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血友病 A 患者大型前瞻性队列的出血模式:Advate 在 HaEmophilia A 结果数据库(AHEAD)研究中的三年随访。

Pattern of bleeding in a large prospective cohort of haemophilia A patients: A three-year follow-up of the AHEAD (Advate in HaEmophilia A outcome Database) study.

机构信息

Haemophilia Comprehensive Care Centre, Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.

Universita' Roma La Sapienza, Policlinico Umberto I, Rome, Italy.

出版信息

Haemophilia. 2018 Jan;24(1):85-96. doi: 10.1111/hae.13361. Epub 2017 Oct 17.

DOI:10.1111/hae.13361
PMID:29044825
Abstract

INTRODUCTION

Outcome data on treatment of patients with haemophilia A spanning several years of real-world evidence collection are currently very limited.

AIM AND METHODS

The global prospective long-term Advate Haemophilia A Outcome Database (AHEAD) cohort study collects real-world data from patients with severe and moderate haemophilia. We report an interim data read-out after three years of observation.

RESULTS

A total of 522 patients were enrolled from 21 countries: 334 completed year 1 follow-up, 238 completed year 2 and 136 completed year 3, with an overall follow-up of 811 patient-years. Median annual bleeding rates (ABR) were 1.7 in the prophylaxis group and 8.9 in the on-demand group at year 1 visit, 1.6 and 13.0, respectively, at year 2 visit and 2.2 and 10.3, respectively, at year 3 visit. Moreover, about 42% of patients on prophylaxis vs 12% of patients on on-demand had zero annual joint bleeding rates (AJBR). Effectiveness of prophylaxis and on-demand treatment was deemed excellent/good in the majority of cases. Octocog alfa (Advate ) was well tolerated. The inhibitors that developed in nine patients all disappeared spontaneously. Three patients had been previously exposed to FVIII for ≤50 exposure days (EDs), 3 for >50 EDs and 3 showed a borderline positive inhibitory activity (≤0.6 BU/mL).

CONCLUSIONS

These data confirm that the goal of zero bleeds is achievable, although not yet achieved in all patients. Understanding reasons behind the lower response to standard prophylaxis regimens in some patients and personalizing prophylactic treatment may further improve outcome in patients with haemophilia A.

摘要

简介

目前,关于血友病 A 患者多年真实世界数据采集的治疗结果数据非常有限。

目的和方法

全球前瞻性长效 Advate 血友病 A 结局数据库(AHEAD)队列研究从重度和中度血友病患者中收集真实世界数据。我们报告了三年观察期后的中期数据结果。

结果

共纳入来自 21 个国家的 522 名患者:334 名患者完成了第 1 年随访,238 名完成了第 2 年随访,136 名完成了第 3 年随访,总体随访时间为 811 患者年。在第 1 年就诊时,预防组和按需组的年出血率(ABR)中位数分别为 1.7 和 8.9,第 2 年就诊时分别为 1.6 和 13.0,第 3 年就诊时分别为 2.2 和 10.3。此外,约 42%接受预防治疗的患者与 12%接受按需治疗的患者的年关节出血率(AJBR)为零。大多数情况下,预防和按需治疗的效果被认为是极好/良好的。奥塔戈阿尔法(Advate)的耐受性良好。在 9 名患者中,所有抑制剂均自发消失。3 名患者此前曾接受过≤50 个暴露日(EDs)的 FVIII 治疗,3 名患者接受过>50 EDs 的治疗,3 名患者的抑制活性呈临界阳性(≤0.6 BU/mL)。

结论

这些数据证实,零出血的目标是可以实现的,尽管并非所有患者都已达到。了解一些患者对标准预防方案反应较低的原因,并对预防治疗进行个体化,可能会进一步改善血友病 A 患者的预后。

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