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淋巴瘤相关噬血细胞综合征:一项 86 例患者的回顾性单中心研究

英文原题:Lymphoma-associated hemophagocytic syndrome: a retrospective, single-center study of 86 patients.

查看英文原题

Lymphoma-associated hemophagocytic syndrome: a retrospective, single-center study of 86 patients.

PubMed 2024/07/30(内容时间) Ann Hematol Q3 · IF 2.3(JCR 2025)

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中文摘要

本研究旨在真实临床环境中探讨淋巴瘤相关噬血细胞综合征(LAHS)患者的临床特征、治疗和预后。回顾性分析本中心2016年1月至2023年8月确诊的LAHS患者,重点评估临床特征、治疗方式、总缓解率(ORR)和总生存期(OS),并结合单变量及多变量分析识别潜在预后因素。共纳入86例LAHS患者进行临床特征和预后评估。与B细胞淋巴瘤患者相比,T/NK细胞淋巴瘤患者在临床过程中发生噬血细胞综合征(HPS)的可能性更高。全体患者中位生存期为55天;T/NK细胞LAHS组和B细胞LAHS组分别为47天和81天(P=0.025)。可评估患者的ORR为42.2%。先开始抗淋巴瘤治疗的患者ORR较先开始抗HPS治疗者更高,但差异未达显著。

单变量分析显示,T/NK细胞LAHS(P=0.027)、复发时出现HPS(P=0.036)、基线血浆EBV-DNA水平较高(>4,000拷贝/mL,P=0.034),以及接受细胞因子吸附和芦可替尼治疗(分别P<0.001和P=0.017),可能与OS较差有关;糖皮质激素治疗则有利于OS。多变量分析显示,T/NK细胞LAHS(校正风险比[aHR]=2.007)、细胞因子吸附治疗(aHR=4.547)和糖皮质激素治疗(aHR=0.118)与死亡独立相关。T/NK细胞淋巴瘤是LAHS的主要病因,且预后更差。抗淋巴瘤或抗HPS治疗何者应先启动,仍需更大样本的前瞻性研究确定。控制HPS的关键是及时阻断细胞因子风暴。糖皮质激素有效且易于获得,应尽早、足量使用。

展开英文摘要原文

To explore the clinical features, treatment, and prognosis of patients with lymphoma-associated hemophagocytic syndrome (LAHS) in a real-world clinical setting.

We retrospectively examined LAHS patients diagnosed at our center between January 2016 and August 2023, focusing primarily on their clinical features, therapeutic approaches, overall response rate (ORR), and overall survival (OS). A combination of univariate and multivariate analyses was conducted to identify potential prognostic factors. A total of 86 patients diagnosed with LAHS were included to evaluate clinical characteristics and prognostic factors. Patients with T/NK cell lymphoma had a higher probability of developing hemophagocytic syndrome (HPS) during the clinical process than those with B cell lymphoma. The median survival time was 55 days for all patients, and 47 and 81 days for the T/NK cell LAHS and B cell LAHS cohorts, respectively (P = 0. 025). Among the patients evaluated, the ORR was 42. 2%. Patients starting with anti-lymphoma treatment had a better, albeit not significant, ORR than those beginning with anti-HPS treatment.

In the univariate analysis, T/NK cell LAHS (P = 0. 027), HPS onset at relapse (P = 0. 036), higher baseline plasma EBV-DNA levels (> 4,000 copies/mL, P = 0. 034), and treatments including cytokine adsorption and ruxolitinib (P < 0. 001 and P = 0. 017, respectively) were potentially associated with worse OS, while corticosteroid therapy benefited OS. In the multivariate analysis, T/NK cell LAHS (adjusted hazard ratio (aHR) = 2. 007), cytokine adsorption therapy (aHR = 4.

547), and corticosteroid therapy (aHR = 0. 118) were independently associated with mortality. T/NK cell lymphoma was the main cause of LAHS and carried a worse prognosis. Whether anti-lymphoma or anti-HPS treatment should start first still requires prospective studies with larger sample sizes. The key point in controlling HPS is to block the cytokine storm promptly. Corticosteroid therapy is both effective and accessible and should be used early and in sufficient quantities.

论文信息

作者
Cheng S、Yan Z、Ma H、Liu Y
第一作者单位
Department of Internal Medicine, The Affiliated Cancer Hospital of Zhengzhou University &amp; Henan Cancer Hospital, Zhengzhou, Henan, 450008, China.China
通讯作者单位
Department of Internal Medicine, The Affiliated Cancer Hospital of Zhengzhou University &amp; Henan Cancer Hospital, Zhengzhou, Henan, 450008, China. yyliu@zzu.edu.cn.China
期刊
Annals of hematology2024 Sep
原文标识
PubMed 39078433 · DOI 10.1007/s00277-024-05900-y