Pamidronate is superior to ibandronate in decreasing bone resorption, interleukin-6 and β2-microglobulin in multiple myeloma

被引:42
作者
Terpos, E
Viniou, N
de la Fuente, J
Meletis, J
Voskaridou, E
Karkantaris, C
Vaiopoulos, G
Palermos, J
Yataganas, X
Goldman, JM
Rahemtulla, A
机构
[1] Hammersmith Hosp, Imperial Coll Sci Technol & Med, Fac Med, Dept Haematol, London W12 0NN, England
[2] Univ Athens, Sch Med, Laikon Gen Hosp, Dept Med 1, GR-11527 Athens, Greece
[3] 251 Gen AF Hosp, Dept Haematol, Athens, Greece
[4] 251 Gen AF Hosp, Dept Immunol, Athens, Greece
关键词
pamidronate; ibandronate; multiple myeloma; tartrate-resistant acid phosphatase type 5b (TRACP-5b); N-terminal cross-linking telopeptide of type-I collagen (NTX); bone markers;
D O I
10.1034/j.1600-0609.2003.02823.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives : Bisphosphonates have been found to reduce skeletal events in patients with multiple myeloma (MM). This is the first randomised trial to compare the efficacy of pamidronate and ibandronate, a third-generation aminobisphosphonate, in bone turnover and disease activity in MM patients. Methods : Patients with MM, stage II or III, were randomly assigned to receive either pamidronate 90 mg (group I: 23 patients) or ibandronate 4 mg (group II: 21 patients) as a monthly intravenous infusion in addition to conventional chemotherapy. Skeletal events, such as pathologic fractures, hypercalcaemia, and bone radiotherapy were analysed. Bone resorption markers [N -terminal cross-linking telopeptide of type-I collagen (NTX) and tartrate-resistant acid phosphatase type 5b (TRACP-5b)], bone formation markers (bone alkaline phosphatase and osteocalcin), markers of disease activity (paraprotein, CRP, beta(2) -microglobulin), and interleukin-6 (IL-6) were also studied. Results : In both groups, the combination of chemotherapy with either pamidronate or ibandronate produced a reduction in bone resorption and tumour burden as measured by NTX, IL-6, paraprotein, CRP, and beta(2) -microglobulin from the second month of treatment, having no effect on bone formation. TRACP-5b also had a significant reduction in the pamidronate group from the second month of treatment and in the ibandronate group from the sixth month. However, there was a greater reduction of NTX, IL-6, and beta(2) -microglobulin in group I than in group II, starting at the second month of treatment (P = 0.002, 0.001, and 0.004, respectively) and of TRACP-5b, starting at the fourth month (P = 0.014), that being continued throughout the 10-month follow-up of this study. There was no difference in skeletal events during this period. A significant correlation was observed between changes of NTX and changes of TRACP-5b, IL-6, and beta(2) -microglobulin from the second month for patients of both groups. Conclusions : These results suggest that a monthly dose of 90 mg of pamidronate is more effective than 4 mg of ibandronate in reducing osteoclast activity, bone resorption, IL-6, and possibly tumour burden in MM. TRACP-5b has also proved to be a useful new marker for monitoring bisphosphonates treatment in MM.
引用
收藏
页码:34 / 42
页数:9
相关论文
共 35 条
[1]  
Abildgaard N, 1998, EUR J HAEMATOL, V61, P128
[2]   Biochemical markers of bone metabolism reflect osteoclastic and osteoblastic activity in multiple myeloma [J].
Abildgaard, N ;
Glerup, H ;
Rungby, J ;
Bendix-Hansen, K ;
Kassem, M ;
Brixen, K ;
Heickendorff, L ;
Nielsen, JL ;
Eriksen, EF .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2000, 64 (02) :121-129
[3]  
Anderson KC, 1999, SEMIN HEMATOL, V36, P14
[4]   EFFECTIVE TREATMENT OF ADVANCED MULTIPLE-MYELOMA REFRACTORY TO ALKYLATING-AGENTS [J].
BARLOGIE, B ;
SMITH, L ;
ALEXANIAN, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 310 (21) :1353-1356
[5]   New advances in the biology and treatment of myeloma bone disease [J].
Berenson, JR .
SEMINARS IN HEMATOLOGY, 2001, 38 (02) :15-20
[6]   Efficacy of pamidronate in reducing skeletal events in patients with advanced multiple myeloma [J].
Berenson, JR ;
Lichtenstein, A ;
Porter, L ;
Dimopoulos, MA ;
Bordoni, R ;
George, S ;
Lipton, A ;
Keller, A ;
Ballester, O ;
Kovacs, MJ ;
Blacklock, HA ;
Bell, R ;
Simeone, J ;
Reitsma, DJ ;
Heffernan, M ;
Seaman, J ;
Knight, RD .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (08) :488-493
[7]   Long-term pamidronate treatment of advanced multiple myeloma patients reduces skeletal events [J].
Berenson, JR ;
Lichtenstein, A ;
Porter, L ;
Dimopoulos, MA ;
Bordoni, R ;
George, S ;
Lipton, A ;
Keller, A ;
Ballester, O ;
Kovacs, M ;
Blacklock, H ;
Bell, R ;
Simeone, JF ;
Reitsma, DJ ;
Heffernan, M ;
Seaman, J ;
Knight, RD .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (02) :593-602
[8]  
Blade Joan, 1998, British Journal of Haematology, V102, P1115, DOI 10.1046/j.1365-2141.1998.00930.x
[9]   Ibandronate decreases bone disease development and osteoclast stimulatory activity in an in vivo model of human myeloma [J].
Cruz, JC ;
Alsina, M ;
Craig, F ;
Yoneda, T ;
Anderson, JL ;
Dallas, M ;
Roodman, GD .
EXPERIMENTAL HEMATOLOGY, 2001, 29 (04) :441-447
[10]   Ibandronate reduces osteolytic lesions but not tumor burden in a murine model of myeloma bone disease [J].
Dallas, SL ;
Garrett, IR ;
Oyajobi, BO ;
Dallas, MR ;
Boyce, BF ;
Bauss, F ;
Radl, J ;
Mundy, GR .
BLOOD, 1999, 93 (05) :1697-1706