CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Serum ferritin as a prognostic biomarker in CAR-T therapy for multiple myeloma: A meta-analysis.
Serum ferritin as a prognostic biomarker in CAR-T therapy for multiple myeloma: A meta-analysis.
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血清铁蛋白是全身炎症和铁代谢指标,与复发/难治性多发性骨髓瘤(R/R MM)患者结局有关,但其在接受嵌合抗原受体修饰T细胞(CAR-T)治疗患者中的预后意义尚不明确。本荟萃分析旨在评估CAR-T 输注前血清铁蛋白水平与生存结局的关系。研究系统检索PubMed、Embase和Web of Science,纳入报告按血清铁蛋白水平分组的无进展生存期(PFS)和/或总生存期(OS)的研究,采用随机效应模型合并风险比(HR)及95%置信区间(CI)。共纳入8项回顾性队列研究、1077例患者。输注前血清铁蛋白水平较高与较差PFS(HR 2.15,95% CI 1.74–2.66,P<.001)和OS(HR 2.86,95% CI 2.20–3.72,P<.001)显著相关,异质性较低(PFS的I²=9%,OS为0%)。逐项排除研究的敏感性分析证实结果稳健。亚组分析显示,不同CAR-T 产品来源(商业或学术机构)、铁蛋白截断值及随访时间的结果一致(亚组差异P值均>.05)。结论:CAR-T 输注前血清铁蛋白升高预示R/R MM患者生存结局较差,提示铁蛋白具有潜在预后价值,并可能有助于优化CAR-T 治疗的患者选择和管理策略。
Serum ferritin, a marker of systemic inflammation and iron metabolism, has been implicated in the outcomes of patients with relapsed/refractory multiple myeloma (R/R MM).
However, its prognostic significance in R/R MM patients undergoing chimeric antigen receptor-modified T-cell (CAR-T) therapy remains unclear. This meta-analysis aimed to evaluate the association between pre-infusion serum ferritin levels and survival outcomes in R/R MM patients treated with CAR-T therapy.
We systematically searched PubMed, Embase, and Web of Science for relevant studies. Studies reporting progression-free survival (PFS) and/or overall survival (OS) based on serum ferritin levels were included. Hazard ratios (HRs) with 95% confidence intervals (CIs) were pooled using a random-effects model. Eight retrospective cohort studies, encompassing 1077 patients, met the inclusion criteria. High pre-infusion serum ferritin levels were significantly associated with worse PFS (HR: 2.
15, 95% CI: 1. 74-2. 66, P < 0. 001) and OS (HR: 2. 86, 95% CI: 2. 20-3. 72, P < 0. 001), with mild heterogeneity (I = 9% for PFS and 0% for OS). Sensitivity analyses, conducted by excluding one study at a time, confirmed the robustness of these findings. Subgroup analyses showed consistent results across different CAR-T product sources (commercial vs academic), ferritin cutoffs, and follow-up durations (P for subgroup differences all >0. 05).
In conclusion, elevated serum ferritin levels before CAR-T infusion predict poorer survival outcomes in R/R MM patients.
These findings highlight the potential prognostic value of ferritin and its role in optimizing patient selection and management strategies in CAR-T therapy.
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