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新型戈谢病患者在家中接受维雷帕酶快速输注治疗。

Rapid home therapy infusion of velaglucerase alfa in naïve patients with Gaucher disease.

机构信息

Gaucher Unit, Shaare Zedek Medical Centre, Jerusalem, Israel.

Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

出版信息

Intern Med J. 2024 Mar;54(3):398-403. doi: 10.1111/imj.16179. Epub 2023 Jul 26.

Abstract

BACKGROUND

Enzyme replacement therapy (ERT) has revolutionised the management of patients with Gaucher disease (GD). In 2018, we published the safety and efficacy of rapid 10-min infusion of velaglucerase alfa in previously treated patients, mostly on low-dose therapy.

AIM

To improve quality of life (QoL) for patients needing lifelong bi-weekly infusions by introducing a 10-min infusion instead of 1 h per label in patients naive to ERT and on high-dose therapy.

METHODS

Fifteen naive patients were enrolled; all received bi-weekly infusions of 60 units/kgBW velaglucerase alfa; the infusion rate was gradually reduced in the hospital, followed by home infusions. Each infusion was followed for safety. Efficacy parameters were assessed every 3 months. Patient-reported outcome questionnaires were collected at baseline and follow-up.

RESULTS

Ten-minute rapid infusions were well tolerated without related severe adverse events (SAEs). Two patients experienced a non-related SAE and another a possibly related AE. In three patients, the infusion rate was increased to 30 or 60 min (two because of suboptimal response and one because of AE). Two patients dropped out because of an unwillingness to attend follow-up visits during the COVID-19 pandemic. All 13 remaining patients reached the 24-month end-point. The platelet counts increased by a median (range) of 68.38% (12.5-300%) and the lyso-Gb1 levels decreased by 62.6% (32.9-89.9%).

CONCLUSION

Home therapy with rapid infusion of high-dose velaglucerase alfa was a safe, effective and preferable alternative for patients with GD naïve to treatment. We believe that shortening the infusion time improves the QoL of patients with GD who have a lifelong commitment to intravenous therapy.

摘要

背景

酶替代疗法(ERT)彻底改变了戈谢病(GD)患者的治疗方式。2018 年,我们发表了快速 10 分钟输注维拉苷酶阿尔法在既往接受治疗的患者中的安全性和有效性数据,这些患者大多接受低剂量治疗。

目的

通过引入 10 分钟输注而不是标签规定的每两周 1 小时输注,改善需要终身接受每两周静脉输注的患者的生活质量(QoL),这些患者对 ERT 治疗无经验且接受高剂量治疗。

方法

入组 15 名无经验的患者;所有患者均接受每两周 60 单位/公斤体重维拉苷酶阿尔法静脉输注;输注速度在医院内逐渐降低,随后在家中进行输注。每次输注均进行安全性随访。每 3 个月评估疗效参数。在基线和随访时收集患者报告的结果问卷。

结果

10 分钟快速输注耐受良好,无相关严重不良事件(SAE)。两名患者发生非相关 SAE,另一名患者发生可能相关的 AE。在三名患者中,输注速度增加至 30 分钟或 60 分钟(两名患者因疗效不佳,一名患者因 AE)。两名患者因 COVID-19 大流行期间不愿参加随访而退出。其余 13 名患者均达到 24 个月终点。血小板计数中位数(范围)增加了 68.38%(12.5-300%),溶酶体-β-葡糖苷酶 1 水平降低了 62.6%(32.9-89.9%)。

结论

高剂量维拉苷酶阿尔法快速输注的家庭治疗是一种安全、有效且更优的选择,适用于无治疗经验的 GD 患者。我们认为,缩短输注时间可以提高需要终身接受静脉治疗的 GD 患者的生活质量。

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