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2
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1
Depth of response and response kinetics of isatuximab plus carfilzomib and dexamethasone in relapsed multiple myeloma.伊沙佐米联合卡非佐米和地塞米松治疗复发多发性骨髓瘤的反应深度和反应动力学。
Blood Adv. 2022 Aug 9;6(15):4506-4515. doi: 10.1182/bloodadvances.2021006713.
2
Biallelic loss of BCMA as a resistance mechanism to CAR T cell therapy in a patient with multiple myeloma.双等位基因 BCMA 缺失导致多发性骨髓瘤患者对 CAR T 细胞治疗产生耐药。
Nat Commun. 2021 Feb 8;12(1):868. doi: 10.1038/s41467-021-21177-5.
3
Bortezomib, lenalidomide, and dexamethasone with or without elotuzumab in patients with untreated, high-risk multiple myeloma (SWOG-1211): primary analysis of a randomised, phase 2 trial.硼替佐米、来那度胺和地塞米松联合或不联合依洛珠单抗治疗未经治疗的高危多发性骨髓瘤患者(SWOG-1211):一项随机、2 期试验的主要分析。
Lancet Haematol. 2021 Jan;8(1):e45-e54. doi: 10.1016/S2352-3026(20)30354-9. Epub 2020 Dec 22.
4
Safety of ninety-minute daratumumab infusion.达雷妥尤单抗 90 分钟输注的安全性。
J Oncol Pharm Pract. 2021 Jul;27(5):1080-1085. doi: 10.1177/1078155220951231. Epub 2020 Aug 30.
5
Subcutaneous versus intravenous daratumumab in multiple myeloma - Authors' reply.皮下注射与静脉注射达雷妥尤单抗治疗多发性骨髓瘤——作者回复
Lancet Haematol. 2020 Aug;7(8):e559. doi: 10.1016/S2352-3026(20)30188-5.
6
Carfilzomib, dexamethasone, and daratumumab versus carfilzomib and dexamethasone for patients with relapsed or refractory multiple myeloma (CANDOR): results from a randomised, multicentre, open-label, phase 3 study.卡非佐米、地塞米松和达雷妥尤单抗与卡非佐米和地塞米松治疗复发或难治性多发性骨髓瘤患者(CANDOR):一项随机、多中心、开放性、3 期研究的结果。
Lancet. 2020 Jul 18;396(10245):186-197. doi: 10.1016/S0140-6736(20)30734-0.
7
Bispecific, T-Cell-Recruiting Antibodies in B-Cell Malignancies.双特异性、T 细胞募集抗体在 B 细胞恶性肿瘤中的应用。
Front Immunol. 2020 May 7;11:762. doi: 10.3389/fimmu.2020.00762. eCollection 2020.
8
Daratumumab, lenalidomide, bortezomib, and dexamethasone for transplant-eligible newly diagnosed multiple myeloma: the GRIFFIN trial.达雷妥尤单抗、来那度胺、硼替佐米和地塞米松用于适合移植的新诊断多发性骨髓瘤:GRIFFIN 试验。
Blood. 2020 Aug 20;136(8):936-945. doi: 10.1182/blood.2020005288.
9
A T-cell-redirecting bispecific G-protein-coupled receptor class 5 member D x CD3 antibody to treat multiple myeloma.一种双特异性 G 蛋白偶联受体家族 5 成员 D x CD3 T 细胞导向抗体,用于治疗多发性骨髓瘤。
Blood. 2020 Apr 9;135(15):1232-1243. doi: 10.1182/blood.2019003342.
10
Mechanisms of Resistance to Anti-CD38 Daratumumab in Multiple Myeloma.多发性骨髓瘤中抗 CD38 达雷妥尤单抗耐药的机制。
Cells. 2020 Jan 9;9(1):167. doi: 10.3390/cells9010167.

基于抗体的多发性骨髓瘤治疗方法。

Antibody-Based Treatment Approaches in Multiple Myeloma.

机构信息

Division of Hematology, Department of Medicine, Stanford University, Stanford, CA, USA.

Stanford Cancer Institute, Stanford, CA, USA.

出版信息

Curr Hematol Malig Rep. 2021 Apr;16(2):183-191. doi: 10.1007/s11899-021-00624-6. Epub 2021 Mar 17.

DOI:10.1007/s11899-021-00624-6
PMID:33730360
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8715952/
Abstract

PURPOSE OF REVIEW

The field of multiple myeloma treatment has entered a new era with antibody-based approaches in clinical practice. In this review, we focus on the clinical approaches of utilizing antibody-based modality, specifically monoclonal antibodies, antibody-drug conjugates, and bispecific T-cell antibodies in the treatment of multiple myeloma.

RECENT FINDINGS

Three monoclonal antibodies (daratumumab, isatuximab, elotuzumab) and one anti-BCMA (B-cell maturation antigen) antibody-drug conjugate (belantamab mafodotin) have been approved by the FDA in the last 5 years for the treatment of multiple myeloma. There are many ongoing clinical trials using novel targets and constructs, including bispecific antibodies against BCMA, GPRC5D, and FCRH5. In addition to exploring efficacy, there are ongoing efforts to overcome the resistance to therapy. Antibody-based therapy has improved the outcomes of patients with multiple myeloma and has been incorporated in the standard of care. We expect to see novel targets and constructs that can achieve a deeper and more durable response while minimizing toxicity, as well as better strategies for toxicity management for existing agents. We also expect that antibody-based strategies will be used in earlier lines of therapy in the future.

摘要

目的综述

随着抗体类药物在临床实践中的应用,多发性骨髓瘤的治疗领域已经进入了一个新时代。在这篇综述中,我们重点关注利用抗体类药物(特别是单克隆抗体、抗体药物偶联物和双特异性 T 细胞抗体)治疗多发性骨髓瘤的临床方法。

最近的发现

在过去的 5 年里,美国食品药品监督管理局(FDA)已经批准了三种单克隆抗体(达雷妥尤单抗、伊沙妥昔单抗、埃罗妥珠单抗)和一种抗 B 细胞成熟抗原(BCMA)抗体药物偶联物(贝兰他单抗马妥珠单抗)用于多发性骨髓瘤的治疗。目前有许多正在进行的临床试验,涉及新型靶点和构建体,包括针对 BCMA、GPRC5D 和 FCRH5 的双特异性抗体。除了探索疗效外,目前还在努力克服治疗耐药性。抗体类药物治疗改善了多发性骨髓瘤患者的预后,并已纳入标准治疗方案。我们期望看到能够实现更深层次和更持久反应的新型靶点和构建体,同时最大限度地降低毒性,以及更好的现有药物毒性管理策略。我们还期望在未来的治疗中更早地使用抗体类药物治疗策略。