Thalidomide has been shown to be an effective treatment for cutaneous forms
of lupus erythematous refractory to other therapies. Thalidomide has very
serious side effects, including teratogenicity and neuropathy, which limit
its clinical use in lupus to such severe refractory cases. Efficacy has bee
n confirmed in several studies, although recurrence after discontinuation o
f treatment is frequent. More recent experience suggests that lower doses t
han originally used may be effective, which may result in a reduction in si
de effects. Much effort has been expended in studying the mechanisms of act
ion of thalidomide, although as yet it is unclear which of the mechanisms i
dentified to date contribute to its efficacy in treating cutaneous forms of
lupus erythematosus. Identification of patients suitable for thalidomide t
herapy requires a rigorous selection process. Potential side effects should
be clearly explained, particularly teratogenicity as many patients are you
ng women. Written consent and a negative pregnancy test must be obtained pr
ior to commencement of therapy. Reliable contraceptive measures should be s
trictly observed by patients taking thalidomide. Close clinical and neuroph
ysiological supervision using nerve conduction studies should be undertaken
.