Hematology transplant Unit - French Reference Center for Aplastic Anemia, Hôpital Saint-Louis, Paris, France.
Stiftung Lichterzellen, Cologne, Germany.
Hematology. 2022 Dec;27(1):1140-1151. doi: 10.1080/16078454.2022.2127630.
To assess the clinical and healthcare resource burden among C5 inhibitor (C5i)-treated patients with paroxysmal nocturnal haemoglobinuria (PNH), using patient-reported data.
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.
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.
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.
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。
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。
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。
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。