Drug intelligence / Profile preview

bleomycin + dexamethasone

Development stage
Unknown
Modality
Cyclic Peptides → Modified Peptides → Peptides, Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Antimicrobial Peptides → Native Peptides → Peptides
Administration
Intralesional, Intravenous, Intramuscular, Subcutaneous, Intracavitary
01

Overview

Bleomycin + dexamethasone is a combination therapy consisting of bleomycin, an antineoplastic glycopeptide antibiotic, and dexamethasone, a synthetic glucocorticoid corticosteroid. Bleomycin acts primarily by inducing DNA strand breaks through free radical formation, leading to inhibition of DNA synthesis and cell death. It is widely used in the treatment of various malignancies and as a sclerosing agent for lymphangiomas. Dexamethasone exerts potent anti-inflammatory and immunosuppressive effects by binding to the glucocorticoid receptor, modulating gene expression to suppress pro-inflammatory cytokines and mediators. The combination has been studied particularly in pediatric lymphangioma sclerotherapy, where it has demonstrated improved response rates compared to bleomycin alone with a favorable safety profile[1]. The rationale for combining these agents includes enhanced efficacy (bleomycin’s cytotoxicity plus dexamethasone’s anti-inflammatory action) and potentially reduced recurrence or side effects.

Other names
intralesional bleomycin with dexamethasonebleomycin-dexamethasone combination
02

Targets

GR (Glucocorticoid receptor)DNA

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