The purine analogs, fludarabine, 2-chlorodeoxy-adenosine, and 2'-deoxy
coformycin, have revolutionized our approach to the treatment of a var
iety of indolent lymphoid malignancies. Because of their impressive si
ngle agent activity, they should be considered as an initial therapeut
ic option, not only for hairy cell leukemia, but also for chronic lymp
hocytic leukemia, indolent non-Hodgkin's lymphomas, and Waldenstrom's
macroglobulinemia. Combinations of purine analogs with alkylatng agent
s, topisomerase II inhibitors, and other new compounds are in developm
ent, and their role as radiation sensitizers is being explored in clin
ical trials. Substantial activity has also been noted in several of th
e rheumatologic and immunologic disorders, and in multiple sclerosis.
Continued progress requires innovative strategies which can modulate t
he biology and immunology of these diseases toward the goal of curing
these patients.