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Invasive Breast Cancer clinical trials

View clinical trials related to Invasive Breast Cancer.

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NCT ID: NCT01765049 Active, not recruiting - Clinical trials for Invasive Breast Cancer

Breast Density Change Predicting Response to Adjuvant Aromatase Inhibitor

DEAR
Start date: January 2013
Phase:
Study type: Observational [Patient Registry]

Breast density change after short term use of aromatase inhibitor in postmenopausal ER positive breast cancer would predict endocrine responsiveness

NCT ID: NCT01717131 Active, not recruiting - Clinical trials for Invasive Breast Cancer

Axillary Node Dissection Versus no Dissection in Breast Cancer With Positive Sentinel Lymph Node

Start date: July 19, 2012
Phase: N/A
Study type: Interventional

Data from cohorts, prospective studies and one randomized trial (ASCOG Z0011) support the hypothesis that omission of additional axillary dissection in case of positive sentinel node has a limited impact on overall survival and relapse free survival. However, these data are not sufficient enough to recommend, as a standard of care, to avoid axillary dissection in case of positive sentinel node. The ASCOG Z0011 trial has been closed before the end of inclusions and the predefined non inferiority margin was found to be too large (5% difference at 5 years for primary endpoint). Prospective randomized trial is then urgently mandatory before omission of axillary node dissection becomes a usual practice without a sufficient scientific level of proof. Indeed, in several reviews, the rate of omission of axillary node dissection in case of micrometastasis increased (Bilimoria) despite any strong proof has been demonstrated. The omission of axillary node dissection in case of positive sentinel node may have strong practical impacts on patients but also on medical and economical aspects: in avoiding a prolonged hospitalisation, secondary morbidities due to axillary dissection requiring secondary care and their costs, as well as costs for secondary axillary dissection (14 to 25% in case of positive sentinel node) and finally shortening surgery duration. The main investigator propose a Non Inferiority Randomized Multicenter Phase III Trial of Axillary Node Dissection Versus no Axillary Node Dissection in Case of Positive Sentinel Lymph Node in Invasive Breast Cancer

NCT ID: NCT01597999 Recruiting - Clinical trials for Invasive Breast Cancer

Benefits of Breast MRI for Predicting of Histopathologic Cell Type of Small Breast Cancer

Start date: February 2011
Phase: Phase 4
Study type: Interventional

This study examines the additional benefits of magnetic resonance imaging (MRI) with Gadovist in early breast cancer with poor prognostic features.

NCT ID: NCT01509781 Recruiting - Clinical trials for Invasive Breast Cancer

Suction Drain Versus the Use of Adaptive Skin Sutures After Mastectomy ± Axillary Lymphadenectomy; a Prospective Randomised Study

Start date: September 2011
Phase: Phase 3
Study type: Interventional

The objective of this prospective randomized study is to perform qualitative and quantitative comparisons between the insertion of traditional suction drains (Arm: Suction drain) versus the application of absorbable adaptive sutures (Arm: Adaptive suture) following simplex mastectomy or modified radical mastectomy in the light of the total volume of withdrawn serum from wound cavity, the extent of early postoperative analgesic requirements and quality of life.

NCT ID: NCT01340495 Active, not recruiting - Clinical trials for Invasive Breast Cancer

Proton Radiation Therapy for Invasive Breast Cancer Following Mastectomy

Start date: June 2011
Phase: N/A
Study type: Interventional

In this study we are looking at a type of radiation called proton radiation which is known to spare surrounding tissue and organs from radiation. The proton radiation will be delivered using 3D conformal proton radiation or scanned beam/IMPT (Intensity Modulated Proton Radiation Treatment). Proton radiation delivers no dose beyond the region requiring treatment. This may reduce side effects that patients would normally experience with conventional radiation therapy or other means of delivering proton radiation therapy. In this study we are evaluating the effectiveness of using proton radiation delivered to reduce side effects association with radiation treatment.

NCT ID: NCT01194427 Terminated - Clinical trials for Stage II Breast Cancer

A Study of Vorinostat and Tamoxifen in Newly Diagnosed Breast Cancer

Start date: March 2011
Phase: Phase 2
Study type: Interventional

This research study is designed to look at the effects of the combination of vorinostat (Suberoylanilide Hydroxamic Acid or Zolinza) and tamoxifen on breast cancer tissue. The investigators will do this by comparing tissues from the original breast biopsy to tissues obtained after taking vorinostat and tamoxifen for 2 weeks.

NCT ID: NCT01138553 Terminated - Clinical trials for Invasive Breast Cancer

Preoperative Testing of the Anti-Progesterone Mifepristone in Early Stage Breast Cancer

Start date: June 2010
Phase: Early Phase 1
Study type: Interventional

The primary objective of this study is to identify the group of women with early stage breast cancer most likely to benefit from treatment with the selective progesterone receptor modulator (SPRM) mifepristone. This will be done by treating women briefly prior to planned surgery and examining the decrease in growth rate (measured by Ki-67 immunohistochemistry) in tumor samples taken before and after exposure to mifepristone.

NCT ID: NCT01060085 Completed - Clinical trials for Invasive Breast Cancer

Digital Breast Tomosynthesis Versus Contrast Enhanced Magnetic Resonance Imaging (MRI) for Breast Cancer Staging

Start date: February 2009
Phase: N/A
Study type: Observational

The primary objective of this study is to compare the diagnostic accuracy of Digital Breast Tomosynthesis (DBT) versus that of Contrast Enhanced Magnetic Resonance Imaging (CEMRI) in determining the size of breast cancer preoperatively. Secondary objectives include: 1. Comparing the operating characteristics of each combined imaging protocol with respect to the reference standard, i.e. histopathologic assessment, of additional non-index lesions. 2. Comparison of re-excision rates based on estimated disease extent from adjunctive CEMRI vs. adjunctive DBT. 3. Evaluation of patient satisfaction with regard to the adjunctive modality (DBT vs. CEMRI).

NCT ID: NCT01004744 Completed - Clinical trials for Invasive Breast Cancer

Pre-Surgical Intervention for Targeted Therapies for Breast Cancer

Start date: July 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the feasibility of a short term administration of a targeted therapy (i.e., anastrozole) in women with newly diagnosed early invasive or non invasive breast cancer during the interval between their breast biopsy and surgery. Anastrozole is a form of hormonal therapy which is part of the standard treatment for hormone sensitive breast cancer in postmenopausal women. This clinical model is being used to evaluate the biologic effects of this drug on a specific molecular pathway called the PI3K/AKT signaling pathway.

NCT ID: NCT00983684 Completed - Breast Cancer Clinical Trials

Comparison of Intra-operative Radiotherapy With Post-operative Radiotherapy for Women With Early Breast Cancer

TARGIT
Start date: March 2000
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate whether a single fraction of radiotherapy given intra-operatively and targeted to the tissues at the highest risk of local recurrence is equivalent to standard post-operative external beam radiotherapy after breast conserving surgery in women with early stage breast cancer in terms of local relapse within the treated breast.