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剂量调整 EPOCH-R 是双打击淋巴瘤安全且耐受良好的门诊治疗方案。

Dose-adjusted EPOCH-R is a safe and well tolerated outpatient treatment regimen in double-hit lymphoma.

机构信息

Department of Haematology, Sunshine Cost University Hospital, Sunshine Coast, Queensland, Australia.

Department of Cancer Care Services, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.

出版信息

Intern Med J. 2023 May;53(5):773-778. doi: 10.1111/imj.15747. Epub 2022 May 27.

Abstract

BACKGROUND

Double-hit lymphoma (DHL) is an aggressive subtype of high-grade B-cell lymphoma with inferior prognosis using standard dose chemotherapy. Controversy remains whether more intensive chemotherapy regimens such as dose-adjusted etoposide, prednisolone, vincristine, cyclophosphamide, doxorubicin and rituximab (DA-EPOCH-R) provide better outcomes in this cohort.

AIMS

To review consecutive cases of DHL treated with DA-EPOCH-R at our institution in comparison to available literature.

METHODS

We conducted a retrospective study of 13 consecutive patients with DHL treated with DA-EPOCH-R at our institution. Primary endpoints included complete response (CR), event-free survival (EFS) and overall survival (OS).

RESULTS

CR rate with DA-EPOCH-R in DHL was 69% in our cohort. Median EFS and OS duration was 61 months (95% CI: 41-86 months) and 64 months (95% CI: 42-86 months) respectively. One patient discontinued DA-EPOCH-R due to recurrent febrile neutropenia and there were no treatment or infection-related deaths during the study.

CONCLUSIONS

This study suggests that DA-EPOCH-R is a well tolerated outpatient regimen for DHL and should be considered for initial treatment in medically fit patients. Further prospective studies are warranted to confirm these findings.

摘要

背景

双打击淋巴瘤(DHL)是一种侵袭性高级别 B 细胞淋巴瘤亚型,采用标准剂量化疗预后较差。是否更强化疗方案,如剂量调整依托泊苷、泼尼松、长春新碱、环磷酰胺、多柔比星和利妥昔单抗(DA-EPOCH-R),能为这一患者群体带来更好的结果,目前仍存在争议。

目的

本研究回顾性分析了我院采用 DA-EPOCH-R 治疗的连续 DHL 病例,并与现有文献进行了比较。

方法

我们对我院采用 DA-EPOCH-R 治疗的 13 例连续 DHL 患者进行了回顾性研究。主要终点包括完全缓解(CR)、无事件生存(EFS)和总生存(OS)。

结果

本研究中,DHL 患者采用 DA-EPOCH-R 治疗的 CR 率为 69%。中位 EFS 和 OS 持续时间分别为 61 个月(95%CI:41-86 个月)和 64 个月(95%CI:42-86 个月)。1 例患者因反复发热性中性粒细胞减少而停止接受 DA-EPOCH-R 治疗,在研究期间无治疗相关或感染相关死亡。

结论

本研究表明,DA-EPOCH-R 是一种耐受良好的门诊治疗方案,适用于身体状况适宜的患者的初始治疗。需要进一步的前瞻性研究来证实这些发现。

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