大 B 细胞淋巴瘤标准治疗方案 Axicabtagene Ciloleucel 的五年随访:美国淋巴瘤CAR T联盟的研究结果。

IF 42.1 1区 医学 Q1 ONCOLOGY Journal of Clinical Oncology Pub Date : 2024-10-20 Epub Date: 2024-08-02 DOI:10.1200/JCO.23.02786
Michael D Jain, Jay Y Spiegel, Loretta J Nastoupil, John Tamaresis, Armin Ghobadi, Yi Lin, Lazaros Lekakis, Patrick Reagan, Olalekan Oluwole, Joseph McGuirk, Abhinav Deol, Kathleen A Dorritie, Alison R Sehgal, Andre Goy, Brian T Hill, Charalambos Andreadis, Javier Munoz, Matthew Ulrickson, Jason Westin, Julio C Chavez, Dilan Patel, Miriam T Jacobs, Radhika Bansal, N Nora Bennani, Vivek G Patel, Aaron P Rapoport, Julie M Vose, David B Miklos, Sattva S Neelapu, Frederick L Locke, Matthew Lunning, Saurabh Dahiya
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引用次数: 0

摘要

目的:Axicabtagene ciloleucel(axi-cel)是一种自体CD19嵌合抗原受体(CAR)T细胞疗法,已被批准用于治疗复发或难治性大B细胞淋巴瘤。人们对CAR T细胞疗法后的长期存活率知之甚少:我们曾报道过 298 例患者的治疗结果,这些患者在接受了两种或两种以上的治疗后进行了白细胞清洗,并打算接受标准疗法 axi-cel(n = 275 例输注),中位随访时间为 12.9 个月。在此,我们报告了对这批患者中位随访58个月的结果,重点关注晚期生存事件:结果:在接受axi-cel治疗的患者中,5年无进展生存率为29%,5年总生存率(OS)为40%。5年淋巴瘤特异性生存率为53%,晚期复发率较低。然而,5年非复发死亡率(NRM)为16.2%,超过一半的NRM事件发生在2年之后。与60岁以下的患者相比,60岁及以上的患者复发风险较低(P = .02),但NRM风险较高(NRM几率比为4.5 [95% CI, 2.1 to 10.8];P < .001)。晚期NRM主要是由于感染和随后的恶性肿瘤(SMN)引起的。共有24名患者(9%)发生了恶性肿瘤,包括与治疗相关的髓系肿瘤(15例)、实体瘤(7例)和无关的淋巴恶性肿瘤(2例):结论:在标准护理环境下,axi-cel的疗效与临床试验报告的结果一致,在5年时间点观察到持续、持久的反应。然而,晚期感染和SMN的发生是降低CAR T细胞疗法长期存活率的关键问题,尤其是对老年人而言。
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Five-Year Follow-Up of Standard-of-Care Axicabtagene Ciloleucel for Large B-Cell Lymphoma: Results From the US Lymphoma CAR T Consortium.

Purpose: Axicabtagene ciloleucel (axi-cel) is an autologous CD19 chimeric antigen receptor (CAR) T-cell therapy that is approved for the treatment of relapsed or refractory large B-cell lymphoma. Little is known about the long-term survivorship after CAR T-cell therapy.

Methods: We previously reported the results of 298 patients who were leukapheresed with the intent to receive standard-of-care axi-cel (n = 275 infused) after two or more previous lines of therapy at a median follow-up of 12.9 months. Here, we report extended follow-up of this cohort to a median of 58 months, with a focus on late survivorship events.

Results: Among axi-cel-infused patients, progression-free survival at 5 years was 29% and overall survival (OS) at 5 years was 40%. The 5-year lymphoma-specific survival was 53% with infrequent late relapses. However, the 5-year nonrelapse mortality (NRM) was 16.2%, with over half of NRM events occurring beyond 2 years. Patients who were 60 years and older had a lower risk of relapse (P = .02), but a higher risk of NRM compared with patients younger than 60 years (NRM odds ratio, 4.5 [95% CI, 2.1 to 10.8]; P < .001). Late NRM was mainly due to infections and subsequent malignant neoplasms (SMNs). In total, SMNs occurred in 24 patients (9%), including therapy-related myeloid neoplasms (n = 15), solid tumors (n = 7), and unrelated lymphoid malignancies (n = 2).

Conclusion: In the standard-of-care setting, axi-cel exhibits outcomes consistent with those reported in clinical trials, with sustained, durable responses observed at the 5-year time point. However, late infections and the development of SMN are key survivorship issues that reduce long-term survival after CAR T-cell therapy, particularly in the elderly.

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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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