Astermark Jan, Baghaei Fariba, Strandberg Karin, Toplican Petra Gabric, Birkedal Maj Friberg, Grahn Emma Engman, Hansson Charlotta, Kampmann Peter, Lehtinen Anna-Elina, Täckström Kinga, Holme Pål Andre, Magnusson Maria
Department of Translational Medicine, Lund University, Malmö, Sweden.
Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Jan Waldenströms gata 14, Malmö, SE-205 02, Sweden.
Ther Adv Hematol. 2023 Oct 17;14:20406207231202306. doi: 10.1177/20406207231202306. eCollection 2023.
Despite improvements in hemophilia care, challenges remain, including treatment burden and impaired quality of life. Gene therapy may overcome these. However, its introduction presents a challenge.
To outline a function-based gene therapy working model describing critical milestones associated with gene therapy handling, administration, and follow-up to facilitate and implement an effective infrastructure for gene therapy introduction.
Literature review and consensus discussion among Hemophilia Comprehensive Care centers (HCCCs) in the Nordic region.
Representatives from six HCCCs sought to pinpoint milestones and key stakeholders for site readiness at the pre-, peri-, and post-infusion stages, including authority and genetically modified organism (GMO) product requirements, awareness, medical eligibility, logistics and product handling for infusion, laboratory monitoring, and follow-up.
A gene therapy transit map was developed with key stakeholders identified. The approach to prepare the vector will differ between the Nordic centers, but the contracted pharmacy unit will be a key stakeholder. Therefore, a pharmacy checklist for the implementation of gene therapy was developed. For the future, Advanced Therapy Medicinal Product centers will also be implemented. Patients' expectations, commitments, and concerns need to be addressed repeatedly and education of patients and the expanded health-care professionals team will be the key to successful and optimal clinical management. Eligibility testing according to the product's summary of product characteristics and frequent follow-up and monitoring post-infusion according to the World Federation of Hemophilia chart will be crucial.
The approach to deliver gene therapy in the Nordic region will differ partly between the hemophilia centers, but the defined road map with checklists for the implementation of this advanced therapy will be applicable to all. The map may also serve as a platform for the use of future GMO product options both within and outside the area of hemophilia.
尽管血友病治疗有所改善,但挑战依然存在,包括治疗负担和生活质量受损。基因疗法或许可以克服这些问题。然而,其引入带来了一项挑战。
概述一个基于功能的基因疗法工作模型,描述与基因疗法处理、给药及随访相关的关键节点,以促进并实施有效的基因疗法引入基础设施。
北欧地区血友病综合治疗中心(HCCC)之间的文献综述与共识讨论。
来自六个HCCC的代表试图确定输注前、输注期间和输注后阶段场地准备就绪的关键节点及主要利益相关者,包括监管机构和转基因生物(GMO)产品要求、认知度、医学适用性、输注的物流与产品处理、实验室监测及随访。
制定了一份基因疗法流程地图,并确定了主要利益相关者。北欧各中心制备载体的方法会有所不同,但签约药房将是主要利益相关者。因此,制定了一份基因疗法实施的药房检查表。未来,还将设立高级治疗药品中心。需要反复关注患者的期望、承诺和担忧,对患者及扩大后的医疗专业人员团队进行教育将是成功且优化临床管理的关键。根据产品特性摘要进行适用性检测,并按照世界血友病联盟图表在输注后进行频繁的随访和监测至关重要。
北欧地区血友病中心提供基因疗法的方法会存在部分差异,但这份定义明确的路线图及该先进疗法实施检查表将适用于所有中心。该路线图还可作为在血友病领域内外使用未来转基因产品选项的平台。