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骨修饰药物在多发性骨髓瘤中的作用:美国临床肿瘤学会临床实践指南更新。

Role of Bone-Modifying Agents in Multiple Myeloma: American Society of Clinical Oncology Clinical Practice Guideline Update.

机构信息

Kenneth Anderson, Dana-Farber Cancer Institute; Noopur Raje, Massachusetts General Hospital, Boston, MA; Nofisat Ismaila, American Society of Clinical Oncology, Alexandria, VA; Patrick J. Flynn, Minnesota Oncology, Woodbury; Robert A. Kyle, Mayo Clinic, Rochester, MN; Susan Halabi, Duke University Medical Center, Durham, NC; Sundar Jagannath, Mount Sinai Medical Center, New York, NY; Mohammed S. Ogaily, Beuamont Center for Hematology and Oncology-Downriver, Brownstown, MI; Jim Omel, Education and Advocacy, Grand Island; Gary C. Yee, University of Nebraska Medical Center, Omaha, NE; and G. David Roodman, Indiana University School of Medicine, Indianapolis, IN.

出版信息

J Clin Oncol. 2018 Mar 10;36(8):812-818. doi: 10.1200/JCO.2017.76.6402. Epub 2018 Jan 17.

Abstract

Purpose To update guideline recommendations on the role of bone-modifying agents in multiple myeloma. Methods An update panel conducted a targeted systematic literature review by searching PubMed and the Cochrane Library for randomized controlled trials, systematic reviews, meta-analyses, clinical practice guidelines, and observational studies. Results Thirty-five relevant studies were identified, and updated evidence supports the current recommendations. Recommendations For patients with active symptomatic multiple myeloma that requires systemic therapy with or without evidence of lytic destruction of bone or compression fracture of the spine from osteopenia on plain radiograph(s) or other imaging studies, intravenous administration of pamidronate 90 mg over at least 2 hours or zoledronic acid 4 mg over at least 15 minutes every 3 to 4 weeks is recommended. Denosumab has shown to be noninferior to zoledronic acid for the prevention of skeletal-related events and provides an alternative. Fewer adverse events related to renal toxicity have been noted with denosumab compared with zoledronic acid and may be preferred in this setting. The update panel recommends that clinicians consider reducing the initial pamidronate dose in patients with preexisting renal impairment. Zoledronic acid has not been studied in patients with severe renal impairment and is not recommended in this setting. The update panel suggests that bone-modifying treatment continue for up to 2 years. Less frequent dosing has been evaluated and should be considered in patients with responsive or stable disease. Continuous use is at the discretion of the treating physician and the risk of ongoing skeletal morbidity. Retreatment should be initiated at the time of disease relapse. The update panel discusses measures regarding osteonecrosis of the jaw. Additional information is available at www.asco.org/hematologic-malignancies-guidelines and www.asco.org/guidelineswiki .

摘要

目的

更新多发性骨髓瘤中骨修饰剂作用的指南推荐。

方法

更新小组通过搜索 PubMed 和 Cochrane 图书馆中的随机对照试验、系统评价、荟萃分析、临床实践指南和观察性研究,进行了有针对性的系统文献回顾。

结果

确定了 35 项相关研究,更新的证据支持当前的推荐。

推荐意见

对于需要全身治疗且有症状的活动性多发性骨髓瘤患者,无论是否存在骨破坏或脊柱压缩性骨折的证据(来自骨质疏松症的平片或其他影像学研究),建议静脉给予帕米膦酸 90mg 至少 2 小时或唑来膦酸 4mg 至少 15 分钟,每 3-4 周一次。地舒单抗在预防骨骼相关事件方面已被证明不劣于唑来膦酸,并提供了一种替代药物。与唑来膦酸相比,地舒单抗与肾毒性相关的不良反应较少,在这种情况下可能更受青睐。更新小组建议临床医生考虑在有预先存在的肾功能损害的患者中减少初始帕米膦酸盐剂量。由于唑来膦酸尚未在严重肾功能损害患者中进行研究,因此不建议在这种情况下使用。更新小组建议骨修饰治疗持续长达 2 年。在有反应或稳定疾病的患者中,已评估了更频繁的剂量,并应予以考虑。连续使用由治疗医生和持续骨骼发病率的风险决定。应在疾病复发时开始重新治疗。更新小组讨论了关于颌骨坏死的措施。其他信息可在 www.asco.org/hematologic-malignancies-guidelineswww.asco.org/guidelineswiki 获得。

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