Zobrazeno 1 - 10
of 19
pro vyhledávání: '"L P Schacter"'
Autor:
N Soni, L P Schacter, D Noel, K E Gunton, Patrick J. Creaven, Lakshmi Pendyala, Neal J. Meropol
Publikováno v:
Journal of Clinical Oncology. 15:766-772
PURPOSE Etoposide has schedule-dependent cytotoxic activity, and clinical resistance may be overcome with prolonged low-dose therapy. Oral bioavailability is variable, and protracted intravenous administration is limited by water insolubility, which
Autor:
John D. Hainsworth, N Levitan, J Randolph, G L Wampler, Chandra P. Belani, F. A. Greco, L P Schacter, M S Seyedsadr
Publikováno v:
Europe PubMed Central
PURPOSE This randomized phase II study evaluated the efficacy and toxicity of etoposide phosphate when used in combination with cisplatin in the treatment of small-cell lung cancer. PATIENTS AND METHODS Patients with previously untreated small-cell l
Autor:
S Z, Fields, D R, Budman, R R, Young, W, Kreis, R, Ingram, P, Schulman, R C, Cherny, J, Wright, J, Behr, C, Snow, L P, Schacter
Publikováno v:
Bone marrow transplantation. 18(5)
Etoposide is a widely used cytotoxic agent with a broad spectrum of activity in human malignancies. This agent has been incorporated into many transplant regimens although toxicity occurs because of its poor water solubility and toxic excipients. Eto
Autor:
S Z, Fields, L N, Igwemezie, S, Kaul, L P, Schacter, R J, Schilder, P P, Litam, B S, Himpler, C, McAleer, J, Wright, R H, Barbhaiya
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 1(1)
Etoposide phophate is a phosphate ester prodrug of etoposide designed to improve the pharmaceutical characteristics of the parent compound. A Phase I dose-escalating study of etoposide phosphate was conducted concurrently at two institutions to deter
Autor:
L P, Schacter, C, Anderson, R M, Canetta, S, Kelley, C, Nicaise, N, Onetto, M, Rozencweig, L, Smaldone, B, Winograd
Publikováno v:
Seminars in oncology. 19(6)
The discovery and development of new anticancer drugs is a complex and largely empirical process. New compounds can be discovered by screening, modification of existing compounds, rational drug design, and serendipitous basic research observations. S
Publikováno v:
Cancer research. 52(6)
Elsamitrucin (BMY-28090) is an antitumor antibiotic first described in 1985 that has significant oncolytic activity against a number of murine tumors including P388, L1210, B16 and M5076, as well as against MX1 and HCT116 xenografts. Preclinical toxi
Autor:
N C Cherng, Harvey J. Cohen, J A Randolph, G O Broun, Bruce J. Roth, David H. Johnson, L P Schacter, Jeffrey Crawford, Lawrence H. Einhorn, J L Goodlow
Publikováno v:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 10(2)
PURPOSE The trial was undertaken to determine (1) the relative efficacy/toxicity of two commonly used combination chemotherapy regimens in patients with extensive small-cell lung cancer (SCLC) and (2) whether the rapid alternation of these two regime
Publikováno v:
Seminars in oncology. 17(6 Suppl 9)
Hormonal therapy of breast cancer is widely used and effective. Although never curative in advanced disease, significant palliation and durable remissions can be obtained with a wide variety of hormonal manipulations. Historically, surgical ablation
Autor:
L. P. Schacter
Publikováno v:
European Journal of Clinical Investigation. 16:204-210
To test the hypothesis that the resistance of sickle trait (AS Hgb) erythrocytes (rbcs) to malaria may be mediated by increased production of activated oxygen species, the production of superoxide anion (O2-) and hydrogen peroxide (H2O2) by AS rbcs a
Autor:
L. P. Schacter
Publikováno v:
JAMA: The Journal of the American Medical Association. 237:1848-1851