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. Author manuscript; available in PMC: 2020 Jul 31.
Published in final edited form as: Crit Rev Toxicol. 2018 Feb 23;48(5):359–374. doi: 10.1080/10408444.2018.1429386

Table 6.

Defined Approach (DA) performance in predicting LLNA sensitizing potency.

Predicting LLNA Potency (Strong, Weak, Non-sensitizers)
Defined Approach: Kao
STS
Kao
ITS
Shiseido ANN
(D_hC)
Shiseido
ANN
(D_hC_KS)
P&G
BN ITS-3
N 126 120 126 126 115
Accuracy (%)* 67.5 66.7 65.1 69.8 67.8
Over-predicted (%) 21.4 14.2 21.4 23.0 12.2
Under-predicted (%) 11.1 19.2 13.5 7.1 20.0
*

Performance was assessed for prediction of three potency classes as described in the main text, and is shown against the maximum subset (N) out of 128 substances with all necessary DA features. With the exception of the P&G BN ITS-3, all DA human potency predictions were off by one class only (i.e. no non-sensitizers predicted as strong or vice versa.) Abbreviations: LLNA: local lymph node assay, STS: sequential testing strategy, ITS: integrated testing strategy, SVM: support vector machine, ANN: artificial neural network, BN: Bayesian network, DKH and D_hC_KS: DPRA/hCLAT/KeratinoSens™, D_hC: DPRA/hCLAT