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Study identifier: NCT07587086 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Fluorocholine PET/MR in Breast Cancer

Condition: Breast Neoplasms · Female  ·  Sponsor: Taipei Veterans General Hospital, Taiwan

PhaseN/A
Planned participants195
Who can joinFemale, 25 Years to 75 Years
Healthy volunteersNo

About this study

Objectives: Our study is conducted to use the pre-treatment Fluorocholine (FCH) Positron emission tomography/magnetic resonance (PET/MR) imaging in breast cancer patients, to investigate whether the conventional PET/MR imaging markers (maximum standardized uptake value \[SUVmax\], MR spectroscopy-derived choline analysis, dynamic contrast-enhanced MRI, apparent diffusion coefficient \[ADC\] analysis), and FCH PET/MR radiomic features, deep learning (DL) analysis are associated with molecular subtypes, clinical outcomes, treatment response, survival, and which parameters are more accurate for predictive purposes. Primary study purposes: -To investigate whether the pre-treatment FCH PET/MR imaging parameters are associated with molecular subtypes of breast cancers, and to evaluate the diagnostic performance for predictive purposes. Secondary study purposes: -To investigate whether the pre-treatment FCH PET/MR imaging parameters are associated with the factors related to clinical outcomes (histologic grade, prognosis) and to analyze which parameters are more accurate for predictive purposes. Test drug: Name: 18F- Fluorocholine (18F-FCH) Dosage form: N-(\[18F\]fluoromethyl)-2-hydroxy-N,N-dimethylethan-1-aminium Strength: 3-5 MBq/kg per patient (5-6 mCi/mL at time of injection (TOI)) Dosage and administration: Intravenous injection.fluoromethyl Selection criteria: 1. Women aged 25-75 years old. 2. Women diagnosed with breast cancer by pathological diagnosis from a core bio…

This description comes directly from the study's public registry record.

Talk to the study team

Jane Wang, M.D.  ·  +886938591583  ·  jwang2@vghtpe.gov.tw

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Locations (1)

Taipei Veterans General HospitalTaipei, Taiwan, TaiwanRecruiting

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Source record: clinicaltrials.gov/study/NCT07587086