Clinical Trials Logo

Breast Neoplasms clinical trials

View clinical trials related to Breast Neoplasms.

Filter by:

NCT ID: NCT03900884 Active, not recruiting - Clinical trials for Breast Neoplasm Female

Palbociclib, Letrozole & Venetoclax in ER and BCL-2 Positive Breast Cancer

PALVEN
Start date: September 25, 2019
Phase: Phase 1
Study type: Interventional

This study is investigating the combination of palbociclib, letrozole and venetoclax in ER and BCL-2 positive locally advanced or metastatic breast cancer. It is hypothesised that venetoclax may augment the actions of palbociclib and letrozole in these patient groups. The primary objective of the study is to determine the maximum tolerated dose of the combination treatment, which can be used in subsequent studies. The study will also investigate disease response and survival. Participants will receive palbociclib (daily, on days 1-21 of each 28 day cycle), letrozole (daily, on days 1-28 of each 28 day cycle) and venetoclax (daily, on days 1-21 of each 28 day cycle) until the last patient has completed 18 months treatment on the study.

NCT ID: NCT03900637 Active, not recruiting - Breast Cancer Clinical Trials

PersonaLized neoAdjuvant Strategy ER Positive and HER2 Negative Breast Cancer TO Increase BCS Rate

Start date: November 8, 2019
Phase: Phase 2
Study type: Interventional

In ER+ and HER2- breast cancer(BC) patients for whom BCS is not feasible, we investigate the rate of BCS can be increased while decreasing unnecessary chemotherapy thru selective neoadjuvant chemotherapy or neoadjuvant endocrine therapy using tools of nodal status, Ki-67, and multigene assay(Mammaprint)

NCT ID: NCT03900299 Active, not recruiting - Breast Cancer Clinical Trials

Evaluating New Surgical Technique in Management of Female Patients With Operable Multifocal Breast Cancer

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

Multi-focal Breast Cancers(MFBC) still have undiscoverable Clinical Significance reflecting on a debatable surgical decision for this Category of breast cancer. A prospective study was conducted using certain surgical technique as a surgical treatment for female patients with operable breast cancer managed at the Surgical Oncology Unit, Alexandria University from May. 2017 to May2018 and will be followed for 3 Years.Analysis will be done to settle a paradigm for surgical management of Multi-focal Breast Cancer

NCT ID: NCT03898947 Completed - Breast Cancer Clinical Trials

Endometrial Changes in Breast Cancer Women With or Without Hormonal Therapies

BETA-1
Start date: January 2007
Phase:
Study type: Observational

A history of breast cancer is a risk factor for the development of endometrial pathologies, such as typical and atypical glandular hyperplasia, endometrial polyps, uterine fibroids, endometrial adenocarcinoma and uterine sarcoma, probably due to some common risk factors (eg. obesity, nulliparity). Even if ethiopathogenesis for breast cancer and endometrial pathologies is not well established, both genetic factors and hyperestrogenic state may be play a pivotal role for their development. Indeed, relative hyperestrogenism is also the main target for the treatment of breast cancer. Currently used therapies for this purpose are selective estrogen receptor (ER) modulators (SERMs), such as Tamoxifen (TAM), and third generation non-steroidal aromatase inhibitors (AIs), such as letrozole and anastrozole. TAM has both agonist and antagonist properties, depending upon the individual target organ and circulating levels of serum estrogens: on the one hand, it blocks estrogen stimulation in breast tissue; on the other hand, TAM shows an ER agonist activity in the endometrium that is able to stimulate proliferation and, in some cases, it causes an increased risk of uterine pathologies. Women with hormone-dependent breast cancer have to use TAM for five to ten years. Many reports suggest that the risk of uterine pathologies increases with the time of administration. Considering these elements, the primary aim of this study will be to investigate the incidence of endometrial pathologies, especially of endometrial cancer, in different groups of breast cancer women undergoing diagnostic hysteroscopy.

NCT ID: NCT03898453 Completed - Clinical trials for Breast Cancer Female

EMDR Psychotherapy for Anxious-depressive Symptoms in Breast Cancer Patient

PSYCANCER
Start date: March 11, 2019
Phase: N/A
Study type: Interventional

The study will consist in an evaluation of the EMDR (Eye Movement Desensitization and Reprocessing) psychotherapy in the context on invasive primitive breast cancer. EMDR could then allow the affected patients to readjust their point of view on the pathology and thus promote more adapted behaviors or additional resources to cope with the disease. 190 Patients are going to be randomized in two groups : one group with EMDR psychotherapists and one group with support psychotherapists. Patients will receive 8 sessions. We expect that patient in EMDR psychotherapists group will have an higher decrease of anxiety score, depressive score (CES-D) and PTSD score, and a higher increase in quality of life.

NCT ID: NCT03897270 Recruiting - Breast Carcinoma Clinical Trials

Photoacoustic Imaging of the Breast in Patients With Breast Cancer and Healthy Subjects

Start date: October 25, 2018
Phase: N/A
Study type: Interventional

This trial studies photoacoustic imaging of the breast in patients with breast cancer and healthy subjects. Dense breasts typically reduce the sensitivity of a mammography and also is associated with a higher risk of breast cancer. Photoacoustic tomography combines light and sound to provide more information about breast tissue.

NCT ID: NCT03894410 Completed - Breast Cancer Clinical Trials

Real World Study of Lapatinib Among Metastatic Breast Cancer Patients

Start date: January 10, 2019
Phase:
Study type: Observational

A multicenter, retrospective, real world study of Lapatinib among Metastatic Breast Cancer (MBC) Patients in Clinical Practice.

NCT ID: NCT03894007 Terminated - Clinical trials for HER2-positive Breast Cancer

Improving Pre-operative Systemic Therapy for Human Epidermal Growth Factor Receptor 2 (HER2) Amplified Breast Cancer

PREDIXIIHER2
Start date: May 23, 2019
Phase: Phase 2
Study type: Interventional

This is a phase 2 study evaluating medical treatment before surgery in HER2-amplified early breast cancer patients. Patients receive chemotherapy with HER2-targeted antibodies and are randomised to receive the checkpoint inhibitor atezolizumab or not.

NCT ID: NCT03892655 Active, not recruiting - Breast Cancer Clinical Trials

Real World Study of Biosimilar Trastuzumab in Her2 Positive Breast Cancer

LB1802
Start date: October 7, 2019
Phase:
Study type: Observational [Patient Registry]

Zedora registration was based on studies of women with metastatic breast cancer, but its approval includes adjuvant treatment. Thus, prospective data of drug use in localized disease are lacking, as well as are real-world safety and efficacy data, taking into consideration comorbidities and compliance difficulties. This will be an observational study of patients receiving adjuvant Zedora at several Brazilian institutions for the purpose of describing its efficacy and safety.

NCT ID: NCT03890744 Completed - Clinical trials for Metastatic Breast Cancer

ModraDoc006/r in Patients With Breast Cancer

Start date: January 30, 2019
Phase: Phase 2
Study type: Interventional

This is a multicenter phase IIa study to evaluate the efficacy and tolerability of ModraDoc006 in combination with ritonavir (denoted ModraDoc006/r) in patients with recurrent or metastatic HER-2 negative breast cancer, that are suitable for treatment with a taxane as 1st-3rd line of therapy.