نتایج جستجو برای: Lomustine

تعداد نتایج: 2060  

Journal: :Neuro-oncology 2016
Kader Yagiz Tiffany T Huang Fernando Lopez Espinoza Daniel Mendoza Carlos E Ibañez Harry E Gruber Douglas J Jolly Joan M Robbins

BACKGROUND Toca 511, a gamma retroviral replicating vector encoding cytosine deaminase, used in combination with 5-fluorocytosine (5-FC) kills tumor by local production of 5-fluorouracil (5-FU), inducing local and systemic immunotherapeutic response resulting in long-term survival after cessation of 5-FC. Toca 511 and Toca FC (oral extended-release 5-FC) are under investigation in patients with...

Journal: :Neuro-oncology practice 2014
Hans-Georg Wirsching Isabel Tritschler Antonella Palla Christoph Renner Michael Weller Ghazaleh Tabatabai

Lomustine is an oral alkylating drug commonly used for brain tumor patients. Recently, the lomustine-containing PCV polychemotherapy regime (procarbazine, CCNU/lomustine, and vincristine) in combination with radiotherapy has become the standard of care for anaplastic oligodendroglioma with 1p/19q codeletion and high-risk low-grade glioma. Here, we review the literature of all reported cases of ...

2016
J.H. Burton S.D. Stanley H.K. Knych C.O. Rodriguez K.A. Skorupski R.B. Rebhun

BACKGROUND Compounded lomustine is used commonly in veterinary patients. However, the potential variability in these formulations is unknown and concern exists that compounded formulations of drugs may differ in potency from Food and Drug Administration (FDA)-approved products. HYPOTHESIS/OBJECTIVES The initial objective of this study was to evaluate the frequency and severity of neutropenia ...

2014
Thushara Chakkath Sidonie N. Lavergne Timothy M. Fan David Bunick Levent Dirikolu

The nitrosourea drug lomustine is used clinically for treating a wide variety of malignancies, most commonly brain tumors and lymphoma. Lomustine undergoes hydrolysis in vivo to form isomeric metabolites, primarily trans-4-hydroxylomustine (trans-4) and cis-4-hydroxylomustine (cis-4) in various animal species including humans. Despite its widespread usage to treat canine lymphoma, the metabolis...

Journal: :Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2013
Tracy T Batchelor Paul Mulholland Bart Neyns L Burt Nabors Mario Campone Antje Wick Warren Mason Tom Mikkelsen Surasak Phuphanich Lynn S Ashby John Degroot Rao Gattamaneni Lawrence Cher Mark Rosenthal Franz Payer Juliane M Jürgensmeier Rakesh K Jain A Gregory Sorensen John Xu Qi Liu Martin van den Bent

PURPOSE A randomized, phase III, placebo-controlled, partially blinded clinical trial (REGAL [Recent in in Glioblastoma Alone and With Lomustine]) was conducted to determine the efficacy of cediranib, an oral pan-vascular endothelial growth factor (VEGF) receptor tyrosine kinase inhibitor, either as monotherapy or in combination with lomustine versus lomustine in patients with recurrent gliobla...

Journal: :The Lancet. Oncology 2014
Walter Taal Hendrika M Oosterkamp Annemiek M E Walenkamp Hendrikus J Dubbink Laurens V Beerepoot Monique C J Hanse Jan Buter Aafke H Honkoop Dolf Boerman Filip Y F de Vos Winand N M Dinjens Roelien H Enting Martin J B Taphoorn Franchette W P J van den Berkmortel Rob L H Jansen Dieta Brandsma Jacoline E C Bromberg Irene van Heuvel René M Vernhout Bronno van der Holt Martin J van den Bent

BACKGROUND Treatment options for recurrent glioblastoma are scarce, with second-line chemotherapy showing only modest activity against the tumour. Despite the absence of well controlled trials, bevacizumab is widely used in the treatment of recurrent glioblastoma. Nonetheless, whether the high response rates reported after treatment with this drug translate into an overall survival benefit rema...

2014
Yun Guo Shuoye Yang

To prepare lomustine-iohexol thermosensetive compound liposomes, and evaluate the properties and in vitro release behaviors of two drugs enveloped. Lomustine-iohexol thermosensetive compound liposomes were prepared by reverse evaporation method, HPLC assays for determination of lomustine and iohexol in vitro were developed, and their release property was studied by using dislysis method. The me...

This study aimed to improve delivery of lomustine as a chemotherapeutic agent and to increase its uptake by U87-MG cancer cells via synthesizes LN-FA-PG-SPIONs (lomustine loaded polyglycerol coated superparamagnetic iron oxide nanoparticles conjugated with folic acid). Nanoparticles were synthesized by thermal decomposition method and characterized using TEM (transmission microscope), FTIR (Fou...

This study aimed to improve delivery of lomustine as a chemotherapeutic agent and to increase its uptake by U87-MG cancer cells via synthesizes LN-FA-PG-SPIONs (lomustine loaded polyglycerol coated superparamagnetic iron oxide nanoparticles conjugated with folic acid). Nanoparticles were synthesized by thermal decomposition method and characterized using TEM (transmission microscope), FTIR (Fou...

Journal: :Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2010
Wolfgang Wick Vinay K Puduvalli Marc C Chamberlain Martin J van den Bent Antoine F Carpentier Lawrence M Cher Warren Mason Michael Weller Shengyan Hong Luna Musib Astra M Liepa Donald E Thornton Howard A Fine

PURPOSE This phase III open-label study compared the efficacy and safety of enzastaurin versus lomustine in patients with recurrent glioblastoma (WHO grade 4). PATIENTS AND METHODS Patients were randomly assigned 2:1 to receive 6-week cycles of enzastaurin 500 mg/d (1,125-mg loading dose, day 1) or lomustine (100 to 130 mg/m(2), day 1). Assuming a 45% improvement in progression-free survival ...

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