Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Judy Chiao"'
Autor:
Parameswaran Venugopal, Elias Jabbour, Stephen A. Strickland, Karen Seiter, Martha Arellano, Gary J. Schiller, Steven Coutre, David F. Claxton, Wendy Stock, Selina M. Luger, Lori J. Maness, Meir Wetzler, Stuart L. Goldberg, Hagop M. Kantarjian, William Plunkett, Stefan Faderl, Judy Chiao, Guillermo Garcia-Manero
Publikováno v:
The Lancet Oncology. 13:1096-1104
Summary Background Available treatments for acute myeloid leukaemia (AML) have limited durable activity and unsatisfactory safety profiles in most elderly patients. We assessed the efficacy and toxicity of sapacitabine, a novel oral cytosine nucleosi
Autor:
Parul Hazarika, Chunlei Zhang, Cecilia Kelly, Stanley R. Frankel, Justin L. Ricker, John F. Reilly, Judy Chiao, Rakhshandra Talpur, Xiao Ni, Madeleine Duvic, Victoria M. Richon
Publikováno v:
Blood. 109:31-39
The activity and safety of the histone deacetylase inhibitor vorinostat (suberoylanilide hydroxamic acid, SAHA) were evaluated in patients with refractory cutaneous T-cell lymphoma (CTCL). Group 1 received vorinostat 400 mg daily, group 2 received vo
Autor:
L. Sun, Eileen Reilly, Syed Rizvi, Carol Oerth, Laura McBride, Constantine S. Mitsiades, Judy Chiao, Kathleen Colson, Ivy Fearen, Justin L. Ricker, Paul G. Richardson, Kenneth C. Anderson, Barbara Atkins, David Siegel
Publikováno v:
Leukemialymphoma. 49(3)
A Phase I trial (NCT00109109) of oral vorinostat 200, 250 or 300 mg twice daily for 5 days/week/4-week cycle or 200, 300, or 400 mg twice daily for 14 days/3-week cycle until progressive disease or intolerable toxicity was conducted. Patients with me
Autor:
Cong Chen, Charles Lu, George R. Blumenschein, Ashok Kumar, Justin L. Ricker, Merrill S. Kies, Judy Chiao, Stanley R. Frankel, Vassiliki A. Papadimitrakopoulou
Publikováno v:
Investigational new drugs. 26(1)
This phase II trial was initiated to assess the efficacy and safety of oral vorinostat (Zolinza™, suberoylanilide hydroxamic acid, SAHA) in patients with recurrent and/or metastatic head and neck cancer. Eligible patients must have recurrent and/or
Publikováno v:
Current Cancer Therapeutics ISBN: 9781573401760
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab0c5cfcba2eeb672ea293f10d18c8cf
https://doi.org/10.1007/978-1-4613-1099-0_2
https://doi.org/10.1007/978-1-4613-1099-0_2
Autor:
Hagop M. Kantarjian, Karen Seiter, Jessica K. Altman, Martha Arellano, Selina M. Luger, Stuart L. Goldberg, Meir Wetzler, Guillermo Garcia-Manero, Judy Chiao
Publikováno v:
Blood. 122:2752-2752
Background Sapacitabine is an orally administered nucleoside analogue which causes single-strand DNA breaks and induces G2 cell cycle arrest. A multi-center, randomized phase 2 study was conducted to evaluate 3 dose regimens in older patients with MD
Autor:
Judy Chiao, Gautam Borthakur, Patricia Ann Boone, Stefan Faderl, Guillermo Garcia-Manero, Tapan M. Kadia, Parameswaran Venugopal, Elias Jabbour, Farhad Ravandi, Hagop M. Kantarjian, Jorge E. Cortes, Meir Wetzler, William G. Wierda
Publikováno v:
Blood. 118:3630-3630
Abstract 3630 Background: Sapacitabine is a novel nucleoside analogue with a unique ability to induce single-strand DNA breaks after incorporation into DNA, leading to production of double strand DNA breaks and/or G2 cell cycle arrest. It is orally a
Autor:
Guillermo Garcia-Manero, Jessica K. Altman, Stuart L. Goldberg, Judy Chiao, James M. Foran, Stephen A. Strickland, Lori J. Maness, David F. Claxton, Hagop M. Kantarjian, Meir Wetzler, P. Venugopal, Selina M. Luger
Publikováno v:
Blood. 116:1857-1857
Abstract 1857 This study is registered with ClinicalTrials.gov, number NCT00590187. Background: Sapacitabine is an orally administered nucleoside analogue with a unique ability to cause irreparable single-strand DNA breaks and induce G2 cell cycle ar
Autor:
Lori J. Maness, Steven Coutre, Wendy Stock, Selina M. Luger, Gautam Borthakur, Parameswaran Venugopal, Hagop M. Kantarjian, Meir Wetzler, Guillermo Garcia-Manero, Judy Chiao
Publikováno v:
Blood. 114:1061-1061
Abstract 1061 Poster Board I-83 Introduction: Sapacitabine is a novel nucleoside analogue with a unique ability to cause irreparable single-strand DNA breaks and induce G2 cell cycle arrest. It is orally administered and has demonstrated promising an
Autor:
Ivy Fearen, Kenneth C. Anderson, Paul G. Richardson, David S. Siegel, Syed Rizvi, L. Sun, Barbara Atkins, Laura McBride, Carol Oerth, Eileen Reilly, Constantine S. Mitsiades, Judy Chiao, Kathleen Colson, Justin L. Ricker
Publikováno v:
Blood. 110:1179-1179
Background: The histone deacetylase inhibitor vorinostat was approved by the United States FDA in October 2006 for the treatment of cutaneous manifestations in patients with cutaneous T-cell lymphoma who have progressive, persistent or recurrent dise