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:Serum sCD25/ferritin ratio combined with MCP-1 is a valid predictor for identifying LAHS with HLH as the first manifestation.
Serum sCD25/ferritin ratio combined with MCP-1 is a valid predictor for identifying LAHS with HLH as the first manifestation.
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我们的研究揭示,血清 sCD25/铁蛋白比值联合 MCP-1 是识别以 HLH 为首发表现的 LAHS 的有效预测指标,并可能有助于预测该淋巴瘤是起源于 B 细胞还是 T/NK 细胞。
淋巴瘤相关噬血细胞综合征(LAHS)是一组进展迅速、死亡率高的恶性疾病。本研究评估血清可溶性CD25/铁蛋白比值及细胞因子辅助诊断LAHS的价值。
回顾分析82例以噬血细胞性淋巴组织细胞增多症(HLH)为首发表现的LAHS患者,依据淋巴瘤病理分为B-LAHS和T/NK-LAHS组进行比较;另按接受DEP/L-DEP诱导治疗两周后的疗效分为应答和未应答组,比较潜在指标。
B-LAHS和T/NK-LAHS组血清sCD25/铁蛋白比值及MCP-1水平显著不同(p分别为0.001和0.022)。比值>7.8倾向提示B-LAHS(AUC 0.71,95% CI 0.596–0.823);与MCP-1联合后预测效能更高(AUC 0.81,95% CI 0.699–0.922)。应答和未应答组的该比值亦显著不同(p=0.002),最佳截点为11.48;高于该值倾向提示LAHS对诱导治疗应答。
血清sCD25/铁蛋白比值联合MCP-1可帮助识别以HLH为首发表现的LAHS,并辅助判断B细胞或T/NK细胞来源。该比值还可预测诱导治疗早期反应。
Lymphoma-associated haemophagocytic syndrome (LAHS) is a group of malignant diseases with rapid progression and a high mortality rate. Our study aimed to discover the significance of serum sCD25/ferritin ratio as well as cytokines in assisting the diagnosis of LAHS.
We retrospectively analyzed the clinical data of 82 patients with LAHS with hemophagocytic lymphohistiocytosis (HLH) as the first manifestation and divided them into B-LAHS group and T/NK-LAHS group according to lymphoma pathological diagnosis for comparison. And patients with LAHS were divided into responding group, non-responding group according to the assessment of efficacy after receiving DEP/L-DEP induction therapy for 2 weeks to compare possible valuable indicators.
Serum sCD25/ferritin ratio and MCP-1 levels were significantly different between B-LAHS and T/NK-LAHS groups (P = 0.001, P = 0.022). An sCD25/ferritin ratio > 7.8 tended to suggest a diagnosis of B-LAHS (AUC = 0.71, 95% CI: 0.596-0.823), and the sCD25/ferritin ratio had better predictive value when combined with MCP-1 (AUC = 0.81, 95% CI: 0.699-0.922). The sCD25/ferritin ratio was also significantly different between the two groups responding or not responding to induction therapy (P = 0.002), yielding an optimal cutoff value of 11.48. An sCD25/ferritin ratio > 11.48 tended to suggest that the patient's LAHS was responsive to induction therapy.
Our study reveals that serum sCD25/ferritin ratio combined with MCP-1 is a valid predictor for identifying LAHS with HLH as the first manifestation and may assist in predicting whether the lymphoma is of B-cell or T/NK-cell origin. The sCD25/ferritin ratio can also be used to predict the early response of LAHS after induction therapy.
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