Ws. Wilke et Jm. Cash, THE USE OF SLOWER-ACTING (CLASS-III) SYMPTOM-MODIFYING ANTIRHEUMATIC DRUGS IN RHEUMATOID-ARTHRITIS, CLINICAL IMMUNOTHERAPEUTICS, 5(4), 1996, pp. 309-325
Slower-acting (class III) symptom-modifying drugs are given in rheumat
oid arthritis to control acute signs and symptoms of the disease, with
the hope of favourably modifying long term outcome. Among these agent
s, methotrexate, sulfasalazine and hydroxychloroquine offer the best e
fficacy/toxicity ratio. Unfortunately, sustained remission with treatm
ent is rare, and most analyses demonstrate long term progressive disab
ility. Clearly, strategies that initiate single-agent therapy with the
currently available class III symptom-modifying drugs only after fail
ure of physical therapy and treatment with nonsteroidal anti-inflammat
ory drugs are successful in only a small proportion of patients. For m
ost patients with moderate to severe disease at the time of diagnosis,
this approach should probably be abandoned. New agents and/or new str
ategies are needed. Newer biological agents have not proven superior t
o existing therapies, nor are they readily available to most practisin
g clinicians. However, novel strategies using existing agents can ofte
n control disease in the short term and might also offer improved long
term outcome. There is reason to believe that both of these goals can
be met by using a strategy in which sufficiently aggressive treatment
is given to decrease the number of swollen joints to less than or equ
al to 5 and to normalise acute phase reactant levels. If combinations
of class III symptom-modifying drugs are necessary to achieve these go
als, methotrexate combined with hydroxychloroquine, sulfasalazine or c
yclosporin seem the best choices today.