Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Hillary Prescott"'
Autor:
Hillary Prescott, Julie Kennerly-Shah, Christopher T Elder, Alexandra Shillingburg, Bhavesh Shah, Michael J Reff
Publikováno v:
Journal of Oncology Pharmacy Practice. 26:156-174
The development of BCR-ABL-targeting tyrosine kinase inhibitors has transformed chronic phase chronic myeloid leukemia (CP CML) from a disease with a terminal prognosis to a treatable chronic illness. Long-term treatment with tyrosine kinase inhibito
Publikováno v:
American Journal of Health-System Pharmacy. 72:439-447
Purpose The pharmacology, pharmacokinetics, efficacy, and safety of the tyrosine kinase inhibitor (TKI) bosutinib in the management of chronic myeloid leukemia (CML) are reviewed. Summary Although clinical outcomes are favorable in patients wth Phila
Publikováno v:
Blood. 132:3234-3234
Introduction: Daratumumab is a first in class immunoglobin G1 kappa human monoclonal antibody that targets the CD38 antigen on the exterior of myeloma cells. Daratumumab provides an important treatment option and has become standard of care for patie
Autor:
Irene M. Ghobrial, Hillary Prescott, Kaitlen Reyes, Jacob P. Laubach, Houry Leblebjian, Paul G. Richardson, Elaine Xiang
Publikováno v:
Blood. 132:2024-2024
Introduction: Multiple Myeloma (MM) is a hematologic cancer caused by malignant plasma cells. Daratumumab is an immunoglobin G1 kappa human monoclonal antibody that targets CD38 antigen which is a cell surface glycoprotein highly expressed on myeloma
The FMS-like tyrosine kinase 3 (FLT3) is highly expressed in acute leukemias. Mutations involving FLT3 are among the most common molecular abnormalities in acute myelogenous leukemia (AML). Available evidence suggests that these molecular lesions con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d09e0d26a761a87759e17dd323d00d73
https://europepmc.org/articles/PMC4122233/
https://europepmc.org/articles/PMC4122233/
Publikováno v:
Seminars in hematology. 47(3)
Thrombocytopenia, common in leukemias and myelodysplastic syndromes (MDS), is responsible for increased risk of bleeding and delay of therapy. Platelet transfusions, although effective in increasing platelet counts, are limited by supply, are associa
Autor:
Jean Pierre J. Issa, Jeffrey Bryan, Hagop M. Kantarjian, Hillary Prescott, Elias Jabbour, Guillermo Garcia-Manero
Publikováno v:
Drugs. 70(11)
The management of the myelodysplastic syndromes (MDS) requires insight into the complex biology of the disease. Despite this challenge, two recent developments have contributed significantly to advancements in the treatment of MDS: (i) improvements i
Autor:
Naval Daver, Daniela Hoehn, Guillermo Garcia-Manero, Hagop M. Kantarjian, Jianhua Hu, Hillary Prescott, Jeffrey Bryan, Jorge E. Cortes, Elias Jabbour, Paolo Strati, Wei Qiao, Susan O'Brien, Navira F Khan, Courtney D. DiNardo, Tapan M. Kadia
Publikováno v:
Blood. 122:2801-2801
Background Epigenetic therapy with HMA is now the standard of care for pts with MDS with complete response (CR) rates of 7% to 35% and median survival of 20 to 24 months (mos). Large studies have demonstrated the relevance of karyotype abnormalities
Autor:
Elias Jabbour, Guillermo Garcia-Manero, Lianchun Xiao, Al Ali Najla, Asmita Mishra, Eric Padron, Jeffrey E Lancet, Jeffery Bryan, Hillary Prescott, David P. Steensma, Mikkael A. Sekeres, Gail J. Roboz, Alan List, Hagop M Kantarjian, Rami S Komrokji
Publikováno v:
Blood. 122:388-388
Background HMA are standard of care in pts with high-risk MDS and commonly used in pts with lower risk. Pts with high-risk disease post HMA failure have a poor prognosis with a median survival of 4-6 months. The prognosis of pts with low and intermed
Publikováno v:
European Oncology & Haematology. :200
Myelodysplastic syndromes (MDS) are a group of heterogeneous haematopoietic stem cell disorders characterised by peripheral blood cytopenias and a risk of transformation to acute myeloid leukaemia. Until recently, treatment of MDS predominately consi