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众多“小型慢性阻塞性肺疾病”:慢性阻塞性肺疾病应属罕见病。

The many "small COPDs": COPD should be an orphan disease.

作者信息

Rennard Stephen I, Vestbo Jørgen

机构信息

University of Nebraska Medical Center, Omaha, NE.

Hvidovre Hospital, Hvidovre, Denmark.

出版信息

Chest. 2008 Sep;134(3):623-627. doi: 10.1378/chest.07-3059.

Abstract

COPD is one of the most common causes of morbidity and mortality. Perhaps paradoxically, COPD also should be an orphan disease. Importantly, this could advance the development of treatments for COPD. There are two criteria for orphan status in the United States. Most widely known is the criterion of < 200,000 affected individuals; however, secondarily, is the impossibility for development costs to be recovered during the patent life of a product. COPD should qualify for the first criterion if the various conditions that comprise COPD are regarded separately. The subphenotyping of COPD into separate groups based on mechanism sets the stage for the rational development of therapeutics. In addition, many candidate treatments may alter the natural history of COPD. Testing them, however, will require large studies for a duration that will compromise the commercial life of any resulting product. Orphan status, therefore, could facilitate the development of treatments for both phenotypic subsets of COPD patients as well as aid the development of agents to alter the natural history of the disease. Post-drug approval regulations could require that agents approved under the orphan provisions are prospectively monitored, assuring that rigorous longitudinal data are generated. This approach could encourage the pharmaceutical industry to stratify studies based on a more detailed characterization of study subjects at baseline, thus approaching "many small COPDs" instead of a single large and heterogeneous COPD. This strategy may help to address the increasing burden that COPD presents and for which no novel clinical class of treatment has been introduced for 30 years.

摘要

慢性阻塞性肺疾病(COPD)是发病和死亡的最常见原因之一。或许自相矛盾的是,COPD也应是一种罕见病。重要的是,这可能会推动COPD治疗方法的发展。在美国,有两个罕见病认定标准。最为人熟知的是受影响个体少于20万这一标准;然而,其次是在产品专利有效期内无法收回研发成本。如果将构成COPD的各种情况分开看待,COPD应符合第一个标准。根据发病机制将COPD亚分型为不同组,为合理开发治疗方法奠定了基础。此外,许多候选治疗方法可能会改变COPD的自然病程。然而,对它们进行测试将需要大规模研究,且研究持续时间会影响任何由此产生的产品的商业寿命。因此,罕见病认定状态有助于开发针对COPD患者两个表型亚组的治疗方法,也有助于开发改变疾病自然病程的药物。药品批准后的监管规定可能要求对根据罕见病条款批准的药物进行前瞻性监测,以确保产生严格的纵向数据。这种方法可能会鼓励制药行业根据研究对象在基线时更详细的特征对研究进行分层,从而接近“许多小型COPD”,而不是单一的大型异质性COPD。这一策略可能有助于应对COPD日益加重的负担,而30年来尚未引入新的临床治疗类别来应对这一负担。

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