The overall aim of this project is to help improve the Health Related Quality of Life (HRQOL) of metastatic breast cancer (MBC) patients. There is currently an urgent and unmet need for specific tools to aid in the evaluation of HRQOL in MBC and this project aims to address these needs by developing a comprehensive EORTC questionnaire for assessing the HRQOL of this group. The new module will be used in conjunction with EORTC QLQ-C30 and will provide better measurement of the quality of life issues experienced by women with MBC. Interviews will be conducted with patients from several centres across Europe, guiding the development process in a patient centred way.
Cardiac Outcomes With Near-Complete Estrogen Deprivation
This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.
This trial is no longer recruiting — here are similar active trials
Matched by cancer type/biomarker, currently recruiting.
This is a Phase III, multicenter, randomized, open-label, global study designed to evaluate the efficacy and safety of inavolisib plus fulvestrant compared with alpelisib plus fulvestrant in patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2) -negative, PIK3CA-mutated, locally advanced (LA) or metastatic breast cancer (mBC), who progressed during or after cyclin dependent kinase 4/6i (CDK4/6i)-based therapy. Enrollment for the main study is now complete.
Open label, multi-centre, Phase Ia/b adaptive design study with an initial 2-stage Dose Escalation Phase followed by a Dose Expansion Phase.
The purpose of this study is to investigate the efficacy, safety, and tolerability of camizestrant in combination with ribociclib in patients with ER+ HER2- BC who have not received any other systemic treatment for advanced disease. Participants will be treated within the trial until they discontinue the study treatment for any reason.
About the trial
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.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Kobieta w wieku do 55 lat, która nie przeszła przesilenia menopauzalnego w chwili rozpoznania raka piersi
- •Planowane leczenie raka piersi hormonalne lub chemioterapią z medycznie lub chirurgicznie wywołanym przesileiem menopauzalnym w ciągu 3 miesięcy od rozpoczęcia leczenia
- •Rak piersi stadium I-III
- •Rak piersi niezależnie od statusu HER2 (dodatni lub ujemny)
- •Możliwość leczenia dodatkowymi lekami takimi jak inhibitory CDK, inhibitory PARP lub immunoterapia
- •Ogólny stan zdrowia pozwalający na uczestnictwo w badaniu (ECOG 0-2)
- •Gotowość do podpisania pisemnej zgody na uczestnictwo w badaniu
- •Jeśli przebyli COVID-19, muszą być w pełni zdrowotnie wyzdrowieni
✗ Disqualifies
- •Alergia na substancje podobne chemicznie do adenozyny
- •Aktywny świszczący oddech
- •Metalowe implanty w mózgu lub urządzenia elektroniczne (rozrusznik, stymulator), które uniemożliwiają badanie MRI
- •Niekontrolowane choroby towarzyszące takie jak aktywne infekcje, niewydolność serca, niestabilna dławica piersiowa, arytmie serca lub zaburzenia psychiczne
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Maximum age
- 55 Years
- Last updated (source)
- August 5, 2026
- Sex
- Female only
Therapies / drugs in trial
Locations (3)
Duke Cancer Center
Durham, United States
Wake Forest Baptist Comprehensive Cancer Center
Winston-Salem, United States
Virginia Commonwealth University Massey Cancer Center
Richmond, United States
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/1/2026.
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