Division of Haematology/Oncology, Department of Paediatrics and Child Health Evaluative Sciences, Research Institute, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Haemophilia Centre Rhine Main, Möerfelden-Walldorf, Germany.
Haemophilia. 2019 Jul;25(4):676-684. doi: 10.1111/hae.13762. Epub 2019 Apr 29.
As a result of the new treatment paradigm that the haemophilia community will face with the availability of novel (non-factor) therapies, an updated consensus on ITI recommendations and inhibitor management strategies is needed.
The Future of Immunotolerance Treatment (FIT) group was established to contemplate, determine and recommend the best management options for patients with haemophilia A and inhibitors.
Despite the considerable success of emicizumab in the management of inhibitor patients, the FIT group still sees the importance of eradicating inhibitors. However, the availability of emicizumab and other non-factor therapies in the future might impact greatly on how ITI is undertaken. Theoretically, concomitant use of emicizumab and FVIII might allow emicizumab to effectively prevent bleeding with lower dose ITI regimens. This might allow for the greater adoption of low-dose/low-frequency FVIII ITI regimens, which may result in a reduced need for central venous access devices while still maintaining a reasonable likelihood of ITI success. The FIT group proposes a new management algorithm for current ITI (without emicizumab) and a hypothetical new approach with the availability of emicizumab. As there are no published data regarding the concomitant use of emicizumab and FVIII for ITI, the FIT Expert group encourages the undertaking of properly conducted prospective studies to explore these approaches further.
由于新型(非因子)疗法的出现,血友病患者将面临新的治疗模式,因此需要更新关于 ITI 建议和抑制剂管理策略的共识。
为了思考、确定和推荐血友病 A 患者和抑制剂患者的最佳管理选择,成立了未来免疫耐受治疗(FIT)小组。
尽管emicizumab 在抑制剂患者管理方面取得了相当大的成功,但 FIT 小组仍然认为消除抑制剂很重要。然而,emicizumab 和其他非因子疗法在未来的可用性可能会极大地影响 ITI 的实施方式。理论上,emicizumab 与 FVIII 的同时使用可能允许 emicizumab 以较低剂量 ITI 方案更有效地预防出血。这可能会导致更多地采用低剂量/低频率的 FVIII ITI 方案,从而减少对中心静脉通路装置的需求,同时仍然保持 ITI 成功的合理可能性。FIT 小组为当前的 ITI(无 emicizumab)提出了新的管理算法,并为 emicizumab 可用性假设了一种新方法。由于尚无关于 emicizumab 和 FVIII 同时用于 ITI 的发表数据,FIT 专家组鼓励进行适当的前瞻性研究,以进一步探索这些方法。