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Breast Cancer clinical trials

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NCT ID: NCT05309655 Recruiting - Breast Cancer Clinical Trials

Cardiac Outcomes With Near-Complete Estrogen Deprivation

CROWN
Start date: September 2, 2022
Phase: Early Phase 1
Study type: Interventional

The purpose of this research study is to understand what effect near complete estrogen deprivation (NCED) therapy has on the heart in breast cancer patients. Investigators want to understand if NCED changes how the heart works.

NCT ID: NCT05309265 Recruiting - Breast Cancer Clinical Trials

Vocational Rehabilitation for the Return to Work of Breast Cancer Patients: a Feasibility Study

VocRehab
Start date: May 9, 2022
Phase: N/A
Study type: Interventional

In Italy, 50% of new breast cancer (BC) diagnosis occur in female of working age. Although return to work (RTW) is strongly desired by BC patients, cancer survivors are more likely to be unemployed than healthy individuals. Moreover, work difficulties may hindrance this process. Since 2018, the investigators have planned a local social-healthcare pathway which provides a multidisciplinary vocational rehabilitation intervention with the aim to help cancer survivors in their RTW process. To date, the feasibility of the multidisciplinary vocational rehabilitation interventions has not been verified for BC patients.

NCT ID: NCT05309252 Recruiting - Breast Cancer Clinical Trials

The Unmet Needs and the Workplace Reintegration of Breast Cancer Patients: the NEW-BreCa Project

NEW-BreCa
Start date: May 9, 2022
Phase:
Study type: Observational

Breast cancer (BC) have unmet needs that can impact negatively on participation in meaningful activities and the overall quality of life, if not addressed by the healthcare services. One of those needs is the return to work (RTW) for female in their working age. The perceived needs of BC patients and RTW process might be influenced by sociodemographic data, disease-related, and work-related factors. Moreover, needs might change (type and priority) from diagnosis onwards. Prospective data regarding these topics have never been collected in Italian BC patients.

NCT ID: NCT05307757 Recruiting - Breast Cancer Clinical Trials

Screening Contralateral Breast Cancers in Patients With Newly Diagnosed Breast Cancer

Start date: May 1, 2022
Phase:
Study type: Observational

In women with newly diagnosed breast cancer, synchronous contralateral breast cancer is reported in 1% to 3%. During the initial diagnosis of breast cancer, it is important to detect the contralateral cancer to avoid second round of cancer therapy. Because breast MRI is a highly sensitive modality, it is used for screening of occult contralateral disease in women newly diagnosed with breast cancer and detects contralateral cancers not seen on clinical or conventional imaging (mammography and ultrasonography) in 4.1% of women. However, the use of breast MRI for screening contralateral breast cancer, is limited not only by high costs and long examination time but also by high false-positive findings resulting in more benign biopsies and extensive surgeries. In addition, the use of intravenous gadolinium-based contrast agent is contraindicated in pregnancy and in women with renal impairment or contrast material allergy contrast. Thus, there is a need to develop a more safe and cost-effective supplemental imaging modality for screening breast cancer. Diffusion-weighted (DW) MRI is a fast, functional modality that measures the movement of water molecules to create tissue contrast without the need for contrast injection. Breast malignancies exhibit hindered diffusion and appear hyperintense on DW MRI with low apparent diffusion coefficient (ADC) compared to normal surrounding tissue. A number of studies have shown that the use of DW MRI can significantly reduce the false positives and unnecessary benign biopsy of breast MRI. Several studies have explored how to use DW MRI as a stand-alone tool for breast cancer screening, and recent results have shown that DW MRI is more useful than conventional imaging in detecting small breast cancer. However, most of these studies were retrospective with inconsistent results. Thus, a prospective multicenter study with standardized acquisition and interpretation protocols in a large population is needed to determine the efficacy of DW MRI for breast cancer screening. The purpose of our study is to determine whether DWI improves the performance of preoperative DCE MRI in detecting clinically occult contralateral breast cancers.

NCT ID: NCT05307705 Recruiting - Breast Cancer Clinical Trials

A Study of LOXO-783 in Patients With Breast Cancer/Other Solid Tumors

PIKASSO-01
Start date: May 11, 2022
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to learn more about the safety, side effects, and effectiveness of LOXO-783. LOXO-783 may be used to treat breast cancer and other solid tumors that have a change in a particular gene (known as the PIK3CA gene). Participation could last up to 36 months (3 years) and possibly longer if the disease does not get worse.

NCT ID: NCT05306600 Recruiting - Breast Cancer Clinical Trials

Onco-Genomas Brasil: Mapping Breast and Prostate Cancer in the Brazilian Public Health System

Start date: November 9, 2022
Phase:
Study type: Observational

This project aims to perform complete sequencing of the somatic (tumor) and germline exomes during clinical investigation of cancer patients treated through the Brazilian Unified Health System to generate genomic and phenotypic data for the Brazilian Ministry of Health's National Precision Genomics and Health Program, called Genomas Brasil, as well as to collect data on the population's ancestry.

NCT ID: NCT05305963 Recruiting - Clinical trials for Breast Cancer Female

Breast CANcer Risk Assessment in Younger Women: BCAN-RAY

BCAN-RAY
Start date: January 31, 2023
Phase:
Study type: Observational

The overarching aim of the proposed research is to develop a comprehensive breast cancer risk assessment strategy for women aged 30-39 years. There are three main objectives to the study. Objective 1 - Mammographic Density and Risk To define the magnitude of BC risk associated with MD in women aged 30-39 and facilitate its incorporation into risk prediction models. Objective 2 - Psychological impact To examine the feasibility of a strategy to offer breast cancer risk-assessment to diverse ethnic and socioeconomic populations of women in their 30s, assessing: - Potential benefits and harms - Impact on health inequalities - Acceptability Objective 3 - DNA Methylation substudy To explore the potential of DNA Methylation (DNAme) signatures from self-obtained cervical samples to further refine risk prediction algorithms

NCT ID: NCT05305365 Recruiting - Breast Cancer Clinical Trials

Study Assessing QBS72S For Treating Brain Metastases

Start date: August 16, 2022
Phase: Phase 2
Study type: Interventional

This study is to evaluate the efficacy and safety of QBS72S in participants with advanced, relapsed, metastatic breast cancer with CNS involvement.

NCT ID: NCT05305092 Recruiting - Breast Cancer Clinical Trials

Assessment of Brain Cognitive Impairment in Breast Cancer

Start date: May 31, 2022
Phase:
Study type: Observational

To explore the cognitive impairment caused by chemotherapy and endocrine therapy in premenopausal breast cancer patients and to find biomarkers with early predictive effect on this cognitive impairment by using multimodal integrated PET/MRI technology combined with psychobehavioral technology.

NCT ID: NCT05304962 Recruiting - Breast Cancer Clinical Trials

First-in-Human Study of RGT-419B Alone and With Endocrine Therapy in Subjects With HR-Positive, HER2-Negative Advanced/Metastatic Breast Cancer

Start date: March 4, 2022
Phase: Phase 1
Study type: Interventional

This is a phase I, First-in-Human (FIH), open-label study to evaluate the safety, tolerability, pharmacokinetic (PK) profile, and preliminary efficacy of RGT-419B administered orally as monotherapy OR in combination with Hormonal Therapy in subjects with HR+, HER2- locally advanced and unresectable (Stage III) or metastatic (Stage IV) breast cancer whose disease has progressed during prior therapy with an approved CDK4/6i plus hormonal therapy.