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Elias Jabbour

Researcher at University of Texas MD Anderson Cancer Center

Publications -  1303
Citations -  29725

Elias Jabbour is an academic researcher from University of Texas MD Anderson Cancer Center. The author has contributed to research in topics: Myeloid leukemia & Medicine. The author has an hindex of 71, co-authored 1108 publications receiving 21641 citations. Previous affiliations of Elias Jabbour include University of Texas Health Science Center at Houston.

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Phase1/2 Single Arm Study of Rigosertib (ON 01910.Na) in Patients (Pts) with Relapsed or Refractory Acute Leukemia or Transformed Myeloproliferative Neoplasms

TL;DR: A study in acute myeloid leukemia (AML) investigating alternative schedules to determine the optimal dose and anti-leukemia efficacy and serious adverse events seen were altered mental status, confusion, delirium, acute respiratory distress, and febrile neutropenia.
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Final Report Of Single-Center Study Of Chemotherapy Plus Dasatinib For The Initial Treatment Of Patients With Philadelphia-Chromosome Positive Acute Lymphoblastic Leukemia

TL;DR: This phase II trial determined the long-term efficacy of the combination of the hyperCVAD regimen with dasatinib for treating patients with Ph+ ALL and found that 45 patients have achieved complete molecular remission (CMR) and another 19 have achieved a major (but not complete) molecular response (MMR).
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Survival Outcomes in Relapsed/Refractory Acute Myeloid Leukemia Patients Who Achieve Less-than-Complete Response After First Salvage Therapy

TL;DR: If less-than-complete remissions (CRi) after salvage therapy impact overall survival in relapsed or refractory AML patients when compared to complete remission and no response is evaluated.
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Response to Frontline Therapy with Second Generation Tyrosine Kinase Inhibitors in Chronic Myeloid Leukemia: Analysis of Outcome for b3a2 Vs. b2a2 Fusion Transcripts

TL;DR: Those with b3a2 have a significantly higher rate of molecular responses and a trend for better EFS, compared with those with b2a2 whether they express b3A2 or b2A2 at diagnosis, which warrant further investigation.