Literature DB >> 10794805

Temozolomide, a novel alkylating agent with activity in the central nervous system, may improve the treatment of advanced metastatic melanoma.

S S Agarwala1, J M Kirkwood.   

Abstract

Temozolomide (TMZ) is the first new chemotherapy agent to be approved for the treatment of high-grade malignant gliomas in more than 20 years. This novel oral alkylating agent has demonstrated promising activity not only in brain tumors, but in a variety of solid tumors, including malignant melanoma. TMZ is 100% bioavailable when taken orally and, because of its small size and lipophilic properties, it is able to cross the blood-brain barrier. Concentrations in the central nervous system are approximately 30% of plasma concentrations. Once it has entered the central nervous system, TMZ can be spontaneously converted to the active metabolite. These pharmacologic properties make it an ideal agent for treating central nervous system malignancies. In patients with advanced metastatic melanoma, brain metastases are a major cause of treatment failure. In this setting, TMZ has been shown to be as effective as dacarbazine, with a similar safety profile. More importantly, there is evidence to suggest that TMZ-treated patients have a lower incidence of central nervous system relapse compared with dacarbazine-treated patients. Therefore, TMZ is actively being investigated for the treatment and prevention of brain metastases in melanoma patients. TMZ may become an important part of treatment regimens for advanced metastatic melanoma.

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Year:  2000        PMID: 10794805     DOI: 10.1634/theoncologist.5-2-144

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  85 in total

1.  Temozolomide (Temodar).

Authors:  J R Wesolowski; P Rajdev; S K Mukherji
Journal:  AJNR Am J Neuroradiol       Date:  2010-06-10       Impact factor: 3.825

Review 2.  Molecular basis of pharmacological therapy in Cushing's disease.

Authors:  Diego Ferone; Claudia Pivonello; Giovanni Vitale; Maria Chiara Zatelli; Annamaria Colao; Rosario Pivonello
Journal:  Endocrine       Date:  2013-11-23       Impact factor: 3.633

3.  Potentiation of temozolomide cytotoxicity by inhibition of DNA polymerase beta is accentuated by BRCA2 mutation.

Authors:  Gregory C Stachelek; Shibani Dalal; Katherine A Donigan; Denise Campisi Hegan; Joann B Sweasy; Peter M Glazer
Journal:  Cancer Res       Date:  2009-12-22       Impact factor: 12.701

Review 4.  Evidence-Based Practice: Temozolomide Beyond Glioblastoma.

Authors:  Jason Chua; Elizabeth Nafziger; Denise Leung
Journal:  Curr Oncol Rep       Date:  2019-03-05       Impact factor: 5.075

Review 5.  Targeting EGFR for treatment of glioblastoma: molecular basis to overcome resistance.

Authors:  T E Taylor; F B Furnari; W K Cavenee
Journal:  Curr Cancer Drug Targets       Date:  2012-03       Impact factor: 3.428

6.  A multicenter phase I dose escalation trial to evaluate safety and tolerability of intra-arterial temozolomide for patients with advanced extremity melanoma using normothermic isolated limb infusion.

Authors:  Georgia M Beasley; Paul Speicher; Christina K Augustine; Paul C Dolber; Bercedis L Peterson; Ketan Sharma; Paul J Mosca; Richard Royal; Merrick Ross; Jonathan S Zager; Douglas S Tyler
Journal:  Ann Surg Oncol       Date:  2014-08-22       Impact factor: 5.344

7.  EMAP-II sensitize U87MG and glioma stem-like cells to temozolomide via induction of autophagy-mediated cell death and G2/M arrest.

Authors:  Qi Yu; Libo Liu; Ping Wang; Yilong Yao; Yixue Xue; Yunhui Liu
Journal:  Cell Cycle       Date:  2017-04-24       Impact factor: 4.534

8.  Temozolomide-mediated radiosensitization of human glioma cells in a zebrafish embryonic system.

Authors:  Geoffrey A Geiger; Weili Fu; Gary D Kao
Journal:  Cancer Res       Date:  2008-05-01       Impact factor: 12.701

9.  Temozolomide as first-line agent in treating high-grade gliomas: phase II study.

Authors:  S Chibbaro; L Benvenuti; A Caprio; S Carnesecchi; F Pulerà; F Faggionato; D Serino; C Galli; M Andreuccetti; N Buxton; R Gagliardi
Journal:  J Neurooncol       Date:  2004 Mar-Apr       Impact factor: 4.130

10.  Glioma-associated endothelial cells are chemoresistant to temozolomide.

Authors:  Jenilyn J Virrey; Encouse B Golden; Walavan Sivakumar; Weijun Wang; Ligaya Pen; Axel H Schönthal; Florence M Hofman; Thomas C Chen
Journal:  J Neurooncol       Date:  2009-04-18       Impact factor: 4.130

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