NIH-funded research R01 grant

Genetics of childhood acute lymphoblastic leukemia

Official title: Genomics of childhood acute lymphoblastic leukemia in the Childhood Cancer and Leukemia International Consortium

Funded at University of Minnesota · NIH-11407899 · Data updated 2026-11-12

This project looks at how inherited genes affect the risk of acute lymphoblastic leukemia in children from many countries and ancestry groups.

More Acute Lymphoblastic Leukemia research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Minnesota
NIH-funded
Lab location1 site (Minneapolis, United States)
Project startAugust 22, 2022
Project endJuly 31, 2027
Funding year2025
Award (this year)$101,629
NIH project number3R01CA266253-04S1
Project IDNIH-11407899 on NIH RePORTER

Who could benefit from this research

Could help

Ideal participants are children and young adults diagnosed with ALL and unaffected children from diverse ancestral backgrounds who can provide DNA samples and basic health information.

Less likely to help

People without available DNA samples or those seeking immediate changes to their current treatment plan are unlikely to receive direct clinical benefit from joining this research.

What this research studies

If your child has or had acute lymphoblastic leukemia (ALL), this project gathers DNA and health information from children around the world to search for genetic differences tied to risk. Researchers compare genomes from children with ALL to those without the disease, use genome-wide scans to find common genetic variants, and build polygenic risk scores to measure inherited risk. The work is done through an international consortium that combines samples and data from many regions, especially places with high ALL burden. By including diverse ancestry groups, the team aims to explain why ALL rates differ across populations.

Why it matters

Potential benefit: If successful, this work could help identify children at higher inherited risk for ALL and inform earlier detection or targeted prevention efforts in the future.

How similar studies have gone: Previous genome-wide studies have already found multiple inherited variants linked to childhood ALL and produced polygenic risk scores, but large, diverse international analyses remain limited.

Where this research is happening

  • University of Minnesota
    Minneapolis, United States
    Active

Researchers

  • Principal investigator: Spector, Logan G. — University of Minnesota
  • Study coordinator: Spector, Logan G.

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.