Drug intelligence / Profile preview

carmustine + cytarabine + etoposide + melphalan

Development stage
Unknown
Lead developer
Bristol Myers Squibb
Modality
Small Molecules
Administration
Intravenous
01

Overview

BEAM is a chemotherapy regimen consisting of four drugs: carmustine (also known as BCNU), cytarabine (also known as Ara-C or cytosine arabinoside), etoposide, and melphalan (also known as Alkeran). This combination is primarily used as a conditioning regimen before autologous or allogeneic stem cell transplantation in patients with lymphoma, including Hodgkin lymphoma and non-Hodgkin lymphoma. Each component has a distinct mechanism of action: - Carmustine is an alkylating agent that cross-links DNA and RNA, inhibiting replication and transcription. - Cytarabine is an antimetabolite that inhibits DNA synthesis by acting as a cytosine analog. - Etoposide inhibits topoisomerase II, leading to DNA strand breaks. - Melphalan is another alkylating agent that cross-links DNA strands. The regimen aims to eradicate malignant cells and suppress the immune system prior to stem cell transplantation. It is considered standard for high-dose chemotherapy in this setting due to its efficacy and tolerability profile[1][2][3][4].

Brand names
BEAM
Other names
BEAMBCNU + Ara-C + VP-16 + Alkeran
02

Targets

TOP2A (DNA topoisomerase II)DNA polymerase familyDNA

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