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嵌合抗原受体 T 细胞疗法治疗 70 岁以上弥漫性大 B 细胞淋巴瘤患者与年轻患者的毒性和疗效比较 - 一项匹配对照多中心队列研究。

Toxicity and efficacy of chimeric antigen receptor T-cell therapy in patients with diffuse large B-cell lymphoma above the age of 70 years compared to younger patients - a matched control multicenter cohort study.

机构信息

BMT Unit, Aviv (Sourasky) Medical Center, Aviv, Israel; Sackler Faculty of Medicine, Aviv University, Aviv.

Department of Bone Marrow Transplantation Hadassah University Hospital and The Hebrew University of Jerusalem Faculty of Medicine.

出版信息

Haematologica. 2022 May 1;107(5):1111-1118. doi: 10.3324/haematol.2021.278288.

Abstract

Data regarding efficacy and toxicity of chimeric antigen receptor T (CAR-T) cell therapy in the elderly, geriatric population are insufficient. In 2019, tisagenlecleucel and axicabtagene-ciloleucel were commercially approved for relapsed/refractory diffuse large B-cell lymphoma. From May 2019 onwards, 47 relapsed/refractory diffuse large Bcell lymphoma patients, ≥70 years underwent lymphopharesis in three Israeli centers. Elderly (n=41, mean age 76.2 years) and young (n=41, mean age 55.4 years) patients were matched based on ECOG performance status and lactose dehydrogenase levels. There were no differences in CD4/CD8 ratio (P=0.94), %CD4 naive (P=0.92), %CD8 naive (P=0.44) and exhaustion markers (both HLA-DR and PD-1) between CAR-T cell products in both cohorts. Forty-one elderly patients (87%) received CAR-T cell infusion. There were no differences in the incidence of grade ≥3 cytokine-release-syndrome (P=0.29), grade≥3 neurotoxicity (P=0.54), and duration of hospitalization (P=0.55) between elderly and younger patients. There was no difference in median D7-CAR-T cell expansion (P=0.145). Response rates were similar between the two groups (complete response 46% and partial response 17% in the elderly group, P=0.337). Non-relapse mortality at 1 and 3 months was 0 in both groups. With a median follow-up of 7 months (range, 1.3-17.2 months), 6- and 12-months progression-free and overall survival in elderly patients were 39% and 32%, and 74% and 69%, respectively. EORTC QLQ-C30 questionnaires, obtained at 1 month, showed worsening of disability and cancer-related-symptoms in elderly versus younger patients. We conclude that outcomes of CAR-T cell therapy are comparable between elderly, geriatric and younger patients, indicating that age as per se should not preclude CAR-T cell administration. Longer rehabilitation therapy is essential to improve disabilities and long-term symptoms.

摘要

关于嵌合抗原受体 T (CAR-T) 细胞疗法在老年人、老年人群体中的疗效和毒性的数据不足。2019 年,tisagenlecleucel 和 axicabtagene-ciloleucel 被商业化批准用于复发/难治性弥漫性大 B 细胞淋巴瘤。自 2019 年 5 月以来,在以色列的三个中心,47 名复发/难治性弥漫性大 B 细胞淋巴瘤患者,年龄≥70 岁,进行了淋巴清除术。老年(n=41,平均年龄 76.2 岁)和年轻(n=41,平均年龄 55.4 岁)患者根据 ECOG 表现状态和乳酸脱氢酶水平进行匹配。两组之间的 CD4/CD8 比值(P=0.94)、%CD4 幼稚细胞(P=0.92)、%CD8 幼稚细胞(P=0.44)和衰竭标志物(HLA-DR 和 PD-1)均无差异。两组患者的 CAR-T 细胞产品均无差异。≥3 级细胞因子释放综合征(P=0.29)、≥3 级神经毒性(P=0.54)和住院时间(P=0.55)的发生率在老年患者和年轻患者之间无差异。中位 D7-CAR-T 细胞扩增无差异(P=0.145)。两组的反应率相似(老年组完全缓解率为 46%,部分缓解率为 17%,P=0.337)。两组在 1 个月和 3 个月时的非复发死亡率均为 0。中位随访 7 个月(范围 1.3-17.2 个月),老年患者 6 个月和 12 个月时的无进展生存率和总生存率分别为 39%和 32%,74%和 69%。在 1 个月时获得的 EORTC QLQ-C30 问卷显示,与年轻患者相比,老年患者的残疾和癌症相关症状恶化。我们得出的结论是,CAR-T 细胞治疗的结果在老年、老年和年轻患者之间是可比的,这表明年龄本身不应该排除 CAR-T 细胞的应用。需要更长的康复治疗来改善残疾和长期症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6b8/9052918/b862c7762980/1071111.fig1.jpg

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