Effect of Baseline Characteristics on the Efficacy and Safety of Once-Daily Darunavir/Ritonavir in HIV-1-Infected, Treatment-Naive ARTEMIS Patients at Week 96


Por: Fourie, J, Flamm, J, Rodriguez-French, A, Kilby, D, Domingo, P, Lazzarin, A, Ballesteros, J, Sosa, N, Van De Casteele, T, DeMasi, R, Spinosa-Guzman, S, Layreys, L

Publicada: 1 nov 2011
Resumen:
Objectives: ARTEMIS demonstrated significantly greater efficacy of once-daily darunavir/ritonavir (DRV/r) 800/100 mg versus lopinavir/ritonavir 800/200 mg (total daily dose) in treatment-naive, HIV-1-infected patients at week 96. The influence of baseline characteristics on efficacy and safety was analyzed in DRV/r patients. Methods: Patients received once-daily DRV/r plus fixed-dose tenofovir/emtricitabine. Week 96 efficacy and safety data were analyzed by gender (males, n = 239; females, n = 104), age (<= 30, n = 115; 31-45, n = 175; >45, n = 53), race (Asian, n = 44; Black, n = 80; Caucasian/White, n = 137; Hispanic, n = 77), and hepatitis B and/or C virus coinfection (n = 43). Results: Week 96 virologic response rates (HIV-1 RNA <50 copies/mL) were as follows: gender: 79% for both males and females; age: 72% (<= 30), 81% (31-45), and 89% (>45); race: 96% (Asian), 71% (Black), 77% (Caucasian/White), and 79% (Hispanic); coinfection status: 72% (coinfected) and 80% (non-coinfected). The incidence of treatment-related adverse drug reactions (ADRs) and laboratory abnormalities were comparable across gender, age, and race subgroups. Coinfected patients had a higher incidence of liver-related ADRs than non-coinfected patients. Conclusions: DRV/r 800/100 mg qd is an effective, well-tolerated treatment option for treatment-naive patients of different gender, age, race, or coinfection status.

Filiaciones:
Fourie, J:
 Dr J Fourie Med Practice, ZA-3000 Dundee, Kzn, South Africa

Flamm, J:
 Kaiser Permanente Med Grp, Sacramento, CA USA

Rodriguez-French, A:
 Hosp Santo Tomas, Panama City, Panama

Kilby, D:
 Univ Ottawa, Hlth Serv, Ottawa, ON, Canada

Domingo, P:
 Autonomous Univ Barcelona, Barcelona, Spain

Lazzarin, A:
 Ist Sci San Raffaele, I-20132 Milan, Italy

Ballesteros, J:
 Hosp Del Salvador, Santiago, Chile

Sosa, N:
 Med & Res Ctr, Panama City, Panama

Van De Casteele, T:
 Tibotec BVBA, Beerse, Belgium

DeMasi, R:
 Tibotec Inc, Titusville, NJ USA

Spinosa-Guzman, S:
 Tibotec BVBA, Beerse, Belgium

Layreys, L:
 Tibotec BVBA, Beerse, Belgium
ISSN: 15284336





HIV CLINICAL TRIALS
Editorial
TAYLOR & FRANCIS LTD, 2-4 PARK SQUARE, MILTON PARK, ABINGDON OR14 4RN, OXON, ENGLAND, Estados Unidos America
Tipo de documento: Article
Volumen: 12 Número: 6
Páginas: 313-322
WOS Id: 000298721800003
ID de PubMed: 22189150

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