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Ciltacabtagene Autoleucel,一种抗 B 细胞成熟抗原嵌合抗原受体 T 细胞疗法,在复发/难治性多发性骨髓瘤(CARTIFAN-1)中国患者中的 II 期、开放标签研究。

Phase II, Open-Label Study of Ciltacabtagene Autoleucel, an Anti-B-Cell Maturation Antigen Chimeric Antigen Receptor-T-Cell Therapy, in Chinese Patients With Relapsed/Refractory Multiple Myeloma (CARTIFAN-1).

机构信息

Shanghai Institute of Hematology, State Key Laboratory of Medical Genomics, National Research Center for Translational Medicine at Shanghai, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, ShaanXi, China.

出版信息

J Clin Oncol. 2023 Feb 20;41(6):1275-1284. doi: 10.1200/JCO.22.00690. Epub 2022 Oct 21.

Abstract

PURPOSE

CARTIFAN-1 aimed to evaluate the efficacy and safety of ciltacabtagene autoleucel (cilta-cel), a B-cell maturation antigen-targeting chimeric antigen receptor T-cell therapy, in Chinese patients with relapsed/refractory multiple myeloma (RRMM).

METHODS

This pivotal phase II, open-label study (ClinicalTrials.gov identifier: NCT03758417), conducted across eight sites in China, enrolled adult patients with RRMM who had received ≥ 3 lines of prior therapy, including a proteasome inhibitor and immunomodulatory drug. Patients received a single infusion of cilta-cel (target dose 0.75 × 10 chimeric antigen receptor-positive viable T cells/kg). The primary end point was overall response rate. Secondary end points included progression-free survival (PFS), overall survival (OS), and incidence and severity of adverse events (AEs).

RESULTS

As of the clinical cutoff of July 19, 2021, 48 patients received a cilta-cel infusion. At an 18-month median follow-up, the overall response rate was 89.6% (95% CI, 77.3 to 96.5), with a median time to first response of approximately 1 month; 77.1% of patients (95% CI, 62.7 to 88.0) achieved complete response or better. Medians for duration of response, PFS, and OS were not reached. The 18-month PFS and OS rates were 66.8% (95% CI, 49.4 to 79.4) and 78.7% (95% CI, 64.0 to 88.0), respectively. Hematologic AEs were common, including anemia (100%), neutropenia (97.9%), lymphopenia (95.8%), and thrombocytopenia (87.5%). Cytokine release syndrome occurred in 97.9% of patients (35.4% grade 3/4); the median time to onset was 7 days, and the median duration was 5 days. Infections occurred in 85.4% of patients (37.5% grade 3/4). Ten deaths occurred after cilta-cel infusion, eight of which were due to treatment-related AEs.

CONCLUSION

These data demonstrate a favorable risk-benefit profile for a single infusion of cilta-cel, resulting in early, deep, and durable responses in heavily pretreated patients with RRMM in China.

摘要

目的

CARTIFAN-1 旨在评估 cilta-cel(一种靶向 B 细胞成熟抗原的嵌合抗原受体 T 细胞疗法)在接受≥3 线既往治疗(包括蛋白酶体抑制剂和免疫调节剂)的中国复发/难治性多发性骨髓瘤(RRMM)患者中的疗效和安全性。

方法

这是一项在中国 8 个地点进行的关键的 II 期、开放标签研究(ClinicalTrials.gov 标识符:NCT03758417),纳入了接受过≥3 线既往治疗(包括蛋白酶体抑制剂和免疫调节剂)的 RRMM 成年患者。患者接受单次 cilta-cel 输注(目标剂量 0.75×106 个嵌合抗原受体阳性活 T 细胞/kg)。主要终点是总缓解率。次要终点包括无进展生存期(PFS)、总生存期(OS)和不良事件(AE)的发生率和严重程度。

结果

截至 2021 年 7 月 19 日的临床截止日期,48 例患者接受了 cilta-cel 输注。在 18 个月的中位随访中,总缓解率为 89.6%(95%CI,77.3 至 96.5),首次缓解的中位时间约为 1 个月;77.1%的患者(95%CI,62.7 至 88.0)达到完全缓解或更好。缓解持续时间、PFS 和 OS 的中位数均未达到。18 个月的 PFS 和 OS 率分别为 66.8%(95%CI,49.4 至 79.4)和 78.7%(95%CI,64.0 至 88.0)。血液学 AE 很常见,包括贫血(100%)、中性粒细胞减少(97.9%)、淋巴细胞减少(95.8%)和血小板减少(87.5%)。细胞因子释放综合征发生在 97.9%的患者中(35.4%为 3/4 级);中位发病时间为 7 天,中位持续时间为 5 天。85.4%的患者发生感染(37.5%为 3/4 级)。10 例患者在 cilta-cel 输注后死亡,其中 8 例死于治疗相关 AE。

结论

这些数据表明,单次输注 cilta-cel 具有良好的风险效益比,可使中国接受过多线治疗的 RRMM 患者产生早期、深度和持久的缓解。

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