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lisocabtagene maraleucel 治疗日本复发/难治性大 B 细胞淋巴瘤的真实世界疗效与安全性

英文原题:Real-world effectiveness and safety of lisocabtagene maraleucel for relapsed/refractory large B cell lymphoma in Japan.

查看英文原题

Real-world effectiveness and safety of lisocabtagene maraleucel for relapsed/refractory large B cell lymphoma in Japan.

PubMed 2026/01/08(内容时间) Int J Clin Oncol Q3 · IF 3(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

商业化 liso-cel 在日本复发/难治性大 B 细胞淋巴瘤患者中显示出高缓解率和良好的安全性。

中文摘要

抗CD19CAR-T 细胞疗法lisocabtagene maraleucel(liso-cel)已显示治疗复发/难治性(R/R)大B细胞淋巴瘤(LBCL)的疗效,但美国以外商业使用的真实世界数据有限。

为评估liso-cel在日本商业使用中的安全性和有效性,对2021年11月至2024年11月在本中心接受治疗的R/R LBCL患者开展单中心回顾性研究。

56例患者接受liso-cel输注,年龄中位数66.5岁,55.4%为原发难治性疾病。14例(25.0%)在二线接受liso-cel,42例(75.0%)在三线或以后接受。最佳总体缓解率为80.4%,完全缓解率为78.6%。中位随访12.3个月时,1年PFS率和OS率分别为69.5%和86.4%。弥漫大B细胞淋巴瘤非特指型、原发性纵隔大B细胞淋巴瘤(PMBCL)和高级别B细胞淋巴瘤(HGBCL)的1年PFS率分别为68.5%、100%和30%。各有1例患者发生3级细胞因子释放综合征和免疫效应细胞相关神经毒性综合征。多变量分析确定HGBCL亚型和输注前代谢肿瘤体积较高是PFS的不良独立因素。

商业使用liso-cel治疗日本R/R LBCL患者显示较高缓解率和良好安全性。PMBCL患者结局极佳,而HGBCL患者预后较差,提示仍需进一步开发治疗策略。

展开英文摘要原文

Lisocabtagene maraleucel (liso-cel), an anti-CD19 CAR T cell therapy, has demonstrated efficacy in relapsed/refractory (R/R) large B cell lymphoma (LBCL). However, real-world data from commercial settings outside the United States remain limited.

To evaluate the safety and effectiveness of commercial-use liso-cel in Japan, we conducted a single-center retrospective study of patients with R/R LBCL who received commercial-use liso-cel at our institution between November 2021 and November 2024.

56 patients received liso-cel infusion. The median age was 66.5 years, and 55.4% had primary refractory disease. Liso-cel was administered as second-line therapy in 14 patients (25.0%) and as third-line or later therapy in 42 patients (75.0%). The best overall response rate was 80.4%, with a complete response rate of 78.6%. At a median follow-up of 12.3 months, 1 year progression-free survival (PFS) and overall survival rates were 69.5% and 86.4%, respectively. The 1 year PFS rates were 68.5% for diffuse large B cell lymphoma not otherwise specified, 100% for primary mediastinal large B cell lymphoma (PMBCL), and 30% for high-grade B cell lymphoma (HGBCL). Grade 3 cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome were observed in one patient each. Multivariate analysis identified HGBCL subtype and higher pre-infusion metabolic tumor volume as independent adverse factors for PFS.

Commercial-use liso-cel demonstrated high response rates and favorable safety in Japanese patients with R/R LBCL. Patients with PMBCL had excellent outcomes, whereas those with HGBCL showed poorer prognosis, indicating a need for further therapeutic strategies.

论文信息

作者
Ochi T、Makita S、Hiratsuka A、Nishiyama R、Ito K、Maeshima AM、Takeda W、Iwaki N
第一作者单位
Department of Hematology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-Ku, Tokyo, 104-0045, Japan.Japan
通讯作者单位
Department of Hematology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-Ku, Tokyo, 104-0045, Japan. smakita@ncc.go.jp.Japan
期刊
International journal of clinical oncology2026 Mar
原文标识
PubMed 41504990 · DOI 10.1007/s10147-025-02946-4