Cyclophosphamide and Docetaxel or Doxorubicin in Treating Women With Newly Diagnosed Breast Cancer That Can Be Removed by Surgery

NCT ID: NCT00801411

Last Updated: 2009-06-17

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 318 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-10-31

Brief Summary

RATIONALE: Drugs used in chemotherapy, such as cyclophosphamide, docetaxel, and doxorubicin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving combination chemotherapy before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. It is not yet known which chemotherapy regimen is more effective in treating breast cancer.

PURPOSE: This randomized phase II trial is studying cyclophosphamide given together with docetaxel to see how well it works compared with cyclophosphamide given together with doxorubicin in treating women with newly diagnosed breast cancer that can be removed by surgery.

Detailed Description

OBJECTIVES:

Primary

• To evaluate tumor pathological complete response rate after neoadjuvant cyclophosphamide in combination with docetaxel vs doxorubicin hydrochloride in women with operable clinically node-negative breast cancer and normal topoisomerase IIα expression.

Secondary

• To assess tumor clinical and pathological overall response rates in patients treated with these regimens.
• To assess the safety and toxicity of these regimens.
• To assess disease-free survival and overall survival of these patients.
• To assess the efficacy of short-course (3 days) filgrastim (G-CSF) as primary and secondary prophylaxis against febrile neutropenia in patients receiving docetaxel and cyclophosphamide.

OUTLINE: This is a multicenter study.

Patients are stratified according to hormone receptor status (estrogen receptor [ER]- or progesterone receptor [PR]-positive vs ER- and PR-negative) and T stage (T2 vs T3). Patients are randomized to 1 of 2 treatment arms.

• Arm I: Patients receive cyclophosphamide IV and docetaxel IV over 1 hour on day 1.
• Arm II: Patients receive cyclophosphamide IV and doxorubicin hydrochloride IV on day 1.

In both arms, treatment repeats every 21 days for 4 courses in the absence of disease progression or unacceptable toxicity. After completion of neoadjuvant chemotherapy, all patients undergo surgery.

Tumor specimens obtained prior to neoadjuvant chemotherapy are analyzed for topoisomerase IIα gene and protein expression by IHC and FISH. Tissue samples are also collected at surgery for future studies.

After completion of study therapy, patients are followed every 3 months for 2 years, every 6 months for 3 years, and then annually for 5 years.

Conditions

Breast Cancer

Study Design

• Allocation Method: RANDOMIZED
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm I

Patients receive cyclophosphamide IV and docetaxel IV over 1 hour on day 1.

Group Type: EXPERIMENTAL

cyclophosphamide

Intervention Type: DRUG

Given IV

docetaxel

Intervention Type: DRUG

Given IV

Arm II

Patients receive cyclophosphamide IV and doxorubicin hydrochloride IV on day 1.

Group Type: ACTIVE_COMPARATOR

cyclophosphamide

Intervention Type: DRUG

Given IV

doxorubicin hydrochloride

Intervention Type: DRUG

Given IV

Interventions

cyclophosphamide

Given IV

Intervention Type: DRUG

docetaxel

Given IV

Intervention Type: DRUG

doxorubicin hydrochloride

Given IV

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed invasive breast cancer

• Newly diagnosed disease
• Operable disease
• Must have clinical T2 (> 2cm) or T3 (> 5 cm) primary tumors with no clinical lymph node involvement (N0)

• No clinical T4 lesion (e.g., peau d'orange, skin ulceration, satellite nodules, or inflammatory breast cancer)
• No evidence of metastatic disease
• Known hormone receptor status

PATIENT CHARACTERISTICS:

• Menopausal status not specified
• ECOG performance status (PS) 0-2 (Karnofsky PS 60-100%)
• Life expectancy > 10 years
• Leukocytes ≥ 3,000/mm³
• ANC ≥ 1,500/mm³
• Platelet count ≥ 100,000/mm³
• Total bilirubin normal
• AST and ALT ≤ 2.5 times upper limit of normal
• Creatinine normal or creatinine clearance ≥ 40 mL/min
• Normal cardiac ejection fraction, defined as ≥ 50% by MUGA scan or 2D-ECHO
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception
• No history of allergic reactions attributed to compounds of similar chemical or biologic composition to docetaxel or other agents used in this study
• No history of pre-existing peripheral neuropathy
• No uncontrolled intercurrent illness including, but not limited to, any of the following:

• Ongoing or active infection
• Symptomatic congestive heart failure
• Unstable angina pectoris
• Cardiac arrhythmia
• Psychiatric illness/social situations that would limit compliance with study requirements
• No prior malignancies except curatively treated basal cell carcinoma of the skin or carcinoma in situ of the cervix

PRIOR CONCURRENT THERAPY:

• No prior chemotherapy or radiotherapy
• No other concurrent investigational or commercial agents or therapies with the intent to treat the patient's malignancy
• No other concurrent chemotherapy, immunotherapy, hormonal cancer therapy, surgery for cancer, or experimental medications
• No concurrent combination antiretroviral therapy for HIV-positive patients
• No other concurrent antitumor therapy

• Minimum Eligible Age: 21 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Centre, Singapore

OTHER

Sponsor Role: lead

Principal Investigators

Wong Nan Soon, MBBS, MRCP, FAMS

Role: PRINCIPAL_INVESTIGATOR

National Cancer Centre, Singapore

Locations

Singapore General Hospital

Singapore, , Singapore

Site Status: RECRUITING

National Cancer Centre - Singapore

Singapore, , Singapore

Site Status: RECRUITING

Countries

Singapore

Facility Contacts

Wong Chow Yin

Role: primary

65-6222-3322

Wong Nan Soon, MBBS, MRCP, FAMS

Role: primary

65-6-436-8088

Other Identifiers

SINGAPORE-NCC0705

Identifier Type: -

Identifier Source: secondary_id

SANOFI-AVENTIS-NCC0705

Identifier Type: -

Identifier Source: secondary_id

CDR0000624374

Identifier Type: -

Identifier Source: org_study_id