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:Pretreatment TyG-BMI predicts CD19 CAR-T persistence and prognosis in diffuse large B-cell lymphoma.
TyG-BMI 是 DLBCL 的独立预后因素,可细化基于 IPI 的分层,并且输注前 TyG-BMI 升高与 CAR-T 细胞持久性减弱和较差结局相关。这一易于获取的代谢指标可能有助于 DLBCL 的风险评估和治疗规划。
尽管CD19 CAR-T细胞疗法改善了复发或难治性弥漫性大B细胞淋巴瘤(DLBCL)的结局,但疗效反应存在差异,且缺乏预测性生物标志物。甘油三酯葡萄糖-体重指数(TyG-BMI)——胰岛素抵抗的替代指标——已在实体瘤中显示出预后价值,但其与DLBCL及CAR-T疗效的相关性仍不清楚。
我们回顾性分析了204例接受含利妥昔单抗方案治疗的新诊断DLBCL患者,按TyG-BMI中位数进行分层。通过Kaplan-Meier和多因素Cox回归评估预后相关性,并构建了列线图。在一项探索性亚组分析中,评估了20例接受CD19 CAR-T治疗的患者。CAR-T细胞持久性通过输注后一周的流式细胞术检测,并与输注前TyG-BMI通过Pearson分析进行相关性分析。CRS和ICANS按ASTCT标准分级。按输注前TyG-BMI中位数分层的Kaplan-Meier分析比较了CAR-T后生存期。
高 TyG-BMI 与较差的 PFS(HR,2.146;95% CI,1.092-4.214;P = 0.027)和 OS(HR,2.531;95% CI,1.084-5.913;P = 0.032)独立相关,并进一步在 IPI 风险组内和不同疾病分期之间进行风险分层。一个纳入 TyG-BMI、IPI 和骨髓受累的列线图预测了 1 年、3 年和 5 年 OS(AUC:0.886、0.799、0.772)。在 CAR-T 亚队列(n = 20)中,输注前 TyG-BMI 升高与输注后一周 CAR-T 细胞持续性显著负相关(r = -0.570,P = 0.009)。与低 TyG-BMI 组相比,输注前高 TyG-BMI 患者对 CAR-T 治疗的反应较差,中位 PFS(5.0 个月 vs. 19.5 个月)和 OS(39.0 个月 vs. 81.0 个月)更短。
BACKGROUND: Although CD19 CAR-T cell therapy has improved outcomes in relapsed or refractory diffuse large B-cell lymphoma (DLBCL), responses are variable and predictive biomarkers are lacking. The triglyceride glucose-body mass index (TyG-BMI)-a surrogate of insulin resistance-has shown prognostic value in solid tumors, but its relevance to DLBCL and CAR-T efficacy remains unknown. METHODS: We retrospectively analyzed 204 newly diagnosed DLBCL patients treated with rituximab-containing regimens, stratified by median TyG-BMI. Prognostic associations were assessed by Kaplan-Meier and multivariate Cox regression, and a nomogram was constructed. In an exploratory sub-analysis, 20 patients who received CD19 CAR-T therapy were assessed. CAR-T cell persistence was measured by flow cytometry one week post-infusion and correlated with pre-infusion TyG-BMI by Pearson analysis. CRS and ICANS were graded per ASTCT criteria. Post-CAR-T survival was compared by Kaplan-Meier analysis stratified by median pre-infusion TyG-BMI. RESULTS: High TyG-BMI was independently associated with poorer PFS (HR, 2.146; 95% CI, 1.092-4.214; P = 0.027) and OS (HR, 2.531; 95% CI, 1.084-5.913; P = 0.032), and further stratified risk within IPI risk groups and across disease stages. A nomogram incorporating TyG-BMI, IPI, and bone marrow involvement predicted 1-, 3-, and 5-year OS (AUC: 0.886, 0.799, 0.772). In the CAR-T subcohort ( n = 20), elevated pre-infusion TyG-BMI was significantly inversely correlated with CAR-T cell persistence at one week post-infusion ( r = -0.570, P = 0.009). Patients with high pre-infusion TyG-BMI experienced inferior responses to CAR-T therapy, with shorter median PFS (5.0 vs. 19.5 months) and OS (39.0 vs. 81.0 months) compared with the low TyG-BMI group. CONCLUSION: TyG-BMI is an independent prognostic factor in DLBCL that refines IPI-based stratification, and elevated pre-infusion TyG-BMI is associated with attenuated CAR-T cell persistence and inferior outcomes. This readily available metabolic index may aid risk assessment and treatment planning in DLBCL.
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