Hoff Ana O, Toth Béla B, Altundag Kadri, Johnson Marcella M, Warneke Carla L, Hu Mimi, Nooka Ajay, Sayegh Gilbert, Guarneri Valentina, Desrouleaux Kimberly, Cui Jeffrey, Adamus Andrea, Gagel Robert F, Hortobagyi Gabriel N
Department of Endocrine Neoplasia and Hormonal Disorders, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, USA.
J Bone Miner Res. 2008 Jun;23(6):826-36. doi: 10.1359/jbmr.080205.
Osteonecrosis of the jaw (ONJ) has been reported in patients treated with bisphosphonates. The incidence and risk factors associated with this disorder have not been clearly defined.
We conducted a retrospective analysis of 4019 patients treated with intravenous bisphosphonates between 1996 and 2004. Our goals were to estimate the frequency, understand the clinical presentation, and identify risk factors associated with ONJ development.
Sixteen of 1338 patients with breast cancer (1.2%) and 13 of 548 patients with multiple myeloma (2.4%) developed ONJ. The median dose and duration of treatment with pamidronate or zoledronic acid were significantly higher in patients with ONJ (p < 0.0001). Multivariate Cox proportional hazards regression analysis identified treatment with zoledronic acid (hazards ratio [HR], 15.01; 95% CI: 2.41-93.48; p = 0.0037), treatment with pamidronate followed by zoledronic acid (HR, 4.00; 95% CI: 0.86-18.70; p = 0.078), and dental extractions (HR, 53.19; 95% CI: 18.20-155.46; p < 0.0001) as significant risks for ONJ in breast cancer. In multiple myeloma, dental extractions (HR, 9.78; 95% CI: 3.07-31.14; p = 0.0001) and osteoporosis (HR, 6.11; 95% CI: 1.56-23.98; p = 0.0095) were significant risk factors while controlling for bisphosphonate therapy. Thirteen of 29 patients were followed for a median of 17.1 mo (range, 7-67 mo); lesions healed in 3 patients during this period.
ONJ is an uncommon but long-lasting disorder that occurs mainly in breast cancer and multiple myeloma patients treated with intravenous bisphosphonates. High cumulative doses of bisphosphonates, poor oral health, and dental extractions may be significant risk factors for ONJ development. ONJ resolved in 23% of patients with conservative therapy.
已有报道称接受双膦酸盐治疗的患者会发生颌骨骨坏死(ONJ)。该疾病的发病率及相关风险因素尚未明确界定。
我们对1996年至2004年间接受静脉注射双膦酸盐治疗的4019例患者进行了回顾性分析。我们的目标是估计其发生率、了解临床表现并确定与ONJ发生相关的风险因素。
1338例乳腺癌患者中有16例(1.2%)发生ONJ,548例多发性骨髓瘤患者中有13例(2.4%)发生ONJ。发生ONJ的患者使用帕米膦酸盐或唑来膦酸治疗的中位剂量和疗程显著更高(p < 0.0001)。多因素Cox比例风险回归分析确定,在乳腺癌患者中,使用唑来膦酸治疗(风险比[HR],15.01;95%置信区间:2.41 - 93.48;p = 0.0037)、先使用帕米膦酸盐后使用唑来膦酸治疗(HR,4.00;95%置信区间:0.86 - 18.70;p = 0.078)以及拔牙(HR,53.19;95%置信区间:18.20 - 155.46;p < 0.0001)是ONJ的显著风险因素。在多发性骨髓瘤患者中,拔牙(HR,9.78;95%置信区间:3.07 - 31.14;p = 0.0001)和骨质疏松(HR,6.11;95%置信区间:1.56 - 23.98;p = 0.0095)是在控制双膦酸盐治疗情况下的显著风险因素。29例患者中的13例接受了中位时间为17.1个月(范围7 - 67个月)的随访;在此期间有3例患者的病变愈合。
ONJ是一种罕见但持续时间长的疾病,主要发生在接受静脉注射双膦酸盐治疗的乳腺癌和多发性骨髓瘤患者中。双膦酸盐的高累积剂量、口腔卫生差和拔牙可能是ONJ发生的显著风险因素。23%的患者经保守治疗后ONJ得到缓解。