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双膦酸盐与抗血管生成因子联合使用比单独使用双膦酸盐更频繁地诱发颌骨坏死。

Combination of bisphosphonates and antiangiogenic factors induces osteonecrosis of the jaw more frequently than bisphosphonates alone.

作者信息

Christodoulou C, Pervena A, Klouvas G, Galani E, Falagas M E, Tsakalos G, Visvikis A, Nikolakopoulou A, Acholos V, Karapanagiotidis G, Batziou E, Skarlos D V

机构信息

Second Oncology Department, Metropolitan Hospital, Athens, Greece.

出版信息

Oncology. 2009;76(3):209-11. doi: 10.1159/000201931. Epub 2009 Feb 12.

Abstract

BACKGROUND

The use of bisphosphonates is associated with osteonecrosis of the jaw (ONJ). Antiangiogenic agents are used with increasing frequency and may induce the risk of ONJ, especially when administered concurrently with bisphosphonates.

PATIENTS AND METHODS

We retrospectively reviewed data of 116 patients receiving bisphosphonates, 78 zoledronic acid and 38 ibandronic acid, with or without antiangiogenic agents for osseous metastases from various tumors in our department from June 2007 to June 2008.

RESULTS

ONJ developed in: 2 patients with breast cancer and 1 with colon cancer receiving concurrently bisphosphonates and bevacizumab, 1 patient with renal cell carcinoma receiving sunitinib and zoledronic acid concurrently, and 1 patient with prostate cancer receiving zoledronic acid without antiangiogenic agents. The incidences of ONJ among patients receiving bisphosphonates with or without antiangiogenic agents were 16 and 1.1%, respectively. The difference was statistically significant (p = 0.008). The treatment duration of bisphosphonates did not differ significantly between the 2 groups.

CONCLUSIONS

The combination of bisphosphonates and antiangiogenic factors induces ONJ more frequently than bisphosphonates alone. These preliminary observations should be evaluated in large cohorts of patients and in prospective studies.

摘要

背景

双膦酸盐的使用与颌骨坏死(ONJ)相关。抗血管生成药物的使用频率日益增加,可能会诱发ONJ风险,尤其是在与双膦酸盐同时使用时。

患者与方法

我们回顾性分析了2007年6月至2008年6月期间在我院接受双膦酸盐治疗的116例患者的数据,其中78例使用唑来膦酸,38例使用伊班膦酸,这些患者伴有或不伴有抗血管生成药物治疗各种肿瘤的骨转移。

结果

发生ONJ的情况如下:2例乳腺癌患者和1例结肠癌患者同时接受双膦酸盐和贝伐单抗治疗,1例肾细胞癌患者同时接受舒尼替尼和唑来膦酸治疗,1例前列腺癌患者接受唑来膦酸治疗但未使用抗血管生成药物。接受双膦酸盐治疗的患者中,使用或未使用抗血管生成药物的ONJ发生率分别为16%和1.1%。差异具有统计学意义(p = 0.008)。两组双膦酸盐的治疗持续时间无显著差异。

结论

双膦酸盐与抗血管生成因子联合使用比单独使用双膦酸盐更易诱发ONJ。这些初步观察结果应在大量患者队列和前瞻性研究中进行评估。

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