Impact of the mutational load on the virological response to a first-line rilpivirine-based regimen
- Dimeglio, Chloé;
- Raymond, Stéphanie;
- Nicot, Florence;
- Jeanne, Nicolas;
- Carcenac, Romain;
- Lefebvre, Caroline;
- Izopet, Jacques;
- Roussel, C;
- Guillou-Guillemette, H Le;
- Alloui, C;
- Bettinger, D;
- Pallier, C;
- Fleury, H;
- Bellecave, P;
- Recordon-Pinson, P;
- Payan, C;
- Vallet, S;
- Vabret, A;
- Dina, J;
- Henquell, C;
- Mirand, A;
- Bouvier-Alias, M;
- de Rougemont, A;
- Si-Mohammed, A;
- Santos, G Dos;
- Morand, P;
- Signori-Schmuck, A;
- Bocket, L;
- Rogez, S;
- Andre, P;
- Tardy, JC;
- Trabaud, MA;
- Tamalet, C;
- Delamare, C;
- Montes, B;
- Schvoerer, E;
- Jeulin, H;
- Ferré, V;
- Rodallec, A;
- Guen, L Le;
- Cottalorda, J;
- Guinard, J;
- Guiguon, A;
- Descamps, D;
- Charpentier, C;
- Visseaux, B;
- Peytavin, G;
- Krivine, A;
- Bouviers-Alias, M;
- Avettand-Fenoel, V;
- Pallier, C;
- Marcelin, AG;
- Calvez, V;
- Soulié, C;
- Wirden, M;
- Morand-Joubert, L;
- Lambert-Niclot, S;
- Fofana, D;
- Delaugerre, C;
- Chaix, ML;
- Mahjoub, N;
- Amiel, C;
- Schneider, V;
- Giraudeau, G;
- Beby-Defaux, A;
- Brodard, V;
- Maillard, A;
- Plantier, JC;
- Mourez, T;
- Leoz, M;
- Chaplain, C;
- Bourlet, T;
- Fafi-Kremer, S;
- Stoll-Keller, F;
- Schmitt, MP;
- Barth, H;
- Yerly, S;
- Poggi, C;
- Izopet, J;
- Raymond, S;
- Barin, F;
- Chaillon, A;
- Marque-Juillet, S;
- Roque-Afonso, AM;
- Haïm-Boukobza, S;
- Flandre, P;
- Grudé, M;
- Assoumou, L;
- Costagliola, D
Published Web Location
https://academic.oup.com/jac/article-abstract/74/3/718/5232574?redirectedFrom=fulltextAbstract
OBJECTIVES: To determine how the load of rilpivirine-resistant variants (mutational load) influences the virological response (VR) of HIV-1-infected patients to a rilpivirine-based first-line regimen. PATIENTS AND METHODS: Four hundred and eighty-nine patients infected with HIV-1 whose reverse transcriptase gene had been successfully resistance genotyped using next-generation sequencing were given a first-line regimen containing rilpivirine. Variables associated with the VR at 12 months were identified using a logistic model. The results were used to build a multivariate model for each mutational load threshold and the R2 variations were analysed to identify the mutational load threshold that best predicted the VR. RESULTS: The mutational load at baseline was the only variable linked to the VR at 12 months (P < 0.01). The VR at 12 months decreased from 96.9% to 83.4% when the mutational load was >1700 copies/mL and to 50% when the mutational load was > 9000 copies/mL. The threshold of 9000 copies/mL was associated with the VR at 12 months with an OR of 36.7 (95% CI 4.7-285.1). The threshold of 1700 copies/mL was associated with the VR at 12 months with an OR of 7.2 (95% CI 1.4-36.8). CONCLUSIONS: There is quantifiable evidence that determining a mutational load threshold can be used to identify those patients on a first-line regimen containing rilpivirine who are at risk of virological failure. The clinical management of HIV-infected patients can be improved by evaluating the frequency of mutant variants at a threshold of < 20% together with the plasma HIV-1 viral load at the time of resistance genotyping.
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