Pomalidomide Is Active in the Treatment of Anemia Associated With Myelofibrosis

被引:154
作者
Tefferi, Ayalew [1 ]
Verstovsek, Srdan
Barosi, Giovanni
Passamonti, Francesco
Roboz, Gail J.
Gisslinger, Heinz
Paquette, Ronald L.
Cervantes, Francisco
Rivera, Candido E.
Deeg, H. Joachim
Thiele, Juergen
Kvasnicka, Hans M.
Vardiman, James W.
Zhang, Yanming
Bekele, B. Nebiyou
Mesa, Ruben A.
Gale, Robert P.
Kantarjian, Hagop M.
机构
[1] Mayo Clin, Rochester, MN 55905 USA
关键词
LENALIDOMIDE PLUS DEXAMETHASONE; MYELOID METAPLASIA; THALIDOMIDE; THERAPY; ERYTHROPOIESIS; CC-4047; CELLS; NEUROPATHY;
D O I
10.1200/JCO.2008.21.7356
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Thalidomide and lenalidomide can alleviate anemia in myelofibrosis. However, their value is undermined by their respective potential to cause peripheral neuropathy and myelosuppression. We therefore evaluated the safety and therapeutic activity of another immunomodulatory drug, pomalidomide. Methods In a phase II randomized, multicenter, double-blind, adaptive design study, four treatment arms were evaluated: pomalidomide (2 mg/d) plus placebo, pomalidomide (2 mg/d) plus prednisone, pomalidomide (0.5 mg/d) plus prednisone, and prednisone plus placebo. Pomalidomide was administered for up to 12 28-day treatment cycles. Prednisone (30 mg/d) was given in a tapering dose schedule during the first three cycles. Response was assessed by International Working Group criteria. Results Eighty-four patients with myelofibrosis-associated anemia were randomly assigned to the aforementioned treatment arms: 22, 19, 22, and 21, respectively. Response in anemia was documented in 20 patients, including 15 who became transfusion independent. Response rates in the four treatment arms were 23% (95% CI, 5% to 41%), 16% (95% CI, 0% to 33%), 36% (95% CI, 16% to 56%), and 19% (95% CI, 2% to 36%). The corresponding figures for patients receiving >= 3 cycles of treatment (n = 62) were 38%, 23%, 40%, and 25%. Response to pomalidomide with or without prednisone was durable (range, 3.2 to 16.9 + months) and significantly better in the absence of leukocytosis (37% v 8%; P = .01); JAK2V617F or cytogenetic status did not affect response. Grade >= 3 toxicities were infrequent and included (in each treatment arm) neutropenia (9%; 16%; 5%; 5%), thrombocytopenia (14%; 16%; 9%; 5%), and thrombosis (9%; 5%; 0%; 0%). Conclusion Pomalidomide therapy at 0.5 or 2 mg/d with or without an abbreviated course of prednisone is well tolerated in patients with myelofibrosis and active in the treatment of anemia. J Clin Oncol 27:4563-4569. (C) 2009 by American Society of Clinical Oncology
引用
收藏
页码:4563 / 4569
页数:7
相关论文
共 31 条
[21]   Phase I study of an immunomodulatory thalidomide analog, CC-4047, in relapsed or refractory multiple myeloma [J].
Schey, SA ;
Fields, P ;
Bartlett, JB ;
Clarke, IA ;
Ashan, G ;
Knight, RD ;
Streetly, M ;
Dalgleish, AG .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (16) :3269-3276
[22]   Alternate day pomalidomide retains anti-myeloma effect with reduced adverse events and evidence of in vivo immunomodulation [J].
Streetly, Matthew J. ;
Gyertson, Kylie ;
Daniel, Yvonne ;
Zeldis, Jerome B. ;
Kazmi, Majid ;
Schey, Stephen A. .
BRITISH JOURNAL OF HAEMATOLOGY, 2008, 141 (01) :41-51
[23]   Lenalidomide therapy in del(5)(q31)-associated myelofibrosis:: cytogenetic and JAK2V617F molecular remissions [J].
Tefferi, A. ;
Lasho, T. L. ;
Mesa, R. A. ;
Pardanani, A. ;
Ketterling, R. P. ;
Hanson, C. A. .
LEUKEMIA, 2007, 21 (08) :1827-1828
[24]   Pathogenesis of myelofibrosis with myeloid metaplasia [J].
Tefferi, A .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (33) :8520-8530
[25]   International Working Group (IWG) consensus criteria for treatment response in myelofibrosis with myeloid metaplasia, for the IWG for Myelofibrosis Research and Treatment (IWG-MRT) [J].
Tefferi, Ayalew ;
Barosi, Giovanni ;
Mesa, Ruben A. ;
Cervantes, Francisco ;
Deeg, H. Joachim ;
Reilly, John T. ;
Verstovsek, Srdan ;
Dupriez, Brigitte ;
Silver, Richard T. ;
Odenike, Olatoyosi ;
Cortes, Jorge ;
Wadleigh, Martha ;
Solberg, Lawrence A., Jr. ;
Camoriano, John K. ;
Gisslinger, Heinz ;
Noel, Pierre ;
Thiele, Juergen ;
Vardiman, James W. ;
Hoffman, Ronald ;
Cross, Nicholas C. P. ;
Gilliland, D. Gary ;
Kantarjian, Hagop .
BLOOD, 2006, 108 (05) :1497-1503
[26]   Lenalidomide therapy in myelofibrosis with myeloid metaplasia [J].
Tefferi, Ayalew ;
Cortes, Jorge ;
Verstovsek, Srdan ;
Mesa, Ruben A. ;
Thomas, Deborah ;
Lasho, Terra L. ;
Hogan, William J. ;
Litzow, Mark R. ;
Allred, Jacob B. ;
Jones, Dan ;
Byrne, Catriona ;
Zeldis, Jerome B. ;
Ketterling, Rhett P. ;
McClure, Rebecca F. ;
Giles, Francis ;
Kantarjian, Hagop M. .
BLOOD, 2006, 108 (04) :1158-1164
[27]   PRACTICAL BAYESIAN GUIDELINES FOR PHASE-IIB CLINICAL-TRIALS [J].
THALL, PF ;
SIMON, R .
BIOMETRICS, 1994, 50 (02) :337-349
[28]   Thalidomide therapy for myelofibrosis with myeloid metaplasia [J].
Thomas, DA ;
Giles, FJ ;
Albitar, M ;
Cortes, JE ;
Verstovsek, S ;
Faderl, S ;
O'Brien, SM ;
Garcia-Manero, G ;
Keating, MJ ;
Pierce, S ;
Zeldis, J ;
Kantarjian, HM .
CANCER, 2006, 106 (09) :1974-1984
[29]  
Vardiman JW, 2001, WHO CLASSIFICATION T, P17
[30]   Lenalidomide and CC-4047 inhibit the proliferation of malignant B cells while expanding normal CD34+ progenitor cells [J].
Verhelle, Dominique ;
Corral, Laura G. ;
Wong, Kevin ;
Mueller, Jessica H. ;
Moutouh-de Parseval, Laure ;
Jensen-Pergakes, Kristen ;
Schafer, Peter H. ;
Chen, Roger ;
Glezer, Emilia ;
Ferguson, Gregory D. ;
Lopez-Girona, Antonia ;
Muller, George W. ;
Brady, Helen A. ;
Chan, Kyle W. H. .
CANCER RESEARCH, 2007, 67 (02) :746-755