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患者在社交媒体上关注以患者为中心的药物研发:患者、行业和监管机构的综合考量

Patient listening on social media for patient-focused drug development: a synthesis of considerations from patients, industry and regulators.

作者信息

Cimiano Philipp, Collins Ben, De Vuono Maria Carmela, Escudier Thierry, Gottowik Jürgen, Hartung Matthias, Leddin Mathias, Neupane Bikalpa, Rodriguez-Esteban Raul, Schmidt Ana Lucia, Starke-Knäusel Cornelius, Voorhaar Maarten, Wieckowski Krzysztof

机构信息

Semalytix GmbH, Bielefeld, Germany.

CITEC, Bielefeld University, Bielefeld, Germany.

出版信息

Front Med (Lausanne). 2024 Mar 6;11:1274688. doi: 10.3389/fmed.2024.1274688. eCollection 2024.

Abstract

Patients, life science industry and regulatory authorities are united in their goal to reduce the disease burden of patients by closing remaining unmet needs. Patients have, however, not always been systematically and consistently involved in the drug development process. Recognizing this gap, regulatory bodies worldwide have initiated patient-focused drug development (PFDD) initiatives to foster a more systematic involvement of patients in the drug development process and to ensure that outcomes measured in clinical trials are truly relevant to patients and represent significant improvements to their quality of life. As a source of real-world evidence (RWE), social media has been consistently shown to capture the first-hand, spontaneous and unfiltered disease and treatment experience of patients and is acknowledged as a valid method for generating patient experience data by the Food and Drug Administration (FDA). While social media listening (SML) methods are increasingly applied to many diseases and use cases, a significant piece of uncertainty remains on how evidence derived from social media can be used in the drug development process and how it can impact regulatory decision making, including legal and ethical aspects. In this policy paper, we review the perspectives of three key stakeholder groups on the role of SML in drug development, namely patients, life science companies and regulators. We also carry out a systematic review of current practices and use cases for SML and, in particular, highlight benefits and drawbacks for the use of SML as a way to identify unmet needs of patients. While we find that the stakeholders are strongly aligned regarding the potential of social media for PFDD, we identify key areas in which regulatory guidance is needed to reduce uncertainty regarding the impact of SML as a source of patient experience data that has impact on regulatory decision making.

摘要

患者、生命科学行业和监管机构都致力于通过满足尚未满足的需求来减轻患者的疾病负担。然而,患者在药物研发过程中并非总是被系统且持续地纳入其中。认识到这一差距后,全球监管机构已启动以患者为中心的药物研发(PFDD)计划,以促进患者更系统地参与药物研发过程,并确保临床试验中衡量的结果真正与患者相关,且能显著改善他们的生活质量。作为真实世界证据(RWE)的来源,社交媒体一直被证明能够捕捉患者的第一手、自发且未经过滤的疾病和治疗体验,美国食品药品监督管理局(FDA)也认可社交媒体是生成患者体验数据的有效方法。虽然社交媒体倾听(SML)方法越来越多地应用于多种疾病和用例,但对于如何将社交媒体得出的证据用于药物研发过程以及它如何影响监管决策,包括法律和伦理方面,仍存在很大的不确定性。在本政策文件中,我们回顾了三个关键利益相关者群体对SML在药物研发中作用的看法,即患者、生命科学公司和监管机构。我们还对SML的当前实践和用例进行了系统回顾,尤其强调了使用SML来识别患者未满足需求的利弊。虽然我们发现利益相关者在社交媒体对PFDD的潜力方面高度一致,但我们确定了需要监管指导的关键领域,以减少关于SML作为影响监管决策的患者体验数据来源所产生影响的不确定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8539/10955474/726859cdbaa3/fmed-11-1274688-g001.jpg

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