Capecitabine Plus Radiotherapy for Local Relapse Breast Cancer With Negative Her2 Tumours

NCT ID: NCT00434941

Last Updated: 2019-02-21

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 1 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-09-30
• Study Completion Date: 2009-01-31

Brief Summary

This is a prospective, open-label, multicenter phase IV.II study. Patients with local relapse breast cancer will receive radiotherapy concomitant to the administration of capecitabine.

Detailed Description

Total dose of radiotherapy will be 50 Gy administered in daily session of 200 centigray (cGy). Radiotherapy treatment will not be longer than 6 weeks.

All patients will receive 1650 mg/m2 by mouth, per day (825 mg/m2 twice a day (p.o. bid) for 35 days.

Tissue samples must be analysed to determinate the human epidermal growth factor receptor-2 (HER2) by fluorescent in situ hybridization (FISH) technical.

Conditions

Breast Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Radiotherapy + Capecitabine

Radiotherapy (for 25 days; Dose: 50 Gy) + Capecitabine (for 35 days; Dose: 825 mg/m2 twice per day p.o.) Experimental treatment consists of administration of 825 mg/m2 x 2 daily p.o., for 7 days simultaneously with daily radiotherapy treatment.Capecitabine will be administered for 35 days as maximum.

Group Type: EXPERIMENTAL

Capecitabine

Intervention Type: DRUG

Radiotherapy

Intervention Type: RADIATION

Interventions

Capecitabine

Intervention Type: DRUG

Radiotherapy

Intervention Type: RADIATION

Other Intervention Names

Xeloda

Eligibility Criteria

Inclusion Criteria

• Written informed consent.
• Histological diagnoses of operable invasive adenocarcinoma of the breast.
• Patients with tumour HER2 negative.
• Previous mastectomy surgery.
• Actual diagnoses of local recurrence of breast cancer.
• Patients must not present evidence of metastatic disease.
• Age >= 18 years old.
• Performance status (Karnofsky index) >= 70.
• Laboratory results (within 14 days prior to randomization):
• Hematology:

• neutrophils >= 1.5 x 10e9/l;
• platelets >= 100x 10e9/l;
• hemoglobin >= 10 mg/dl
• Hepatic function:

• total bilirubin <= 1,5 upper normal limit (UNL);
• Alanine transaminase (SGOT) and aspartate aminotransferase (SGPT) <= 1.5 UNL;
• alkaline phosphatase <= 1.5 UNL.
• Renal Function:

• creatinine <= 175 µmol/l (2 mg/dl)or creatinine clearance >= 60 ml/min.

Exclusion Criteria

• Distant metastasis or metastatic disease in organs.
• Metastasis in internal mammary chain lymph nodes
• Previous radiation treatment on the breast or other locations (30% or greater of the bone marrow).
• Prior treatment with continuous (greater than 24h) 5-fluorouracil (5-FU) infusion, capecitabine or other oral fluoropyrimidines such as eniluracil/5-FU , uracil/tegafur, S1 or emitefur.
• Known hypersensitivity to capecitabine, doxifluridine or any of its components.
• Organ allografts that require an immunosuppressor therapy.
• History of neurological or psychiatric disorders, which could preclude the patients to free informed consent.
• Clinically significant cardiac disease such as congestive heart failure, symptomatic coronary artery disease and cardiac arrhythmia not well controlled with medication or history of myocardial infarction within the last 12 months or uncontrolled hypertension.
• Evidence of central nervous system (CNS) metastases. Pts with a history of uncontrolled seizures, CNS disorders or psychiatric disability judged by the investigator to be clinically significant precluding informed consent or interfering with compliance should be excluded from the study.
• Pregnant or lactating women. Adequate contraceptive methods must be used during chemotherapy and hormone therapy treatments. Negative pregnancy test in the 14 previous days to randomization.
• Active uncontrolled infection or other severe pathologies such as active peptic ulcer, unstable diabetes mellitus.
• Major surgery during 4 weeks prior to treatment.
• Patients lacking physical integrity of upper gastrointestinal tract or with history of bad absorption syndrome.
• Anticoagulant treatment with coumadin anticoagulants.
• Concomitant treatment with other investigational products. Participation in other clinical trials with a non-marketed drug in the 30 previous days before randomization.
• Concomitant treatment with other therapy for cancer.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Hoffmann-La Roche

INDUSTRY

Sponsor Role: collaborator

Spanish Breast Cancer Research Group

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Study Director

Role: STUDY_DIRECTOR

Hospital Clínico Universitario San Carlos

Locations

Hospital Infanta Cristina

Badajoz, , Spain

Hospital de la Esperanza

Barcelona, , Spain

Hospital Universitario de la Princesa

Madrid, , Spain

Hospital Clínico Universitario San Carlos

Madrid, , Spain

Hospital Universitario La Paz

Madrid, , Spain

Hospital Universitario Virgen de la Arrixaca

Murcia, , Spain

Hospital Universitario La Fe

Valencia, , Spain

Countries

Spain

Related Links

http://www.geicam.org

Sponsor's website

Other Identifiers

GEICAM/2005-01

Identifier Type: -

Identifier Source: org_study_id