Outcomes by sex following treatment initiation with darunavir/cobicistat in a large Spanish cohort of the CODAR study (GeSIDA 9316)


Por: Perez Elias, M, Alejos, B, Vivancos, M, Ribera, E, Galindo, M, Vilanova-Trillo, L, Fraile, L, Moral, S, De Lomas, J, Lozano, F, Garcia, M, Pitarch, M, Martinez, M, Rojas, J, Raya-Cruz, M, Sepulveda, M, Troya, J, Del Campo, S, Martinez, E, Callau, P, Moreno, A, Casado, J, Sanchez, J, Ayerbe, C, Negredo, E, Campos, I, Puig, J, Ribera, E, Torrella, A, Planas, B, Knobel, H, Ferrando, R, Crespo, M, Sanz, J, de Los Santos, I, Moreno, A, Diaz, A, Carbonero, L, de la Torre, J, Reina, M, Santos, J, Maria, C, Domenech, G, Gutierrez, M, Montero, M, Cuellar, S, Boix, V, Payeras, A, Ryan, P, Torralba, M and Cuadra, F

Publicada: 1 oct 2019
Resumen:
Background Few women have been included in darunavir/cobicistat clinical development studies, and hardly any of them were antiretroviral experienced or treated with anything other than triple-based therapies. Objectives Our aim was to increase our knowledge about women living with HIV undergoing darunavir/cobicistat-based regimens. Methods A multicentre (21 hospitals), retrospective study including a centrally selected random sample of HIV-1 patients starting a darunavir/cobicistat-based regimen from June 2014 to March 2017 was planned. Baseline characteristics, 24 and 48week viral load response (<50 copies/mL), CD4+ lymphocyte count increase, time to change darunavir/cobicistat and adverse event occurrence were all compared by sex. The study was approved by each of the 21 ethics committees, and patients signed informed consent. Results Out of 761 participants, 193 were women. Similar characteristics were found for both sexes, except that the women had a longer duration of HIV infection (P=0.001), and were less frequently pre-treated with darunavir/cobicistat in their previous regimen (P=0.02). The main reason for using a darunavir/cobicistat-based regimen was simplification, without differences by sex, while monotherapy seems to be more frequently prescribed in women than in men (P=0.067). The main outcomes, HIV viral load response, CD4+ lymphocyte count increase at 24 or 48weeks, occurrence of adverse events, main reasons for changing and time to the modify darunavir/cobicistat regimen, did not show differences between the sexes. Conclusions No sex disparities were found in the main study outcomes. These results support the use of a darunavir/cobicistat-based regimen in long-term pre-treated women. Clinical Trial.gov No. NCT03042390.

Filiaciones:
Perez Elias, M:
 Hosp Ramon & Cajal, IRYCIS, Infect Dis, Madrid, Spain

Alejos, B:
 Inst Salud Carlos III, Madrid, Spain

Vivancos, M:
 Hosp Ramon & Cajal, IRYCIS, Infect Dis, Madrid, Spain

Ribera, E:
 Hosp Univ Vall dHebron, Barcelona, Spain

 Hosp Valle De Hebron, Madrid, Spain

Galindo, M:
 Hosp Clin Univ Valencia, Valencia, Spain

Vilanova-Trillo, L:
 Hosp Alvaro Cunqueiro, Vigo, Spain

Fraile, L:
 Hosp Univ La Princesa, Madrid, Spain

Moral, S:
 Hosp Univ Puerta Hierro Majadahonda, Majadahonda, Spain

De Lomas, J:
 Hosp Costa Sol, Marbella, Spain

Lozano, F:
 Hosp Virgen Valme, Seville, Spain

Garcia, M:
 Hosp Santa Creu & Sant Pau, Barcelona, Spain

Pitarch, M:
 Hosp Univ & Politecn La Fe, Valencia, Spain

:
 Hosp Gen Univ Alicante, Alicante, Spain

Rojas, J:
 Hosp Clin Barcelona, Barcelona, Spain

Raya-Cruz, M:
 Hosp Sont Llatzer, Mallorca, Spain

Sepulveda, M:
 Complejo Hosp Toledo, Toledo, Spain

Troya, J:
 Hosp Infanta Leonor, Madrid, Spain

Del Campo, S:
 Hosp Ramon & Cajal, IRYCIS, Infect Dis, Madrid, Spain

Martinez, E:
 Hosp Clin Barcelona, Barcelona, Spain

Callau, P:
 Hosp Clin Madrid, Madrid, Spain

Moreno, A:
 Hosp Univ Puerta Hierro Majadahonda, Majadahonda, Spain

 Ramon & Cajal, Madrid, Spain

Casado, J:
 Ramon & Cajal, Madrid, Spain

Sanchez, J:
 Ramon & Cajal, Madrid, Spain

Ayerbe, C:
 Ramon & Cajal, Madrid, Spain

Negredo, E:
 Germans Trias, Barcelona, Spain

Campos, I:
 Germans Trias, Barcelona, Spain

Puig, J:
 Germans Trias, Barcelona, Spain

Ribera, E:
 Hosp Univ Vall dHebron, Barcelona, Spain

 Hosp Valle De Hebron, Madrid, Spain

Torrella, A:
 Hosp Valle De Hebron, Madrid, Spain

Planas, B:
 Hosp Valle De Hebron, Madrid, Spain

Knobel, H:
 Hosp Mar, Madrid, Spain

Ferrando, R:
 Clin Valencia, Valencia, Spain

Crespo, M:
 Hosp Alvaro Cunqueiro, Vigo, Spain

Sanz, J:
 Hosp Univ Principe Asturias, Madrid, Spain

de Los Santos, I:
 Hosp Univ La Princesa, Madrid, Spain

Moreno, A:
 Hosp Univ Puerta Hierro Majadahonda, Majadahonda, Spain

 Ramon & Cajal, Madrid, Spain

Diaz, A:
 Hosp Univ Puerta Hierro Majadahonda, Majadahonda, Spain

Carbonero, L:
 Hosp Univ La Paz, Madrid, Spain

de la Torre, J:
 Hosp Costa Sol, Marbella, Spain

Reina, M:
 Hosp Virgen Valme, Seville, Spain

Santos, J:
 Hosp Univ Virgen Victoria, Malaga, Spain

Maria, C:
 Hosp Univ Virgen Victoria, Malaga, Spain

Domenech, G:
 Hosp Univ Virgen Victoria, Malaga, Spain

Gutierrez, M:
 Hosp Santa Creu & Sant Pau, Barcelona, Spain

Montero, M:
 Hosp Univ & Politecn La Fe, Valencia, Spain

Cuellar, S:
 Hosp Univ & Politecn La Fe, Valencia, Spain

:
 Hosp Gen Univ Alicante, Alicante, Spain

Payeras, A:
 Hosp Sont Llatzer, Mallorca, Spain

Ryan, P:
 Hosp Univ Infanta Leonor, Madrid, Spain

Torralba, M:
 Hosp Univ Guadalajara, Guadalajara, Spain

Cuadra, F:
 Complejo Hosp Toledo, Toledo, Spain
ISSN: 03057453





JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
Editorial
OXFORD UNIV PRESS, GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 74 Número: 10
Páginas: 3044-3048
WOS Id: 000491253800031
ID de PubMed: 31236601
imagen Open Access

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