Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Debra Resta"'
Autor:
Franck E. Nicolini, Gert J. Ossenkoppele, Philipp le Coutre, Ariful Haque, Kapil N. Bhalla, Mark R. Litzow, Francesca Palandri, Yaping Shou, Stephen G. O'Brien, Giuliana Alimena, Hagop M. Kantarjian, Norbert Gattermann, Aaron Weitzman, Francis J. Giles, Francisco Cervantes, Andreas Hochhaus, Ravi Bhatia, Debra Resta
Publikováno v:
Blood. 110:3540-3546
Nilotinib, an orally bioavailable, selective Bcr-Abl tyrosine kinase inhibitor, is 30-fold more potent than imatinib in pre-clinical models, and overcomes most imatinib resistant BCR-ABL mutations. In this phase 2 open-label study, 400 mg nilotinib w
Autor:
Mary Beth Riley, John L. Frater, Martin S. Tallman, Mary Ann Hrisinko, Debra Resta, Brian J. Druker, Daina Variakojis, LoAnn Peterson
Publikováno v:
American Journal of Clinical Pathology. 119:833-841
We evaluated bone marrow pathologic features and cytogenetic and molecular genetic status of 13 patients with interferon-resistant, chronic-phase chronic myeloid leukemia (CML), treated with imatinib mesylate (Gleevec). All had morphologic evidence o
Autor:
R N Debra Resta, Thomas B. Sneed, R N Mary Beth Rios, Jorge E. Cortes, Moshe Talpaz, Stefan Faderl, B. Nebiyou Bekele, Xian Zhou, Susan O'Brien, Francis Giles, William G. Wierda, Hagop Kantarjian
Publikováno v:
Cancer. 100:116-121
BACKGROUND Imatinib mesylate induces high rates of hematologic and cytogenetic response in patients with chronic myelogenous leukemia (CML). During therapy with imatinib, up to 45% of patients with CML reportedly experience myelosuppression ≥ Grade
Autor:
Charles L. Sawyers, Sayuri Ohno-Jones, Hagop M. Kantarjian, Elisabeth Buchdunger, John Ford, Bin Peng, Brian J. Druker, Debra Resta, Nicholas B. Lydon, Renaud Capdeville, Moshe Talpaz
Publikováno v:
New England Journal of Medicine. 344:1031-1037
BCR-ABL is a constitutively activated tyrosine kinase that causes chronic myeloid leukemia (CML). Since tyrosine kinase activity is essential to the transforming function of BCR-ABL, an inhibitor of the kinase could be an effective treatment for CML.
Autor:
Moshe Talpaz, Renaud Capdeville, Peter Lloyd, Charles L. Sawyers, Amy Racine-Poon, Michael Hayes, Debra Resta, Brian J. Druker, Bin Peng, Marianne Rosamilia, John Ford
Publikováno v:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 22(5)
Purpose To evaluate the basic pharmacokinetic (PK) characteristics of imatinib mesylate and assess the relationship between the PK and pharmacodynamic (PD) properties of the drug. Patients and Methods The PK and PD properties of imatinib were investi
Autor:
John L, Frater, Martin S, Tallman, Daina, Variakojis, Brian J, Druker, Debra, Resta, Mary Beth, Riley, Mary Ann, Hrisinko, LoAnn C, Peterson
Publikováno v:
American journal of clinical pathology. 119(6)
We evaluated bone marrow pathologic features and cytogenetic and molecular genetic status of 13 patients with interferon-resistant, chronic-phase chronic myeloid leukemia (CML), treated with imatinib mesylate (Gleevec). All had morphologic evidence o
Autor:
Hagop M, Kantarjian, Susan, O'Brien, Jorge E, Cortes, Terry L, Smith, Mary Beth, Rios, Jianqin, Shan, Ying, Yang, Francis J, Giles, Deborah A, Thomas, Stefan, Faderl, Guillermo, Garcia-Manero, Sima, Jeha, William, Wierda, Jean-Pierre J, Issa, Steven M, Kornblau, Michael, Keating, Debra, Resta, Renaud, Capdeville, Moshe, Talpaz
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 8(7)
Imatinib mesylate, a specific Bcr-Abl tyrosine kinase inhibitor, has shown encouraging activity in chronic myelogenous leukemia (CML).We treated 237 patients (median age, 50 years; age range, 18-82 years) with Philadelphia chromosome (Ph)-positive ac
Autor:
M. Talpaz, Stefan Faderl, D. A. Thomas, Debra Resta, M. Albitar, Francis Giles, Guillermo Garcia-Manero, Jianqin Shan, Hagop M. Kantarjian, Jorge E. Cortes, Mary Beth Rios, Susan O'Brien
Publikováno v:
Blood. 99(10)
Molecular abnormalities caused by the hybrid Bcr-Abl gene are causally associated with the development and progression of Philadelphia chromosome–positive (Ph+) chronic myelogenous leukemia (CML). Imatinib mesylate (STI571), a specific Bcr-Abl tyro
Autor:
Hagop, Kantarjian, Charles, Sawyers, Andreas, Hochhaus, Francois, Guilhot, Charles, Schiffer, Carlo, Gambacorti-Passerini, Dietger, Niederwieser, Debra, Resta, Renaud, Capdeville, Ulrike, Zoellner, Moshe, Talpaz, Brian, Druker, John, Goldman, Stephen G, O'Brien, Nigel, Russell, Thomas, Fischer, Oliver, Ottmann, Pascale, Cony-Makhoul, Thierry, Facon, Richard, Stone, Carole, Miller, Martin, Tallman, Randy, Brown, Michael, Schuster, Thomas, Loughran, Alois, Gratwohl, Franco, Mandelli, Giuseppe, Saglio, Mario, Lazzarino, Domenico, Russo, Michele, Baccarani, Enrica, Morra
Publikováno v:
The New England journal of medicine. 346(9)
Chronic myelogenous leukemia (CML) is caused by the BCR-ABL tyrosine kinase, the product of the Philadelphia chromosome. Imatinib mesylate, formerly STI571, is a selective inhibitor of this kinase.A total of 532 patients with late--chronic-phase CML
Autor:
David T. Scadden, Debra Resta, Zhengyu Wang, Scott M. Hammer, Jocelyn Bresnahan, John Gere, James D. Levine, Jacqueline McGRATH, Diane Young
Publikováno v:
AIDS research and human retroviruses. 11(6)
To determine the safety, tolerance, and hematological and virological effects of the recombinant hematopoietic growth factor interleukin 3 (IL-3) in HIV-1-infected individuals with cytopenia.A phase I single-center trial was conducted with patients i