NIH-funded research R01 grant

Childhood acute lymphoblastic leukemia genetics around the world

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

Funded at University of Minnesota · NIH-11407900 · Data updated 2026-11-12

This project compares inherited genetic differences in children with and without acute lymphoblastic leukemia across many countries to learn who is at higher risk.

More 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)$100,003
NIH project number3R01CA266253-04S2
Project IDNIH-11407900 on NIH RePORTER

Who could benefit from this research

Could help

Children diagnosed with acute lymphoblastic leukemia, survivors, and children from diverse ancestral backgrounds may be eligible to provide genetic samples or medical data through participating consortium sites.

Less likely to help

Because this is genetic and epidemiologic research rather than a treatment trial, participants should not expect direct therapeutic benefit or immediate changes to their care.

What this research studies

If you join, researchers will collect genetic samples (for example, blood or saliva) and medical information from children with ALL and from comparison groups across many countries. They will scan the whole genome to find common inherited differences and create polygenic risk scores to see how genetic patterns relate to who develops ALL. The work combines existing data from the Childhood Cancer and Leukemia International Consortium with new samples from under-studied regions such as south/southeast/east Asia, the Middle East, North Africa, and sub-Saharan Africa. Understanding these genetic patterns may explain differences in ALL rates by ancestry and suggest markers to find high-risk children earlier.

Why it matters

Potential benefit: If successful, this could identify inherited genetic markers that help predict which children are more likely to develop ALL and guide earlier monitoring or prevention research.

How similar studies have gone: Previous genome-wide studies have already found over 15 genetic variants linked to childhood B‑cell ALL and shown that polygenic risk scores can separate higher- and lower-risk groups, though many global populations remain understudied.

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.