Predictive Efficacy of Dual Therapies Combining Integrase Strand Transfer Inhibitors with Second-Generation Non-Nucleoside Reverse Transcriptase Inhibitors Following HIV-1 Treatment Failure in Cameroon: Implications for the Use of a Long-Acting Therapeutic Strategy in Low- and Middle-Income Countries

被引:0
作者
Gouissi Anguechia, Davy-Hyacinthe [1 ,2 ]
Bouba, Yagai [1 ,3 ]
Semengue, Ezechiel Ngoufack Jagni [1 ,4 ]
Ka'e, Aude Christelle [1 ]
Takou, Desire [1 ,4 ]
Ambe Chenwi, Collins [1 ,4 ,5 ]
Beloumou, Grace [1 ]
Nka, Alex Durand [1 ]
Basseck Wome, Ulrich Roland [1 ]
Santoro, Maria Mercedes [5 ]
Ceccherini-Silberstein, Francesca [5 ]
Chatte, Adawaye [6 ]
Montesano, Carla [7 ]
Cappelli, Giulia [8 ,9 ]
Colizzi, Vittorio [1 ,9 ,10 ,11 ]
Ndjolo, Alexis [1 ,2 ]
Mbanya, Dora [2 ]
Ndembi, Nicaise [12 ,13 ]
Perno, Carlo-Federico [1 ,14 ]
Fokam, Joseph [1 ,4 ,15 ,16 ]
机构
[1] Chantal BIYA Int Reference Ctr Res HIV AIDS Preven, POB 3077, Yaounde, Cameroon
[2] Univ Yaounde I, Fac Med & Biomed Sci, POB 337, Yaounde, Cameroon
[3] UniCamillus St Camillus Int Univ Hlth Sci, Fac Med, I-00131 Rome, Italy
[4] Natl HIV Drug Resistance Working Grp, POB 1459, Yaounde, Cameroon
[5] Univ Roma Tor Vergata, Dept Expt Med, I-00133 Rome, Italy
[6] Minist Hlth, Project Management Unit, POB 548, Ndjamena, Chad
[7] Univ Roma Tor Vergata, Dept Biol, I-00133 Rome, Italy
[8] CNR, I-00185 Rome, Italy
[9] Ctr Hosp Univ Reference Natl CHU RN, POB 456, Ndjamena, Chad
[10] Univ Roma Tor Vergata, EUROBIOPARK & UNSECO Board Biotechnol, I-00133 Rome, Italy
[11] Evangel Univ Cameroon, Fac Sci & Technol, POB 127, Bandjoun, Cameroon
[12] Africa Ctr Dis Control & Prevent, POB 3243, Addis Ababa, Ethiopia
[13] Inst Human Virol, Baltimore, MD 21201 USA
[14] IRCCS, Bambino Gesu Children Hosp, I-00146 Rome, Italy
[15] Univ Buea, Fac Hlth Sci, POB 63, Buea, Cameroon
[16] Natl AIDS Control Comm, Cent Tech Grp, POB 1459, Yaounde, Cameroon
来源
VIRUSES-BASEL | 2024年 / 16卷 / 12期
关键词
HIV-1; dual therapies; predictive efficacy; non-nucleosides reverse transcriptase inhibitors; integrase strand transfer inhibitor; Cameroon; VIROLOGICAL FAILURE; DRUG-RESISTANCE; RILPIVIRINE; DOLUTEGRAVIR; PREVALENCE; ETRAVIRINE; REGIMENS; TOXICITY; SAFETY;
D O I
10.3390/v16121853
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Dual therapies (DT) combining integrase strand transfer inhibitors (INSTIs) with second-generation non-nucleoside reverse transcriptase inhibitors (2nd-Gen-NNRTIs) offer new possibilities for HIV treatment to improve adherence. However, drug resistance associated mutations (RAMs) to prior antiretrovirals may jeopardize the efficacy of DT. We herein describe the predicted efficacy of DT combining INSTIs + 2nd-Gen-NNRTI following treatment failure among Cameroonian patients. We genotyped the HIV-1 pol gene using Sanger sequencing and assessed acquired RAMs to NNRTIs and INSTIs in patients failing treatment from March 2019 to December 2023. Drug susceptibility was interpreted using Stanford HIVdb v9.5, and statistical analyses were performed using SPSS v22. Of 130 successfully genotyped participants (median age (IQR): 38 (27-46) years; 59.2% female), 92.3% had RAMs to NNRTIs and 1.5% to INSTIs. Prevailing RAMs were Y181C (32.3%) among NNRTIs and R263K (0.7%) among INSTIs. Among 2nd-Gen-NNRTIs, etravirine, doravirine and rilpivirine had 43.85%, 41.54% and 38.46% genotypic sensitivity, respectively. Among INSTIs, we found 97.69% efficacy for dolutegravir/bictegravir, 96.15% for cabotegravir and 92.31% for elvitegravir/raltegravir. The overall predictive efficacy of DT was lower among participants who failed 1st-Gen-NNRTI (p < 0.001); with etravirine + dolutegravir/bictegravir combination showing the highest score (43.8%). Conclusively, DT combining INSTIs + 2nd-Gen-NNRTIs might be suboptimal in the context of previous ART failure, especially with NNRTI-based treatment in low- and middle-income countries. The general data clearly indicate that without resistance testing, it is nearly impossible to use long-acting dual therapies in previously failing patients.
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页数:12
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