A. Rieth et A. Ludascher, PENTOSTATIN (2'-DEOXYCOFORMYCIN, NIPENT(R)) - A STRUCTURAL ANALOG OF THE PURINE ADENOSINE ACTING AS POTENT ADENOSINE-DEAMINASE INHIBITOR, Onkologie, 18(4), 1995, pp. 302-309
Pentostatin, a structural analogue of the purine adenosine, is acting
as a potent inhibitor of adenosine deaminase. It has been studied in t
he treatment of various lymphoproliferative disorders and proved to be
very effective in the treatment of hairy-cell leukemia achieving comp
lete remissions in up to 93%, complete or partial remissions in 63 to
100% of patients. Furthermore, pentostatin has shown activity in treat
ing chronic lymphocytic leukemia, prolymphocytic leukemia, adult T cel
l leukemia/lymphoma and especially cutaneous T cell lymphoma refractor
y to conventional chemotherapy. Randomized clinical studies show that
in the treatment of hairy-cell leukemia pentostatin achieves a faster
response, significantly higher response rates and longer duration of r
emissions than interferon-alpha. Nevertheless it remains uncertain if
patients with complete remission have finally been cured. Since pentos
tatin does produce a substantial response in a highly practicable ther
apy with low toxicity it should be applied as standard first-line trea
tment of hairy-cell leukemia.