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芦可替尼联合多柔比星、依托泊苷和地塞米松治疗淋巴瘤相关噬血细胞综合征。

Ruxolitinib combined with doxorubicin, etoposide, and dexamethasone for the treatment of the lymphoma-associated hemophagocytic syndrome.

机构信息

Department of Hematology, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangdong, China.

出版信息

J Cancer Res Clin Oncol. 2020 Nov;146(11):3063-3074. doi: 10.1007/s00432-020-03301-y. Epub 2020 Jul 2.

Abstract

PURPOSE

Case reports suggest that ruxolitinib-containing treatment could increase the clinical response rate of patients with hemophagocytic syndrome (HPS). This study aimed to explore the effect of ruxolitinib-containing treatment for patients with lymphoma-associated hemophagocytic syndrome (LAHS).

METHODS

This was a retrospective study of patients with LAHS hospitalized at the First Affiliated Hospital of Guangdong Pharmaceutical University between October 2017 and September 2019. Patients were treated with HLH-94 (etoposide and dexamethasone) or R-DED regimen (ruxolitinib, doxorubicin, etoposide, and dexamethasone). The clinical characteristics, treatment responses, and overall survival (OS) were compared. The patients were divided into the HLH-94 group (n = 34) and the R-DED group (n = 36).

RESULTS

Compared with HLH-94, R-DED might effectively improve the clinical manifestations, including fever and splenomegaly in patients with LAHS, and control the systemic cytokine storm. The response rate at 2 weeks was 54.8% in the HLH-94 group, which was lower than in the R-DED group (83.3%) (p = 0.011). The OS was significantly prolonged in the R-DED group compared with the HLH-94 group (median, 5 vs. 1.5 months, p = 0.003). The multivariable analysis showed that lower IL-10 levels [hazard ratio (HR)] = 1.000, [95% confidence interval (CI)] 1.000-1.000, p = 0.012), R-DED regimen (HR = 0.196, 95% CI 0.084-0.457, p < 0.001), and non-NK/T-cell lymphoma (HR = 0.254, 95% CI 0.102-0.628, p = 0.003) were associated with better OS. The prognosis of patients with LAHS was generally poor.

CONCLUSION

Ruxolitinib can be combined with chemotherapy in HPS. It is feasible, with no early signals of increased toxicity.

摘要

目的

病例报告表明,含有鲁索利替尼的治疗方法可提高噬血细胞综合征(HPS)患者的临床缓解率。本研究旨在探讨含有鲁索利替尼的治疗方法对淋巴瘤相关噬血细胞综合征(LAHS)患者的疗效。

方法

这是一项回顾性研究,纳入了 2017 年 10 月至 2019 年 9 月在广东药科大学附属第一医院住院的 LAHS 患者。患者接受 HLH-94(依托泊苷和地塞米松)或 R-DED 方案(鲁索利替尼、多柔比星、依托泊苷和地塞米松)治疗。比较了两组患者的临床特征、治疗反应和总生存(OS)。患者分为 HLH-94 组(n=34)和 R-DED 组(n=36)。

结果

与 HLH-94 相比,R-DED 可能有效改善 LAHS 患者的临床表现,包括发热和脾肿大,并控制全身细胞因子风暴。HLH-94 组的 2 周缓解率为 54.8%,低于 R-DED 组(83.3%)(p=0.011)。与 HLH-94 组相比,R-DED 组的 OS 明显延长(中位时间,5 个月比 1.5 个月,p=0.003)。多变量分析显示,较低的 IL-10 水平[风险比(HR)=1.000,95%置信区间(CI)1.000-1.000,p=0.012)、R-DED 方案(HR=0.196,95%CI 0.084-0.457,p<0.001)和非 NK/T 细胞淋巴瘤(HR=0.254,95%CI 0.102-0.628,p=0.003)与更好的 OS 相关。LAHS 患者的预后一般较差。

结论

鲁索利替尼可与 HPS 中的化疗联合使用。它是可行的,且早期无毒性增加的迹象。

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