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靶向BCMA或GPRC5D的双特异性抗体在CAR T细胞治疗后的复发骨髓瘤中具有高度疗效。

Bispecific antibodies targeting BCMA or GPRC5D are highly effective in relapsed myeloma after CAR T-cell therapy.

作者信息

Merz Maximilian, Dima Danai, Hashmi Hamza, Ahmed Nausheen, Stölzel Friedrich, Holderried Tobias A W, Fenk Roland, Müller Fabian, Tovar Natalia, Oliver-Cáldes Aina, Rathje Kristin, Davis James A, Fandrei David, Vucinic Vladan, Kharboutli Soraya, Baermann Ben-Niklas, Ayuk Francis, Platzbecker Uwe, Albici Anca-Maria, Schub Nathalie, Schmitz Friederike, Shune Leyla, Khouri Jack, Anwer Faiz, Raza Shahzad, McGuirk Joseph, Mahmoudjafari Zahra, Green Kimberly, Khandanpour Cyrus, Teichert Marcel, Jeker Barbara, Hoffmann Michele, Kröger Nicolaus, von Tresckow Bastian, de Larrea Carlos Fernández, Pabst Thomas, Abdallah Al-Ola, Gagelmann Nico

机构信息

Department of Hematology, Cellular Therapy, Hemasteseology and Infectious Disease, University Hospital of Leipzig and Fraunhofer IZI, Leipzig, Germany.

Cleveland Clinic, Cleveland, OH, USA.

出版信息

Blood Cancer J. 2024 Dec 5;14(1):214. doi: 10.1038/s41408-024-01197-2.

Abstract

Despite the astonishing outcomes after chimeric antigen receptor (CAR) T-cell therapy for relapsed refractory multiple myeloma (RRMM), most patients eventually relapse. There are only limited data available on salvage therapies following relapse after BCMA-directed CAR T-cell therapy. Here, we analyzed outcomes of post-CAR T-cell therapy relapse and impact of different salvage strategies in an international cohort of 139 patients (n = 130 ide-cel, n = 9 cilta-cel), receiving talquetamab (n = 28), teclistamab (n = 37), combinations of immunomodulating drugs (IMiDs), proteasome inhibitors (PIs) or CD38 monoclonal antibodies (n = 43), and others (n = 31). The median time to relapse after CAR T-cell therapy was 5 months, 53% had the extramedullary disease (EMD) at relapse, associated with dismal post-relapse outcome (P = 0.005). Overall response and complete response upon salvage therapies were 79% and 39% for talquetamab, 64% and 32% for teclistamab, 30% and 0% for IMiDs/PIs/CD38, and 26% and 3% for others (P < 0.001). Duration of response, as well as median survival, was significantly improved with bispecific antibodies (P < 0.001, respectively). Bispecific antibodies seemed to overcome the poor prognosis associated with early relapse and EMD, and were independent predictors for improved survival in multivariable analysis. In summary, these results suggest bispecific antibodies as the standard of care for relapse after CAR T-cell therapy for RRMM.

摘要

尽管嵌合抗原受体(CAR)T细胞疗法治疗复发难治性多发性骨髓瘤(RRMM)取得了惊人的效果,但大多数患者最终仍会复发。关于BCMA导向的CAR T细胞疗法后复发的挽救治疗,可用数据有限。在此,我们分析了139例患者(n = 130例ide-cel,n = 9例cilta-cel)的国际队列中CAR T细胞治疗后复发的结果以及不同挽救策略的影响,这些患者接受了talquetamab(n = 28)、teclistamab(n = 37)、免疫调节药物(IMiDs)、蛋白酶体抑制剂(PIs)或CD38单克隆抗体的联合治疗(n = 43),以及其他治疗(n = 31)。CAR T细胞治疗后复发的中位时间为5个月,53%的患者在复发时有髓外疾病(EMD),这与复发后的不良预后相关(P = 0.005)。挽救治疗后的总体缓解率和完全缓解率分别为:talquetamab为79%和39%,teclistamab为64%和32%,IMiDs/PIs/CD38为30%和0%,其他治疗为26%和3%(P < 0.001)。双特异性抗体显著改善了缓解持续时间以及中位生存期(分别为P < 0.001)。双特异性抗体似乎克服了与早期复发和EMD相关的不良预后,并且在多变量分析中是生存改善的独立预测因素。总之,这些结果表明双特异性抗体是RRMM的CAR T细胞治疗后复发的标准治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a574/11618392/169b4874f314/41408_2024_1197_Fig1_HTML.jpg

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