Gefitinib With or Without Tamoxifen in Treating Patients With Tamoxifen-Resistant Metastatic Breast Cancer

Breast Cancer Clinical Trial

Official title:

ZD1839 (IRESSA) In Tamoxifen-Resistant Metastatic Breast Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00080743
• Other study ID #: CDR0000355145
• Secondary ID: DMS-0236ZENECA-I
• Status: Completed
• Phase: Phase 2
• First received: April 7, 2004
• Last updated: August 4, 2009
• Start date: January 2004
• Est. completion date: November 2005

Study information

• Verified date: August 2009
• Source: Dartmouth-Hitchcock Medical Center
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Gefitinib may stop the growth of tumor cells by blocking the enzymes necessary for their growth. Hormone therapy using tamoxifen may fight breast cancer by blocking the use of estrogen by the tumor cells. Combining gefitinib with tamoxifen may be effective in killing tumor cells that have become resistant (stopped responding) to tamoxifen.

PURPOSE: This randomized phase II trial is studying how well giving gefitinib together with tamoxifen works compared to gefitinib alone in treating patients with metastatic breast cancer that has stopped responding to tamoxifen.

Description:

OBJECTIVES:

Primary

• Compare the rate of clinical benefit in patients with tamoxifen-resistant breast cancer treated with gefitinib with or without tamoxifen.

Secondary

• Determine the toxic effects of these regimens in these patients.

• Determine whether changes in fludeoxyglucose F 18 uptake by positron emission tomography scan and changes in plasma DNA levels are indicators of an early response to gefitinib in these patients.

• Determine the pharmacokinetics of these regimens in these patients.

OUTLINE: This is a randomized, double-blind, placebo-controlled study. Patients are stratified according to population (intent-to-treat population comprising all patients who receive 1 dose of treatment vs a subset of the intent-to-treat population, excluding patients with nonmeasurable/evaluable only disease). Patients are randomized to 1 of 2 treatment arms.

• Arm I: Patients receive oral tamoxifen once daily. Beginning 14 days after the start of tamoxifen, patients receive oral gefitinib once daily.

• Arm II: Patients receive oral placebo once daily. Beginning 14 days after the start of placebo, patients receive oral gefitinib as in arm I.

In both arms, treatment continues for 26 weeks in the absence of disease progression or unacceptable toxicity.

Patients are followed for 6 months.

PROJECTED ACCRUAL: A total of 46 patients (23 per treatment arm) will be accrued for this study within 23 months.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 2
• Est. completion date: November 2005
• Est. primary completion date: April 2005
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• Histologically confirmed breast cancer

• Metastatic disease

• Initial clinical benefit from tamoxifen for metastatic disease, defined by 1 of the following:

• Stable disease for 24 weeks or longer

• Objective tumor response

• Documentation of clinical progression on tamoxifen within the past 6 weeks

• Hormone receptor status:

• Estrogen or progesterone receptor positive on most recently analyzed biopsy

PATIENT CHARACTERISTICS:

Age

• 18 and over

Sex

• Not specified

Menopausal status

• Not specified

Performance status

• ECOG 0-2

Life expectancy

• At least 6 months

Hematopoietic

• Absolute neutrophil count = 1,500/mm^3

• Platelet count = 100,000/mm^3

Hepatic

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

• Bilirubin = 1.5 times ULN

Renal

• Creatinine = 1.5 times ULN OR

• Creatinine clearance = 50 mL/min

Pulmonary

• No clinically active interstitial lung disease

• Patients with asymptomatic chronic stable radiographic changes are eligible

Other

• Not pregnant or nursing

• Fertile patients must use effective contraception

• No known hypersensitivity to gefitinib

• No other malignancy within the past 5 years except basal cell carcinoma or carcinoma in situ of the cervix

PRIOR CONCURRENT THERAPY:

Biologic therapy

• No concurrent trastuzumab (Herceptin®)

Chemotherapy

• No concurrent cytotoxic chemotherapy

Endocrine therapy

• See Disease Characteristics

• At least 2 weeks since other prior tamoxifen

• No concurrent hormone replacement therapy

• No other concurrent antiestrogens, including raloxifene

• No concurrent aromatase inhibitors

• No concurrent megestrol

• Concurrent systemic steroids for reasons other than skin toxicity allowed provided the steroids were initiated before study entry AND dose remains stable

Radiotherapy

• Concurrent palliative radiotherapy as short-term treatment for symptomatic bone metastases allowed provided other evaluable sites of disease are present AND treatment lasts no more than 14 days

Surgery

• Recovered from prior oncologic or other major surgery

• No concurrent surgery during and for 7 days after study treatment

• No concurrent ophthalmic surgery

Other

• Recovered from all prior therapy (except alopecia)

• More than 30 days since prior investigational drugs

• No other concurrent investigational agents

• No concurrent administration of any of the following:

• Phenytoin

• Carbamazepine

• Barbiturates

• Rifampin

• Phenobarbital

• Hypericum perforatum (St. John's wort)

• Systemic retinoids

• CYP3A4 inhibitors (e.g., itraconazole)

• Drugs that cause significant sustained elevation in gastric pH = 5

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Drug:
• gefitinib
250 mg po once daily
• tamoxifen citrate
20 mg po once daily
• Placebo
One pill po once daily

Locations

Country	Name	City	State
United States	Norris Cotton Cancer Center at Dartmouth-Hitchcock Medical Center	Lebanon	New Hampshire

Sponsors (3)

Lead Sponsor	Collaborator
Dartmouth-Hitchcock Medical Center	National Cancer Institute (NCI), Norris Cotton Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical benefit rate (complete response, partial response, and stable disease) for 26 weeks		26 weeks	No