Thalidomide maintenance treatment increases progression-free but not overall survival in elderly patients with myeloma

被引:56
|
作者
Ludwig, Heinz [1 ]
Adam, Zdenek [2 ,3 ]
Tothova, Elena [4 ]
Hajek, Roman [2 ,3 ]
Labar, Boris [5 ]
Egyed, Miklos [6 ]
Spicka, Ivan [7 ]
Gisslinger, Heinz [8 ]
Drach, Johannes [9 ]
Kuhn, Ingrid [10 ]
Hinke, Axel [11 ]
Zojer, Niklas
机构
[1] Wilhelminenspital Stadt Wien, Ctr Oncol & Hematol, Dept Med 1, Vienna, Austria
[2] Masaryk Univ, Fac Med, Brno, Czech Republic
[3] Masaryk Univ, Fac Hosp Brno, Dept Internal Med & Hematooncol, Brno, Czech Republic
[4] Univ Hosp L Pasteur, Dept Hematol & Oncohematol, Kosice, Slovakia
[5] Clin Hosp Rebro, Dept Internal Med, Zagreb, Croatia
[6] Kaposi Mor Teaching Hosp, Dept Internal Med, Kaposvar, Hungary
[7] Charles Univ Prague, Internal Clin 1, Prague, Czech Republic
[8] Med Univ Vienna, Dept Med 1, Div Hematol & Hemostaseol, Vienna, Austria
[9] Med Univ Vienna, Dept Med 1, Div Oncol, Vienna, Austria
[10] Schering Plough Inc, Vienna, Austria
[11] WISP Res Inst, Langenfeld, Germany
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2010年 / 95卷 / 09期
关键词
thalidomide; thalidomide-interferon; progression-free survival; overall survival; MULTIPLE-MYELOMA; CELL TRANSPLANTATION; RANDOMIZED TRIALS; IMPROVES SURVIVAL; THERAPY; MELPHALAN; DEXAMETHASONE; PREDNISONE; INTERFERON; INDUCTION;
D O I
10.3324/haematol.2009.020586
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Thalidomide maintenance therapy after stem cell transplantation resulted in increased progression-free survival and overall survival in a few trials, but its role in non-transplant eligible patients with multiple myeloma remains unclear. This study assessed the impact of thalidomide-interferon in comparison to interferon maintenance therapy in elderly patients with multiple myeloma. Design and Methods Of 289 elderly patients with multiple myeloma who were randomized to thalidomide-dexamethasone or melphalan-prednisolone induction therapy, 137 finally completed 9 cycles of induction therapy with stable disease or better and thereby qualified for maintenance treatment. Of these, 128 have been randomized to either thalidomide-interferon or interferon alone. Primary study endpoints were progression-free survival and response rates; secondary endpoints were overall survival, toxicity and quality of life. Results Thalidomide-interferon maintenance therapy led to a significantly longer progression-free survival compared to interferon (27.7 vs. 13.2 months, P=0.0068), but overall survival was similar in both groups (52.6 vs. 51.4 months, P=0.81) and did not differ between patients aged 75 years or older, or younger patients (P=0.39). Survival after disease progression tended to be shorter in patients on thalidomide-interferon maintenance therapy (P=0.056). Progression-free survival and overall survival tended to be shorter in patients with adverse cytogenetic (FISH) findings compared to the standard risk group but differences were not significant (P=0.084 and P=0.082, respectively). Patients on thalidomide-interferon presented with more neuropathy (P=0.0015), constipation (P=0.0004), skin toxicity (P=0.0041) and elevated creatinine (P=0.026). Conclusions Thalidomide plus interferon maintenance therapy increased progression-free survival but not overall survival and was associated with slightly more toxicity than maintenance with interferon alone.
引用
收藏
页码:1548 / 1554
页数:7
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