Clinically evaluating genotypic interpretation systems is essential to provide optimal guidance in designing potent individualized HIV-regimens. This study aimed at investigating the ability of the latest Rega algorithm to predict virological response on a short and longer period. MATERIALS METHODS: 9231 treatment changes episodes were extracted from an integrated patient database. The virological response after 8, 24 and 48 weeks was dichotomized to success and failure. Success was defined as a viral load below 50 copies/ml or alternatively, a 2 log decrease from the baseline viral load at 8 weeks. The predictive ability of Rega version 8 was analysed in comparison with that of previous evaluated version Rega 5 and two other algorithms (ANRS v2011.05 and Stanford HIVdb v6.0.11). A logistic model based on the genotypic susceptibility score was used to predict virological response, and additionally, confounding factors were added to the model. Performance of the models was compared using the area under the ROC curve (AUC) and a Wilcoxon signed-rank test.

Vercauteren, J., Beheydt, G., Prosperi, M., Libin, P., Imbrechts, S., Camacho, R., Clotet, B., De Luca, A., Grossman, Z., Kaiser, R., Sönnerborg, A., Torti, C., Van Wijngaerden, E., Schmit, J., Zazzi, M., Geretti, A., Vandamme, A., Van Laethem, K., Clinical evaluation of Rega 8: an updated genotypic interpretation system that significantly predicts HIV-therapy response, <<PLOS ONE>>, 2013; 8 (4): e61436-e61436. [doi:10.1371/journal.pone.0061436] [http://hdl.handle.net/10807/54173]

Clinical evaluation of Rega 8: an updated genotypic interpretation system that significantly predicts HIV-therapy response

De Luca, Andrea;Torti, Carlo;
2013

Abstract

Clinically evaluating genotypic interpretation systems is essential to provide optimal guidance in designing potent individualized HIV-regimens. This study aimed at investigating the ability of the latest Rega algorithm to predict virological response on a short and longer period. MATERIALS METHODS: 9231 treatment changes episodes were extracted from an integrated patient database. The virological response after 8, 24 and 48 weeks was dichotomized to success and failure. Success was defined as a viral load below 50 copies/ml or alternatively, a 2 log decrease from the baseline viral load at 8 weeks. The predictive ability of Rega version 8 was analysed in comparison with that of previous evaluated version Rega 5 and two other algorithms (ANRS v2011.05 and Stanford HIVdb v6.0.11). A logistic model based on the genotypic susceptibility score was used to predict virological response, and additionally, confounding factors were added to the model. Performance of the models was compared using the area under the ROC curve (AUC) and a Wilcoxon signed-rank test.
2013
Inglese
Vercauteren, J., Beheydt, G., Prosperi, M., Libin, P., Imbrechts, S., Camacho, R., Clotet, B., De Luca, A., Grossman, Z., Kaiser, R., Sönnerborg, A., Torti, C., Van Wijngaerden, E., Schmit, J., Zazzi, M., Geretti, A., Vandamme, A., Van Laethem, K., Clinical evaluation of Rega 8: an updated genotypic interpretation system that significantly predicts HIV-therapy response, <<PLOS ONE>>, 2013; 8 (4): e61436-e61436. [doi:10.1371/journal.pone.0061436] [http://hdl.handle.net/10807/54173]
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