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Breast Neoplasms clinical trials

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NCT ID: NCT00301730 Completed - Breast Cancer Clinical Trials

Cellular Adoptive Immunotherapy in Treating a Patient Who Has Undergone a Donor Stem Cell Transplant for Breast Cancer That Has Spread to the Lung

Start date: October 2005
Phase: Phase 1
Study type: Interventional

RATIONALE: Biological therapy, such as cellular adoptive immunotherapy, may stimulate the immune system in different ways and stop tumor cells from growing. PURPOSE: This phase I trial is studying how well cellular adoptive immunotherapy works in treating a patient who has undergone a donor stem cell transplant for breast cancer that has spread to the lung.

NCT ID: NCT00301548 Completed - Breast Neoplasms Clinical Trials

Perioperative Chemotherapy After Primary Chemotherapy for Locally Advanced Breast Cancer

Start date: February 2000
Phase: Phase 2
Study type: Interventional

The role of early timing of adjuvant chemotherapy was postulated to be particularly important for patients with endocrine non-responsive disease. The role of cytotoxicity during the period of breast surgery itself and immediately after (perioperative chemotherapy) remained unknown. We investigated in a randomized trial the role of perioperative chemotherapy in patients treated with a preoperative chemotherapy for locally advanced breast cancer and compare it to the preoperative chemotherapy without additional cytotoxic therapy during and immediately after definitive surgery. Patients with T2-3 N0-2 M0 breast cancer, with both estrogen receptors (ER) and progesterone receptors (PgR) expressed in less than 20% of tumor cells, or with absence of progesterone receptors, received up to 6 courses of primary systemic therapy with epirubicin 25 mg/m2 intravenously (i.v.) on days 1 and 2, cisplatin 60 mg/m2 i.v. on day 1, and 5-fluorouracil 200 mg/m2 i.v. daily as continuous infusion (ECF). Patients achieving a partial or complete remission were randomized to continue the infusion of fluorouracil until 2 weeks after surgery (perioperative treatment arm) or to stop fluorouracil infusion one week before surgery, on day 21 of the sixth cycle (control arm).

NCT ID: NCT00301457 Completed - Breast Cancer Clinical Trials

Different Durations of Adjuvant Anastrozole Therapy After 2 to 3 Years Tamoxifen Therapy in Breast Cancer

DATA
Start date: June 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether 6 years adjuvant anastrozole will improve the disease free survival compared to 3 years adjuvant anastrozole in postmenopausal hormone sensitive breast cancer patients, subsequent to 2-3 years tamoxifen

NCT ID: NCT00301106 Terminated - Breast Cancer Clinical Trials

Biological Therapy in Treating Women With Breast Cancer That Has Spread to the Liver

Start date: October 2005
Phase: Phase 1
Study type: Interventional

RATIONALE: Biological therapy using a gene-modified virus that can make interleukin-12 may help the body build an effective immune response to kill tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of a gene-modified virus that can make interleukin-12 in treating women with breast cancer that has spread to the liver.

NCT ID: NCT00301080 Terminated - Breast Cancer Clinical Trials

D-cycloserine in the Management of Chemotherapy-Induced Peripheral Neuropathic Pain

Start date: February 2006
Phase: Phase 3
Study type: Interventional

D-cycloserine may help lessen pain and other symptoms of peripheral neuropathy caused by chemotherapy. It is not yet known whether D-cycloserine is more effective than a placebo in treating peripheral neuropathy caused by chemotherapy. This randomized, double-blind, placebo-controlled clinical trial was designed to study D-cycloserine at 2 different doses to see how well each works compared to the other and to a placebo in treating cancer patients with peripheral neuropathy caused by chemotherapy.

NCT ID: NCT00301041 Completed - Breast Cancer Clinical Trials

Radiation Therapy in Treating Women With Invasive Breast Cancer

Start date: April 2004
Phase: Phase 0
Study type: Interventional

RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Giving radiation therapy in different ways may kill more tumor cells. PURPOSE: This randomized clinical trial is studying the side effects and best way to give radiation therapy and to see how well it works in treating patients with invasive breast cancer.

NCT ID: NCT00300781 Completed - Neoplasms Clinical Trials

Study Evaluating HKI-272 (Neratinib) In Subjects With Advanced Breast Cancer

Start date: August 4, 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to learn whether neratinib is safe and effective in treating women with advanced human epidermal growth factor receptor 2 (HER2) positive breast cancer.

NCT ID: NCT00300508 Completed - Breast Neoplasms Clinical Trials

3 Years of Anastrozole vs. no Treatment as Extended Adjuvant Therapy for Postmenopausal Women With Breast Cancer

Start date: January 1996
Phase: Phase 3
Study type: Interventional

The study assesses the effect of a further 3 years adjuvant treatment with anastrozole vs. an untreated control group after initial 5 years of adjuvant hormone-therapy.

NCT ID: NCT00299286 Completed - Breast Cancer Clinical Trials

Short-term Presurgical Study to Assess Molecular Predictors of Lapatinib's Effects in Primary Breast Cancer

MAPLE
Start date: June 2007
Phase: Phase 2
Study type: Interventional

To provide an in vivo measure of the activity of lapatinib. To assess the antiproliferative effects of lapatinib in breast cancer, ie how much lapatinib slows down the growth of cancer cells by measuring K167 (a marker of proliferation) in breast tumours before and after a short treatment with lapatinib.

NCT ID: NCT00299117 Completed - Breast Cancer Clinical Trials

Brief Smoking Intervention for Women Undergoing Breast Cancer Surgery

Start date: April 2006
Phase: N/A
Study type: Interventional

The primary purpose of this study is to examine the effect of a brief preoperative smoking intervention on postoperative complications in women undergoing breast cancer surgery. Secondary purposes are to examine long-term smoking cessation rates and experienced stress and nicotine withdrawal symptoms during the smoking cessation period.