不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Clinical significance of high-density lipoprotein cholesterol and its dynamic change in patients with lymphoma-associated hemophagocytic lymphohistiocytosis.
Clinical significance of high-density lipoprotein cholesterol and its dynamic change in patients with lymphoma-associated hemophagocytic lymphohistiocytosis.
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HDL-c 及其动态变化是预测 LA-HLH 患者结局的临床可行标志物。
噬血细胞性淋巴组织细胞增多症(HLH)是一种以失控炎症为特征的致命性疾病。成人HLH最常见的基础病因是淋巴瘤。淋巴瘤相关HLH(LA-HLH)患者的脂质谱常发生失调,但其临床意义仍有待确定。
评估基线脂质谱及高密度脂蛋白胆固醇(HDL-c)动态变化对成人LA-HLH患者的预后价值。 设计:多中心回顾性队列研究。
分析2015至2023年27家医疗中心的277例成人LA-HLH患者。测量基线脂质水平和治疗后HDL-c水平。采用X-tile软件确定最佳预后截点。使用Kaplan-Meier法和Cox回归进行生存分析。
诊断时93.9%(260/277)的患者HDL-c偏低(<1.03 mmol/L)。基线HDL-c<0.48 mmol/L与总生存期(OS)降低(风险比HR=1.51,95%置信区间CI:1.10–2.09,p=0.012)和60天生存率降低(HR=1.66,95% CI:1.10–2.49,p=0.015)独立相关。T/NK细胞恶性肿瘤患者治疗后/基线HDL-c比值显著低于B细胞非霍奇金淋巴瘤患者。比值较低(<1.71)与生存率显著降低相关。基线HDL-c低(<0.48 mmol/L)且比值低(<1.71)的患者构成高危组,结局最差(60天生存率:46.7% vs. 81.8%,p=0.004;中位OS:52天 vs. 尚未达到,p<0.001)。
HDL-c及其动态变化是预测LA-HLH患者结局的临床可行指标。 淋巴瘤相关严重免疫性疾病中,“好胆固醇”水平可预测生存。噬血细胞性淋巴组织细胞增多症(HLH)是一种危及生命的疾病,患者免疫系统危险性过度活化并导致炎症失控。成人HLH最常由淋巴瘤诱发。我们发现,93.9%(260/277)的成人淋巴瘤相关HLH(LA-HLH)患者诊断时“好胆固醇”(HDL-c)水平极低。HDL-c较低的患者总生存期显著缩短,60天生存率也较低;而“坏胆固醇”(LDL-c)不影响生存。治疗后,81.2%的患者HDL-c水平上升;HDL-c升幅较小的患者生存结局也较差。结合基线HDL-c水平和治疗后HDL-c恢复程度,可将患者划分为不同风险组;基线水平低且治疗后升幅很小的患者生存最差。这些发现表明,测量HDL-c并追踪其治疗期间的变化,是一种简单且成本效益高的LA-HLH生存预测方法,可帮助医生及早识别高危患者并调整治疗。
Hemophagocytic lymphohistiocytosis (HLH) is a fatal disorder characterized by uncontrolled inflammation. In adults, lymphoma is the most common underlying cause. The lipid profile is frequently dysregulated in lymphoma-associated HLH (LA-HLH), and the clinical significance remains to be determined.
This study aimed to evaluate the prognostic value of baseline lipid profiles and the dynamic changes in high-density lipoprotein cholesterol (HDL-c) in adult patients with LA-HLH. DESIGN: A multicenter, retrospective cohort study.
We analyzed 277 adult patients with LA-HLH from 27 medical centers (2015-2023). Baseline lipid levels and post-treatment HDL-c levels were measured. The optimal prognostic cutoff was determined using X-tile software. Survival analysis was performed using Kaplan-Meier and Cox regression methods.
Low HDL-c (<1.03 mmol/L) was observed in 93.9% (260/277) patients at diagnosis. A baseline HDL-c <0.48 mmol/L was independently associated with reduced overall survival (OS; hazard ratio, HR = 1.51, 95% confidence interval, CI: 1.10-2.09, p = 0.012) and 60-day survival (HR = 1.66, 95% CI: 1.10-2.49, p = 0.015). The post-treatment/baseline HDL-c ratio was significantly lower in patients with T/NK-cell malignancies than in those with B-cell non-Hodgkin lymphoma. A lower ratio (<1.71) was significantly associated with reduced survival. Patients with both low baseline HDL-c (<0.48 mmol/L) and low ratio (<1.71) constituted a high-risk group with the worst outcomes (60-day survival: 46.7% vs 81.8%, p = 0.004; median OS: 52 days vs not reached, p < 0.001).
HDL-c and its dynamic changes are clinically feasible markers for predicting outcomes in patients with LA-HLH. Good cholesterol levels predict survival in lymphoma-linked severe immune disorders Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening condition where the immune system becomes dangerously overactive, leading to uncontrolled inflammation. In adults, this is most commonly triggered by lymphoma. We found that 93.9% (260/277) of adult patients with lymphoma-associated HLH (LA-HLH) had very low levels of good cholesterol (HDL-c) at diagnosis. Patients with lower HDL-c had significantly shorter overall survival and lower 60-day survival rates, while bad cholesterol (LDL-c) did not impact survival. After treatment, 81.2% of patients saw their HDL-c levels increase. Those with smaller post-treatment HDL-c increases also had worse survival outcomes. By combining baseline HDL-c levels and the degree of HDL-c recovery after treatment, patients were divided into risk groups: those with both low starting HDL-c and minimal post-treatment increases faced the poorest survival. These findings show that measuring HDL-c levels and tracking their changes during treatment offer a simple, cost-effective way to predict survival in LA-HLH, helping doctors identify high-risk patients early and adjust therapies accordingly.
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