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五例既往接受抗 C38 达妥木单抗治疗的复发多发性骨髓瘤患者中抗-CD38 依沙妥昔单抗联合泊马度胺和地塞米松的疗效:病例系列。

Outcomes of anti-CD38 isatuximab plus pomalidomide and dexamethasone in five relapsed myeloma patients with prior exposure to anti-C38 daratumumab: case series.

机构信息

Department of Clinical Haematology, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

Royal Berkshire Hospital, Reading, UK.

出版信息

Hematology. 2022 Dec;27(1):204-207. doi: 10.1080/16078454.2022.2028978.

Abstract

Daratumumab is the first anti-CD38 monoclonal antibody (Mab) used to treat myeloma in the newly diagnosed setting and in the relapsed setting. Isatuximab, another Mab targeting a specific epitope on the CD38 receptor, was recently approved in the UK in combination with pomalidomide and dexamethasone (IsaPomDex) to treat myeloma patients who received three prior lines of therapy. However, there is a lack of understanding of whether using a prior anti-CD38 Mab (e.g. daratumumab) can affect the efficacy of another Mab (e.g. isatuximab), when the latter is used to treat a subsequent relapse. We performed a UK-wide outcomes study of IsaPomDex in the real-world. In this case series, we report a detailed descriptive analysis of the characteristics and clinical outcomes of five IsaPomDex patients in UK routine practice (Patients I to V), with a prior exposure to daratumumab. Age range was 51-77 years with two patients >70 and three patients <70 years. The cytogenetic risk was standard in two patients, high in two patients and not known in one patient. Prior daratumumab regimen were monotherapy (dara-mono) in one patient (II), and daratumumab with bortezomib and dexamethasone (DVd) in four patients. Responses to prior daratumumab were: very good partial response (VGPR) in two patients (I and III), minor response-stable disease (MR-SD) in one patient (II), and progressive disease (PD) in two patients (IV and V). Median (range) number of IsaPomDex cycles received was 2 (1-4). Outcomes of IsaPomDex were PD in three patients (II, IV and V) and a response in two patients. Response categories were: MR-SD in patient I and PR in patient III. Despite the limitations of our case series, we described the first UK real-world report of IsaPomDex outcomes in myeloma patients with a prior exposure to daratumumab. Large prospective studies are required to further evaluate myeloma outcomes in this setting.

摘要

达雷妥尤单抗是首个用于治疗初诊和复发多发性骨髓瘤的抗 CD38 单克隆抗体(Mab)。另一种靶向 CD38 受体特定表位的 Mab 药物依沙妥昔单抗,最近在英国获批与泊马度胺和地塞米松联合使用(IsaPomDex),用于治疗已接受三线以上治疗的多发性骨髓瘤患者。然而,目前尚不清楚当使用另一种 Mab(例如依沙妥昔单抗)治疗随后的复发时,先前使用抗 CD38 Mab(例如达雷妥尤单抗)是否会影响后者的疗效。我们在英国开展了一项 IsaPomDex 的真实世界结局研究。在本病例系列中,我们报告了 5 例在英国常规实践中接受 IsaPomDex 治疗的多发性骨髓瘤患者(患者 I-V)的详细描述性分析,这些患者均有达雷妥尤单抗治疗史。年龄范围为 51-77 岁,其中 2 例患者年龄大于 70 岁,3 例患者年龄小于 70 岁。2 例患者细胞遗传学风险为标准风险,2 例患者为高风险,1 例患者风险未知。先前的达雷妥尤单抗治疗方案为:1 例患者(II 期)接受单药治疗(dara-mono),4 例患者接受达雷妥尤单抗联合硼替佐米和地塞米松(DVd)治疗。先前达雷妥尤单抗的反应为:2 例患者(I 期和 III 期)为非常好的部分缓解(VGPR),1 例患者(II 期)为轻微缓解-疾病稳定(MR-SD),2 例患者(IV 期和 V 期)为疾病进展(PD)。中位(范围)接受的 IsaPomDex 周期数为 2(1-4)。3 例患者(II 期、IV 期和 V 期)出现 PD,2 例患者出现反应。反应类别为:I 期患者为 MR-SD,III 期患者为 PR。尽管我们的病例系列存在局限性,但我们描述了英国首个真实世界报告的多发性骨髓瘤患者在先前接受达雷妥尤单抗治疗后的 IsaPomDex 结局。需要开展大型前瞻性研究进一步评估该情况下多发性骨髓瘤的结局。

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