Standardizing in vitro diagnostics tasks in clinical trials: a call for action

被引:19
作者
Lippi, Giuseppe [1 ,2 ,8 ]
Simundic, Ana-Maria [1 ,3 ]
Rodriguez-Manas, Leocadio [4 ]
Bossuyt, Patrick [5 ,6 ]
Banfi, Giuseppe [7 ,8 ]
机构
[1] Univ Verona, Working Grp Preanalyt Phase WG PRE, European Federat Clin Chem & Lab Med EFLM, Verona, Italy
[2] Univ Verona, Sect Clin Biochem, Verona, Italy
[3] Univ Hosp Sveti Duh, Dept Med Lab Diagnost, Zagreb, Croatia
[4] Hosp Univ Getafe, Dept Geriatr, Getafe, Spain
[5] Univ Amsterdam, Acad Med Ctr, Dept Clin Epidemiol Biostat & Bioinform, Amsterdam, Netherlands
[6] STARD Stand Reporting Diagnost Accuracy Grp, Amsterdam, Netherlands
[7] IRCCS Galeazzi, Milan, Italy
[8] Vita & Salute San Raffaele Univ, Milan, Italy
关键词
Clinical trials; quality; preanalytical variability; safety; CHEMISTRY; HEMOLYSIS; INTERFERENCE; GUIDELINES; COLLECTION; QUALITY;
D O I
10.21037/atm.2016.04.10
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Translational research is defined as the process of applying ideas, insights and discoveries generated through basic scientific inquiry to treatment or prevention of human diseases. Although precise information is lacking, several lines of evidence attest that up to 95% early-phase studies may not translate into tangible outcomes for improving clinical management. Major theoretical hurdles exist in the translational process, but is it also undeniable that many studies may have failed for practical reasons, such as the use of inappropriate diagnostic testing for evaluating efficacy, effectiveness or safety of a given medical intervention, or poor quality in laboratory testing. This can generate biased test results and result in misconceptions during data interpretation, eventually leading to no clinical benefit, possible harm, and a waste of valuable resources. From a genuine economic perspective, it can be estimated that over 10 million euros of funding may be lost each year in clinical trials in the European Union due to preanalytical and analytical problems. These are mostly attributions to the heterogeneity of current guidelines and recommendations for the testing process, to the poor evidence base for basic preanalytical, analytical and post-analytical requirements in clinical trials, and to the failure to thoughtfully integrate the perspectives of clinicians, patients, nurses and diagnostic companies in laboratory best practices. The most rational means for filling the gap between what we know and what we practice in clinical trials cannot discount the development of multidisciplinary teams including research scientists, clinicians, nurses, patients associations and representative of in vitro diagnostic (IVD) companies, who should actively interplay and collaborate with laboratory professionals to adapt and disseminate evidence-based recommendations about biospecimen collection and management into the research settings, from preclinical to phase III studies.
引用
收藏
页数:7
相关论文
共 30 条
[1]   Effect of interference from hemolysis, icterus and lipemia on routine pediatric clinical chemistry assays [J].
Agarwal, Shweta ;
Vargas, German ;
Nordstrom, Cristina ;
Tam, Estella ;
Buffone, Gregory J. ;
Devaraj, Sridevi .
CLINICA CHIMICA ACTA, 2015, 438 :241-245
[2]   Lost in clinical translation [J].
不详 .
NATURE MEDICINE, 2004, 10 (09) :879-879
[3]   The impact of preanalytical variability in clinical trials: are we underestimating the issue? [J].
Banfi, Giuseppe ;
Lippi, Giuseppe .
ANNALS OF TRANSLATIONAL MEDICINE, 2016, 4 (03)
[4]   STARD 2015: updated reporting guidelines for all diagnostic accuracy studies [J].
Bossuyt, Patrick M. ;
Cohen, Jeremie F. ;
Gatsonis, Constantine A. ;
Korevaar, Daniel A. .
ANNALS OF TRANSLATIONAL MEDICINE, 2016, 4 (04)
[5]   Interferences from blood collection tube components on clinical chemistry assays [J].
Bowen, Raffick A. R. ;
Remaley, Alan T. .
BIOCHEMIA MEDICA, 2014, 24 (01) :31-44
[6]   Methodological and Analytic Considerations for Blood Biomarkers [J].
Christenson, Robert H. ;
Duh, Show-Hong .
PROGRESS IN CARDIOVASCULAR DISEASES, 2012, 55 (01) :25-33
[7]   The degree of acceptability of swine blood values at increasing levels of hemolysis evaluated through visual inspection versus automated quantification [J].
Di Martino, Guido ;
Stefani, Anna Lisa ;
Lippi, Giuseppe ;
Gagliazzo, Laura ;
McCormick, Wanda ;
Gabai, Gianfranco ;
Bonfanti, Lebana .
JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2015, 27 (03) :306-312
[8]   In Search of 'Omics'-Based Biomarkers to Predict Risk of Frailty and Its Consequences in Older Individuals: The FRAILOMIC Initiative [J].
Erusalimsky, Jorge D. ;
Grillari, Johannes ;
Grune, Tilman ;
Jansen-Duerr, Pidder ;
Lippi, Giuseppe ;
Sinclair, Alan J. ;
Tegner, Jesper ;
Vina, Jose ;
Durrance-Bagale, Anna ;
Minambres, Rebeca ;
Viegas, Marcelo ;
Rodriguez-Manas, Leocadio .
GERONTOLOGY, 2016, 62 (02) :182-190
[9]  
EudraCT, ENDRACT STAT
[10]  
European Medicines Agency, REFL PAP NONCL EV DR