美国未分化多形性肉瘤 (UPS) 的发病率。

Q2 Medicine Sarcoma Pub Date : 2024-10-29 eCollection Date: 2024-01-01 DOI:10.1155/2024/6735002
Jiemin Ma, Roman Groisberg, Changxia Shao, Wenjun Zhong
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引用次数: 0

摘要

过去 20 年来,随着免疫组化和基因组分析技术的进步,未分化多形性肉瘤(UPS)的分类也在不断发展。目前缺乏有关 UPS 发病率的信息。由于监测、流行病学和最终结果(SEERs)计划中缺乏指定的 UPS 组织学代码,我们利用 SEER 计划 22 个登记处 2000-2020 年的数据,根据临床意见,按照三种不同的定义估算了 UPS 的发病率。三种定义的发病率差异很大,包容性最小的定义在2016-2020年的发病率为每10万人中0.06例,包容性最大的定义为每10万人中0.67例,因此估算UPS的确切发病率具有挑战性。无论如何,2000 年至 2020 年间,所有发病率均有所下降。美国需要更好地执行 UPS 诊断和分类指南。
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Incidence of Undifferentiated Pleomorphic Sarcoma (UPS) in the United States.

The classification of undifferentiated pleomorphic sarcoma (UPS) has been evolving with advances in immunohistochemistry and genomic profiling over the past 20 years. There is a lack of current information on UPS incidence. Due to the lack of designated histology codes for UPS in the Surveillance, Epidemiology, and End Results (SEERs) program, we estimated UPS incidence by three different definitions based on clinical opinions using the 2000-2020 data from 22 registries of the SEER program. The incidence varied widely across the three definitions with 0.06 per 100,000 persons for the least inclusive definition and 0.67 per 100,000 persons for the most inclusive definition in 2016-2020, making it challenging to estimate the exact incidence of UPS. Regardless, all the incidences decreased between 2000 and 2020. Guidelines in UPS diagnosis and classification need to be better implemented in the US.

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来源期刊
Sarcoma
Sarcoma Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
5.00
自引率
0.00%
发文量
15
审稿时长
14 weeks
期刊介绍: Sarcoma is dedicated to publishing papers covering all aspects of connective tissue oncology research. It brings together work from scientists and clinicians carrying out a broad range of research in this field, including the basic sciences, molecular biology and pathology and the clinical sciences of epidemiology, surgery, radiotherapy and chemotherapy. High-quality papers concerning the entire range of bone and soft tissue sarcomas in both adults and children, including Kaposi"s sarcoma, are published as well as preclinical and animal studies. This journal provides a central forum for the description of advances in diagnosis, assessment and treatment of this rarely seen, but often mismanaged, group of patients.
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