Overview
A cell-cycle phase nonspecific alkylating antineoplastic agent. It is used in the treatment of brain tumors and various other malignant neoplasms. (From Martindale, The Extra Pharmacopoeia, 30th ed, p462) This substance may reasonably be anticipated to be a carcinogen according to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985). (From Merck Index, 11th ed)
Indication
For the treatment of brain tumors, multiple myeloma, Hodgkin's disease and Non-Hodgkin's lymphomas.
Associated Conditions
- Astrocytoma
- Brain Stem Gliomas
- Ependymoma
- High Grade Glioma: Glioblastoma (GBM)
- Medulloblastomas
- Metastatic Brain Tumors
- Mycosis Fungoides (MF)
- Newly Diagnosed High-Grade Glioma
- Recurrent Glioblastoma Multiforme (GBM)
- Refractory Hodgkin Lymphoma
- Refractory Multiple Myeloma
- Refractory Non-Hodgkin's lymphoma
Research Report
An Expert Report on Carmustine (BCNU): Pharmacology, Clinical Applications, and Evolving Therapeutic Landscape
Executive Summary
Carmustine, a nitrosourea alkylating agent identified by the DrugBank ID DB00262, represents a cornerstone in the chemotherapeutic management of central nervous system (CNS) malignancies. For nearly five decades, its clinical utility has been fundamentally defined by its high lipophilicity, which facilitates penetration of the blood-brain barrier (BBB)—a characteristic that distinguishes it from many other cytotoxic agents. This report provides an exhaustive analysis of Carmustine, synthesizing its physicochemical properties, multifaceted mechanism of action, complex pharmacokinetics, clinical efficacy, and extensive safety profile.
The drug operates primarily through the alkylation and subsequent cross-linking of DNA and RNA, a process that physically obstructs replication and transcription, leading to cancer cell death. This direct cytotoxic assault is synergistically amplified by Carmustine's ability to inhibit key cellular defense and repair pathways, including glutathione reductase and O6-methylguanine-DNA methyltransferase (MGMT), effectively disarming the cell while damaging it.
Clinical Trials
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Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2007/05/11 | Phase 2 | Completed | |||
2007/02/23 | Phase 2 | Completed | |||
2006/10/16 | Phase 2 | Completed | |||
2006/08/15 | Phase 2 | Completed | |||
2006/07/10 | Phase 2 | Completed | |||
2006/07/10 | Phase 2 | Completed | |||
2006/06/29 | Phase 2 | Completed | |||
2006/04/24 | Not Applicable | UNKNOWN | European Inter-group Cooperation on Childhood and Adolescent Non Hodgkin Lymphoma | ||
2006/01/30 | Phase 2 | UNKNOWN | Kentuckiana Cancer Institute | ||
2006/01/25 | Phase 2 | Terminated |
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