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Study identifier: NCT06087120 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Predicting BReast cAncer Response to neoadjuVant Therapy by ctDNA Assessment

Condition: Breast Cancer Female · Stage II Breast Cancer · Stage III Breast Cancer  ·  Sponsor: Gene Solutions

PhaseN/A
Planned participants125
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a prospective and observational study, aiming to determine the detection rate and change of CtDNA in blood samples of cancer patients before, during and after neoadjuvant treatment. * Determine the rate of ctDNA positivity at the time before treatment, * Determine the rate of ctDNA positivity at the time during treatment, * Determine the rate of ctDNA positivity at the time after neoadjuvant therapy, whether there is a change in ctDNA expression of the study population during treatment. And aiming to investigate the relationship between ctDNA expression and MRI imaging with pCR response in neo-adjuvant therapy: * Correlation between ctDNA detection and pCR response. Determine the percentage of Positive Prediction Value - PPV, Negative Prediction Value - NPV of ctDNA, * Correlation between MRI imaging and pCR response. Determination of PPV, NPV of MRI * Combination of ctDNA detection and MRI imaging in the prognosis of pCR. Determination of PPV, NPV ratio of ctDNA combined with MRI.

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

Talk to the study team

Lan NL Tu, PHD  ·  +84888843489  ·  lantu@genesolutions.vn

Van T. Phan, MSc  ·  +84908145990  ·  vanphan@genesolutions.vn

Always discuss trial participation with your own doctor first.

Locations (3)

MRCCC Siloam Hospitals SemanggiJakarta, IndonesiaRecruiting
Medical Genetics InstituteHo Chi Minh City, VietnamRecruiting
University Medical Center HCMCHo Chi Minh City, VietnamRecruiting

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Source record: clinicaltrials.gov/study/NCT06087120