TY - JOUR
T1 - Implementation of proteomic biomarkers
T2 - making it work
AU - Mischak, Harald
AU - Ioannidis, John P A
AU - Argilés, Angel
AU - Attwood, Teresa K
AU - Bongcam-Rudloff, Erik
AU - Broenstrup, Mark
AU - Charonis, Aristidis
AU - Chrousos, George P
AU - Delles, Christian
AU - Dominiczak, Anna
AU - Dylag, Tomasz
AU - Ehrich, Jochen H H
AU - Egido, Jesus
AU - Findeisen, Peter
AU - Jankowski, Joachim
AU - Johnson, Robert W
AU - Julien, Bruce A
AU - Lankisch, Tim
AU - Leung, Hing Y
AU - Maahs, David M
AU - Magni, Fulvio
AU - Manns, Michael P
AU - Manolis, Efthymios
AU - Mayer, Gert
AU - Navis, Gerjan
AU - Novak, Jan
AU - Ortiz, Alberto
AU - Persson, Frederik
AU - Peter, Karlheinz
AU - Riese, Hans H
AU - Rossing, Peter
AU - Sattar, Naveed
AU - Spasovski, Goce
AU - Thongboonkerd, Visith
AU - Vanholder, Raymond
AU - Schanstra, Joost P
AU - Vlahou, Antonia
N1 - © 2012 The Authors. European Journal of Clinical Investigation © 2012 Stichting European Society for Clinical Investigation Journal Foundation.
PY - 2012/9
Y1 - 2012/9
N2 - While large numbers of proteomic biomarkers have been described, they are generally not implemented in medical practice. We have investigated the reasons for this shortcoming, focusing on hurdles downstream of biomarker verification, and describe major obstacles and possible solutions to ease valid biomarker implementation. Some of the problems lie in suboptimal biomarker discovery and validation, especially lack of validated platforms with well-described performance characteristics to support biomarker qualification. These issues have been acknowledged and are being addressed, raising the hope that valid biomarkers may start accumulating in the foreseeable future. However, successful biomarker discovery and qualification alone does not suffice for successful implementation. Additional challenges include, among others, limited access to appropriate specimens and insufficient funding, the need to validate new biomarker utility in interventional trials, and large communication gaps between the parties involved in implementation. To address this problem, we propose an implementation roadmap. The implementation effort needs to involve a wide variety of stakeholders (clinicians, statisticians, health economists, and representatives of patient groups, health insurance, pharmaceutical companies, biobanks, and regulatory agencies). Knowledgeable panels with adequate representation of all these stakeholders may facilitate biomarker evaluation and guide implementation for the specific context of use. This approach may avoid unwarranted delays or failure to implement potentially useful biomarkers, and may expedite meaningful contributions of the biomarker community to healthcare.
AB - While large numbers of proteomic biomarkers have been described, they are generally not implemented in medical practice. We have investigated the reasons for this shortcoming, focusing on hurdles downstream of biomarker verification, and describe major obstacles and possible solutions to ease valid biomarker implementation. Some of the problems lie in suboptimal biomarker discovery and validation, especially lack of validated platforms with well-described performance characteristics to support biomarker qualification. These issues have been acknowledged and are being addressed, raising the hope that valid biomarkers may start accumulating in the foreseeable future. However, successful biomarker discovery and qualification alone does not suffice for successful implementation. Additional challenges include, among others, limited access to appropriate specimens and insufficient funding, the need to validate new biomarker utility in interventional trials, and large communication gaps between the parties involved in implementation. To address this problem, we propose an implementation roadmap. The implementation effort needs to involve a wide variety of stakeholders (clinicians, statisticians, health economists, and representatives of patient groups, health insurance, pharmaceutical companies, biobanks, and regulatory agencies). Knowledgeable panels with adequate representation of all these stakeholders may facilitate biomarker evaluation and guide implementation for the specific context of use. This approach may avoid unwarranted delays or failure to implement potentially useful biomarkers, and may expedite meaningful contributions of the biomarker community to healthcare.
KW - Biomarkers
KW - Biomedical Research
KW - Clinical Trials as Topic
KW - Drug Discovery
KW - Humans
KW - Proteomics
KW - Journal Article
KW - Research Support, Non-U.S. Gov't
UR - https://www.scopus.com/pages/publications/84865194855
U2 - 10.1111/j.1365-2362.2012.02674.x
DO - 10.1111/j.1365-2362.2012.02674.x
M3 - Journal article
C2 - 22519700
SN - 0014-2972
VL - 42
SP - 1027
EP - 1036
JO - European Journal of Clinical Investigation
JF - European Journal of Clinical Investigation
IS - 9
ER -