Cytarabine liposomal (DepoCyt)
General information
Class/mechanism: Pyrimidine analog, mimics cytosine. Converted intracellularly into cytarabine-5-triphosphate (ara-CTP). Exact mechanism of action not known; believed to inhibit DNA polymerase, incorporate into DNA and RNA, and kill cells undergoing DNA synthesis (S-phase) and sometimes block cells from progressing from the G1 phase to the S-phase.[1][2][3]
Route: IT
Extravasation: irritant
- "In-line filters must not be used when administering DepoCyt."[1]
For conciseness and simplicity, HemOnc.org currently will focus on treatment regimens and not list information such as: renal/hepatic dose adjustments, metabolism (including CYP450), excretion, monitoring parameters (although this will be considered for checklists), or manufacturer. Instead, for the most current information, please refer to your preferred pharmacopeias or the prescribing information.[1]
Diseases for which it is used
Patient drug information
History of changes in FDA indication
- 1999-04-01: Initial accelerated approval for intrathecal treatment of lymphomatous meningitis. (Based on Glantz et al. 1999)
- 2007-04-19: Converted to regular approval for intrathecal treatment of lymphomatous meningitis.
- 2011-08-11 (oldest label available at Drugs @ FDA): indicated for the intrathecal treatment of lymphomatous meningitis.
History of changes in EMA indication
- 2001-07-11: Initial authorization as DepoCyte
- 2018-07-10: Withdrawn on request from the manufacturer, for commercial reasons
Also known as
- Generic name: Liposomal Ara-C
- Brand name: DepoCyt, DepoCyte
References
- ↑ 1.0 1.1 1.2 1.3 Cytarabine liposomal (DepoCyt) package insert
- ↑ Cytarabine liposomal (DepoCyt) package insert (locally hosted backup)
- ↑ DepoCyt manufacturer's website
- ↑ Cytarabine liposomal (DepoCyt) patient drug information (Chemocare)
- ↑ Cytarabine liposomal (DepoCyt) patient drug information (UpToDate)