Letrozole and Celecoxib in Treating Postmenopausal Women With Locally Advanced or Metastatic Breast Cancer

Breast Cancer Clinical Trial

Official title:

Phase II Study of Letrozole (Femara) and Celecoxib (Celebrex) in Postmenopausal Women With Hormone Receptor-Positive Locally Advanced or Metastatic Breast Cancer

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00101062
• Other study ID #: 040402-4671; CDR0000407502
• Secondary ID: P30CA072720CINJ-
• Status: Terminated
• Phase: Phase 2
• First received: January 7, 2005
• Last updated: June 3, 2011
• Start date: January 2004
• Est. completion date: December 2005

Study information

• Verified date: June 2011
• Source: Rutgers, The State University of New Jersey
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Estrogen can cause the growth of breast cancer cells. Hormone therapy using letrozole may fight breast cancer by lowering the amount of estrogen the body makes. Celecoxib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Giving letrozole with celecoxib may kill more tumor cells.

PURPOSE: This phase II trial is studying how well letrozole and celecoxib work in treating postmenopausal women with locally advanced or metastatic breast cancer.

Description:

OBJECTIVES:

Primary

• Determine the response rate in postmenopausal women with hormone receptor-positive locally advanced or metastatic adenocarcinoma of the breast treated with letrozole and celecoxib as first-line therapy.

Secondary

• Determine the time to disease progression and overall survival of patients treated with this regimen.

• Determine the toxicity of this regimen in these patients.

• Compare cyclooxygenase activity in blood and tumor cells from these patients before and after treatment with this regimen.

• Determine the effect of this regimen on aromatase activity, tumor proliferation, and angiogenesis in tumor samples from these patients.

OUTLINE: This is a multicenter study.

Patients receive oral letrozole once daily and oral celecoxib twice daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

Patients are followed for survival.

PROJECTED ACCRUAL: A total of 45-72 patients will be accrued for this study.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 0
• Est. completion date: December 2005
• Est. primary completion date: December 2005
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• Histologically or cytologically confirmed adenocarcinoma of the breast

• Locally advanced or metastatic disease

• Measurable disease

• No bone disease only

• No history of brain metastases unless controlled with radiotherapy or surgical resection for = 6 months before study entry

• Hormone receptor status:

• Estrogen receptor- OR progesterone receptor-positive

PATIENT CHARACTERISTICS:

Age

• 18 and over

Sex

• Female

Menopausal status

• Postmenopausal, as defined by 1 of the following:

• Prior bilateral oophorectomy

• Prior bilateral ovarian irradiation

• No spontaneous menstrual bleeding within the past 12 months

• Age 55 and over AND prior hysterectomy without oophorectomy

• Age 54 and under AND prior hysterectomy without oophorectomy (or status of ovaries is unknown) AND documented follicle-stimulating hormone level in postmenopausal range

Performance status

• ECOG 0-2

Life expectancy

• At least 3 months

Hematopoietic

• Granulocyte count = 1,000/mm^3

• Platelet count = 100,000/mm^3

Hepatic

• Bilirubin = 1.5 times upper limit of normal (ULN)

• AST and ALT = 2.5 times ULN

Renal

• Creatinine = 1.5 times ULN

Other

• No prior allergic reaction attributed to compounds of similar chemical or biologic composition to study drugs

• No prior allergic reaction to sulfonamides

• No active peptic ulcer disease

• No active infection

• No other medical condition that would preclude study participation

• Able to swallow oral medication

PRIOR CONCURRENT THERAPY:

Biologic therapy

• Not specified

Chemotherapy

• No prior chemotherapy for metastatic or recurrent disease

Endocrine therapy

• No prior endocrine therapy for metastatic disease

• Prior adjuvant tamoxifen allowed

• No prior aromatase inhibitors

• No prior hormonal therapy for recurrent disease

• No other concurrent hormonal therapy

Radiotherapy

• See Disease Characteristics

• See Menopausal status

• No concurrent radiotherapy

Surgery

• See Disease Characteristics

• See Menopausal status

Other

• No concurrent fluconazole or lithium

• No concurrent aspirin, non-steroidal anti-inflammatory drugs, or other cyclooxygenase-2 inhibitors

• Concurrent chronic cardioprotective low-dose aspirin allowed

• No other concurrent investigational agents

Study Design

Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Drug:
• celecoxib

• letrozole

Locations

Country	Name	City	State
United States	Cancer Institute of New Jersey at UMDNJ - Robert Wood Johnson Medical School	New Brunswick	New Jersey

Sponsors (2)

Lead Sponsor	Collaborator
University of Medicine and Dentistry of New Jersey	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

External Links

•   Clinical trial summary from the National Cancer Institute's PDQ® database