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本文引用的文献

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Randomized, double-blind study of denosumab versus zoledronic acid in the treatment of bone metastases in patients with advanced cancer (excluding breast and prostate cancer) or multiple myeloma.随机、双盲研究地舒单抗与唑来膦酸治疗晚期癌症(不包括乳腺癌和前列腺癌)或多发性骨髓瘤患者的骨转移。
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Anti-tumour effects of bisphosphonates--what have we learned from in vivo models?双膦酸盐的抗肿瘤作用——从体内模型中学到了什么?
Curr Cancer Drug Targets. 2009 Nov;9(7):807-23. doi: 10.2174/156800909789760339.
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Osteoclasts are important for bone angiogenesis.破骨细胞对于骨血管生成很重要。
Blood. 2010 Jan 7;115(1):140-9. doi: 10.1182/blood-2009-08-237628. Epub 2009 Nov 3.
4
Denosumab in men receiving androgen-deprivation therapy for prostate cancer.地诺单抗用于接受雄激素剥夺治疗的前列腺癌男性患者。
N Engl J Med. 2009 Aug 20;361(8):745-55. doi: 10.1056/NEJMoa0809003. Epub 2009 Aug 11.
5
Extracellular engagement of alpha6 integrin inhibited urokinase-type plasminogen activator-mediated cleavage and delayed human prostate bone metastasis.α6整合素的细胞外结合抑制了尿激酶型纤溶酶原激活剂介导的裂解,并延缓了人前列腺癌骨转移。
Cancer Res. 2009 Jun 15;69(12):5007-14. doi: 10.1158/0008-5472.CAN-09-0354. Epub 2009 Jun 2.
6
Zoledronic acid effectively prevents aromatase inhibitor-associated bone loss in postmenopausal women with early breast cancer receiving adjuvant letrozole: Z-FAST study 36-month follow-up results.唑来膦酸可有效预防接受辅助来曲唑治疗的绝经后早期乳腺癌女性患者出现芳香化酶抑制剂相关的骨质流失:Z-FAST研究36个月随访结果
Clin Breast Cancer. 2009 May;9(2):77-85. doi: 10.3816/CBC.2009.n.015.
7
Effect of denosumab on bone mineral density in women receiving adjuvant aromatase inhibitors for non-metastatic breast cancer: subgroup analyses of a phase 3 study.地舒单抗对接受非转移性乳腺癌辅助芳香化酶抑制剂治疗的女性骨密度的影响:一项 3 期研究的亚组分析。
Breast Cancer Res Treat. 2009 Nov;118(1):81-7. doi: 10.1007/s10549-009-0352-y. Epub 2009 Mar 24.
8
Endocrine therapy plus zoledronic acid in premenopausal breast cancer.绝经前乳腺癌的内分泌治疗加唑来膦酸
N Engl J Med. 2009 Feb 12;360(7):679-91. doi: 10.1056/NEJMoa0806285.
9
Zerumbone abolishes RANKL-induced NF-kappaB activation, inhibits osteoclastogenesis, and suppresses human breast cancer-induced bone loss in athymic nude mice.姜黄二酮可消除RANKL诱导的NF-κB激活,抑制破骨细胞生成,并抑制人乳腺癌诱导的无胸腺裸鼠骨质流失。
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10
Inhibiting Dickkopf-1 (Dkk1) removes suppression of bone formation and prevents the development of osteolytic bone disease in multiple myeloma.抑制Dickkopf-1(Dkk1)可消除对骨形成的抑制,并预防多发性骨髓瘤中溶骨性骨病的发展。
J Bone Miner Res. 2009 Mar;24(3):425-36. doi: 10.1359/jbmr.081104.

转移和骨质流失:推进治疗和预防。

Metastasis and bone loss: advancing treatment and prevention.

机构信息

Yorkshire Cancer Research Professor of Medical Oncology, Academic Unit of Clinical Oncology, Weston Park Hospital, Whitham Road, Sheffield S102SJ, UK.

出版信息

Cancer Treat Rev. 2010 Dec;36(8):615-20. doi: 10.1016/j.ctrv.2010.04.003. Epub 2010 May 15.

DOI:10.1016/j.ctrv.2010.04.003
PMID:20478658
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3047387/
Abstract

Tumor metastasis to the skeleton affects over 400,000 individuals in the United States annually, more than any other site of metastasis, including significant proportions of patients with breast, prostate, lung and other solid tumors. Research on the bone microenvironment and its role in metastasis suggests a complex role in tumor growth. Parallel preclinical and clinical investigations into the role of adjuvant bone-targeted agents in preventing metastasis and avoiding cancer therapy-induced bone loss have recently reported exciting and intriguing results. A multidisciplinary consensus conference convened to review recent progress in basic and clinical research, assess gaps in current knowledge and prioritize recommendations to advance research over the next 5 years. The program addressed three topics: advancing understanding of metastasis prevention in the context of bone pathophysiology; developing therapeutic approaches to prevent metastasis and defining strategies to prevent cancer therapy-induced bone loss. Several priorities were identified: (1) further investigate the effects of bone-targeted therapies on tumor and immune cell interactions within the bone microenvironment; (2) utilize and further develop preclinical models to study combination therapies; (3) conduct clinical studies of bone-targeted therapies with radiation and chemotherapy across a range of solid tumors; (4) develop biomarkers to identify patients most likely to benefit from bone-targeted therapies; (5) educate physicians on bone loss and fracture risk; (6) define optimal endpoints and new measures of efficacy for future clinical trials; and (7) define the optimum type, dose and schedule of adjuvant bone-targeted therapy.

摘要

肿瘤转移至骨骼影响了美国每年超过 40 万人,比其他任何转移部位都多,包括大量患有乳腺癌、前列腺癌、肺癌和其他实体瘤的患者。对骨骼微环境及其在转移中的作用的研究表明,它在肿瘤生长中起着复杂的作用。最近,对辅助骨靶向药物在预防转移和避免癌症治疗引起的骨丢失中的作用的平行临床前和临床研究报告了令人兴奋和有趣的结果。一个多学科共识会议召开,以审查基础和临床研究的最新进展,评估当前知识的差距,并确定未来 5 年推进研究的建议。该计划涉及三个主题:在骨骼病理生理学的背景下推进对转移预防的理解;开发预防转移的治疗方法,并确定预防癌症治疗引起的骨丢失的策略。确定了几个优先事项:(1)进一步研究骨靶向疗法对骨骼微环境中肿瘤和免疫细胞相互作用的影响;(2)利用和进一步开发临床前模型来研究联合疗法;(3)在一系列实体瘤中开展骨靶向治疗与放疗和化疗的临床研究;(4)开发生物标志物以确定最有可能从骨靶向治疗中获益的患者;(5)教育医生关注骨丢失和骨折风险;(6)定义未来临床试验的最佳终点和新疗效衡量标准;(7)定义辅助骨靶向治疗的最佳类型、剂量和方案。