Literature DB >> 3934968

Primary systemic amyloidosis. Comparison of melphalan/prednisone versus colchicine.

R A Kyle, P R Greipp, J P Garton, M A Gertz.   

Abstract

This is the first prospectively randomized study of the use of melphalan/prednisone and colchicine in the treatment of primary systemic amyloidosis. One hundred one patients were stratified according to their dominant clinical manifestation. Forty-nine patients initially received melphalan/prednisone and eight subsequently had colchicine added to their regimen. Fifty-two patients initially received colchicine and 35 subsequently required melphalan/prednisone because of progressive disease. There was no difference in survival when the two groups were analyzed in aggregate (melphalan/prednisone, 25.2 months versus colchicine, 18 months; p = 0.23). When the survival of patients receiving only one regimen was analyzed or when survival was analyzed from the time of entry into the study to the time of death or progression of disease, significant differences (p less than 0.001 and p less than 0.0001, respectively) were evident, favoring melphalan/prednisone. This study suggests that melphalan/prednisone is superior to colchicine in the treatment of primary amyloidosis, but to confirm this impression, a study without a crossover group is necessary.

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Year:  1985        PMID: 3934968     DOI: 10.1016/0002-9343(85)90521-2

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


  15 in total

Review 1.  Amyloidosis.

Authors:  M F Khan; R H Falk
Journal:  Postgrad Med J       Date:  2001-11       Impact factor: 2.401

Review 2.  Colchicine--expanding horizons.

Authors:  A Schattner
Journal:  Postgrad Med J       Date:  1991-03       Impact factor: 2.401

3.  AL amyloid deposits in temporal artery mimicking giant cell arteritis.

Authors:  B Taillan; J G Fuzibet; H Vinti; A Pesce; P Dujardin
Journal:  Clin Rheumatol       Date:  1990-06       Impact factor: 2.980

4.  Phase II trial of high-dose dexamethasone for untreated patients with primary systemic amyloidosis.

Authors:  M A Gertz; M Q Lacy; J A Lust; P R Greipp; T E Witzig; R A Kyle
Journal:  Med Oncol       Date:  1999-07       Impact factor: 3.064

Review 5.  Anti-amyloid drugs: potential in the treatment of diseases associated with aging.

Authors:  R Kisilevsky
Journal:  Drugs Aging       Date:  1996-02       Impact factor: 3.923

6.  Cholestasis and liver failure with lambda-AL amyloidosis.

Authors:  F Konikoff; C Mor; S Stern; M Shaklai; J Halevy; E Theodor
Journal:  Gut       Date:  1987-07       Impact factor: 23.059

Review 7.  Frequency and genetic background of the position 122 (Val----Ile) variant transthyretin gene in the black population.

Authors:  D R Jacobson; J D Reveille; J N Buxbaum
Journal:  Am J Hum Genet       Date:  1991-07       Impact factor: 11.025

8.  [An unusual cause of hepatorenal symptoms].

Authors:  H Frank; M Krammer; W Fierlbeck; R Riess; H Geiger
Journal:  Med Klin (Munich)       Date:  1999-05-15

9.  Etanercept therapy in patients with advanced primary amyloidosis.

Authors:  M A Hussein; J V Juturi; L Rybicki; S Lutton; B R Murphy; M A Karam
Journal:  Med Oncol       Date:  2003       Impact factor: 3.064

10.  A case of prominent hepatic cholestasis developing to hepatic failure in lambda-AL amyloidosis.

Authors:  K Dohmen; M Nagano; R Iwakiri; Y Yamano; Y Kikuchi; M Mizoguchi; Y Iwata; Y Mori; H Ishibashi
Journal:  Gastroenterol Jpn       Date:  1991-06
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