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阵发性睡眠性血红蛋白尿症患者接受 C5 抑制剂治疗的疾病负担:从患者角度看临床结局和医疗接触。

The burden of illness of patients with paroxysmal nocturnal haemoglobinuria receiving C5 inhibitors: clinical outcomes and medical encounters from the patient perspective.

机构信息

Hematology transplant Unit - French Reference Center for Aplastic Anemia, Hôpital Saint-Louis, Paris, France.

Stiftung Lichterzellen, Cologne, Germany.

出版信息

Hematology. 2022 Dec;27(1):1140-1151. doi: 10.1080/16078454.2022.2127630.

Abstract

OBJECTIVES

To assess the clinical and healthcare resource burden among C5 inhibitor (C5i)-treated patients with paroxysmal nocturnal haemoglobinuria (PNH), using patient-reported data.

METHODS

This web-based, cross-sectional survey (01FEB2021-31MAR2021) of adults with PNH treated with eculizumab (France, Germany, UK) or ravulizumab (Germany) included: patient characteristics; treatment patterns/dosage; haematological outcomes (haemoglobin [Hb] levels, transfusions, thrombotic events, breakthrough haemolysis); and medical encounters. Treatment and Hb-level subgroup differences were assessed with statistical significance tests.

RESULTS

Among 71 patients, 98.6% were C5i-treated for ≥3 months. The majority (with reported Hb levels) had levels ≤12.0 g/dL (85.7%;  = 54/63). The mean Hb level was 10.2 g/dL (standard deviation [SD]: 2.0; median 10.0 g/dL). Treatment with above label-recommended doses was reported by 30.4% (eculizumab) and 5.3% (ravulizumab) of patients. Within the past 12 months among patients treated with C5i for ≥1 year: 24.1% had ≥1 transfusion; 3.2% had ≥1 thrombosis; and 28.6% had ≥1 breakthrough haemolysis. Among all patients, 26.8% and 31.0% reported emergency department/room [ER] and inpatient visits, respectively. Mean annual, per-patient all-cause medical encounters were: 0.5 (ER); 1.9 (inpatient); and overall outpatient visits ranged by setting from 2.0 to 6.4. Most encounters were PNH-related, with means of 0.4 (ER); 1.8 (inpatient); and 1.6-5.4 (outpatient). Primary haematological and medical encounter outcomes were similar between treatment as well as Hb-level subgroups, with almost no statistically significant differences.

CONCLUSIONS

Despite at least 3 months of C5i treatment, high proportions of patients with PNH reported low haemoglobin levels and required transfusions and hospitalizations, which suggests remaining unmet needs.

摘要

目的

使用患者报告数据评估 C5 抑制剂(C5i)治疗阵发性夜间血红蛋白尿症(PNH)患者的临床和医疗资源负担。

方法

本项基于网络的横断面研究(2021 年 2 月 1 日至 3 月 31 日)纳入了接受依库珠单抗(法国、德国、英国)或拉维珠单抗(德国)治疗的成年 PNH 患者,评估内容包括:患者特征;治疗方案/剂量;血液学结局(血红蛋白[Hb]水平、输血、血栓事件、突破性溶血);以及医疗就诊情况。使用统计学意义检验评估治疗和 Hb 水平亚组之间的差异。

结果

在 71 例患者中,98.6%的患者接受 C5i 治疗至少 3 个月。大多数(报告 Hb 水平的患者)Hb 水平≤12.0 g/dL(85.7%;54/63)。平均 Hb 水平为 10.2 g/dL(标准差[SD]:2.0;中位数 10.0 g/dL)。30.4%(依库珠单抗)和 5.3%(拉维珠单抗)的患者接受了标签推荐剂量以上的治疗。在过去 12 个月中,接受 C5i 治疗至少 1 年的患者中:24.1%有≥1 次输血;3.2%有≥1 次血栓事件;28.6%有≥1 次突破性溶血。所有患者中,26.8%和 31.0%分别报告了急诊/病房[ER]就诊和住院。每位患者的年平均所有原因医疗就诊情况为:0.5 次 ER;1.9 次住院;总体门诊就诊次数按就诊地点从 2.0 次到 6.4 次不等。大多数就诊与 PNH 相关,ER 就诊均值为 0.4 次;住院就诊均值为 1.8 次;门诊就诊均值为 1.6-5.4 次。根据 Hb 水平亚组和治疗方案的主要血液学和医疗就诊结局相似,几乎没有统计学显著差异。

结论

尽管接受了至少 3 个月的 C5i 治疗,但仍有相当大比例的 PNH 患者报告低血红蛋白水平,并需要输血和住院治疗,这表明仍存在未满足的需求。

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