TY - JOUR
T1 - Recommendation on test readiness criteria for new approach methods in toxicology
T2 - Exemplified for developmental neurotoxicity
AU - Bal-Price, Anna
AU - Hogberg, Helena T.
AU - Crofton, Kevin M.
AU - Daneshian, Mardas
AU - FitzGerald, Rex E.
AU - Fritsche, Ellen
AU - Heinonen, Tuula
AU - Hougaard Bennekou, Susanne
AU - Klima, Stefanie
AU - Piersma, Aldert H.
AU - Sachana, Magdalini
AU - Shafer, Timothy J.
AU - Terron, Andrea
AU - Monnet-Tschudi, Florianne
AU - Viviani, Barbara
AU - Waldmann, Tanja
AU - Westerink, Remco H.S.
AU - Wilks, Martin F.
AU - Witters, Hilda
AU - Zurich, Marie Gabrielle
AU - Leist, Marcel
PY - 2018
Y1 - 2018
N2 - Multiple non-animal-based test methods have never been formally validated. In order to use such new approach methods (NAMs) in a regulatory context, criteria to define their readiness are necessary. The field of developmental neurotoxicity (DNT) testing is used to exemplify the application of readiness criteria. The costs and number of untested chemicals are overwhelming for in vivo DNT testing. Thus, there is a need for inexpensive, high-throughput NAMs, to obtain initial information on potential hazards, and to allow prioritization for further testing. A background on the regulatory and scientific status of DNT testing is provided showing different types of test readiness levels, depending on the intended use of data from NAMs. Readiness criteria, compiled during a stakeholder workshop, uniting scientists from academia, industry and regulatory authorities are presented. An important step beyond the listing of criteria, was the suggestion for a preliminary scoring scheme. On this basis a (semi)-quantitative analysis process was assembled on test readiness of 17 NAMs with respect to various uses (e.g. prioritization/screening, risk assessment). The scoring results suggest that several assays are currently at high readiness levels. Therefore, suggestions are made on how DNT NAMs may be assembled into an integrated approach to testing and assessment (IATA). In parallel, the testing state in these assays was compiled for more than 1000 compounds. Finally, a vision is presented on how further NAM development may be guided by knowledge of signaling pathways necessary for brain development, DNT pathophysiology, and relevant adverse outcome pathways (AOP).
AB - Multiple non-animal-based test methods have never been formally validated. In order to use such new approach methods (NAMs) in a regulatory context, criteria to define their readiness are necessary. The field of developmental neurotoxicity (DNT) testing is used to exemplify the application of readiness criteria. The costs and number of untested chemicals are overwhelming for in vivo DNT testing. Thus, there is a need for inexpensive, high-throughput NAMs, to obtain initial information on potential hazards, and to allow prioritization for further testing. A background on the regulatory and scientific status of DNT testing is provided showing different types of test readiness levels, depending on the intended use of data from NAMs. Readiness criteria, compiled during a stakeholder workshop, uniting scientists from academia, industry and regulatory authorities are presented. An important step beyond the listing of criteria, was the suggestion for a preliminary scoring scheme. On this basis a (semi)-quantitative analysis process was assembled on test readiness of 17 NAMs with respect to various uses (e.g. prioritization/screening, risk assessment). The scoring results suggest that several assays are currently at high readiness levels. Therefore, suggestions are made on how DNT NAMs may be assembled into an integrated approach to testing and assessment (IATA). In parallel, the testing state in these assays was compiled for more than 1000 compounds. Finally, a vision is presented on how further NAM development may be guided by knowledge of signaling pathways necessary for brain development, DNT pathophysiology, and relevant adverse outcome pathways (AOP).
KW - developmental in vitro neurotoxicity testing
KW - quality assurance
KW - regulatory toxicology
KW - toxicity screening
UR - http://www.scopus.com/inward/record.url?scp=85051034983&partnerID=8YFLogxK
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U2 - 10.14573/altex.1712081
DO - 10.14573/altex.1712081
M3 - Article
C2 - 29485663
AN - SCOPUS:85051034983
SN - 1868-596X
VL - 35
SP - 306
EP - 352
JO - ALTEX
JF - ALTEX
IS - 3
ER -