Understanding how trastuzumab deruxtecan works in HER2 positive breast cancer
Official title: Spatial Transcriptomic Approach for Revealing the Resistance Mechanism of Trastuzumab Deruxtexan in HER2 Positive Breast Cancer Patients.
Run by Samsung Medical Center · NCT06330012 · Data updated 2026-11-12
This study is trying to understand why some people with HER2 positive breast cancer don’t respond to the treatment trastuzumab deruxtecan, to help improve future treatment options.
Quick facts
| Study type | Interventional |
|---|---|
| Sex | Women only |
| Enrollment | 50 (estimated) |
| Sponsor | Samsung Medical Center Academic / other |
| Drugs / interventions | trastuzumab |
| Locations | 1 site (Seoul) |
| Status | Recruiting |
| Started | March 18, 2024 |
| Main results expected | January 15, 2025 |
| Study ends | December 31, 2027 |
| Registry record updated | March 26, 2024 |
| Trial ID | NCT06330012 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients with stage IV HER2 positive breast cancer who have been treated with trastuzumab deruxtecan and have available FFPE samples.
✕Probably not a fit
Patients with triple-negative breast cancer or hormone receptor positive breast cancer may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study utilizes a spatial transcriptomic approach to investigate the mechanisms of resistance to trastuzumab deruxtecan in patients with HER2 positive breast cancer. By analyzing formalin-fixed paraffin-embedded (FFPE) samples from patients who have undergone treatment, the study aims to uncover the biological factors that contribute to treatment resistance. The findings could provide insights into improving therapeutic strategies for this patient population.
Why it matters
Potential benefit: If successful, this study could lead to enhanced treatment options for patients with HER2 positive breast cancer by identifying resistance mechanisms.
How similar studies have gone: While the specific approach of this study may be novel, similar studies investigating resistance mechanisms in cancer treatments have shown promise in the past.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * HER2 positive breast cancer * Stage IV disease * Treated with T-Dxd * Available FFPE samples Exclusion Criteria: * TNBC breast cancer * Hormone receptor positive breast cancer * Non-available FFPE samples * Treated except T-Dxd
Where it's running
-
Ji-Yeon Kim
Seoul, South Korea Recruiting
Study contacts
- Study coordinator: Ji-Yeon Kim
- Email: jyeon25@skku.edu
- Phone: 82-2-3410-3459
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Entinostat with Pyrotinib and Endocrine Therapy in HER2-positive, HR-positive Advanced Breast Cancer after Trastuzumab Failure
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This trial tests whether adding trastuzumab rezetecan after an initial THP treatment helps patients with HER2-positive breast cancer decide if they should switch therapies based on response.
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Pyrotinib plus trastuzumab and chemotherapy for HER2-positive early breast cancer
This study tests a treatment combination of Pyrotinib, Trastuzumab and chemo given before surgery to see if it can improve responses in HER2-positive breast cancer patients who have not yet been treated.
-
BL-M07D1 plus pertuzumab vs standard therapy in first-line HER2-positive breast cancer
A Phase 3 trial tests whether adding BL-M07D1 to pertuzumab is as good as or better than docetaxel plus trastuzumab and pertuzumab in patients with newly diagnosed, unresectable or metastatic HER2-positive breast cancer.
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RO7771950 versus tucatinib with trastuzumab and capecitabine for HER2-positive locally advanced or metastatic breast cancer
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.