Related Websites
Degrees
Fellowship Training, University of Washington, Pediatic Hematology and Oncology, 2000.
Fellowship Training, Fred Hutchinson Cancer Research Center, Pediatic Hematology and Oncology, 2000.
Residency Training, Johns Hopkins Hospitals, Pediatrics, 1997.
M.D., Wayne State University, 1994.
Ph.D., University of Michigan, Pharmacology/Protein Biochemistry, 1990.
Research Interests
A. Clinical Expertise:
- Identification and therapy of high-risk leukemias - Management of post transplant relapse in childhood leukemias - Stem cell transplantation in leukemias - Therapy of relapsed AML - Targeted therapy in pediatric AML B. Laboratory Interests: Genomic alterations in AML and their role in the Pathogenesis of AML - Biologic implications of disease associated mutations in AML - Prelavence and clinical significance of FLT3 and other RTK mutations in AML - Biologic consequence of RTK mutations in normal and malignant hematopoiesis TARGET Initiative - TARGET (Therapeutically Applicable Research to Generate Effective Treatments) Initiative, seeks to identify valid therapeutic targets so that new, more effective treatments can be developed for children with cancer. AML is one of the 5 diseases selected for comprehensive mutli-platform genomic and epi-genomic evaluation to identify biomarkers associated with disease outcome as well those who are viable candidates for targeted therapy. As part of this initiative, several hundred specimens from children with AML will undergo whole genome, whole transcriptome and exome capture sequencing to identify disease associated alterations. Upstream gene, transcript, methylation and miRNA profiling will be performed for integration with the sequencing data. Identified biomarkers will be rapidly validated and translated into clinical application. Identification of novel markers of high risk disease in AML. - Using state of the art molecular biologic techniques putative high risk markers are being identified and validated in a large cohort of pediatric and adult AML patients. This information will be used to create a patient-specific risk profile to be used in treatment assignment Minimal Residual Disease (MRD) as a marker of high-risk disease in Pediatric AML - Evaluation of flow cytometric evidence of MRD and its correlation with outcome - Evaluation of molecular evidence of MRD and correlation with outcome - Stem Cell origin of myeloid leukemias and role of RTK mutations in the evolution of AML - Role of activating mutations of the signal transduction pathway in myeloid malignancies LanguagesReading, Writing, Speaking
Farsi: Functional, Functional, Fluent
Memberships
American Society of Clinical Oncology
American Society of Hematology
Children's Oncology Group Myeloid Disease Committee
Childrens Oncology Group
Honors and Awards
Jose Carrera's International Leukemia Fellow, Jose Carrera's Leukemia Foundation, Fred Hutchinson Cancer Research Center, Molecular Pathogenesis of FLT3 Mutations in AML
Child Health Research Center Scholar, National Institutes of Health (NIH), University of Washington
COG Young Investigator Award, Childrens Oncology Group
Previous Positions
Acting Instructor, Fred Hutchinson Cancer Research Center
Assistant Professor and Attending Physician, Children's Hospital and Regional Medical Center, Pediatric Hematology and Oncology
Assistant Member, Fred Hutchinson Cancer Research Center, Clinical Research Division, Pediatric Oncology/Stem Cell Transplantation
Assistant Professor, University of Washington, School of Medicine, Pediatrics, Pediatric Hematology and Oncology, Stem Cell Transplantation
Funding
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