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达雷妥尤单抗优化抗骨髓瘤治疗结局

Optimizing the Outcome of Anti-Myeloma Treatment with Daratumumab.

作者信息

Plesner Torben

机构信息

Department of Hematology, Vejle Hospital, Institute of Regional Health Science, University of Southern Denmark, Beriderbakken 4 DK, 7100 Vejle, Denmark.

出版信息

J Clin Med. 2021 Mar 2;10(5):1002. doi: 10.3390/jcm10051002.

DOI:10.3390/jcm10051002
PMID:33801271
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7958124/
Abstract

A search of the scientific literature for and gives more than 600 results (January 2021), which reflects the interest and activity around this antibody, an interest that was also reflected by the assignment of breakthrough designation for Daratumumab as a treatment for multiple myeloma by FDA in 2013. The high expectations have been supported and met due to a very active clinical development program, and our insight into Daratumumab's modes of action have been expanded by a concomitant, systematic activity of translational research. The scope of this article is to point to some areas where the outcome of treatment with Daratumumab for multiple myeloma may be improved with a focus on areas such as when to initiate treatment with Daratumumab, the use of supportive treatment, duration of therapy and some general thoughts about anti-myeloma treatment as a two-step process involving initial de-bulking followed by reprogramming of the host's immune system and immune-mediated control of myeloma.

摘要

在科学文献中搜索[具体药物名称]和[具体药物名称],得到了600多个结果(2021年1月),这反映了围绕这种抗体的关注度和研究活跃度,这种关注也体现在2013年美国食品药品监督管理局(FDA)将达雷妥尤单抗指定为治疗多发性骨髓瘤的突破性疗法上。由于非常活跃的临床开发项目,这些高期望得到了支持并得以实现,同时,伴随的系统性转化研究活动也扩展了我们对达雷妥尤单抗作用模式的认识。本文的范围是指出一些领域,在这些领域中,针对多发性骨髓瘤使用达雷妥尤单抗治疗的结果可能会得到改善,重点关注的领域包括何时开始使用达雷妥尤单抗治疗、支持性治疗的使用、治疗持续时间,以及关于抗骨髓瘤治疗作为一个两步过程的一些总体思考,该过程包括初始减瘤,随后对宿主免疫系统进行重新编程以及通过免疫介导控制骨髓瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e290/7958124/0af1601d7ee5/jcm-10-01002-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e290/7958124/1218ad58c91b/jcm-10-01002-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e290/7958124/d4fb06dfa1eb/jcm-10-01002-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e290/7958124/6955ee213cc6/jcm-10-01002-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e290/7958124/96de29c6749e/jcm-10-01002-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e290/7958124/9ea5deb9d0a1/jcm-10-01002-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e290/7958124/0af1601d7ee5/jcm-10-01002-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e290/7958124/1218ad58c91b/jcm-10-01002-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e290/7958124/d4fb06dfa1eb/jcm-10-01002-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e290/7958124/6955ee213cc6/jcm-10-01002-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e290/7958124/96de29c6749e/jcm-10-01002-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e290/7958124/9ea5deb9d0a1/jcm-10-01002-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e290/7958124/0af1601d7ee5/jcm-10-01002-g006.jpg

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本文引用的文献

1
The Clinical Course of Multiple Myeloma in the Era of Novel Agents: A Retrospective, Single-Center, Real-World Study.新型药物时代多发性骨髓瘤的临床病程:一项回顾性、单中心、真实世界研究。
Clin Hematol Int. 2019 Aug 12;1(4):220-228. doi: 10.2991/chi.d.190805.002. eCollection 2019 Dec.
2
Cost-Effectiveness of First-Line Versus Second-Line Use of Daratumumab in Older, Transplant-Ineligible Patients With Multiple Myeloma.一线与二线使用达雷妥尤单抗治疗不适合移植的老年多发性骨髓瘤患者的成本效益比较。
J Clin Oncol. 2021 Apr 1;39(10):1119-1128. doi: 10.1200/JCO.20.01849. Epub 2021 Jan 7.
3
Daratumumab plus lenalidomide and dexamethasone in relapsed/refractory multiple myeloma: extended follow-up of POLLUX, a randomized, open-label, phase 3 study.
达雷妥尤单抗联合来那度胺和地塞米松治疗复发/难治性多发性骨髓瘤:随机、开放标签、3 期 POLLUX 研究的扩展随访。
Leukemia. 2020 Jul;34(7):1875-1884. doi: 10.1038/s41375-020-0711-6. Epub 2020 Jan 30.
4
Daratumumab prevents programmed death ligand-1 expression on antigen-presenting cells in de novo multiple myeloma.达雷妥尤单抗可防止初发多发性骨髓瘤中抗原呈递细胞表达程序性死亡配体 1。
Cancer Med. 2020 Mar;9(6):2077-2084. doi: 10.1002/cam4.2827. Epub 2020 Jan 28.
5
Daratumumab plus Lenalidomide and Dexamethasone for Untreated Myeloma.达雷妥尤单抗联合来那度胺和地塞米松治疗初治多发性骨髓瘤。
N Engl J Med. 2019 May 30;380(22):2104-2115. doi: 10.1056/NEJMoa1817249.
6
CD38 in Adenosinergic Pathways and Metabolic Re-programming in Human Multiple Myeloma Cells: In-tandem Insights From Basic Science to Therapy.CD38 在人类多发性骨髓瘤细胞中的腺苷能途径和代谢重编程中的作用:从基础科学到治疗的同步见解。
Front Immunol. 2019 Apr 24;10:760. doi: 10.3389/fimmu.2019.00760. eCollection 2019.
7
CD38-Driven Mitochondrial Trafficking Promotes Bioenergetic Plasticity in Multiple Myeloma.CD38 驱动的线粒体转运促进多发性骨髓瘤中的生物能量可塑性。
Cancer Res. 2019 May 1;79(9):2285-2297. doi: 10.1158/0008-5472.CAN-18-0773. Epub 2019 Jan 8.
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Clin Immunol. 2018 Jun;191:110-115. doi: 10.1016/j.clim.2017.11.014. Epub 2017 Nov 28.
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