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Article

The Use of Computational Models to Predict Response to HIV Therapy for Clinical Cases in Romania †

by
Andrew D Revell
1,*,
LuminiŢA Ene
2,
Dan Duiculescu
2,
Dechao Wang
1,
Mike Youle
4,
Anton Pozniak
5,
Julio Montaner
6 and
Brendan A Larder
1
1
RDI, 14 Union Square, London N1 7DH, UK
2
‘Dr. Victor Babeş’ Hospital for Infectious and Tropical Diseases, 030303 Bucharest, Romania
3
HIV Training and Resource Initiative, London SE1 0BB, UK
4
Chelsea and Westminster Hospital, London SW10 9NH, UK
5
BC Centre for Excellence in HIV and AIDS, Vancouver, BC V6Z 1Y6, Canada
*
Author to whom correspondence should be addressed.
Presented in part: 18th Conference on Retroviruses and Opportunistic Infections (CROI), Boston, USA, March 2011 (Abstract L-208).
Submission received: 13 December 2011 / Accepted: 19 January 2012 / Published: 1 March 2012

Abstract

Introduction: A major challenge in Romania is the optimisation of antiretroviral therapy for the many HIV-infected adults with, on average, a decade of treatment experience. The RDI has developed computational models that predict virological response to therapy but these require a genotype, which is not routinely available in Romania. Moreover the models, which were trained without any Romanian data, have proved most accurate for patients from the healthcare settings that contributed the training data. Here we develop and test a novel model that does not require a genotype, with test data from Romania. Methods: A random forest (RF) model was developed to predict the probability of the HIV viral load (VL) being reduced to <50 copies/ml following therapy change. The input variables were baseline VL, CD4 count, treatment history and time to follow-up. The model was developed with 3188 treatment changes episodes (TCEs) from North America, Western Europe and Australia. The model’s predictions for 100 independent TCEs from the RDI database were compared to those of a model trained with the same data plus genotypes and then tested using 39 TCEs from Romania in terms of the area under the ROC curve (AUC). Results: When tested with the 100 independent RDI TCEs, the AUC values for the models with and without genotypes were 0.88 and 0.86 respectively. For the 39 Romanian TCEs the AUC was 0.60. However, when 14 cases with viral loads that may have been between 50 and 400 copies were removed, the AUC increased to 0.83. Discussion: Despite having been trained without data from Romania, the model predicted treatment responses in treatment-experienced Romanian patients with clade F virus accurately without the need for a genotype. The results suggest that this approach might be generalisable and useful in helping design optimal salvage regimens for treatment-experienced patients in countries with limited resources where genotyping is not always available.
Keywords: HIV; treatment response prediction; computational models HIV; treatment response prediction; computational models

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MDPI and ACS Style

Revell, A.D.; Ene, L.; Duiculescu, D.; Wang, D.; Youle, M.; Pozniak, A.; Montaner, J.; A Larder, B. The Use of Computational Models to Predict Response to HIV Therapy for Clinical Cases in Romania. GERMS 2012, 2, 6-11. https://doi.org/10.11599/germs.2012.1007

AMA Style

Revell AD, Ene L, Duiculescu D, Wang D, Youle M, Pozniak A, Montaner J, A Larder B. The Use of Computational Models to Predict Response to HIV Therapy for Clinical Cases in Romania. GERMS. 2012; 2(1):6-11. https://doi.org/10.11599/germs.2012.1007

Chicago/Turabian Style

Revell, Andrew D, LuminiŢA Ene, Dan Duiculescu, Dechao Wang, Mike Youle, Anton Pozniak, Julio Montaner, and Brendan A Larder. 2012. "The Use of Computational Models to Predict Response to HIV Therapy for Clinical Cases in Romania" GERMS 2, no. 1: 6-11. https://doi.org/10.11599/germs.2012.1007

APA Style

Revell, A. D., Ene, L., Duiculescu, D., Wang, D., Youle, M., Pozniak, A., Montaner, J., & A Larder, B. (2012). The Use of Computational Models to Predict Response to HIV Therapy for Clinical Cases in Romania. GERMS, 2(1), 6-11. https://doi.org/10.11599/germs.2012.1007

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