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Multiple myeloma: comparison of two dose-intensive melphalan regimens (100 vs 200?mg/m2).

Authors :
Palumbo, A.
Bringhen, S.
Bertola, A.
Cavallo, F.
Falco, P.
Massaia, M.
Bruno, B.
Rus, C.
Barbui, A.
Caravita, T.
Musto, P.
Pescota, N.
Rossini, F.
Vignetti, M.
Boccadoro, M.
Source :
Leukemia (08876924); Jan2004, Vol. 18 Issue 1, p133-138, 6p
Publication Year :
2004

Abstract

Several trials have shown the superior impact of high-dose melphalan (usually 200?mg/m<superscript>2</superscript>, MEL200) vs standard therapy in myeloma patients. Intermediate-dose melphalan (100?mg/m<superscript>2</superscript>, MEL100) is also superior to the standard dose, but has not been clinically compared with MEL200. A total of 90 patients at diagnosis were treated with two MEL100 courses. Their clinical outcome was compared with that of a control group of 90 pair mates matched for serum ß2-microglobulin levels and Durie and Salmon clinical stage. These patients were treated at diagnosis with two MEL200 courses. Patient characteristics were similar in both groups except that the median age of the MEL100 group was significantly higher (P<0.0001). Complete remission was 35% after MEL100 and 48% after MEL200 (P=0.08). Median event-free survival (EFS) was 32 months in the MEL100 group and 42 months in the MEL200 group (P<0.005), but overall survival (OS) was not different. Transplant-related mortality was not significantly different. Haematological and extra-haematological toxicity was significantly reduced after MEL100. Despite the significant age difference, tandem MEL100 was less toxic than tandem MEL200, and MEL100 was inferior to MEL200 in terms of EFS but not in terms of OS. The intensified nonmyeloablative MEL100 regimen is an effective first-line treatment.Leukemia (2004) 18, 133-138. doi:10.1038/sj.leu.2403196 Published online 30 October 2003 [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08876924
Volume :
18
Issue :
1
Database :
Complementary Index
Journal :
Leukemia (08876924)
Publication Type :
Academic Journal
Accession number :
11724172
Full Text :
https://doi.org/10.1038/sj.leu.2403196