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| Sponsor: | National Center for Research Resources (NCRR) |
|---|---|
| Information provided by: | National Center for Research Resources (NCRR) |
| ClinicalTrials.gov Identifier: | NCT00006433 |
Purpose
Purpose: The purpose of this protocol is to evaluate the combination of Doxil chemotherapy and heat treatment for recurrent breast cancer located on the chestwall following mastectomy. This protocol also includes patients with metastatic breast cancer who have not had mastectomy but have advanced tumor remaining within the breast. Doxil is the drug adriamycin (also called doxorubicin) encapsulated in liposomes, which coats the drug with a small amount of lipid (fat). This chemotherapy is in a newer form which can be better delivered to the tumor tissue without causing as much systemic toxicity. We are combining heat treatment with this drug in an effort to further increase the delivery of drug to the tumor, which may give an increased tumor response.
Methods: The patients will be treated with chemotherapy followed by heat treatment. This will be given for 6 cycles approximately every 4 weeks. For the first cycle patients will need to be hospitalized 3 days for measurement of blood levels of drug as well as some additional radiology studies which will help us to determine whether the drug is preferentially distributed within tumor.
| Condition | Intervention | Phase |
|---|---|---|
|
Breast Cancer |
Drug: Doxil Procedure: heat treatment |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment |
Eligibility| Ages Eligible for Study: | 18 Years to 90 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Contacts and Locations| Contact: Janye Blivin, R.N., M.S.N. | 1-919-660-2174 |
| United States, North Carolina | |
| Radiation Oncology, Duke University Medical Center | Recruiting |
| Durham, North Carolina, United States, 21170 | |
| Contact: Janye Blivin, RN, MSN 919-660-2174 | |
| Principal Investigator: Leonard R. Prosnitz, MD | |
| Principal Investigator: | Leonard R. Prosnitz, M.D. |
More Information
| Study ID Numbers: | NCRR-M01RR00030-0156, M01RR00030 |
| Study First Received: | November 3, 2000 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00006433 History of Changes |
| Health Authority: | United States: Federal Government |
|
Neoplasms Neoplasms by Site Skin Diseases Breast Neoplasms Breast Diseases |