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从挑战到机遇:施瓦赫曼-戴蒙德综合征如何成为治疗开发的一个有前景的靶点。

From Challenge to Opportunity: How Shwachman-Diamond Syndrome Became a Promising Target for Therapy Development.

作者信息

Hars Eszter S, McReynolds Lisa J

机构信息

Shwachman-Diamond Syndrome Alliance Inc, Woburn, Massachusetts, USA.

Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland, USA.

出版信息

Clin Pharmacol Ther. 2024 Dec;116(6):1377-1380. doi: 10.1002/cpt.3393. Epub 2024 Jul 22.

DOI:10.1002/cpt.3393
PMID:39039619
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11567794/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3195/11567794/23893add48b9/nihms-2010253-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3195/11567794/96b41ed52c91/nihms-2010253-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3195/11567794/23893add48b9/nihms-2010253-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3195/11567794/96b41ed52c91/nihms-2010253-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3195/11567794/23893add48b9/nihms-2010253-f0002.jpg

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Blood. 2024 Aug 29;144(9):931-939. doi: 10.1182/blood.2023019986.
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Br J Haematol. 2024 Jan;204(1):292-305. doi: 10.1111/bjh.19134. Epub 2023 Oct 24.
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对孤儿药设计和批准在孤儿药法案的四十年中针对的罕见疾病和病症进行全面研究。
Orphanet J Rare Dis. 2023 Jun 23;18(1):163. doi: 10.1186/s13023-023-02790-7.
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