Clinical trial · Interventional
Trial of ZD1839 (Iressa) and Tamoxifen in Breast Cancer Patients
A Neoadjuvant Phase II Trial of ZD1839 (Iressa) and Tamoxifen in Inoperable Locally Advanced HER2-Overexpressing, ER-Positive Breast Cancer Patients: Biologic Correlative Study (AZ #1839US/0303)
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): halted by the PI only 3 of 45 subjects were accrued.
Summary
Brief summary (as posted)
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
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Iressa and Tamoxifen
- description
- Iressa and Tamoxifen
- interventionNames
- Drug: Iressa
- Drug: Tamoxifen
Primary outcomes (1)
- measure
- cellular response
- timeFrame
- 10 years
- description
- mechanisms of the cellular response, markers predicting response, by investigating whether ZD1839 with or without tamoxifen treatment is associated with altered biomarkers in cells isolated by core needle biopsy
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. All patients must be female and must have signed an informed consent form. 2. 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. 3. Negative serum pregnancy test (bHCG) within 7 days of starting study, if of child-bearing potential. 4. 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. 5. Renal function tests: * creatinine within 1.5 times the institution's upper limit of normal (ULN). 6. Liver function tests: * Total serum bilirubin within ULN, * liver transaminases within 2.5 x ULN, * alkaline phosphatase within 5 x ULN. 7. Performance status (WHO scale) \<2. 8. Age \> 18 years. Exclusion Criteria: 1. Pregnancy or unwillingness to use a reliable contraceptive method in women of child-bearing potential. 2. Women who are lactating or breastfeeding. 3. Severe underlying chronic illness or disease. 4. Patients on other investigational drugs while on study will be excluded. 5. Severe or uncontrolled hypertension, history of congestive heart failure, acute myocardial infarction, or severe coronary arterial disease. 6. 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. 7. Any evidence of ongoing interstitial lung disease. 8. Concomitant use of phenytoin, carbamazepine, rifampicin, barbiturates, or St John's Wort. 9. Treatment with a non-approved or investigational drug within 30 days before Day 1 of study treatment. 10. Known severe hypersensitivity to ZD1839 or any of the excipients of this product.
References
Publications (0)
Data not yet available