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Influenza: Aktuelles und State of the Art - Österreichische ...

Influenza: Aktuelles und State of the Art - Österreichische ...

Influenza: Aktuelles und State of the Art - Österreichische ...

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| kongress<br />

Fighting HIV<br />

New antiretroviral agents<br />

and novel regimens<br />

Improvements in antiretroviral <strong>the</strong>rapy (ART) have made <strong>the</strong> treatment <strong>of</strong> HIV infections more potent and<br />

better tolerated. While current treatment regimens still have limitations, <strong>the</strong>y are more effective, more<br />

convenient, and less toxic than those that were used in <strong>the</strong> early ART era. Joel E. Gallant, MD, MPH, Johns<br />

Hopkins University School <strong>of</strong> Medicine, Baltimore, Maryland, USA, discussed studies that have shown<br />

<strong>the</strong> effectiveness <strong>of</strong> new and potential ART <strong>the</strong>rapies, including single-tablet regimens, c<strong>of</strong>ormulations,<br />

nucleoside reverse transcriptase inhibitor (NRTI)-sparing regimens, CCR5 antagonists as initial <strong>the</strong>rapy,<br />

and new entry inhibitors.<br />

ECHO [NCT00540449] and THRIVE<br />

[NCT00543725], two randomized Phase<br />

3 trials, showed that <strong>the</strong> recently approved<br />

non-nucleoside reverse trans criptase<br />

inhibitor (NNRTI) rilpivirine (RPV) has<br />

sustained efficacy that is noninferior to<br />

efavirenze (EFV) in ART-naïve adults<br />

who are infected with HIV-1 [Cohen CJ<br />

et al, Lancet 2011; Molina JM et al, Lancet<br />

2011]. There were fewer discontinuations<br />

that were due to adverse events<br />

and fewer treatment-limiting side effects<br />

(especially neurological and dermatological)<br />

in <strong>the</strong> RPV arm but more virologic<br />

failure and resistance compared<br />

with <strong>the</strong> EFV arm,<br />

most notably in participants<br />

with baseline viral loads<br />

>100,000 copies/mL (Fig. 1).<br />

RPV has been approved<br />

both as a single agent and<br />

in a c<strong>of</strong>ormula tion with<br />

ten<strong>of</strong>ovir DF (TDF) and<br />

emtricitabine (FTC). It is<br />

taken once daily with a<br />

meal and is contraindi cated<br />

in patients who are taking<br />

proton pump inhibitors.<br />

In <strong>the</strong> MERIT study<br />

[NCT00098293], maraviroc<br />

(MVC) BID was not<br />

nonin ferior to EFV at

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