决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Anti-metabolic agent pegaspargase plus PD-1 antibody sintilimab for first-line treatment in advanced natural killer T cell lymphoma.
无化疗方案培门冬酶联合信迪利单抗在新诊断的晚期NKTCL中有效且安全。
自然杀伤T细胞淋巴瘤(NKTCL)具有高度侵袭性,晚期患者对强化化疗反应不佳。为探索初诊晚期NKTCL有效且安全的治疗方法,我们开展了一项抗代谢药物培门冬酶联合PD-1抗体信迪利单抗的II期研究(NCT04096690)。共入组22例患者,中位年龄51岁(范围24-74岁),接受诱导治疗:第1天肌肉注射培门冬酶2500 IU/m²,第2天静脉注射信迪利单抗200 mg,21天为1周期,共6周期;随后维持治疗:信迪利单抗200 mg,21天为1周期,共28周期。诱导治疗后的完全缓解率和总缓解率分别为59%(95%CI,43-79%)和68%(95%CI,47-84%)。中位随访30个月,2年无进展生存率和总生存率分别为68%(95%CI,45-83%)和86%(95%CI,63-95%)。最常见的3/4级不良事件为中性粒细胞减少(32%,n=7)和低纤维蛋白原血症(18%,n=4),均可管理,未导致治疗中断。PD-L1肿瘤比例评分、外周血高密度脂蛋白胆固醇和载脂蛋白A-I与良好缓解相关,而TIL(肿瘤浸润淋巴细胞)上的PD-1和外周Treg细胞与培门冬酶联合信迪利单抗治疗反应不佳相关。总之,无化疗方案培门冬酶联合信迪利单抗在初诊晚期NKTCL中有效且安全。脂质谱失调和免疫抑制特征导致治疗耐药,为NKTCL中双重靶向脂肪酸代谢和CTLA-4提供了替代治疗策略。
Natural killer T cell lymphoma (NKTCL) is highly aggressive, with advanced stage patients poorly responding to intensive chemotherapy. To explore effective and safe treatment for newly diagnosed advanced stage NKTCL, we conducted a phase II study of anti-metabolic agent pegaspargase plus PD-1 antibody sintilimab (NCT04096690). Twenty-two patients with a median age of 51 years (range, 24-74) were enrolled and treated with induction treatment of pegaspargase 2500 IU/m 2 intramuscularly on day 1 and sintilimab 200 mg intravenously on day 2 for 6 cycles of 21 days, followed by maintenance treatment of sintilimab 200 mg for 28 cycles of 21 days. The complete response and overall response rate after induction treatment were 59% (95%CI, 43-79%) and 68% (95%CI, 47-84%), respectively. With a median follow-up of 30 months, the 2 year progression-free and overall survival rates were 68% (95%CI, 45-83%) and 86% (95%CI, 63-95%), respectively. The most frequently grade 3/4 adverse events were neutropenia (32%, n = 7) and hypofibrinogenemia (18%, n = 4), which were manageable and led to no discontinuation of treatment. Tumor proportion score of PD-L1, peripheral blood high-density lipoprotein cholesterol, and apolipoprotein A-I correlated with good response, while PD-1 on tumor infiltrating lymphocytes and peripheral Treg cells with poor response to pegaspargase plus sintilimab treatment. In conclusion, the chemo-free regimen pegaspargase plus sintilimab was effective and safe in newly diagnosed, advanced stage NKTCL. Dysregulated lipid profile and immunosuppressive signature contributed to treatment resistance, providing an alternative therapeutic approach dual targeting fatty acid metabolism and CTLA-4 in NKTCL.
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