Centre Hospitalier Universitaire de Lille, Groupe de Recherche sur les formes Injectables et les Technologies Associées, Lille, France.
Stanford University School of Medicine, Stanford, CA, USA.
Nat Med. 2024 Aug;30(8):2199-2207. doi: 10.1038/s41591-024-02986-9. Epub 2024 Jun 3.
An unmet need exists for patients with relapsed/refractory (R/R) follicular lymphoma (FL) and high-risk disease features, such as progression of disease within 24 months (POD24) from first-line immunochemotherapy or disease refractory to both CD20-targeting agent and alkylator (double refractory), due to no established standard of care and poor outcomes. Chimeric antigen receptor (CAR) T cell therapy is an option in R/R FL after two or more lines of prior systemic therapy, but there is no consensus on its optimal timing in the disease course of FL, and there are no data in second-line (2L) treatment of patients with high-risk features. Lisocabtagene maraleucel (liso-cel) is an autologous, CD19-directed, 4-1BB CAR T cell product. The phase 2 TRANSCEND FL study evaluated liso-cel in patients with R/R FL, including 2L patients who all had POD24 from diagnosis after treatment with anti-CD20 antibody and alkylator ≤6 months of FL diagnosis and/or met modified Groupe d'Etude des Lymphomes Folliculaires criteria. Primary/key secondary endpoints were independent review committee-assessed overall response rate (ORR)/complete response (CR) rate. At data cutoff, 130 patients had received liso-cel (median follow-up, 18.9 months). Primary/key secondary endpoints were met. In third-line or later FL (n = 101), ORR was 97% (95% confidence interval (CI): 91.6‒99.4), and CR rate was 94% (95% CI: 87.5‒97.8). In 2L FL (n = 23), ORR was 96% (95% CI: 78.1‒99.9); all responders achieved CR. Cytokine release syndrome occurred in 58% of patients (grade ≥3, 1%); neurological events occurred in 15% of patients (grade ≥3, 2%). Liso-cel demonstrated efficacy and safety in patients with R/R FL, including high-risk 2L FL. ClinicalTrials.gov identifier: NCT04245839 .
对于复发/难治性(R/R)滤泡性淋巴瘤(FL)患者和具有高危疾病特征的患者,例如一线免疫化疗后 24 个月内(POD24)疾病进展或对 CD20 靶向药物和烷化剂均耐药(双重耐药),存在未满足的需求,因为尚无既定的治疗标准且预后较差。嵌合抗原受体(CAR)T 细胞疗法是 R/R FL 患者在二线或以上系统治疗后的选择,但在 FL 病程中其最佳时机尚无共识,并且在具有高危特征的二线(2L)治疗患者中尚无数据。Lisocabtagene maraleucel(liso-cel)是一种自体、CD19 定向、4-1BB CAR T 细胞产品。2 期 TRANSCEND FL 研究评估了 liso-cel 在 R/R FL 患者中的应用,包括所有在诊断后经抗 CD20 抗体和烷化剂治疗且 FL 诊断后<6 个月时发生 POD24 和/或符合改良的 Groupe d'Etude des Lymphomes Folliculaires 标准的 2L 患者。主要/关键次要终点是独立审查委员会评估的总缓解率(ORR)/完全缓解(CR)率。在数据截止时,130 例患者接受了 liso-cel 治疗(中位随访时间,18.9 个月)。主要/关键次要终点均达到。在三线或以上 FL(n=101)中,ORR 为 97%(95%置信区间[CI]:91.6-99.4),CR 率为 94%(95% CI:87.5-97.8)。在 2L FL(n=23)中,ORR 为 96%(95% CI:78.1-99.9);所有应答者均达到 CR。58%的患者发生细胞因子释放综合征(≥3 级,1%);15%的患者发生神经事件(≥3 级,2%)。Liso-cel 在 R/R FL 患者中显示出疗效和安全性,包括高危 2L FL。ClinicalTrials.gov 标识符:NCT04245839。