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Stefan Faderl

Researcher at University of Texas MD Anderson Cancer Center

Publications -  586
Citations -  36426

Stefan Faderl is an academic researcher from University of Texas MD Anderson Cancer Center. The author has contributed to research in topics: Myeloid leukemia & Leukemia. The author has an hindex of 96, co-authored 577 publications receiving 34155 citations. Previous affiliations of Stefan Faderl include Penn State Milton S. Hershey Medical Center & Hackensack University Medical Center.

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Phase I study of TH-302, a hypoxia-activated cytotoxic prodrug, in subjects with advanced leukemias.

TL;DR: A phase 1 study of TH-302, a 2-nitroimidazole prodrug of the DNA alkylator, bromo-isophosphoramide mustard designed to be selectively activated in hypoxic conditions, was designed for advanced leukemias with no standard therapy options available and preliminary clinical activity was assessed.
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Time from Diagnosis to Treatment Initiation Predicts Survival in Acute Myeloid Leukemia (AML).

TL;DR: AML should be considered a medical emergency in younger AML patients, as delaying induction therapy significantly affects CR rates and OS, and the harm in delaying therapy in young AML pts is offset by the potentially greater harm in giving standard therapy to those later found to have unfavorable cytogenetics.
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Pediatric-Based Therapy for Young Adults with Newly Diagnosed Lymphoblastic Leukemia.

TL;DR: 48 young adult patients between the ages of 12 to 40 years with de novo Philadelphia chromosome negative ALL treated with the augmented Berlin-Frankfurt-Munster (BFM) chemotherapy regimen effectively induces remission, both by morphology and by flow cytometry.
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The Heterogeneous Prognosis of Patients with Myelodysplastic Syndrome (MDS) and Chromosome 5 Abnormalities: How Does It Relate to the Original Lenalidomide Experience in MDS?.

TL;DR: This study provides baseline expectations of outcome in different MDS subsets and deletion 5q, which could be used for comparative purposes with the lenalidomide experience to define the prognosis in MDS and deletion5q with or without other cytogenetic abnormalities.