Hars Eszter S, McReynolds Lisa J
Shwachman-Diamond Syndrome Alliance Inc, Woburn, Massachusetts, USA.
Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland, USA.
Clin Pharmacol Ther. 2024 Dec;116(6):1377-1380. doi: 10.1002/cpt.3393. Epub 2024 Jul 22.
Rare diseases affect over 30 million people in the US and 300 million globally, yet 95% lack FDA-approved treatments. Rare disease therapy development poses unique challenges and opportunities. Shwachman-Diamond Syndrome (SDS) is emerging as a model rare disease due to its uniform genetics, robust molecular understanding, and mature research infrastructure—including de-risking through model development, regulatory engagement, patient community development, ICD-10 implementation, and data access, driven by the SDS Alliance —a research-focused patient advocacy organization.
在美国,罕见病影响着超过3000万人,全球受影响人数达3亿,但其中95%的患者缺乏美国食品药品监督管理局(FDA)批准的治疗方法。罕见病治疗的研发带来了独特的挑战与机遇。施瓦赫曼-戴蒙德综合征(SDS)正逐渐成为一种典型的罕见病,这得益于其一致的遗传学特征、深入的分子层面理解以及成熟的研究基础设施,包括通过模型开发、监管机构参与、患者群体发展、国际疾病分类第十版(ICD - 10)实施以及数据获取来降低风险,这些工作由施瓦赫曼-戴蒙德综合征联盟推动,该联盟是一个专注于研究的患者权益倡导组织。