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硬纤维瘤研究基金会患者登记与自然史研究的启动、设计及建立。

The initiation, design, and establishment of the Desmoid Tumor Research Foundation Patient Registry and Natural History Study.

作者信息

Mercier Kelly A, Walsh Darragh M

机构信息

Department of Orthopaedic Surgery, Duke University Medical Center, Durham, NC, USA.

School of Computing, Insight Center for Data Analytics, Dublin City University, Dublin, Ireland.

出版信息

Rare Tumors. 2019 Oct 14;11:2036361319880978. doi: 10.1177/2036361319880978. eCollection 2019.

Abstract

Desmoid tumors are locally invasive sarcoma, affecting 5-6 individuals out of 1,000,000 per year. The desmoid tumors have high rates of recurrence after resection and can lead to significant deterioration of the quality of life of patients. There is a need for a better understanding of the desmoid tumors' patient experience from first symptoms through diagnosis, disease monitoring, and clinical treatment options. With the National Organization of Rare Disorders, the Desmoid Tumor Research Foundation Natural History Study was designed to be collected through the registry. This article describes the protocol for the Desmoid Tumor Research Foundation Natural History Study and some initial findings. The Desmoid Tumor Research Foundation Natural History Study Advisory Committee developed a series of questionnaires and longitudinal surveys, in addition to those from the National Organization of Rare Disorders for all of the rare diseases. These 13 surveys are designed to uncover initial symptoms, diagnosis process, disease monitoring, quality of life, treatments, as well as socioeconomic information. Since launching the Desmoid Tumor Research Foundation Registry and Natural History Study (https://dtrf.iamrare.org), more than 300 desmoid tumor patients have consented to the Desmoid Tumor Research Foundation Natural History Study and completed the Participant Profile. The majority of the respondents are between the ages of 21 and 50 years (76%), female (81.2%), White (91.5%), and live in the United States (47.1%). The majority of tumors are in the lower or upper extremity, (22.9%) followed closely by abdominal desmoid tumors (21.5%). Most are willing to donate specimens (89.9%) and participate in trials (97.2%). Ongoing efforts are addressing the demographic differences between the respondents and non-respondents and any selection bias based on access to the registry and study. The Desmoid Tumor Research Foundation Natural History Study is built on the largest desmoid tumors registry and has recruited more desmoid tumors participants since launching in September 2017. It will serve to fill desmoid tumors knowledge gaps and assist other researchers in their recruitment efforts for additional studies.

摘要

韧带样瘤是一种局部侵袭性肉瘤,每年每100万人中有5至6人受其影响。韧带样瘤切除后复发率很高,会导致患者生活质量显著下降。有必要更好地了解韧带样瘤患者从首发症状到诊断、疾病监测及临床治疗选择的经历。与罕见病国家组织合作,韧带样瘤研究基金会自然史研究旨在通过登记处收集数据。本文介绍了韧带样瘤研究基金会自然史研究的方案及一些初步研究结果。韧带样瘤研究基金会自然史研究咨询委员会除了采用罕见病国家组织针对所有罕见病的问卷外,还制定了一系列问卷和纵向调查。这13项调查旨在揭示首发症状、诊断过程、疾病监测、生活质量、治疗方法以及社会经济信息。自韧带样瘤研究基金会登记处和自然史研究(https://dtrf.iamrare.org)启动以来, 已有300多名韧带样瘤患者同意参与韧带样瘤研究基金会自然史研究并完成了参与者概况调查。大多数受访者年龄在21至50岁之间(76%),女性(81.2%),白人(91.5%),且居住在美国(47.1%)。大多数肿瘤位于下肢或上肢(22.9%),其次是腹部韧带样瘤(21.5%)。大多数人愿意捐赠标本(89.9%)并参与试验(97.2%)。目前正在努力解决受访者与未受访者之间的人口统计学差异以及基于登记处和研究获取情况的任何选择偏倚问题。韧带样瘤研究基金会自然史研究建立在最大的韧带样瘤登记处基础上,自2017年9月启动以来招募了更多的韧带样瘤参与者。它将有助于填补韧带样瘤的知识空白,并协助其他研究人员开展更多研究的招募工作。

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