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Blood Adv. 2021 Aug 10;5(15):3016-3020. doi: 10.1182/bloodadvances.2021004176.
2
Longer term outcomes with single-agent belantamab mafodotin in patients with relapsed or refractory multiple myeloma: 13-month follow-up from the pivotal DREAMM-2 study.在复发或难治性多发性骨髓瘤患者中单用 belantamab mafodotin 的长期疗效:关键性 DREAMM-2 研究的 13 个月随访结果。
Cancer. 2021 Nov 15;127(22):4198-4212. doi: 10.1002/cncr.33809. Epub 2021 Jul 27.
3
Belantamab Mafodotin (GSK2857916) Drives Immunogenic Cell Death and Immune-mediated Antitumor Responses .贝兰他单抗马妥昔单抗(GSK2857916)诱导免疫原性细胞死亡和免疫介导的抗肿瘤反应。
Mol Cancer Ther. 2021 Oct;20(10):1941-1955. doi: 10.1158/1535-7163.MCT-21-0035. Epub 2021 Jul 12.
4
Ciltacabtagene autoleucel, a B-cell maturation antigen-directed chimeric antigen receptor T-cell therapy in patients with relapsed or refractory multiple myeloma (CARTITUDE-1): a phase 1b/2 open-label study.西达基奥仑赛,一种针对 B 细胞成熟抗原的嵌合抗原受体 T 细胞疗法,用于治疗复发或难治性多发性骨髓瘤患者(CARTITUDE-1):一项 1b/2 期开放标签研究。
Lancet. 2021 Jul 24;398(10297):314-324. doi: 10.1016/S0140-6736(21)00933-8. Epub 2021 Jun 24.
5
Ocular Toxicity of Belantamab Mafodotin, an Oncological Perspective of Management in Relapsed and Refractory Multiple Myeloma.贝兰他单抗莫福汀的眼部毒性:复发难治性多发性骨髓瘤治疗的肿瘤学视角
Front Oncol. 2021 May 11;11:678634. doi: 10.3389/fonc.2021.678634. eCollection 2021.
6
Management of belantamab mafodotin-associated corneal events in patients with relapsed or refractory multiple myeloma (RRMM).贝兰他单抗mafodotin 相关角膜事件的管理在复发或难治性多发性骨髓瘤(RRMM)患者中的应用。
Blood Cancer J. 2021 May 26;11(5):103. doi: 10.1038/s41408-021-00494-4.
7
Belantamab mafodotin in combination with novel agents in relapsed/refractory multiple myeloma: DREAMM-5 study design.贝兰他单抗马妥昔单抗联合新型药物治疗复发/难治性多发性骨髓瘤:DREAMM-5 研究设计。
Future Oncol. 2021 Jun;17(16):1987-2003. doi: 10.2217/fon-2020-1269. Epub 2021 Mar 8.
8
Idecabtagene Vicleucel in Relapsed and Refractory Multiple Myeloma.伊达比星脂质体注射用多柔比星治疗复发/难治性多发性骨髓瘤
N Engl J Med. 2021 Feb 25;384(8):705-716. doi: 10.1056/NEJMoa2024850.
9
Homozygous BCMA gene deletion in response to anti-BCMA CAR T cells in a patient with multiple myeloma.一名多发性骨髓瘤患者中,针对抗BCMA嵌合抗原受体T细胞的纯合BCMA基因缺失。
Nat Med. 2021 Apr;27(4):616-619. doi: 10.1038/s41591-021-01245-5. Epub 2021 Feb 22.
10
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.

硼替佐米、卡非佐米和来那度胺联合方案治疗多发性骨髓瘤患者的真实世界研究:梅奥诊所的经验

"Real-life" data of the efficacy and safety of belantamab mafodotin in relapsed multiple myeloma-the Mayo Clinic experience.

机构信息

Division of Hematology, Mayo Clinic, Rochester, MN, USA.

Institute of Hematology, Davidoff Cancer Center, Rabin Medical Center, Petah- Tikvah, Israel.

出版信息

Blood Cancer J. 2021 Dec 7;11(12):196. doi: 10.1038/s41408-021-00592-3.

DOI:10.1038/s41408-021-00592-3
PMID:34876555
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8651684/
Abstract

Belantamab mafodotin is a highly selective targeted therapy for multiple myeloma. It targets the B cell maturation antigen (BCMA) on plasma cells and showed promising results in several randomized clinical trials. We report the outcomes of 36 patients treated at Mayo Clinic. Our cohort received a median of eight prior lines of therapy. Six patients received belantamab in combination with other medications (pomalidomide, cyclophosphamide, thalidomide), 13 patients (36%) were 70 years or older, two patients had a creatinine of >2.5 mg/dL, and one patient was on dialysis. All three patients with renal failure received full dose belantamab. Chimeric antigen receptor (CAR-T) therapy was used prior to belantamab in seven patients and none of them responded to belantamab therapy. The overall response rate (ORR) was 33% (CR 6%, VGPR 8%, PR 19%), like the ORR reported in the DREAMM-2 trial. Keratopathy developed in 16 patients (43%), grade 1 in six patients, grade 2 in seven patients, and grade 3 in three patients. Eight percent discontinued therapy due to keratopathy. The median PFS and OS was 2 months and 6.5 months, respectively.

摘要

贝兰他单抗马妥昔单抗是一种针对多发性骨髓瘤的高度选择性靶向治疗药物。它针对浆细胞上的 B 细胞成熟抗原 (BCMA),并在几项随机临床试验中显示出良好的效果。我们报告了在 Mayo 诊所接受治疗的 36 名患者的结果。我们的队列接受了中位数为 8 线的治疗。6 名患者接受了贝兰他单抗联合其他药物(泊马度胺、环磷酰胺、沙利度胺)治疗,13 名患者(36%)年龄在 70 岁或以上,2 名患者的肌酐>2.5mg/dL,1 名患者正在接受透析。所有 3 名肾功能衰竭患者均接受了全剂量贝兰他单抗治疗。在接受贝兰他单抗治疗之前,有 7 名患者接受了嵌合抗原受体 (CAR-T) 治疗,他们均未对贝兰他单抗治疗产生反应。总缓解率(ORR)为 33%(完全缓解率 6%,非常好的部分缓解率 8%,部分缓解率 19%),与 DREAMM-2 试验报告的 ORR 相似。16 名患者(43%)出现角膜病,6 名患者为 1 级,7 名患者为 2 级,3 名患者为 3 级。8%的患者因角膜病停止治疗。中位无进展生存期和总生存期分别为 2 个月和 6.5 个月。