Mayo Clin Proc. 2000 Sep;75(9):897-901. Unique Identifier : AIDSLINE
OBJECTIVE: To describe the efficacy of therapy with thalidomide, a drug
that has antiangiogenic properties, in patients with relapsed multiple
myeloma. PATIENTS AND METHODS: We studied 16 patients (median age, 64
years) who received thalidomide for relapsed myeloma at the Mayo Clinic
in Rochester, Minn, between November 1998 and August 1999. Treatment
consisted of thalidomide given orally at a dose of 200 mg/d for 2 weeks,
then increased by 200 mg/d every 2 weeks, up to a maximal dose of 800
mg/d. RESULTS: The stage of myeloma at treatment was Durie-Salmon IIIA
in 9 patients (56%) and IIIB in 7 (44%). The median time from myeloma
diagnosis to initiation of thalidomide therapy was 32 months. In 4
patients (25%) prior stem cell transplantation had failed, and 14 (88%)
had received 2 or more prior chemotherapeutic regimens before
institution of thalidomide. All patients were evaluable for response.
Four (25%) achieved a partial response to therapy, with a greater than
50% reduction in the serum or urine M protein level. Responses lasted 2,
4+, 8, and 10+ months. Major adverse effects included constipation,
sedation, rash, and peripheral neuropathy. CONCLUSION: Thalidomide is an
active agent in the treatment of patients with advanced myeloma.
JOURNAL ARTICLE Administration, Oral Aged Aged, 80 and over
Angiogenesis Inhibitors/PHARMACOLOGY/*THERAPEUTIC USE Case Report
Disease-Free Survival Female Follow-Up Studies Hematopoietic Stem
Cell Transplantation Human Male Middle Age Multiple
Myeloma/CLASSIFICATION/*DRUG THERAPY/METABOLISM Muscle
Proteins/BLOOD/URINE Recurrence Severity of Illness Index Support,
Non-U.S. Gov't Support, U.S. Gov't, P.H.S.
Thalidomide/PHARMACOLOGY/*THERAPEUTIC USE Treatment Failure