Adverse drug reactions to integrase strand transfer inhibitors

被引:37
作者
Lepik, Katherine J. [1 ,2 ]
Yip, Benita [1 ]
Ulloa, Ana C. [1 ]
Wang, Lu [1 ]
Toy, Junine [1 ,2 ]
Akagi, Linda [1 ,2 ]
Lima, Viviane Dias [1 ,3 ]
Guillemi, Silvia [1 ]
Montaner, Julio S. G. [1 ,3 ]
Barrios, Rolando [1 ,4 ]
机构
[1] BC Ctr Excellence HIV AIDS, 1081 Burrard St, Vancouver, BC V6Z 1Y6, Canada
[2] St Pauls Hosp, Pharm Dept, Vancouver, BC, Canada
[3] Univ British Columbia, Fac Med, Dept Med, Div Aids, Vancouver, BC, Canada
[4] Univ British Columbia, Sch Populat & Publ Hlth, Fac Med, Vancouver, BC, Canada
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
dolutegravir; drug-related side effects and adverse reactions; elvitegravir; HIV integrase inhibitors; raltegravir; HIV-INFECTED PATIENTS; COMBINATION ANTIRETROVIRAL THERAPY; CO-FORMULATED ELVITEGRAVIR; DOUBLE-BLIND; INITIAL TREATMENT; WEIGHT-GAIN; DOLUTEGRAVIR; REGIMENS; EFFICACY; EVENTS;
D O I
10.1097/QAD.0000000000001781
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objectives: To describe and compare integrase strand transfer inhibitor (INSTI) adverse drug reactions (ADRs) for raltegravir, elvitegravir-cobicistat, and dolutegravir. Design: Population-based, retrospective cohort. Methods: Antiretroviral-experienced and naive persons at least 19 years old were included if they received their first prescription for raltegravir, elvitegravir-cobicistat, or dolutegravir in British Columbia, Canada, in 2012-2014, and were followed for 2 years until 31 December 2016. The primary outcome was an ADR resulting in INSTI discontinuation. ADR rates and 95% confidence intervals (95% CIs) were calculated by Poisson method. Cox proportional-hazards regression estimated the hazard ratio for ADR-related INSTI discontinuation, adjusted for confounders. ADR symptoms were compared across INSTIs. Results: There were 1344 persons contributing 1464 person-INSTI exposures. The cohort was predominantly male (79%) and antiretroviral therapy-experienced (85%). ADR events and unadjusted ADR rates (95% CI) per 100 person-years were raltegravir 24 of 551 (4.4%), 2.91 (1.95, 4.35); elvitegravir-cobicistat 38 of 394 (9.6%), 5.94 (4.32, 8.16); and dolutegravir 27 of 519 (5.2%), 2.96 (2.03, 4.31). The ADR rate for elvitegravir-cobicistat was double that of dolutegravir (adjusted hazard ratio 2.24, 95% CI 1.13, 4.44), but not significantly different for either dolutegravir or elvitegravir versus raltegravir. Elvitegravir-cobicistat-treated persons had a significantly higher proportion of gastrointestinal and general (fatigue, malaise) ADRs. Neuropsychiatric ADRs were more frequent with dolutegravir, but not significantly different between INSTIs. Among those switching between INSTIs, there was no apparent relationship between experiencing an ADR to one INSTI and subsequent intolerance to another. Conclusions: This study affirms INSTIs are well tolerated during routine clinical use. Consideration of differences in side effect profiles can inform antiretroviral therapy individualization. Copyright (C) 2018 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:903 / 912
页数:10
相关论文
共 31 条
[1]   The impact of specific HIV treatment-related adverse events on adherence to antiretroviral therapy: A systematic review and meta-analysis [J].
Al-Dakkak, Imad ;
Patel, Seema ;
McCann, Eilish ;
Gadkari, Abhijit ;
Prajapati, Girish ;
Maiese, Eric M. .
AIDS CARE-PSYCHOLOGICAL AND SOCIO-MEDICAL ASPECTS OF AIDS/HIV, 2013, 25 (04) :400-414
[2]  
[Anonymous], DRUG TREATM PROGR
[3]  
[Anonymous], C RETR OPP INF CROI
[4]  
[Anonymous], GUID US ANT AG HIV 1
[5]  
BC Centre for Excellence in HIV/AIDS, PHARM IN
[6]   Discontinuation of treatment and adverse events in an Italian cohort of patients on dolutegravir [J].
Bonfanti, Paolo ;
Madeddu, Giordano ;
Gulminetti, Roberto ;
Squillace, Nicola ;
Orofino, Giancarlo ;
Vitiello, Paola ;
Rusconi, Stefano ;
Celesia, Benedetto M. ;
Maggi, Paolo ;
Ricci, Elena .
AIDS, 2017, 31 (03) :455-457
[7]   Efficacy and tolerability of dolutegravir and two nucleos(t) ide reverse transcriptase inhibitors in HIV-1-positive, virologically suppressed patients [J].
Borghetti, Alberto ;
Baldin, Gianmaria ;
Capetti, Amedeo ;
Sterrantino, Gaetana ;
Rusconi, Stefano ;
Latini, Alessandra ;
Giacometti, Andrea ;
Madeddu, Giordano ;
Picarelli, Chiara ;
De Marco, Ramona ;
Cossu, Maria V. ;
Lagi, Filippo ;
Cauda, Roberto ;
De Luca, Andrea ;
Di Giambenedetto, Simona .
AIDS, 2017, 31 (03) :457-459
[8]   Clinical Experience with the Integrase Inhibitors Dolutegravir and Elvitegravir in HIV-infected Patients: Efficacy, Safety and Tolerance [J].
Cid-Silva, Purificacion ;
Llibre, Josep M. ;
Fernandez-Bargiela, Noelia ;
Margusino-Framinan, Luis ;
Balboa-Barreiro, Vanesa ;
Pernas-Souto, Berta ;
Martin-Herranz, Isabel ;
Castro-Iglesias, Angeles ;
Poveda, Eva .
BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2017, 121 (05) :442-446
[9]   Once-daily dolutegravir versus darunavir plus ritonavir in antiretroviral-naive adults with HIV-1 infection (FLAMINGO): 48 week results from the randomised open-label phase 3b study [J].
Clotet, Bonaventura ;
Feinberg, Judith ;
van Lunzen, Jan ;
Khuong-Josses, Marie-Aude ;
Antinori, Andrea ;
Dumitru, Irina ;
Pokrovskiy, Vadim ;
Fehr, Jan ;
Ortiz, Roberto ;
Saag, Michael ;
Harris, Julia ;
Brennan, Clare ;
Fujiwara, Tamio ;
Min, Sherene .
LANCET, 2014, 383 (9936) :2222-2231
[10]   Intolerance of dolutegravir-containing combination antiretroviral therapy regimens in real-life clinical practice [J].
de Boer, Mark G. J. ;
van den Berk, Guido E. L. ;
van Holten, Natasja ;
Oryszcyn, Josephine E. ;
Dorama, Willemien ;
Moha, Daoud Ait ;
Brinkman, Kees .
AIDS, 2016, 30 (18) :2831-2834