NIH-funded research R01 grant

A broader genomic risk picture to guide AML treatment

Official title: Towards a more generalizable genomic risk classification for acute myeloid leukemia (AML)

Funded at Ohio State University · NIH-11389404 · Data updated 2026-11-12

AIM to refine how genetic information guides treatment decisions for adults with acute myeloid leukemia by looking at how inherited and recurrent mutations affect risk.

More Acute Myeloid Leukemia (AML) research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionOhio State University
NIH-funded
Lab location1 site (Columbus, UNITED STATES)
Project startSeptember 18, 2023
Project endJuly 31, 2028
Funding year2026
Award (this year)$648,220
NIH project number5R01CA284595-04
Project IDNIH-11389404 on NIH RePORTER

Who could benefit from this research

Could help

Adults with acute myeloid leukemia who will undergo genomic testing as part of their clinical care.

Less likely to help

Patients without access to comprehensive genomic testing or whose treatment decisions are not influenced by genetic risk may see limited benefit.

What this research studies

This project focuses on adults with AML and analyzes both inherited and tumor-related genetic features to improve how risk is classified in everyday care. Researchers plan to extend previous genome studies to better understand how genetic backgrounds modify the prognostic value of AML mutations and to identify new molecular features that may influence disease development or therapy response. The work will use large-scale genomic data and statistical methods to strengthen confidence in which genes matter for prognosis, potentially tailoring treatment choices to the individual patient. The study is grounded in real-world clinical practice and aims to translate complex genetics into clearer guidance for clinicians and patients.

Why it matters

Potential benefit: If successful, patients could receive more accurate risk stratification and personalized treatment plans based on their unique genetic profile.

How similar studies have gone: Previous studies showed that incorporating genetic context improves prognostic models, and this work aims to strengthen and broaden that approach.

Where this research is happening

  • Ohio State University
    Columbus, United States
    Active

Researchers

  • Principal investigator: Eisfeld, Ann-Kathrin — Ohio State University
  • Study coordinator: Eisfeld, Ann-Kathrin

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.