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Myeloid Malignancies Program

A trans-NIH multidisciplinary network of researchers and clinicians dedicated to improving early detection, diagnosis, prognosis and development of novel therapeutics for myeloid malignancies.

About

Our Vision

The vision of the NIH Myeloid Malignancies Program is to successfully control, cure and prevent MDS and AML.

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MDS with multi-lineage dysplasia and ringed sideroblasts.
MDS with multi-lineage dysplasia and ringed sideroblasts. Image courtesy of Kathy Calvo, M.D., Ph.D.

The mission of the trans-NIH Myeloid Malignancies Program (MMP) is to develop a comprehensive program aimed at understanding, diagnosing, and treating the heterogeneous collection of myeloid malignancies that arise in children and adults, especially the Myelodysplastic Syndromes (MDS) and secondary or therapy-related Acute Myelogenous Leukemia (AML). Our objective is to establish a trans-NIH clinical research program at the NIH Clinical Center to allow rapid translation of intramural science and the development of novel therapies for patients with MDS and AML.

This program functions as a clinical scientific unit with regular protocol and research progress meetings. It also serves as a focal point for fellows and medical staff education in the practice of translational clinical research in the myeloid malignancies. We aim to utilize new intramural opportunities and initiatives to stimulate translational research in MDS and AML.  

There are more than 10,000 new cases of MDS diagnosed in the U.S. every year. These blood cancers remain difficult to treat due to vast differences in the patient population including great genetic diversity, complicated clinical presentation with similarities to several overlap syndromes, and lack of highly effective and long-lasting treatments. These difficulties inspired the trans-NIH MMP to consolidate expertise and create an interactive and collaborative environment to foster myeloid malignancy care and research through innovative laboratory studies, state-of-the-art research, and promising clinical applications. The overarching goal is to develop novel therapeutic targeting strategies that may significantly alter the natural history of these disorders.


Join Our Email List

To join the Myeloid Malignancy Interest Group email list, please visit the Myeloid Malignancy Interest Group Listserv homepage, then click the “Subscribe or Unsubscribe” link in the right sidebar.

Interns and doctors

Patients & Providers

The NIH Myeloid Malignancies Clinical Program focuses on the rapid translation of science to novel, first-in-disease clinical trials with the aim of developing new science-driven therapy approaches in adult and pediatric patients with myeloid malignancies, especially MDS and secondary AML.

Have questions about Myeloid Malignancies Program clinical trials?

Please contact Ashley Carpenter via email.

carpentera@mail.nih.gov

Team

The Myeloid Malignancies Program consists of physician-scientists and investigators from multiple institutes within the National Institutes of Health (NIH), including the National Cancer Institutes (NCI), the National Heart, Lung, and Blood Institute (NHLBI), and others. If you are interested in participating in this trans-NIH program, please contact a member of our leadership team.  View a list of participating NIH investigators.

Core biopsy H & E dysplastic megakaryocites

Our Research Program

We are developing a comprehensive program aimed at understanding and treating myeloid malignancies in children and adults. Our research program has four overarching themes:

  • Pre-clinical models to study MDS biology and therapy
  • Post-transcriptional regulation in MDS/AML
  • Germline predispositions to myeloid malignancies
  • Role of the immune system in control of MDS/AML

Join Our Email List
To join the Myeloid Malignancy Interest Group email list, please visit the Myeloid Malignancy Interest Group Listserv homepage, then click the “Subscribe or Unsubscribe” link in the right sidebar.

News

March 7, 2023
Myeloid Malignancies Members Publish in JAMA on Residual Disease in AML

Congratulations to the Pre-MEASURE project team for their outstanding contributions to understanding the impact of residual disease before transplant in AML!

DNA Sequencing to Detect Residual Disease in Adults With Acute Myeloid Leukemia Prior to Hematopoietic Cell Transplant. Dillon LW, Gui G, Page KM, Ravindra N, Wong ZC, Andrew G, Mukherjee D, Zeger SL, El Chaer F, Spellman S, Howard A, Chen K, Auletta J, Devine SM, Jimenez Jimenez AM, De Lima MJG, Litzow MR, Kebriaei P, Saber W, Weisdorf DJ, Hourigan CS. JAMA. 2023 Mar 7;329(9):745-755. doi: 10.1001/jama.2023.1363. PMID: 36881031

Laura Dillon PhD FACMG (left), Chris Hourigan, MD, PhD (center), Gege Gui ScM (right)

July 22, 2022
Myeloid Malignancies Program Awarded CCR Special Act Award

Congratulations to the Myeloid Malignancies Program Steering Committee for being awarded a CCR Group Special Act Award for their initiative in implementing a comprehensive program aimed at understanding, diagnosing, and treating pediatric and adult Myelodysplastic Syndromes (MDS) and secondary Acute Myelogenous Leukemia (AML). The CCR Group Special Act Award is given in recognition for a significant contribution in the public interest.

(Left to right: Dr. Steven Pavletic, Dr. Murali Palangat, Dr. Kathy McGraw, Dr. Peter Aplan, Dr. Nirali Shah, Dr. Chris Hourigan, Dr. Kathy Calvo, Dr. Dan Larson, Dr. Lea Cunningham)