کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5528189 1547959 2017 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Economic burden of clinical trials in lung cancer in a German Comprehensive Cancer Center
ترجمه فارسی عنوان
بار اقتصادی از آزمایشات بالینی در سرطان ریه در یک مرکز سرطان آلمان
کلمات کلیدی
سرطان ریه، آزمایشات بالینی، درمان فردی، پزشکی دقیق، محاسبه هزینه، مرکز سرطان،
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی تحقیقات سرطان
چکیده انگلیسی


- Lung cancer research has a strong focus on early proof of concept trials.
- Trials with low patient numbers/investigator-initiated trials are economic risks.
- There is a need for full cost compensation by pharmaceutical companies.
- There is a need for novel structures in public funding in precision medicine.

ObjectivesThe recent success of individualized lung cancer therapy has triggered fundamental changes in clinical research strategies. To date there is a strong focus on early proof of concept trials in genetically preselected small patient subgroups. This analysis focuses on the economic burden caused by such trials for advanced lung cancer patients in a German Comprehensive Cancer Center (CCC).MethodsThe profit margins between recruiting groups with ≤3 and >3 patients were compared. Clinical and economic data from clinical trials for advanced lung cancer (LC), pharma-sponsored trials (PhST) as well as investigator initiated trials (IIT), conducted between 2011 and 2015 at the Center for Integrated Oncology (CIO) Cologne, were analyzed using a profit-center calculation model.Results161 patients were enrolled in 27 clinical trials. The key economic parameter determining costs and payments was the 'trial visits'. In comparison of the two groups (A ≤ 3; B > 3 patients enrolled) we found negative profit margins for the low recruiting group (€ −1444). Concerning the number of visits significant differences were found between PhST and IIT (p = 0.009). Additionally, sub-analysis show structural differences in cost composition by conducting PhST and IIT.ConclusionTrials with low patient numbers and IIT, do not cover the cost. To ensure adequate, cost-covering compensation by pharmaceutical companies CCCs have to thoroughly calculate the cost of early proof of concept trials. The findings of this study also underline the need for novel structures in public funding for investigator-initiated clinical trials in precision medicine.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Lung Cancer - Volume 108, June 2017, Pages 134-139
نویسندگان
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