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12902 Usf Magnolia DrTampa, FL 33612
Overview of Dr. Sallman
Dr. David Sallman is an oncologist in Tampa, FL and is affiliated with H. Lee Moffitt Cancer Center and Research Institute. He received his medical degree from University of South Florida College of Medicine and has been in practice 7 years. He is one of 183 doctors at H. Lee Moffitt Cancer Center and Research Institute who specialize in Oncology. He has more than 100 publications and over 500 citings.
Education & Training
University of South Florida Morsani College of Medicine/Moffitt Cancer Center/Tampa General HospitalFellowship, Hematology and Medical Oncology, 2013 - 2016
Mass General Brigham/Massachusetts General HospitalResidency, Internal Medicine, 2010 - 2013
University of South Florida College of MedicineClass of 2010
Certifications & Licensure
FL State Medical License 2013 - 2027
MA State Medical License 2012 - 2015
American Board of Internal Medicine Internal Medicine
American Board of Internal Medicine Hematology
American Board of Internal Medicine Medical Oncology
Awards, Honors, & Recognition
- Junior Faculty Research Award for Clinical Science 2020
- Best Abstract Award Winner Moffitt Research Symposium 2016
- Alpine Oncology Foundation Young Investigator 2015
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Clinical Trials
- Phase 1b/2 Safety and Efficacy of APR-246 w/Azacitidine for tx of TP53 Mutant Myeloid Neoplasms Start of enrollment: 2017 May 18
- DEPLETHINK - LymphoDEPLEtion and THerapeutic Immunotherapy With NKR-2 Start of enrollment: 2018 Sep 18
- CPX-351 (Vyxeos™) for Transplant Eligible, Higher Risk Patients With Myelodysplastic Syndrome Start of enrollment: 2018 Dec 14
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Publications & Presentations
PubMed
- 1 citationsA comparative assessment of molecular-based prognostic models in CMML.Luis E Aguirre, Najla Al Ali, Somedeb Ball, Akriti G Jain, David A Sallman
Blood Neoplasia. 2025-11-01 - Transfusion Independence Corresponds With Survival in Patients With Lower-Risk Myelodysplastic Syndrome: Real-World Evidence From United States Insurance Claims.Rami S Komrokji, Dylan Supina, Shyamala Navada, Ravi Potluri, Rohit Tyagi
Clinical Lymphoma, Myeloma & Leukemia. 2025-10-01 - Hypomethylating Agent and Venetoclax Combination Is a Safe and Effective Alternative to Intensive Chemotherapy in Older (≥ 70 Years) Patients With Newly Diagnosed Favo...Somedeb Ball, Akriti G Jain, Najla Al Ali, Luis E Aguirre, Jan Philipp Bewersdorf
American Journal of Hematology. 2025-10-01
Abstracts/Posters
- A Phase 1 Study of Lenzilumab, a humaneered recombinant Anti_Human Granulocyte-Macrophage Colony- Stimulating Factor (anti-hGM-CSF) Antibody, for Chronic Myelomonocyti...David A Sallman, 61st Annual American Society of Hematology Meeting, Orlando, FL, 12/9/2019
- WHO-Defined Chronic Myelomonocytic Leukemia-2 (CMML-2) Patients Rapidly Progress to AML Suggesting This Entity Represents a Transitory Clinical StateDavid A Sallman, 61st Annual American Society of Hematology Meeting, Orlando, FL, 12/7/2019
- Marrow Ring Sideroblasts Are Highly Predictive for TP53 Mutation in MDS with Excess BlastsDavid A Sallman, 61st Annual American Society of Hematology Meeting, Orlando, FL, 12/9/2019
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Lectures
- The first-in-class anti-CD47 antibody Hu5F9-G4 is active and well tolerated alone or with azacitidine in AML and MDS patients: Initial phase 1b results.2019 ASCO Annual Meeting - 6/1/2019
- Geno-Clinical Model to Aid in the Diagnosis of Myelodysplastic Syndrome (MDS) Versus Chronic Myelomonocytic Leukemia (CMML)2018 ASH Annual Meeting - San Diego, CA - 12/1/2018
- Clonal Suppression of TP53 Mutant MDS and Oligoblastic AML with Hypomethylating Agent Therapy Improves Overall Survival2018 ASH Annual Meeting - San Diego, CA - 12/1/2018
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Press Mentions
Addressing Frequency of Care to Improve Quality of Life in Patients with Low-Risk AnemiaJuly 25th, 2024
Magrolimab plus Azacitidine Results in Promising Activity in Higher-Risk MDS PatientsMarch 9th, 2023
First-in-Class Investigational SX-682 Demonstrates Single-Agent Efficacy in Patients with Hypomethylating Agent Failure Myelodysplastic SyndromesDecember 9th, 2022- Join now to see all
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