alkaline phosphatase no greater than 2.5 times ULN (5 times ULN if liver metastases present OR 10 times ULN if bone metastases present)

• No hepatitis

Renal:

• Creatinine no greater than 1.5 times ULN

• Creatinine clearance at least 50 mL/min

Cardiovascular:

• No clinically significant cardiac disease

• No congestive heart failure

• No symptomatic coronary artery disease

• No cardiac arrhythmias poorly controlled with medication

• No myocardial infarction within the past 12 months even if adequately controlled with medication

Other:

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

• HIV negative

• No severe pain inadequately controlled by analgesics

• No prior severe and unexpected reaction to fluoropyrimidine therapy

• No known hypersensitivity to fluorouracil

• No impaired physical integrity of the upper gastrointestinal tract

• No malabsorption syndrome

• No inability to swallow tablets

• No history of uncontrolled seizures, central nervous system disorder, or psychiatric disability that would preclude study participation

• No serious uncontrolled infection

PRIOR CONCURRENT THERAPY:

Biologic therapy:

• Not specified

Chemotherapy:

• At least 2 but no more than 3 prior chemotherapy regimens

• At least 1 prior chemotherapy regimen containing paclitaxel and an anthracycline as adjuvant therapy or for advanced and/or metastatic disease

Endocrine therapy:

• Not specified

Radiotherapy:

• No prior radiotherapy to target lesions unless there is evidence of new disease within the irradiated field

• No concurrent radiotherapy

Surgery:

• No prior organ allografts

Other:

• At least 4 weeks since prior investigational drug

• No concurrent enrollment on other investigational study

• No other concurrent anticancer agents

Study Design

Primary Purpose: Treatment

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Drug:
• capecitabine

Locations

Country	Name	City	State
United States	Maryland Hematology/Oncology Associates	Baltimore	Maryland
United States	Charleston Hematology-Oncology, P.A.	Charleston	South Carolina
United States	Family Cancer Center	Collierville	Tennessee
United States	Oncology Clinic, P.C.	Colorado Springs	Colorado
United States	Antelope Valley Hospital	Lancaster	California
United States	Logan Regional Hospital	Logan	Utah
United States	Medical Oncology Care Associates	Orange	California
United States	Hematology Oncology Associates of theTreasure Coast - Port St. Lucie	Port Saint Lucie	Florida
United States	North Florida Cancer Center	St. Augustine	Florida
United States	California Cancer Medical Center	West Covina	California

Sponsors (1)

Lead Sponsor	Collaborator
Pharmatech Oncology

Country where clinical trial is conducted

United States,