Dalia Mahmoud
Celgene
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Publication
Featured researches published by Dalia Mahmoud.
Cancer | 2013
Amer M. Zeidan; Steven D. Gore; Diane L. McNally; Maria R. Baer; Franklin Hendrick; Dalia Mahmoud; Amy J. Davidoff
Lenalidomide is approved for the treatment of anemia with transfusion dependence (TD) in patients with lower‐risk myelodysplastic syndrome (MDS) with 5q deletion (del5q‐MDS), but its “real‐life” use and effect on transfusion needs are unclear. In the current study, the authors examined its use in the Medicare population.
Experimental hematology & oncology | 2014
B. Douglas Smith; C.L. Beach; Dalia Mahmoud; Laura Weber; Henry J. Henk
BackgroundThis study examined patient outcomes using real world data for acute myeloid leukemia (AML) patients initiating treatment.MethodsA retrospective, administrative claims-based, comparative analysis was developed to study outcomes for AML patients initiating treatment with decitabine or azacitidine between January 2006 and June 2012.ResultsTreatment with azacitidine was associated with a longer median overall survival (10.1 versus 6.9 mos., p = 0.007) and a lower risk of hospitalization (HR 0.787, p = 0.02) compared to treatment with decitabine.ConclusionsThis analysis of the outcomes of real-world treatment of AML patients with demethylating agents suggests that azacitidine may result in clinically superior outcomes than decitabine.
Expert Review of Hematology | 2016
Amer M. Zeidan; Dalia Mahmoud; Izabela Kucmin-Bemelmans; Cathelijne J M Alleman; Marja Hensen; Barry S. Skikne; B. Douglas Smith
The economic burden associated with acute myeloid leukemia (AML) is poorly defined and understudied. The goal of this study is estimate the direct cost of illness for AML in the United States (US) and the United Kingdom (UK), by conducting a comprehensive literature review and calculating the average direct cost-of-illness per patient for the first 6 months of therapy. Patients were grouped by therapy: intensive chemotherapy alone; induction chemotherapy followed by allogeneic stem cell transplantation (alloSCT); low intensity therapy; and best supportive care. Data suggest that the pathways alloSCT, followed by intensive chemotherapy, are associated with the highest direct costs. Calculated direct costs suggest that they are higher in the US (
Leukemia & Lymphoma | 2014
B. Douglas Smith; Dalia Mahmoud; Stacey Dacosta-Byfield; Virginia M. Rosen
14,014 for BSC-only to
Experimental hematology & oncology | 2014
B. Douglas Smith; C.L. Beach; Dalia Mahmoud; Laura Weber; Henry J. Henk
352,682 for alloSCT) than in the UK (£3708 [
Blood | 2012
Dalia Mahmoud; Barry S. Skikne; Izabela Kucmin-Bemelmans; Cathelijne J.M. Alleman; Marja Hensen
5837] for BSC-only to £112,545 [
Blood | 2013
Roberto Ovilla; Maria Guadalupe Rodríguez-González; Renée Arnold; Dalia Mahmoud
177,187]). AML appears to be associated with significant direct economic costs, but more studies are needed to fully assess the economic impact especially in relation to total and indirect costs.
Blood | 2012
B. Douglas Smith; Dalia Mahmoud; Stacey Dacosta Byfield; Henry J. Henk
Abstract This study utilized claims data from a national US commercial health insurer to examine rates of cytopenia-related complications (significant bleeding, infection) and health care utilization (emergency room visits, inpatient hospitalizations) among patients with myelodysplastic syndromes (MDS) within predefined periods of transfusion activity and active therapy. Periods with no transfusions, regardless of relationship to treatment intervention, were associated with lower rates of cytopenia-related complications. These data suggest that eliminating or reducing the need for transfusions may help to reduce MDS-related medical problems, and treatment toward that goal should be considered in patients with MDS needing transfusions.
Blood | 2012
Dalia Mahmoud; Stacie Hudgens; Fiona Taylor; Farrah Pompilus; Steve Hwang; C.L. Beach
After the publication of this work [1], it was brought to our attention that a statement in the article is not consistent with the data. The statement “Prior RBC transfusions were found to significantly increase the time to hospitalization (adjusted HR 1.373, p = 0.018) while no other covariates examined were found to impact the risk of hospitalization” is not a correct reflection of the results from the data analysis in Table 2 of the article. The corrected statement is provided here as follows: “Prior RBC transfusions were found to significantly shorten the time to hospitalization (adjusted HR 1.373, p = 0.018) while no other covariates examined were found to impact the risk of hospitalization.”
Blood | 2011
B. Douglas Smith; Dalia Mahmoud; Henry J Henk; Zeba M. Khan