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:Increased visceral fat distribution and body composition impact cytokine release syndrome onset and severity after CD19 chimeric antigen receptor T-cell therapy in advanced B-cell malignancies.
Increased visceral fat distribution and body composition impact cytokine release syndrome onset and severity after CD19 chimeric antigen receptor T-cell therapy in advanced B-cell malignancies.
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CAR-T 细胞治疗与一种独特的毒性特征相关,包括细胞因子释放综合征(CRS)和免疫效应细胞相关神经毒性综合征(ICANS)。CRS的特征是释放促炎细胞因子如白细胞介素6(IL-6),并与CAR-T 扩增及旁观者细胞如单核细胞/巨噬细胞密切相关。在其他高炎症状态下,肥胖促进炎症级联反应,并作为疾病严重程度的风险因素。
我们旨在研究64例接受CD19靶向CAR-T 治疗复发/难治性B细胞恶性肿瘤患者的人体测量学和身体成分(BC)指标对CAR-T 相关免疫毒性的影响。2级CRS患者的中位体重指数(BMI)、腰围、腰高比(WtHR)和内脏脂肪组织(VAT)显著更高。这些参数也与CRS更早发生相关。其他脂肪沉积和肌肉质量在0-1级CRS与2级CRS患者之间无差异。
此外,BC参数未影响ICANS的严重程度或发生时间。在纳入已知免疫毒性风险因素的多变量二元逻辑回归中,BMI、腰围、WtHR和VAT增加了2级CRS的概率。采用受试者工作特征分析确定这些参数的最佳判别阈值。高于这些阈值的患者显示出显著升高的IL-6峰值水平。
我们的数据表明,身体成分增加,尤其是VAT增加,代表了严重和早期CRS的额外风险因素。这些发现对CD19 CAR-T 前的风险分层具有意义,并可能被整合到已有的风险模型中。
Chimeric antigen receptor T-cell (CAR-T) therapy is associated with a distinct toxicity profile that includes cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS). CRS is characterized by the release of pro-inflammatory cytokines such as interleukin 6 (IL-6) and is closely linked to CAR-T expansion and bystander cells like monocytes/macrophages. In other hyperinflammatory states, obesity contributes to inflammatory cascades and acts as a risk factor for disease severity.
We aimed to study the influence of anthropometric and body composition (BC) measurements on CAR-T-related immunotoxicity in 64 patients receiving CD19-directed CAR-T for relapsed/refractory Bcell malignancies.
Patients with grade 2 CRS presented with a significantly higher median body mass index (BMI), waist circumference, waist-to-height ratio (WtHR) and visceral adipose tissue (VAT). These parameters were also found to be associated with an earlier CRS onset. Other adipose deposits and muscle mass did not differ between patients with grade 0-1 CRS versus grade 2 CRS.
Moreover, BC parameters did not influence ICANS severity or onset. In a multivariate binary logistic regression incorporating known risk factors of immunotoxicity, the factors BMI, waist circumference, WtHR and VAT increased the probability of grade 2 CRS. Receiver operating characteristic analyses were utilized to determine optimal discriminatory thresholds for these parameters. Patients above these thresholds displayed markedly increased peak IL-6 levels.
Our data imply that increased body composition and VAT in particular represent an additional risk factor for severe and early CRS.
These findings carry implications for risk-stratification prior to CD19 CAR-T and may be integrated into established risk models.
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