Boosted Protease Inhibitor Monotherapy. What Have We Learnt after Seven Years of Research?
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作者:
Pulido, Federico
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Hosp 12 Octubre, HIV Unit, E-28041 Madrid, Spain
Univ Complutense Madrid, Fac Med, Madrid, SpainHosp 12 Octubre, HIV Unit, E-28041 Madrid, Spain
Pulido, Federico
[1
,2
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Matarranz, Mariano
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Hosp 12 Octubre, HIV Unit, E-28041 Madrid, SpainHosp 12 Octubre, HIV Unit, E-28041 Madrid, Spain
Matarranz, Mariano
[1
]
Rodriguez-Rivera, Violeta
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Hosp 12 Octubre, HIV Unit, E-28041 Madrid, SpainHosp 12 Octubre, HIV Unit, E-28041 Madrid, Spain
Rodriguez-Rivera, Violeta
[1
]
Fiorante, Silvana
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Hosp 12 Octubre, HIV Unit, E-28041 Madrid, Spain
Univ Europea Madrid, Dept Med Specialties, Madrid, SpainHosp 12 Octubre, HIV Unit, E-28041 Madrid, Spain
Fiorante, Silvana
[1
,3
]
Hemando, Asuncion
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Hosp 12 Octubre, HIV Unit, E-28041 Madrid, Spain
Univ Europea Madrid, Dept Med Specialties, Madrid, SpainHosp 12 Octubre, HIV Unit, E-28041 Madrid, Spain
Hemando, Asuncion
[1
,3
]
机构:
[1] Hosp 12 Octubre, HIV Unit, E-28041 Madrid, Spain
[2] Univ Complutense Madrid, Fac Med, Madrid, Spain
[3] Univ Europea Madrid, Dept Med Specialties, Madrid, Spain
Boosted protease inhibitor monotherapy has emerged as an antiretroviral alternative option to avoid the use of nucleosides. After more than seven years of research with hundreds of patients exposed to this kind of therapy, controversy about its use remains. While European and Spanish guidelines for the use of antiretroviral therapy in adults include monotherapy as an alternative for simplification, experts in the USA express the view that this strategy cannot be currently recommended. Our conclusion, after more than seven years of research, is that simplification of a suppressive triple antiretroviral therapy to boosted protease inhibitor monotherapy has demonstrated safety and efficacy in a high proportion of patients. Although this is not a strategy to implement indiscriminately in all patients, it could be a good option for those patients with toxicity related to nucleoside reverse transcriptase inhibitors, or for trying to avoid such toxicities in virologically controlled patients without previous failure to protease inhibitors, restarting nucleosides if the viral load does not remain undetectable. If simplification to monotherapy is selected to treat some patients, twice-daily lopinavir/ritonavir, or preferably once-daily darunavir/ritonavir, should be chosen as data with other boosted protease inhibitors are inconclusive or even nonexistent. Nevertheless, more studies focusing on the control of HIV replication in viral reservoirs with monotherapy, as with triple therapy, are warranted. (AIDS Rev. 2010;12:127-34)
机构:
Univ Illinois, Linguist, Urbana, IL 61801 USA
Univ Illinois, CMCLL, Urbana, IL 61801 USA
Univ Illinois, VWLL, Urbana, IL 61801 USA
Univ Illinois, Teaching Reading & Writing 2, Urbana, IL 61801 USAUniv Illinois, Linguist, Urbana, IL 61801 USA
Sadler, Randall
Dooly, Melinda
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Univ Autonoma Barcelona, Fac Educ, Barcelona, SpainUniv Illinois, Linguist, Urbana, IL 61801 USA