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Breast Neoplasms clinical trials

View clinical trials related to Breast Neoplasms.

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NCT ID: NCT00169533 Completed - Neoplasms, Breast Clinical Trials

Rollover Study Of Lapatinib In Cancer Patients

Start date: August 19, 2004
Phase: Phase 1
Study type: Interventional

The EGF19060 study is a rollover study to evaluate the long term safety of lapatinib and to provide lapatinib to patients who had a positive response in previous lapatinib studies until lapatinib is available pending FDA approval.

NCT ID: NCT00169104 Terminated - Clinical trials for Metastatic Breast Cancer

Effects of Granulocyte Colony-stimulating Factor (G-CSF), Trastuzumab, and Vinorelbine on Immune Cell Function

Start date: July 2002
Phase: Phase 2/Phase 3
Study type: Interventional

Trastuzumab or Herceptin is an antibody directed against Her-2. Her-2 is a growth factor receptor which is present on the tumors of 25% of patients with breast cancer. The addition of trastuzumab to chemotherapy has been shown in a randomized clinical trial to increase the response rate to chemotherapy, the duration of response to chemotherapy, and to improve the duration of survival of patients with metastatic breast cancer. The anticancer mechanism of action of trastuzumab is unknown, but it is possible that trastuzumab acts by promoting antibody-dependent cell mediated cytotoxicity (ADCC), or direct killing of cancer cells by immune cells, triggered by antibodies bound to the surface of the cancer cell. G-CSF is a drug which is a growth factor for certain types of immune cells. G-CSF has two favorable effects on ADCC. G-CSF increases the pool of circulating cancer-killing immune cells, and G-CSF increases the strength of binding of cancer-killing immune cells to a specific part of the antibody. Therefore, priming with G-CSF significantly increases the efficiency of ADCC, and four days of treatment with G-CSF has been shown to optimize ADCC in some studies. Recent data from the investigators' laboratory indicates that chemotherapy can augment ADCC directed against tumor cells. The investigators' hypothesis is that pre-treatment with the drug G-CSF would increase the effectiveness of chemotherapy given with trastuzumab.

NCT ID: NCT00167414 Completed - Clinical trials for Breast Cancer, Metastatic

Study for Using Radiosurgery on Limited Metastases of Breast Cancer

Start date: December 2000
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate whether radiosurgery, along with standard chemotherapy, immunotherapy (the treatment of cancer by modulating the immune system and immune response), or hormonal therapy, affects the quality and length of life. The standard therapy is surgery, radiation therapy, or chemotherapy alone or in any combination. A second purpose of this study is to determine if the levels of a special type of protein (called cytokines) found in the blood are related to the quality of life while on this treatment.

NCT ID: NCT00166998 Recruiting - Breast Neoplasms Clinical Trials

The Study of Infrared Imaging on Breast Cancer

Start date: March 2005
Phase: N/A
Study type: Observational

Breast cancer can cause focal temperature increase on the breast skin due to vasodilatation mediated by NO secretion from cancer cells. Our study is to evaluate this situation and to assess the diagnostic efficacy of infrared imaging (thermography)on breast cancer.

NCT ID: NCT00166543 Completed - Breast Cancer Clinical Trials

Three Doses of TAS-108 to Treat Recurrent or Recurrent Inoperable Breast Cancer

Start date: May 2004
Phase: Phase 2
Study type: Interventional

This study is being done to find out how safe TAS-108 is and how well TAS-108 works on recurrent or recurrent inoperable breast cancer.

NCT ID: NCT00165581 Terminated - Breast Cancer Clinical Trials

High Dose Rate Intracavitary Brachytherapy as the Sole Method of Radiation Therapy for Breast Carcinoma

Start date: December 2002
Phase: N/A
Study type: Interventional

The purpose of this study is to understand the side effects (skin reaction, infection and abscess formation) at the site of radiation treatment, which my occur during the treatment and following 2 months using a new method of radiation therapy for breast cancer.

NCT ID: NCT00165308 Completed - Breast Cancer Clinical Trials

Tamoxifen in the Prevention of Breast Cancer in Hodgkin's Disease Survivors

Start date: April 2001
Phase: N/A
Study type: Interventional

The purpose of this study is determine whether or not tamoxifen reduces the chance of Hodgkin's Disease survivors developing breast cancer.

NCT ID: NCT00165243 Completed - Clinical trials for Early-Stage Breast Cancer

Tangential Radiation Therapy Without Axillary Dissection in Breast Cancer

Start date: September 1998
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate whether treatment to the axilla (area under the arm) can be safely minimized by omitting axillary surgery and full axillary radiation therapy and replacing it with radiation therapy to the breast and lower axilla.

NCT ID: NCT00162929 Completed - Clinical trials for Metastatic Breast Cancer

Her-2/Neu in Patients With Metastatic Breast Cancer (AdHERe)

AdHERe
Start date: January 2005
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the maximum tolerated dose and/or maximum attainable dose of a vaccine consisting of human autologous dendritic cells transduced by an adenovector expressing rat Her-2/neu (AdHer-2/neu) in patients with metastatic breast cancer.

NCT ID: NCT00162812 Terminated - Breast Cancer Clinical Trials

Topoisomerase II Alpha Gene Amplification and Protein Overexpression Predicting Efficacy of Epirubicin

TOP
Start date: January 2003
Phase: Phase 2
Study type: Interventional

prospective evaluation of topoisomerase II alpha gene amplification and protein overexpression as markers predicting the efficacy of epirubicin in the primary treatment of breast cancer patients.