Temozolomide for treating brain metastases Journal Article


Authors: Abrey, L. E.; Christodoulou, C.
Article Title: Temozolomide for treating brain metastases
Abstract: The metastasis of solid tumors to the brain is associated with a poor prognosis despite aggressive treatment. Available treatment options are limited, as many chemotherapeutic agents do not penetrate the blood-brain barrier. Temozolomide (Temodar in the United States, Temodal globally; Schering Corporation, Kenilworth, NJ) is a novel chemotherapeutic agent with a good safety profile that crosses the blood-brain barrier and has shown activity against many human solid tumors. In two phase II trials of temozolomide in heavily pretreated patients with various solid tumor brain metastases, temozolomide was safe and generally well tolerated and showed clinical activity, with three partial responses and 19 disease stabilizations. Results of a third randomized phase II trial of concurrent administration of temozolomide and radiation therapy followed by adjuvant temozolomide therapy compared with radiation alone showed a higher rate of complete and partial responses (objective response of 96% v 67%) and significantly more complete responses (38% v 33%, P = .017), primarily in patients with newly diagnosed brain and lung metastases. Copyright © 2001 by W.B. Saunders Company.
Keywords: controlled study; aged; middle aged; clinical trial; drug activity; review; drug safety; cancer radiotherapy; chemotherapy, adjuvant; temozolomide; brain neoplasms; cancer diagnosis; dacarbazine; controlled clinical trial; neoplasm recurrence, local; leukopenia; thrombocytopenia; carcinoma, non-small-cell lung; lung neoplasms; antineoplastic activity; pneumonia; lung metastasis; blood brain barrier; antineoplastic agents, alkylating; brain metastasis; liver disease; neurologic disease; drug tolerance; clinical trials; whole-body irradiation; humans; prognosis; human; male; female; priority journal
Journal Title: Seminars in Oncology
Volume: 28
Issue: Suppl. 13
ISSN: 0093-7754
Publisher: Elsevier Inc.  
Date Published: 2001-08-01
Start Page: 34
End Page: 42
Language: English
PUBMED: 11550137
PROVIDER: scopus
DOI: 10.1016/S0093-7754(01)90069-7
DOI/URL:
Notes: Export Date: 21 May 2015 -- Source: Scopus
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  1. Lauren E Abrey
    278 Abrey