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

被引:157
作者
Ludwig, Heinz [1 ]
Hajek, Roman [2 ,3 ]
Tothova, Elena [4 ]
Drach, Johannes [5 ]
Adam, Zdenek [2 ,3 ]
Labar, Boris [6 ]
Egyed, Miklos [7 ]
Spicka, Ivan [8 ]
Gisslinger, Heinz [9 ]
Greil, Richard [10 ]
Kuhn, Ingrid [11 ]
Zojer, Niklas
Hinke, Axel [12 ]
机构
[1] Wilhelminenspital Stadt Wien, Ctr Oncol & Hematol, Dept Med 1, A-1171 Vienna, Austria
[2] Fac Hosp Brno, Internal Hematooncol Clin, Brno, Czech Republic
[3] Fac Med MU, Brno, Czech Republic
[4] Fac Hosp Policlin, Clin Hematol, Kosice, Slovakia
[5] Med Univ Vienna, Div Clin Oncol, Vienna, Austria
[6] Clin Hosp Rebro, Zagreb, Croatia
[7] Kaposi Mor Teaching Hosp, Dept Internal Med, Kaposvar, Hungary
[8] Charles Univ Prague, Internal Clin 1, Prague, Czech Republic
[9] Univ Clin, Dept Hematol, Vienna, Austria
[10] Univ Clin, Salzburg, Austria
[11] Schering Plough AESCA Pharma, Traiskirchen, Austria
[12] Wissensch Serv Pharma Res Inst, Langenfeld, Germany
关键词
CELL TRANSPLANTATION; PLUS THALIDOMIDE; PHASE; LENALIDOMIDE; THERAPY; TRIALS;
D O I
10.1182/blood-2008-07-169565
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We 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 alpha-2b thrice weekly or to 3 MU interferon alpha-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. (Blood. 2009; 113: 3435-3442)
引用
收藏
页码:3435 / 3442
页数:8
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