Personalized stem cell transplant aims to beat inherited blood cancers

NCT ID NCT07524530

First seen Jun 25, 2026 · Last updated Aug 14, 2026 · Updated 35 times

Summary

This study tests whether adjusting chemotherapy doses for each patient can improve outcomes after a stem cell transplant for blood cancers caused by a RUNX1 gene mutation. Up to 98 people aged 4 to 70 with these cancers will receive a transplant from a half-matched donor. The goal is to see if this personalized approach leads to better disease-free survival at one year compared to past results.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance
stem cell transplant with chemotherapy drugs (cyclophosphamide, busulfan, fludarabine)
What this could lead to
If successful, this could show that personalized chemotherapy doses improve survival after stem cell transplant for people with RUNX1-related blood cancers.
What could go wrong
This is a Phase II trial with only 98 participants, so results may not apply to everyone. Stem cell transplants carry serious risks like infection and graft-versus-host disease.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for CORE BINDING FACTOR ALPHA SUBUNITS are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

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

Locations

  • National Institutes of Health Clinical Center

    Bethesda, Maryland, 20892, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.