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Evaluation of Cardiovascular Disease Risk in HIV-1-Infected Patients Treated with Darunavir
Magda Opsomer1, Dessislava Dimitrova2, Johan Verspeelt3
1Janssen Research and Development, Beerse, Belgium. mopsomer@its.jnj.com.
Insights
Cardiovascular disease (CVD) risk was evaluated in darunavir users. Data from clinical trials and post-marketing surveillance suggest CVD is not a significant risk associated with darunavir treatment.
Area of Science:
- HIV/AIDS research
- Cardiovascular disease epidemiology
- Pharmacovigilance
Background:
- Cardiovascular disease (CVD) is a concern in HIV-1 infected patients.
- Darunavir is an antiretroviral medication used to treat HIV-1 infection.
- Understanding the CVD risk profile of darunavir is crucial for patient management.
Purpose of the Study:
- To evaluate the cardiovascular disease (CVD) risk associated with darunavir treatment.
- To examine the demographic and clinical characteristics of darunavir users.
- To analyze data from clinical trials, post-marketing surveillance, and claims databases.
Main Methods:
- Analysis of CVD events in 19 Janssen-sponsored clinical trials.
- Evaluation of spontaneously reported CVD events in post-marketing pharmacovigilance databases.
- Exploration of baseline characteristics of HIV-1 infected patients using US administrative claims databases.
Main Results:
- CVD event rates in clinical trials varied by dosing frequency, with once-daily darunavir/ritonavir showing lower rates.
- Post-marketing data indicated a general decline in CVD event reporting rates over time.
- Darunavir users were generally older, male, and had more CVD risk comorbidities compared to other groups.
Conclusions:
- Comprehensive data from clinical trials, post-marketing surveillance, and epidemiological studies do not indicate significant CVD risk with darunavir.
- Darunavir is not associated with disproportionately reported CVD events compared to other protease inhibitors.
- Further research may explore CVD risk in specific patient subgroups.
Introduction:
We evaluated cardiovascular disease (CVD) risk associated with darunavir treatment and examined the demographic/clinical characteristics of darunavir users based on data from Janssen-sponsored clinical trials, post-marketing pharmacovigilance databases, and administrative claims databases.
Methods:
First, selected CVD events [myocardial infarction, stroke, sudden death, invasive cardiovascular procedures (coronary artery angioplasty or bypass, or carotid endarterectomy)] were analyzed in 19 Janssen-sponsored phase 2-4 studies (incidence rates estimated from pooled data; 95% confidence intervals derived from Poisson distribution). Second, analyses were conducted to identify spontaneously reported CVD events in post-marketing pharmacovigilance databases and evaluate disproportional reporting of CVD events for darunavir (using Empirical Bayesian Geometric Mean scores). Third, baseline demographic/clinical characteristics of human immunodeficiency virus-1 (HIV-1)-infected patients in general and new users of darunavir and atazanavir were explored using three US administrative claims databases.
Results:
Among 19 Janssen-sponsored clinical trials (treatment durations ≤ 6 years), the CVD event rate (95% CI) per 1000 person-years (pooled population; n = 5713) was 6.15 (2.91-11.89), and was lower for patients who used once-daily darunavir/ritonavir 800/100 mg [0.71 (0.16-3.05); n = 1326] versus twice-daily darunavir/ritonavir 600/100 mg [9.21 (4.94-16.04); n = 3058]. Trend analysis of post-marketing pharmacovigilance data showed that cumulative CVD event reporting rates for darunavir users (any dose) generally declined over time. Spontaneously reported CVD events were not disproportionately reported with darunavir versus other protease inhibitors. Compared with the general HIV-1-infected population and atazanavir users, higher proportions of darunavir users were male, older, and had comorbidities associated with CVD risk based on results from US administrative claims databases.
Conclusions:
This comprehensive review of Janssen-sponsored clinical trial, post-marketing, and epidemiological data does not suggest that CVD should be considered an important risk for users of darunavir.
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