Harmonization of immune biomarker assays for clinical studies.


Autoria(s): van der Burg S.H.; Kalos M.; Gouttefangeas C.; Janetzki S.; Ottensmeier C.; Welters M.J.; Romero P.; Britten C.M.; Hoos A.
Data(s)

2011

Resumo

Assays that measure a patient's immune response play an increasingly important role in the development of immunotherapies. The inherent complexity of these assays and independent protocol development between laboratories result in high data variability and poor reproducibility. Quality control through harmonization--based on integration of laboratory-specific protocols with standard operating procedures and assay performance benchmarks--is one way to overcome these limitations. Harmonization guidelines can be widely implemented to address assay performance variables. This process enables objective interpretation and comparison of data across clinical trial sites and also facilitates the identification of relevant immune biomarkers, guiding the development of new therapies.

Identificador

https://serval.unil.ch/?id=serval:BIB_03DCFBBD2035

isbn:1946-6242 (Electronic)

pmid:22072636

doi:10.1126/scitranslmed.3002785

isiid:000296765800002

Idioma(s)

en

Fonte

Science Translational Medicine, vol. 3, no. 108, pp. 108ps44

Tipo

info:eu-repo/semantics/article

article