Treatment of al amyloidosis with melphalan, prednisone, and colchicine
Open Access
- 1 May 1986
- journal article
- research article
- Published by Wiley in Arthritis & Rheumatism
- Vol. 29 (5), 683-687
- https://doi.org/10.1002/art.1780290515
Abstract
Seven patients with immunoglobulin type (AL) amyloidosis were treated with combination chemotherapy, including melphalan, prednisone, and colchicine. Two patients died within 5 months of the beginning of therapy. Both had amyloid cardiomyopathy. Five patients were alive 17–60 months after the start of therapy, and none had shown progression of disease. The most significant findings were the resolution of the nephrotic syndrome in 2 patients, and improvement of liver function, as demonstrated by excretion of indocyanine green, in 2 patients. These results are encouraging and support the need for further studies of this regimen of combination chemotherapy for patients with AL amyloidosis.This publication has 13 references indexed in Scilit:
- Prolonged dimethylsulphoxide treatment in 13 patients with systemic amyloidosis.Annals Of The Rheumatic Diseases, 1982
- Primary systemic amyloidosis: resolution of the nephrotic syndrome with melphalan and prednisoneArchives of Internal Medicine, 1982
- Amyloid Deposits and AmyloidosisNew England Journal of Medicine, 1980
- Amyloidosis of the AL typeThe American Journal of Medicine, 1979
- Colchicine in Familial Mediterranean FeverNew England Journal of Medicine, 1976
- AMYLOIDOSIS: REVIEW OP 236 CASESMedicine, 1975
- Resolution of Primary Amyloidosis During ChemotherapyAnnals of Internal Medicine, 1975
- BLOCKAGE OF AMYLOID INDUCTION BY COLCHICINE IN AN ANIMAL MODELThe Journal of Experimental Medicine, 1974
- Primary Amyloidosis and Acute Leukemia Associated With Melphalan TherapyBlood, 1974
- A clinical analysis of the course and prognosis of forty-two patients with amyloidosisThe American Journal of Medicine, 1968