New trial aims to outsmart cancer by adjusting chemo doses in real time
NCT ID NCT06525766
First seen Jun 27, 2026 · Last updated Aug 13, 2026 · Updated 2 times
Summary
This phase 2 trial tests whether giving the chemotherapy drug capecitabine in a flexible, response-based way (adaptive therapy) can better control metastatic ER-positive breast cancer. About 35 adults with advanced, hormone-resistant disease will receive doses that are adjusted based on tumor scans and blood markers. The goal is to see if this personalized dosing can slow tumor growth while reducing side effects.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- capecitabine (Xeloda)
- What this could lead to
- If successful, this approach could offer a way to control metastatic breast cancer with fewer side effects by adjusting doses based on tumor response.
- What could go wrong
- This is a small, early-phase pilot study with only 35 participants. It may not show a clear benefit, and capecitabine can cause side effects like hand-foot syndrome and fatigue.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
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Study contacts
-
Contact
Email: •••••@•••••
Locations
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Mayo Clinic in Arizona
RECRUITINGScottsdale, Arizona, 85259, United States
Contact Email: •••••@•••••
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