Wessel John H, Dodson Thomas B, Zavras Athanasios I
Harvard School of Dental Medicine, Boston, MA 02115, USA.
J Oral Maxillofac Surg. 2008 Apr;66(4):625-31. doi: 10.1016/j.joms.2007.11.032.
Bisphosphonates (BPs) effectively treat metastatic bone disease, hypercalcemia, and osteoporosis. BP exposure, however, may be associated with osteonecrosis of the jaw (ONJ). The aim of the present study was to estimate the magnitude of the association between intravenous (IV) BP exposure and ONJ, and to identify potential confounders.
Using a case-control study design, the investigators identified and adjudicated a sample of cases with ONJ and matched them randomly with 5 controls per case. The controls were matched to cases on age, gender, cancer type, and date of cancer diagnosis. The medical records were abstracted and data on BP exposure, cancer therapy, and comorbidities were recorded. Statistical analyses were carried out using conditional logistic regression in Stata 9.0 (Stata Corp, College Station, TX).
Thirty cases of ONJ were identified at Massachusetts General Hospital from February 2003 through February 2007. Zoledronate was found to confer significant risk toward development of ONJ (adjusted odds ratio = 31.8, P < .05). Although a trend toward increased risk was noted for pamidronate, this association was not significant after controlling for zoledronate. Obesity and smoking were associated significantly with ONJ development, whereas oral BPs had no effect.
In this study, cancer patients who had received zoledronate exhibited a significant 30-fold increase in their risk to develop ONJ. More studies are needed to elucidate the exact role of obesity and smoking in the development of ONJ, and the complex interactions of IV BPs with other chemotherapies during cancer treatment.
双膦酸盐(BPs)可有效治疗转移性骨病、高钙血症和骨质疏松症。然而,接触双膦酸盐可能与颌骨坏死(ONJ)有关。本研究的目的是评估静脉注射(IV)双膦酸盐暴露与颌骨坏死之间关联的程度,并确定潜在的混杂因素。
采用病例对照研究设计,研究人员识别并判定了一组颌骨坏死病例样本,并为每个病例随机匹配5名对照。对照在年龄、性别、癌症类型和癌症诊断日期方面与病例进行匹配。提取病历并记录有关双膦酸盐暴露、癌症治疗和合并症的数据。使用Stata 9.0(Stata公司,德克萨斯州大学城)中的条件逻辑回归进行统计分析。
2003年2月至2007年2月期间,在马萨诸塞州总医院共识别出30例颌骨坏死病例。发现唑来膦酸会显著增加发生颌骨坏死的风险(调整后的优势比 = 31.8,P < 0.05)。尽管帕米膦酸有增加风险的趋势,但在控制唑来膦酸后,这种关联并不显著。肥胖和吸烟与颌骨坏死的发生显著相关,而口服双膦酸盐则无影响。
在本研究中,接受唑来膦酸治疗的癌症患者发生颌骨坏死的风险显著增加了30倍。需要更多研究来阐明肥胖和吸烟在颌骨坏死发生中的确切作用,以及静脉注射双膦酸盐在癌症治疗期间与其他化疗药物的复杂相互作用。