Pentostatin Explained
Pentostatin (or deoxycoformycin, trade name Nipent, manufactured by SuperGen) is an anticancer chemotherapeutic drug.[1]
Mechanism
It is classified as a purine analog, which is a type of antimetabolite.
It mimics the nucleoside adenosine and thus inhibits the enzyme adenosine deaminase, interfering with the cell's ability to process DNA.[2]
Cancer cells generally divide more often than healthy cells; DNA is highly involved in cell division (mitosis) and drugs which target DNA-related processes are therefore more toxic to cancer cells than healthy cells.
Uses
Pentostatin is used to treat hairy cell leukemia.[3] It is given by intravenous infusion once every two weeks for three to six months.
Additionally, pentostatin has been used to treat steroid-refractory acute and chronic graft-versus-host disease.[4]
Pentostatin is also used in chronic lymphocytic leukemia (CLL) patients who have relapsed.
Synthesis
This is the original synthetic pathway although improvements were made.
Notes and References
- Kay NE, Geyer SM, Call TG, etal . Combination chemoimmunotherapy with pentostatin, cyclophosphamide, and rituximab shows significant clinical activity with low accompanying toxicity in previously untreated B chronic lymphocytic leukemia . Blood . 109 . 2 . 405–11 . January 2007 . 17008537 . 1785105 . 10.1182/blood-2006-07-033274 .
- Sauter C, Lamanna N, Weiss MA . Pentostatin in chronic lymphocytic leukemia . Expert Opin Drug Metab Toxicol . 4 . 9 . 1217–22 . September 2008 . 18721115 . 10.1517/17425255.4.9.1217 .
- Cannon T, Mobarek D, Wegge J, Tabbara IA . Hairy cell leukemia: current concepts . Cancer Invest. . 26 . 8 . 860–5 . October 2008 . 18798068 . 10.1080/07357900801965034 .
- Bolaños-Meade J, Jacobsohn DA, Margolis J, Ogden A, Wientjes MG, Byrd JC, Lucas DM, Anders V, Phelps M, Grever MR, Vogelsang GB . Pentostatin in steroid-refractory acute graft-versus-host disease . J Clin Oncol . 23 . 12 . 2661–8 . April 2005 . 15837980 . 10.1200/JCO.2005.06.130. free .