NIH-funded research R01 grant

Targeting genetic changes in aggressive lymphoma for better treatment

Official title: Functional characterization and rational therapeutic targeting of 18q DNA copy number gains in diffuse large B-cell lymphoma

Funded at University of Tx Md Anderson Can Ctr · NIH-10986115 · Data updated 2026-11-12

This study is looking at how certain changes in genes on chromosome 18 can make diffuse large B-cell lymphoma (DLBCL) more aggressive, and it aims to create personalized treatments using new medicines that target these genetic markers to help improve outcomes for patients.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Tx Md Anderson Can Ctr
NIH-funded
Lab location1 site (Houston, United States)
Project startDecember 1, 2020
Project endNovember 30, 2025
Funding year2025
Award (this year)$396,838
NIH project number5R01CA240839-05
Project IDNIH-10986115 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for this research are patients diagnosed with diffuse large B-cell lymphoma, particularly those with aggressive subtypes associated with genetic alterations on chromosome 18.

Less likely to help

Patients with other types of lymphoma or those whose DLBCL does not exhibit the specific genetic changes being targeted may not benefit from this research.

What this research studies

This research focuses on diffuse large B-cell lymphoma (DLBCL), the most common type of lymphoma, which is often treated with chemotherapy and the anti-CD20 antibody, Rituximab. The study aims to identify genetic alterations on chromosome 18 that are linked to more aggressive forms of DLBCL, particularly focusing on the TCF4 and BCL2 genes. By using innovative protein-degrader molecules and inhibitors, the researchers hope to develop a precision medicine approach that tailors treatment based on these genetic markers, potentially improving outcomes for patients with this challenging disease.

Why it matters

Potential benefit: If successful, this research could lead to more effective and personalized treatment options for patients with aggressive forms of DLBCL.

How similar studies have gone: Previous research has shown promise in targeting genetic alterations in various cancers, suggesting that this approach could be effective, although the specific targeting of 18q alterations in DLBCL is relatively novel.

Where this research is happening

  • University of Tx Md Anderson Can Ctr
    Houston, United States
    Active

Researchers

  • Principal investigator: Green, Michael Richard — University of Tx Md Anderson Can Ctr
  • Study coordinator: Green, Michael Richard

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.