Background and Objectives. Thalidomide is currently used as a very promisin
g drug in patients with recurrent multiple myeloma or those refractory to c
hemotherapy. Literature data show prolonged survival in patients with advan
ced multiple myeloma treated with thalidomide but the optimal time and dose
of thalidomide treatment remain to be established.
Design and Methods. We have treated 53 refractory or relapsed myeloma patie
nts with thalidomide (Grunenthal, Aachen). The patients received thalidomid
e orally as monotherapy at a starting dose of 200 mg daily, with a dose inc
rease of 100 mg every week to a maximum well-tolerated dose of 400 mg. All
the patients qualified for the therapy underwent clinical and laboratory as
sessments every 4 weeks. Laboratory tests included complete blood count, el
ectrophoresis, immunoglobulin level, lactate dehydrogenase (LDH), C-reactiv
e protein, beta (2) microglobulin concentration, liver and renal function t
ests and there was also a monthly neurological examination. Bone marrow asp
iration was performed every 3 months during the 12-month treatment.
Results. Among 53 evaluable patients, a clinical response was observed in 2
7 (51%): there was a major response in 7 patients, a partial response in 12
and a minor response in 8.
Interpretation and Conclusions. In responding patients the earliest respons
e was observed after 4 weeks of treatment and the latest after 12 weeks of
treatment, Our results, obtained during a long observation period, show tha
t thalidomide is an effective drug, with an acceptable degree of toxicity,
in patients with refractory multiple myeloma (C) 2001, Ferrata Storti Found
ation.