Thalidomide-dexamethasone compared with melphalan-prednisolone in elderly patients with multiple myeloma

Author:

Ludwig Heinz1,Hajek Roman2,Tóthová Elena3,Drach Johannes4,Adam Zdenek2,Labar Boris5,Egyed Miklós6,Spicka Ivan7,Gisslinger Heinz8,Greil Richard9,Kuhn Ingrid10,Zojer Niklas1,Hinke Axel11

Affiliation:

1. Department of Medicine I, Wilhelminenspital Vienna, Vienna, Austria;

2. Internal Hematooncological Clinic, Faculty Hospital Brno and Faculty of Medicine MU, Brno, Czech Republic;

3. Clinic of Hematology, Faculty Hospital with Policlinic, Kosice, Slovakia;

4. Clinical Division of Oncology, Medical University of Vienna, Vienna, Austria;

5. Clinical Hospital “Rebro,” Zagreb, Croatia;

6. Department of Internal Medicine, Kaposi Mór Teaching Hospital, Kaposvár, Hungary;

7. First Internal Clinic, Charles University, Prague, Czech Republic;

8. Department of Hematology, University Clinic, Vienna, Austria;

9. University Clinic, Salzburg, Austria;

10. Schering-Plough AESCA Pharma, Traiskirchen, Austria; and

11. Wissenschaftlicher Service Pharma Research Institute, Langenfeld, Germany

Abstract

AbstractWe compared thalidomide-dexamethasone (TD) with melphalan-prednisolone (MP) in 289 elderly patients with multiple myeloma (MM). Patients received either thalidomide 200 mg plus dexamethasone 40 mg, days 1 to 4 and 15 to 18 on even cycles and days 1 to 4 on odd cycles, during a 28-day cycle or to melphalan 0.25 mg/kg and prednisolone 2 mg/kg orally on days 1 to 4 during a 28- to 42-day cycle. Patients achieving stable disease or better were randomly assigned to maintenance therapy with either thalidomide 100 mg daily and 3 MU interferon α-2b thrice weekly or to 3 MU interferon α-2b thrice weekly only. TD resulted in a higher proportion of complete and very good remissions (26% vs 13%; P = .006) and overall responses (68% vs 50%; P = .002) compared with MP. Time to progression (21.2 vs 29.1 months; P = .2), and progression-free survival was similar (16.7 vs 20.7 months; P = .1), but overall survival was significantly shorter in the TD group (41.5 vs 49.4 months; P = .024). Toxicity was higher with TD, particularly in patients older than 75 years with poor performance status. The study was registered at ClinicalTrials.gov as NCT00205751.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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