The Forteo Patient Registry linkage to multiple state cancer registries: study design and results from the first 8 years
Autor: | David Harris, Elizabeth Andrews, Alicia Gilsenan, Kirk Midkiff, N Kellier-Steele, Abenah Harding |
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Rok vydání: | 2018 |
Předmět: |
Adult
Male Registry medicine.medical_specialty Adolescent Endocrinology Diabetes and Metabolism Bone Neoplasms 030209 endocrinology & metabolism Young Adult 03 medical and health sciences 0302 clinical medicine Study methods Teriparatide Internal medicine Product Surveillance Postmarketing Humans Medicine Registries 030212 general & internal medicine Link data Aged Aged 80 and over Linkage (software) Osteosarcoma Bone Density Conservation Agents Patient registry Linkage business.industry Patient Selection Incidence (epidemiology) Cancer Middle Aged medicine.disease United States Cancer registry Research Design Original Article Female Medical Record Linkage business medicine.drug |
Zdroj: | Osteoporosis International |
ISSN: | 1433-2965 0937-941X |
DOI: | 10.1007/s00198-018-4604-8 |
Popis: | Summary The Forteo Patient Registry (FPR) aims to estimate the incidence of osteosarcoma in US patients treated with teriparatide. Enrollment began in 2009 and will continue through 2019, with linkage planned through 2024. To date, no incident cases of osteosarcoma have been identified among patients registered in the FPR. Introduction The Forteo Patient Registry (FPR) was established in 2009 to estimate the incidence of osteosarcoma in US patients treated with teriparatide. The objective of this paper is to describe study methods, challenges encountered, and progress to date. Methods The FPR is a prospective US registry designed to link data from participants annually with state cancer registries. Patient enrollment is planned for 10 years (2009–2019) and annual linkage with US state cancer registries for 15 years (2010–2024). All US state cancer registries and DC were invited to participate. Patients are recruited using pre-enrollment materials included in teriparatide device packaging, kits, and brochures distributed by health-care providers; a toll-free number; and a study website. A linkage algorithm is used to match data from enrolled participants with cancer registry data. Results For the eighth annual linkage in 2017, information necessary for linkage with 63,270 patients in the FPR was submitted to each of the 42 participating registries. These patients contributed approximately 242,782 person-years of follow-up. A total of 5268 adult osteosarcoma cases diagnosed since January 1, 2009, were available for linkage from participating state cancer registries. To date, no incident cases of osteosarcoma have been identified among patients registered in the FPR. Conclusions Based on the estimated 242,782 person-years of observation as of the eighth annual linkage and projecting current enrollment rate to study end in 2024, it is anticipated that the completed study will be able to detect a fourfold increase in the risk of osteosarcoma if one exists. Electronic supplementary material The online version of this article (10.1007/s00198-018-4604-8) contains supplementary material, which is available to authorized users. |
Databáze: | OpenAIRE |
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