Trial of ZD1839 (Iressa) and Tamoxifen in Breast Cancer Patients

Stopped early · Phase 2

Conditions studied: Breast Cancer

In brief

The researchers want to learn whether ZD1839 can improve the activity of tamoxifen, a drug that participants will receive for the treatment of the type of breast cancer being studied. Tamoxifen medicine is part of the standard treatment for the type of breast cancer being studied. It is approved for the treatment of this problem. In order to help the researchers understand how the cancer responds to these medicines, the researchers will take a small tissue sample (biopsy) of the breast cancer before beginning treatment and after two weeks of treatment, at 6 weeks and when surgery is done as part of treatment for the cancer. If participants do not respond to treatment, another biopsy will be done to see why the participants did not respond. These samples will also be collected to look at different characteristics of the cancer. The researchers cannot and do not guarantee that participants will benefit if they take part in this study

Key facts

Study ID

NCT00206492

Run by

Baylor Breast Care Center

People needed

3

Starts

2003-07-01

Expected to finish

2006-10-01

Last updated by the study team

2017-08-01

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• All patients must be female and must have signed an informed consent form.
• Primary breast cancers must be human epidermal growth factor receptor (HER2) overexpressing (2+ or 3+, or both, as determined by immunohistochemistry [IHC]), and estrogen receptor (ER) positive. Primary breast cancers must be of clinical and/or radiologic size >4 cm, with or without gross metastatic disease according to the International Union against Cancer (UICC) modified World Health Organization (WHO) criteria.
• Negative serum pregnancy test (bHCG) within 7 days of starting study, if of child-bearing potential.
• Adequate bone marrow function:
• Hematocrit >30%,
• total neutrophil count must be >1.5 x 10\^9/L, and
• platelet count >100 x 10\^9/L.
• Renal function tests:
• creatinine within 1.5 times the institution's upper limit of normal (ULN).
• Liver function tests:
• Total serum bilirubin within ULN,
• liver transaminases within 2.5 x ULN,
• alkaline phosphatase within 5 x ULN.
• Performance status (WHO scale) <2.
• Age > 18 years.

You may not qualify if…

• Pregnancy or unwillingness to use a reliable contraceptive method in women of child-bearing potential.
• Women who are lactating or breastfeeding.
• Severe underlying chronic illness or disease.
• Patients on other investigational drugs while on study will be excluded.
• Severe or uncontrolled hypertension, history of congestive heart failure, acute myocardial infarction, or severe coronary arterial disease.
• No previous or current malignancies at other sites within the preceding 5 years, with the exception of adequately treated, cone-biopsied in situ carcinoma of the cervix uteri and basal or squamous cell carcinoma of the skin.
• Any evidence of ongoing interstitial lung disease.
• Concomitant use of phenytoin, carbamazepine, rifampicin, barbiturates, or St John's Wort.
• Treatment with a non-approved or investigational drug within 30 days before Day 1 of study treatment.
• Known severe hypersensitivity to ZD1839 or any of the excipients of this product.

Where it is running

• Baylor Breast Center — Houston, Texas, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.