The combination of intermediate doses of thalidomide and dexamethasone reduces bone marrow micro-vessel density but not serum levels of angiogenic cytokines in patients with refractory/relapsed multiple myeloma

被引:23
作者
Hatjiharissi, E
Terpos, E
Papaioannou, M
Hatjileontis, C
Kaloutsi, V
Galaktidou, G
Gerotziafas, G
Christakis, J
Zervas, K
机构
[1] Theagene Anticanc Ctr, Dept Hematol, Thessaloniki, Greece
[2] Gen Airforce Hosp 251, Dept Med Res, Athens, Greece
[3] Gen Airforce Hosp 251, Dept Hematol, Athens, Greece
[4] Aristotle Univ Thessaloniki, Dept Pathol, Sch Med, GR-54006 Thessaloniki, Greece
关键词
thalidomide; dexamethasone multiple myeloma; angiogenesis; microvessel density;
D O I
10.1002/hon.738
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of the study was the evaluation of anti-angiogenic activity of the combination of intermediate doses of thalidomide and dexamethasone in patients with refractory/relapsed myeloma. Twenty-five patients were included in the study. Microvessel density (MVD) was evaluated in marrow biopsies before and after treatment. Serum levels of vascular endothelial growth factor (VEGF), basic fibroblast growth factor (b-FGF), tumor necrosis factor-alpha (TNF-alpha), which have angiogenic potential and interleukin-6 (IL-6), IL-1 beta, soluble IL-6 receptor (sIL-6R), and transforming growth factor-beta (TGF-beta) which are involved in the disease biology, were measured before treatment and then every 2 weeks for 8 weeks. Pretreatment levels of MVD, VEGF, b-FGF, IL-6, sIL-6R were increased in the patients compared to controls. The overall response rate to therapy was 72%. The administration of the combined regimen produced a significant reduction in MVD in responders. However, an increase in serum levels of VEGF, b-FGF, IL-6, sIL-6R was observed post-treatment in responders. In contrast, serum levels of TNF-alpha, TGF-beta, IL-1 beta did not differ between patients and controls and remained unchanged during the study. These results suggest that the combination of thalidomide plus dexamethasone is an effective treatment for myeloma reducing MVD marrow levels but not serum levels of angiogenic cytokines or cytokines implicated in myeloma biology. Copyright (C) 2005 John Wiley & Sons, Ltd.
引用
收藏
页码:159 / 168
页数:10
相关论文
共 46 条
[1]  
Anderson KC, 1999, SEMIN HEMATOL, V36, P3
[2]   Release of the angiogenic cytokine vascular endothelial growth factor (VEGF) from platelets: significance for VEGF measurements and cancer biology [J].
Banks, RE ;
Forbes, MA ;
Kinsey, SE ;
Stanley, A ;
Ingham, E ;
Walters, C ;
Selby, PJ .
BRITISH JOURNAL OF CANCER, 1998, 77 (06) :956-964
[3]   Thalidomide in multiple myeloma, myelodysplastic syndromes and histiocytosis. Analysis of clinical results and of surrogate angiogenesis markers [J].
Bertolini, F ;
Mingrone, W ;
Alietti, A ;
Ferrucci, PF ;
Cocorocchio, E ;
Peccatori, F ;
Cineri, S ;
Mancuso, P ;
Corsini, C ;
Burlini, A ;
Zucca, E ;
Martinelli, G .
ANNALS OF ONCOLOGY, 2001, 12 (07) :987-990
[4]  
Blade J, 2001, Hematol J, V2, P272, DOI 10.1038/sj.thj.6200115
[5]  
Blade Joan, 1998, British Journal of Haematology, V102, P1115, DOI 10.1046/j.1365-2141.1998.00930.x
[6]  
Browder T, 2000, CANCER RES, V60, P1878
[7]  
BRUNNER G, 1993, BLOOD, V81, P631
[8]   High-dose chemotherapy with hematopoietic stem-cell rescue for multiple myeloma [J].
Child, JA ;
Morgan, GJ ;
Davies, FE ;
Owen, RG ;
Bell, SE ;
Hawkins, K ;
Brown, J ;
Drayson, MT ;
Selby, PJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (19) :1875-1883
[9]   THALIDOMIDE IS AN INHIBITOR OF ANGIOGENESIS [J].
DAMATO, RJ ;
LOUGHNAN, MS ;
FLYNN, E ;
FOLKMAN, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (09) :4082-4085
[10]   Vascular endothelial growth factor and interleukin-6 in paracrine tumor-stromal cell interactions in multiple myeloma [J].
Dankbar, B ;
Padró, T ;
Leo, R ;
Feldmann, B ;
Kropff, M ;
Mesters, RM ;
Serve, H ;
Berdel, WE ;
Kienast, J .
BLOOD, 2000, 95 (08) :2630-2636