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7例因药物相关性颌骨坏死接受下颌骨节段性切除术患者,采用免疫组化研究高剂量地诺单抗药物假期及破骨细胞抑制恢复情况。

Drug holiday of high-dose denosumab and recovery from osteoclast inhibition using immunohistochemical investigation of 7 patients with medication-related osteonecrosis of the jaw undergoing segmental mandibulectomy.

作者信息

Sawada Shunsuke, Sakamoto Yuki, Kirihigashi Mako, Kojima Yuka

机构信息

Department of Dentistry and Oral Surgery, Kansai Medical University Hospital, Osaka, Japan.

Department of Dentistry and Oral Surgery, Kansai Medical University Medical Center, Osaka, Japan.

出版信息

J Dent Sci. 2023 Oct;18(4):1645-1650. doi: 10.1016/j.jds.2023.01.021. Epub 2023 Feb 11.

Abstract

BACKGROUND/PURPOSE: Denosumab is used to treat bone metastases from malignant tumors. Unlike bisphosphonates, denosumab is not deposited in the bone; thus, withdrawal for a relatively short period would help recovery from osteoclast suppression. This study investigated the relationship between drug holidays and recovery from osteoclast suppression.

MATERIALS AND METHODS

Seven patients who received high-dose denosumab and underwent segmental mandibulectomy for medication-related osteonecrosis of the jaw were enrolled in this study. Osteoclast suppression (+) was defined as the absence of cathepsin K-positive cells or cathepsin K-positive mononuclear or small multinucleated cells observed on the bone surface of both mesial and distal specimens. When normal osteoclasts were found, osteoclast suppression was defined as (-); when both suppressed cathepsin K-positive cells and normal morphological osteoclasts were found, it was defined as (±).

RESULTS

Osteoclast suppression was: (+) in four patients, three without a drug holiday and one with a 9-month drug holiday; (±) in one patient with an 8-month drug holiday, and (-) in two patients with drug holidays for 13 and 20 months.

CONCLUSION

These findings suggest that a long-term drug holiday, such as 12 months, is required for recovery from osteoclast suppression in patients with cancer receiving high-dose denosumab.

摘要

背景/目的:地诺单抗用于治疗恶性肿瘤的骨转移。与双膦酸盐不同,地诺单抗不会沉积在骨中;因此,相对短期的停药有助于从破骨细胞抑制中恢复。本研究调查了药物假期与破骨细胞抑制恢复之间的关系。

材料与方法

本研究纳入了7例接受高剂量地诺单抗并因药物相关性颌骨坏死接受节段性下颌骨切除术的患者。破骨细胞抑制(+)定义为在近中和远中标本的骨表面均未观察到组织蛋白酶K阳性细胞或组织蛋白酶K阳性单核或小多核细胞。当发现正常破骨细胞时,破骨细胞抑制定义为(-);当同时发现受抑制的组织蛋白酶K阳性细胞和正常形态的破骨细胞时,定义为(±)。

结果

破骨细胞抑制情况为:4例患者为(+),其中3例未进行药物假期,1例有9个月的药物假期;1例有8个月药物假期的患者为(±),2例分别有13个月和20个月药物假期的患者为(-)。

结论

这些发现表明,接受高剂量地诺单抗的癌症患者从破骨细胞抑制中恢复需要12个月这样的长期药物假期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae0f/10547948/7c8e2aaed8f2/gr1.jpg

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