Osteonecrosis of the jaw in multiple myeloma patients: Clinical features and risk factors

被引:413
作者
Badros, A
Weikel, D
Salama, A
Goloubeva, O
Schneider, A
Rapoport, A
Fenton, R
Gahres, N
Sausville, E
Ord, R
Meiller, T
机构
[1] Univ Maryland, Marlene & Stewart Greenebaum Canc Ctr, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Dent, Baltimore, MD 21201 USA
关键词
D O I
10.1200/JCO.2005.04.2465
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To describe the clinical, radiologic, and pathologic features and risk factors for osteonecrosis of the jaw (ONJ) in multiple myeloma (MM) patients. Patients and Methods A retrospective review of 90 MM patients who had dental assessments, including 22 patients with ONJ. There were 62 men; the median age was 61 years in ONJ patients and 58 years among the rest. Prior MM therapy included thalidomide (n = 67) and stem-cell transplantation (n = 72). Bisphosphonate therapy included zoledronate (n = 34) or pamidronate (n = 17) and pamidronate followed by zoledronate (n = 33). Twenty-seven patients had recent dental extraction, including 12 patients in the ONJ group. Median time from MM diagnosis to ONJ was 8.4 years for the whole group. Results Patients usually presented with pain. ONJ occurred posterior to the cuspids (n = 20) mostly in the mandible. Debridement and sequestrectomy with primary closure were performed in 14 patients; of these, four patients had major infections and four patients had recurrent ONJ. Bone histology revealed necrosis and osteomyelitis. Microbiology showed actinomycetes (n = 7) and mixed bacteria (n = 9). More than a third of ONJ patients also suffered from long bone fractures (n = 4) and/or avascular necrosis of the hip (n = 4). The variables predictive of developing ONJ were dental extraction (P = .009), treatment with pamidronate/zoledronate (P = .009), longer follow-up time (P = .03), and older age at diagnosis of MM (P = .006). Conclusion ONJ appears to be time-dependent with higher risk after long-term use of bisphosphonates in older MM patients often after dental extractions. No satisfactory therapy is currently available. Trials addressing the benefits/risks of continuing bisphosphonate therapy are needed.
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页码:945 / 952
页数:8
相关论文
共 43 条
[1]   Efficacy of alendronate, a bisphosphonate, in the treatment of AVN of the hip. A prospective open-label study [J].
Agarwala, S ;
Jain, D ;
Joshi, VR ;
Sule, A .
RHEUMATOLOGY, 2005, 44 (03) :352-359
[2]   New foundations in understanding osteonecrosis of the jaws [J].
Assael, LA .
JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 2004, 62 (02) :125-126
[3]   Avascular jaw osteonecrosis in association with cancer chemotherapy: series of 10 cases [J].
Bagan, JV ;
Murillo, J ;
Jimenez, Y ;
Poveda, R ;
Milian, MA ;
Sanchis, JM ;
Silvestre, FJ ;
Scully, C .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 2005, 34 (02) :120-123
[4]   American Society of Clinical Oncology clinical practice guidelines: The role of bisphosphonates in multiple myeloma [J].
Berenson, JR ;
Hillner, BE ;
Kyle, RA ;
Anderson, K ;
Lipton, A ;
Yee, GC ;
Biermann, JS .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (17) :3719-3736
[5]   Myeloma bone disease [J].
Berenson, JR .
BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY, 2005, 18 (04) :653-672
[6]   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
[7]  
Boivin G., 2002, Journal of Musculoskeletal & Neuronal Interactions, V2, P538
[8]   Bisphosphonates and avascular necrosis of the jaw: a possible association [J].
Carter, G ;
Goss, AN ;
Doecke, C .
MEDICAL JOURNAL OF AUSTRALIA, 2005, 182 (08) :413-415
[9]  
Carter GD, 2003, AUST DENT J, V48, P268
[10]  
Choi SJ, 2000, BLOOD, V96, P671