Effects of long-term intravenous ibandronate therapy on skeletal-related events, survival, and bone resorption markers in patients with advanced multiple myeloma

被引:109
作者
Menssen, HD
Sakalová, A
Fontana, A
Herrmann, Z
Boewer, C
Facon, T
Lichinitser, MR
Singer, CRJ
Euller-Ziegler, L
Wetterwald, M
Fiere, D
Hrubisko, M
Thiel, E
Delmas, PD
机构
[1] Free Univ Berlin, Benjamin Franklin Klin, Dept Hematol, D-1000 Berlin, Germany
[2] Free Univ Berlin, Benjamin Franklin Klin, Dept Oncol, D-1000 Berlin, Germany
[3] Roche Diagnost GmbH, Mannheim, Germany
[4] St Hedwig Krankenhaus, Berlin, Germany
[5] Inst Hematol & Blood Transfus, Bratislava, Slovakia
[6] CHR Claude Huriez, Lille, France
[7] CHU Hop Archet, Serv Rhumatol, Nice, France
[8] Ctr Hosp, Serv Med Interne A, Dunkerque, France
[9] Hop Edouard Herriot, Lyon, France
[10] Canc Res Ctr, Moscow, Russia
[11] Royal United Hosp, Bath BA1 3NG, Avon, England
关键词
D O I
10.1200/JCO.2002.02.032
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Bisphosphonates have been found to reduce the incidence of skeletal-related events (SREs) in patients with multiple myeloma. This is the first double-blind, randomized, placebo-controlled study to assess the efficacy of ibandronate, a third-generation amino-bisphosphonate, in preventing SREs in advanced-stage multiple myeloma patients. Patients and Methods: Patients with multiple myeloma stage 11 or III were randomly assigned to receive either ibandronate 2 mg or placebo as a monthly intravenous (IV) bolus injection for 12 to 24 months in addition to conventional chemotherapy. SREs such as peripheral pathologic or vertebral fractures, hypercalcemia, severe bone pain, and bone radiotherapy or surgery were analyzed. Bone-turnover markers were also studied. Finally, post hoc analyses of bone morbidity and survival were performed. Results: Ninety-nine patients per treatment group were assessable for efficacy analysis. The occurrence of SIZE per patient year and the time to first SIZE were not significantly different between the two treatment groups. in overall evaluation, no differences were found between the treatment groups regarding bone pain, analgesic drug use, quality of life, and median survival (33.1 v 28.2 months, respectively). Explorative post hoc analyses revealed that ibandronate patients with strongly suppressed bone-turnover markers (2: 30% and greater than or equal to 50% mean reduction of serum osteocalcin and urinary C-terminal telopeptides) developed significantly less bone morbidity. Ibandronate was tolerated well during as many as 25 therapy cycles. Conclusion: Monthly injections of ibandronate 2 mg lV neither reduced bone morbidity nor prolonged survival in the overall population of stage II/III multiple myeloma patients.
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页码:2353 / 2359
页数:7
相关论文
共 37 条
[1]  
Abildgaard N, 1998, EUR J HAEMATOL, V61, P128
[2]  
Adami S, 1997, CANCER, V80, P1674, DOI 10.1002/(SICI)1097-0142(19971015)80:8+<1674::AID-CNCR18>3.3.CO
[3]  
2-D
[4]   TREATMENT FOR MULTIPLE MYELOMA - COMBINATION CHEMOTHERAPY WITH DIFFERENT MELPHALAN DOSE REGIMENS [J].
ALEXANIAN, R ;
HAUT, A ;
KHAN, AU ;
LANE, M ;
MCKELVEY, EM ;
MIGLIORE, PJ ;
STUCKEY, WJ ;
WILSON, HE .
JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1969, 208 (09) :1680-+
[5]  
ALEXANIAN R, 1995, SEMIN HEMATOL, V32, P20
[6]   In vitro cytoreductive effects on multiple myeloma cells induced by bisphosphonates [J].
Aparicio, A ;
Gardner, A ;
Tu, Y ;
Savage, A ;
Berenson, J ;
Lichtenstein, A .
LEUKEMIA, 1998, 12 (02) :220-229
[7]   A prospective, randomized trial of autologous bone marrow transplantation and chemotherapy in multiple myeloma [J].
Attal, M ;
Harousseau, JL ;
Stoppa, AM ;
Sotto, JJ ;
Fuzibet, JG ;
Rossi, JF ;
Casassus, P ;
Maisonneuve, H ;
Facon, T ;
Ifrah, N ;
Payen, C ;
Bataille, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (02) :91-97
[8]  
AVERBUCH SD, 1993, CANCER-AM CANCER SOC, V72, P3443, DOI 10.1002/1097-0142(19931201)72:11+<3443::AID-CNCR2820721611>3.0.CO
[9]  
2-3
[10]   PLASMA-CELL DYSCRASIAS [J].
BARLOGIE, B ;
ALEXANIAN, R ;
JAGANNATH, S .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1992, 268 (20) :2946-2951