Delisle Jean-Sébastien, Fournier Diane, Santerre Kim, Rochette Samuel, Zawati Ma'n H, Dumont-Lagacé Maude, Turcotte Simon, Guertin Jason Robert, Vermette Patrick, Tremblay Jacques P, Parisotto Maxime, Beauséjour Christian, Petropoulos Louisa, Kekre Natasha, Michaud Stéphanie, Dieudé Mélanie
Centre de recherche de l'Hôpital Maisonneuve-Rosemont, Montreal, QC, Canada.
Institut d'hématologie, oncologie et thérapie cellulaire (iHOT), Hôpital Maisonneuve-Rosemont, Montreal, QC, Canada.
Front Med (Lausanne). 2025 Jun 3;12:1581058. doi: 10.3389/fmed.2025.1581058. eCollection 2025.
The last decade has witnessed tremendous progress in the fields of cell and gene therapy and regenerative medicine (CGT/RM). However, these advances came with their own challenges and opportunities, which may vary among jurisdictions depending on infrastructures, laws, regulations, access to funding, and socioeconomic, political and cultural aspects. In September 2023, the Québec cell, tissue and gene therapy network (ThéCell) and Héma-Québec held a symposium on the opportunities and challenges of CGT/RM in Québec, Canada. We collected and synthetized the views of scientists, CGT/RM manufacturers, business representatives, and experts in ethics and law, pharmacoeconomics, and regulatory affairs expressed during and after this symposium. Comments were grouped into seven strategic orientations: (1) a framework should be built for the development of CGT/RM products based on principles that will enable fair and timely access for all; (2) governments should spur private and public research investments in CGT/RM; (3) the skillsets of developers should be mobilized to foster the development and production of CGT/RM products in the academic and industrial settings, and the training of Québec's workforce could be better aligned with industry and population needs to facilitate the industrialization of the sector, with the aim of reducing production costs and improving accessibility to patients; (4) Québec should ensure that the province's production and healthcare capacity is aligned with current and future needs in CGT/RM products, considering the rapidly evolving landscape of CGT/RM; (5) regulatory awareness may be improved among developers through outreach approaches and early consultations; (6) the regulations governing the development of CGT/RM could be streamlined and adapted to the needs of these emerging products; (7) ongoing efforts to reform the clinical reimbursement framework could be continued in Québec's public, single-payer healthcare system. This symposium provided guidance addressing current limitations and taking advantage of opportunities in CGT/RM in Québec. These considerations should help guide the development of new policies for CGT/RM products in Québec, keeping with principles of universal healthcare in Canada. We surmise that other jurisdictions face similar challenges, and the global CGT/RM community could benefit from these shared experiences to promote the optimal development and access to these promising therapies.
过去十年见证了细胞与基因治疗以及再生医学(CGT/RM)领域的巨大进展。然而,这些进展也伴随着自身的挑战与机遇,在不同司法管辖区,这些挑战和机遇可能因基础设施、法律、法规、资金获取以及社会经济、政治和文化等方面的差异而有所不同。2023年9月,魁北克细胞、组织与基因治疗网络(ThéCell)和魁北克血液中心(Héma-Québec)在加拿大魁北克举办了一场关于CGT/RM在魁北克的机遇与挑战的研讨会。我们收集并综合了科学家、CGT/RM制造商、商业代表以及伦理与法律、药物经济学和监管事务方面的专家在此次研讨会期间及之后表达的观点。评论被归纳为七个战略方向:(1)应基于能让所有人公平且及时获得治疗的原则,构建一个CGT/RM产品开发框架;(2)政府应刺激对CGT/RM的私人和公共研究投资;(3)应调动开发者的技能,以促进学术和工业环境中CGT/RM产品的开发与生产,并且魁北克劳动力的培训可以更好地与行业和民众需求相匹配,以推动该领域的产业化,目标是降低生产成本并提高患者可及性;(4)考虑到CGT/RM迅速演变的形势,魁北克应确保该省的生产和医疗保健能力与CGT/RM产品当前及未来的需求相匹配;(5)可通过推广方法和早期磋商提高开发者的监管意识;(6)可简化CGT/RM开发的相关法规,并使其适应这些新兴产品的需求;(7)魁北克公共的单一支付者医疗保健系统中正在进行的临床报销框架改革工作可以继续推进。此次研讨会为解决魁北克CGT/RM当前的局限性并利用其机遇提供了指导。这些考量应有助于指导魁北克CGT/RM产品新政策的制定,符合加拿大全民医疗保健的原则。我们推测其他司法管辖区也面临类似挑战,全球CGT/RM界可以从这些共同经验中受益,以促进这些有前景疗法的最佳开发与可及性。