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在三药暴露复发/难治性多发性骨髓瘤中,特里斯他单抗与现实世界中医生治疗选择的比较疗效:LocoMMotion 和 MoMMent 研究。

Comparative Effectiveness of Teclistamab Versus Real-World Physician's Choice of Therapy in LocoMMotion and MoMMent in Triple-Class Exposed Relapsed/Refractory Multiple Myeloma.

机构信息

Hematology Clinic, University Hospital Hotel-Dieu, Nantes, France.

University Hospital of Salamanca/IBSAL/CIC/CIBERONC, Salamanca, Spain.

出版信息

Adv Ther. 2024 Feb;41(2):696-715. doi: 10.1007/s12325-023-02738-0. Epub 2023 Dec 19.

Abstract

INTRODUCTION

Teclistamab is the first approved B cell maturation antigen × CD3 bispecific antibody with precision dosing for the treatment of triple-class exposed (TCE) relapsed/refractory multiple myeloma (RRMM). We compared the effectiveness of teclistamab in MajesTEC-1 versus real-world physician's choice of therapy (RWPC) in patients from the prospective, non-interventional LocoMMotion and MoMMent studies.

METHODS

Patients treated with teclistamab from MajesTEC-1 (N = 165) were compared with an external control arm from LocoMMotion (N = 248) or LocoMMotion + MoMMent pooled (N = 302). Inverse probability of treatment weighting adjusted for imbalances in prognostic baseline characteristics. The relative effect of teclistamab versus RWPC for overall response rate (ORR), very good partial response or better (≥ VGPR) rate, and complete response or better (≥ CR) rate was estimated with an odds ratio using weighted logistic regression transformed into a response-rate ratio (RR) and 95% confidence interval (CI). Weighted proportional hazards regression was used to estimate hazard ratios (HRs) and 95% CIs for duration of response (DOR), progression-free survival (PFS), and overall survival (OS).

RESULTS

Baseline characteristics were well balanced between treatment cohorts after reweighting. Patients treated with teclistamab had significantly improved outcomes versus RWPC in LocoMMotion: ORR (RR [95% CI], 2.44 [1.79-3.33]; p < 0.0001), ≥ VGPR (RR 5.78 [3.74-8.93]; p < 0.0001), ≥ CR (RR 113.73 [15.68-825.13]; p < 0.0001), DOR (HR 0.39 [0.24-0.64]; p = 0.0002), PFS (HR 0.48 [0.35-0.64]; p < 0.0001), and OS (HR 0.64 [0.46-0.88]; p = 0.0055). Teclistamab versus RWPC in LocoMMotion + MoMMent also had significantly improved outcomes: ORR (RR 2.41 [1.80-3.23]; p < 0.0001), ≥ VGPR (RR 5.91 [3.93-8.88]; p < 0.0001), ≥ CR (RR 132.32 [19.06-918.47]; p < 0.0001), DOR (HR 0.43 [0.26-0.71]; p = 0.0011), PFS (HR 0.49 [0.37-0.66]; p < 0.0001), and OS (HR 0.69 [0.50-0.95]; p = 0.0247).

CONCLUSION

Teclistamab demonstrated significantly improved effectiveness over RWPC in LocoMMotion ± MoMMent, emphasizing its clinical benefit as a highly effective treatment for patients with TCE RRMM.

TRIAL REGISTRATION

MajesTEC-1, ClinicalTrials.gov NCT03145181 (phase 1) and NCT04557098 (phase 2); LocoMMotion, ClinicalTrials.gov NCT04035226; MoMMent, ClinicalTrials.gov NCT05160584.

摘要

简介

特卡昔单抗是首个获批的用于治疗三药暴露(TCE)复发/难治性多发性骨髓瘤(RRMM)的 B 细胞成熟抗原 × CD3 双特异性抗体,具有精准剂量。我们比较了特卡昔单抗在 MajesTEC-1 中的疗效与现实世界中医生选择的治疗方案(RWPC)在前瞻性、非干预性 LocoMMotion 和 MoMMent 研究中的疗效。

方法

从 MajesTEC-1 中接受特卡昔单抗治疗的患者(N=165)与来自 LocoMMotion 的外部对照臂(N=248)或 LocoMMotion+MoMMent 汇总(N=302)进行比较。采用逆概率治疗加权法调整预后基线特征的不平衡。使用加权逻辑回归转化为反应率比(RR)和 95%置信区间(CI),采用比值比估计特卡昔单抗与 RWPC 的总体反应率(ORR)、非常好的部分缓解或更好(≥VGPR)率和完全缓解或更好(≥CR)率。使用加权比例风险回归估计反应持续时间(DOR)、无进展生存期(PFS)和总生存期(OS)的风险比(HR)和 95%CI。

结果

经过重新加权后,治疗队列之间的基线特征得到了很好的平衡。与 RWPC 相比,LocoMMotion 中接受特卡昔单抗治疗的患者有显著改善的疗效:ORR(RR[95%CI],2.44[1.79-3.33];p<0.0001)、≥VGPR(RR 5.78[3.74-8.93];p<0.0001)、≥CR(RR 113.73[15.68-825.13];p<0.0001)、DOR(HR 0.39[0.24-0.64];p=0.0002)、PFS(HR 0.48[0.35-0.64];p<0.0001)和 OS(HR 0.64[0.46-0.88];p=0.0055)。LocoMMotion+MoMMent 中特卡昔单抗与 RWPC 相比也有显著改善的疗效:ORR(RR 2.41[1.80-3.23];p<0.0001)、≥VGPR(RR 5.91[3.93-8.88];p<0.0001)、≥CR(RR 132.32[19.06-918.47];p<0.0001)、DOR(HR 0.43[0.26-0.71];p=0.0011)、PFS(HR 0.49[0.37-0.66];p<0.0001)和 OS(HR 0.69[0.50-0.95];p=0.0247)。

结论

特卡昔单抗在 LocoMMotion±MoMMent 中与 RWPC 相比显示出显著改善的疗效,强调了其作为治疗 TCE RRMM 患者的高效治疗方法的临床获益。

试验注册

MajesTEC-1,ClinicalTrials.gov NCT03145181(I 期)和 NCT04557098(II 期);LocoMMotion,ClinicalTrials.gov NCT04035226;MoMMent,ClinicalTrials.gov NCT05160584。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f55/10838813/c38cb37f46cc/12325_2023_2738_Fig1_HTML.jpg

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