Berning Philipp, Shumilov Evgenii, Maulhardt Markus, Boyadzhiev Hristo, Kerkhoff Andrea, Call Simon, Reicherts Christian, Saidy Anna O, Aydilek Enver, Hoffmann Michèle, Novak Urban, Daskalakis Michael, Schmitz Norbert, Stelljes Matthias, Wulf Gerald, Bacher Ulrike, Lenz Georg, Pabst Thomas
Department of Hematology and Oncology University Hospital Muenster Muenster Germany.
Department of Hematology and Medical Oncology University Hospital Göttingen Göttingen Germany.
Hemasphere. 2024 Mar 20;8(3):e54. doi: 10.1002/hem3.54. eCollection 2024 Mar.
CD19-directed chimeric antigen receptor (CAR)-T cell therapy has become a standard treatment for relapsed/refractory diffuse large B-cell lymphoma (r/r DLBCL). While the benefits of CAR-T cell treatment are clear in the general patient population, there remains a relative scarcity of real-world evidence regarding its efficacy and toxicity in patients (pts) aged ≥70 years with DLBCL. We conducted a multicenter retrospective analysis including 172 r/r DLBCL pts with CAR-T cell treatment, axicabtagene ciloleucel or tisagenlecleucel, between 2019 and 2023 at three tertiary centers. Pts were grouped by age at CAR-T infusion (<70 vs. ≥70 years). Subsequently, descriptive and survival analyses, including propensity score matching, were performed to compare outcomes between both age groups. We identified 109 pts aged <70 and 63 pts aged ≥70 years. Overall response rates for both age groups were comparable (77.7% vs. 78.3%; = 0.63). With a median follow-up of 8.3 months, median progression-free survival was 10.2 months (95% confidence interval [CI]: 6.5-21.8) and 11.1 months (95% CI: 4.9-NR) ( = 0.93) for both cohorts. Median overall survival reached 21.8 months (95% CI: 11.8-NR) and 34.4 months (95% CI: 10.1-NR) ( = 0.97), respectively. No significant differences in the incidence of cytokine release syndrome ( = 0.53) or grade ≥3 neurotoxicity ( = 0.56) were observed. Relapse and nonrelapse mortality were not significantly different between both groups. Our findings provide additional support that CAR-T cell therapy is feasible and effective in patients with r/r DLBCL aged 70 years or older, demonstrating outcomes comparable to those observed in younger patients. CAR-T cell therapy should be not withheld for elderly patients with r/r DLBCL.
靶向CD19的嵌合抗原受体(CAR)-T细胞疗法已成为复发/难治性弥漫性大B细胞淋巴瘤(r/r DLBCL)的标准治疗方法。虽然CAR-T细胞治疗在一般患者群体中的益处是显而易见的,但对于年龄≥70岁的DLBCL患者,其疗效和毒性方面的真实世界证据仍然相对匮乏。我们进行了一项多中心回顾性分析,纳入了2019年至2023年期间在三个三级中心接受CAR-T细胞治疗(阿基仑赛或替雷利珠单抗)的172例r/r DLBCL患者。患者按CAR-T输注时的年龄分组(<70岁与≥70岁)。随后,进行了描述性和生存分析,包括倾向评分匹配,以比较两个年龄组的结果。我们确定了109例年龄<70岁的患者和63例年龄≥70岁的患者。两个年龄组的总体缓解率相当(77.7%对78.3%;P = 0.63)。中位随访8.3个月,两个队列的中位无进展生存期分别为10.2个月(95%置信区间[CI]:6.5 - 21.8)和11.1个月(95% CI:4.9 - NR)(P = 0.93)。中位总生存期分别达到21.8个月(95% CI:11.8 - NR)和34.4个月(95% CI:10.1 - NR)(P = 0.97)。细胞因子释放综合征的发生率(P = 0.53)或≥3级神经毒性的发生率(P = 0.56)均未观察到显著差异。两组之间的复发和非复发死亡率也没有显著差异。我们的研究结果进一步支持了CAR-T细胞疗法在70岁及以上的r/r DLBCL患者中是可行且有效的,其结果与年轻患者相当。对于老年r/r DLBCL患者不应拒绝给予CAR-T细胞治疗。