Indication |
Used orally for the treatment of skin manifestations of cutaneous
T-cell lymphoma (CTCL) in patients who are refractory to at least one
prior systemic therapy. Also used topically for the treatment of skin
lesions in early (stage IA and IB) CTCL in patients who experience
refractory or persistent disease with the use of other therapies or are
intolerant of other therapies. |
Pharmacodynamics |
Bexarotene is a member of a subclass of retinoids that
selectively activate retinoid X receptors (RXRs). These retinoid
receptors have biologic activity distinct from that of retinoic acid
receptors (RARs). Bexarotene is indicated for the treatment of cutaneous
manifestations of cutaneous T-cell lymphoma in patients who are
refractory to at least one prior systemic therapy. Bexarotene
selectively binds and activates retinoid X receptor subtypes (RXRα, RXRβ, RXRγ).
RXRs can form heterodimers with various receptor partners such as
retinoic acid receptors (RARs), vitamin D receptor, thyroid receptor,
and peroxisome proliferator activator receptors (PPARs). Once activated,
these receptors function as transcription factors that regulate the
expression of genes that control cellular differentiation and
proliferation. Bexarotene inhibits the growth in vitro of some tumor cell lines of hematopoietic and squamous cell origin. It also induces tumor regression in vivo in some animal models. |
Mechanism of action |
Bexarotene selectively binds with and activates retinoid X receptor subtypes. There are three subtypes in total: RXRα, RXRβ, RXRγ.
The exact mechanism of action of bexarotene in the treatment of CTCL is
unknown but the drug has activity in all clinical stages of CTCL. |
Absorption |
Not Available |
Volume of distribution |
Not Available |
Protein binding |
>99% |
Metabolism |
Not Available |
Route of elimination |
Urinary elimination of bexarotene and its known metabolites is a minor excretory pathway (<1% of administered dose). |
Half life |
7 hours |
Clearance |
Not Available |
Toxicity |
Not Available |