Division of Laboratory and Transfusion Medicine, Hokkaido University Hospital, Sapporo, Japan.
Department of Hematology and Oncology, Kyoto University Hospital, Kyoto, Japan.
Int J Clin Oncol. 2023 Jun;28(6):816-826. doi: 10.1007/s10147-023-02334-w. Epub 2023 Apr 18.
Tisagenlecleucel, an autologous CD19-directed T-cell immunotherapy, can induce a durable response in adult patients with relapsed/refractory (r/r) B-cell lymphoma.
To elucidate the outcome of chimeric antigen receptor (CAR) T-cell therapy in Japanese, we retrospectively analyzed the outcomes of 89 patients who received tisagenlecleucel for r/r diffuse large B-cell lymphoma (n = 71) or transformed follicular lymphoma (n = 18).
With a median follow-up of 6.6-months, 65 (73.0%) patients achieved a clinical response. The overall survival (OS) and event-free survival (EFS) rates at 12 months were 67.0% and 46.3%, respectively. Overall, 80 patients (89.9%) had cytokine release syndrome (CRS), and 6 patients (6.7%) had a grade ≥ 3 event. ICANS occurred in 5 patients (5.6%); only 1 patient had grade 4 ICANS. Representative infectious events of any grade were cytomegalovirus viremia, bacteremia and sepsis. The most common other adverse events were ALT elevation, AST elevation, diarrhea, edema, and creatinine elevation. No treatment-related mortality was observed. A Sub-analysis showed that a high metabolic tumor volume (MTV; ≥ 80 ml) and stable disease /progressive disease before tisagenlecleucel infusion were both significantly associated with a poor EFS and OS in a multivariate analysis (P < 0.05). Notably, the combination of these 2 factors efficiently stratified the prognosis of these patients (HR 6.87 [95% CI 2.4-19.65; P < 0.05] into a high-risk group).
We report the first real-world data on tisagenlecleucel for r/r B-cell lymphoma in Japan. Tisagenlecleucel is feasible and effective, even in late line treatment. In addition, our results support a new algorithm for predicting the outcomes of tisagenlecleucel.
Tisagenlecleucel 是一种自体 CD19 定向 T 细胞免疫疗法,可在复发/难治性(r/r)B 细胞淋巴瘤的成年患者中诱导持久缓解。
为了阐明嵌合抗原受体(CAR)T 细胞疗法在日本的结果,我们回顾性分析了 89 例接受 tisagenlecleucel 治疗 r/r 弥漫性大 B 细胞淋巴瘤(n=71)或转化滤泡性淋巴瘤(n=18)患者的结果。
中位随访 6.6 个月时,65(73.0%)例患者达到临床缓解。12 个月时的总生存率(OS)和无事件生存率(EFS)分别为 67.0%和 46.3%。总体而言,80 例(89.9%)患者发生细胞因子释放综合征(CRS),6 例(6.7%)患者发生≥3 级事件。发生免疫效应细胞相关神经毒性综合征(ICANS)的患者有 5 例(5.6%);仅有 1 例患者发生 4 级 ICANS。任何级别均有代表性的感染事件为巨细胞病毒血症、菌血症和败血症。最常见的其他不良事件为丙氨酸氨基转移酶升高、天冬氨酸氨基转移酶升高、腹泻、水肿和肌酐升高。未观察到治疗相关死亡。亚分析显示,高代谢肿瘤体积(MTV;≥80ml)和 tisagenlecleucel 输注前疾病稳定/进展在多变量分析中均与较差的 EFS 和 OS 显著相关(P<0.05)。值得注意的是,这 2 个因素的组合有效地对这些患者的预后进行了分层(HR 6.87 [95%CI 2.4-19.65;P<0.05),分为高危组)。
我们报告了日本首例 tisagenlecleucel 治疗 r/r B 细胞淋巴瘤的真实世界数据。Tisagenlecleucel 是可行且有效的,即使在晚期治疗中也是如此。此外,我们的结果支持一种新的预测 tisagenlecleucel 治疗结果的算法。