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Personalized transplant approach targets genetic blood cancers

NCT ID NCT07524530

First seen Apr 18, 2026 · Last updated Jun 23, 2026 · Updated 13 times

Summary

This study tests whether adjusting chemotherapy and supportive care doses for each patient can improve outcomes after a stem cell transplant for blood cancers caused by RUNX1 gene mutations. 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 tailored approach increases the number of patients who are alive and cancer-free one year later.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • National Institutes of Health Clinical Center

    Bethesda, Maryland, 20892, United States

    Contact Phone: •••-•••-•••• Email: •••••@•••••

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 (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 risks like infection, graft-versus-host disease, and organ damage.

Conditions

The condition(s) this trial relates to.

hematopoietic and lymphoid system neoplasm leukemia lymphoma

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.