Heavy arv exposure and exhausted/limited arv options: predictors and clinical outcomes

Author:

Mocroft Amanda12,Pelchen-Matthews Annegret2,Hoy Jennifer3,Llibre Josep M.4,Neesgaard Bastian1,Jaschinski Nadine1,Domingo Pere5,Rasmussen Line Dahlerup6,Günthard Huldrych F.78,Surial Bernard9,Öllinger Angela10,Knappik Michael11,De Wit Stephan12,Wit Ferdinand13,Mussini Cristina14,Vehreschild Joerg15,Monforte Antonella D’Arminio16,Sonnerborg Anders17,Castagna Antonella18,Anne Alain Volny19,Vannappagari Vani20,Cohen Cal21,Greaves Wayne22,Wasmuth Jan C.23,Spagnuolo Vincenzo18,Ryom Lene12425

Affiliation:

1. CHIP, Section 2100, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark

2. Centre for Clinical Research, Epidemiology, Modelling and Evaluation, University College London, London, UK

3. Department of Infectious Diseases, Alfred Hospital and Monash University, Melbourne, Victoria, Australia

4. Department of Infectious Diseases, Hospital Universitari Germans Trias i Pujol

5. Department of Infectious Diseases, Hospital of the Holy Cross and Saint Paul, Barcelona, Spain

6. Department of Infectious Diseases, Odense University Hospital, Odense, Denmark

7. Department of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich

8. Institute of Medical Virology, University of Zurich, Zurich

9. Department of Infectious Diseases, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland

10. Department of Dermatology and Venerology, Kepler University Hospital, Linz

11. Department of Respiratory Medicine, Klinik Penzing, Vienna, Austria

12. CHU Saint-Pierre, Centre de Recherche en Maladies Infectieuses a.s.b.l., Brussels, Belgium

13. AIDS Therapy Evaluation in the Netherlands (ATHENA) cohort, HIV Monitoring Foundation, Amsterdam, the Netherlands

14. Modena HIV Cohort, Università degli Studi di Modena, Modena, Italy

15. Department I of Internal Medicine, Faculty of Medicine and University Hospital Cologne, Cologne, Germany

16. Italian Cohort Naive Antiretrovirals (ICONA), ASST Santi Paolo e Carlo, Milan, Italy

17. Swedish InfCare HIV Cohort, Karolinska University Hospital, Karolinska, Sweden

18. San Raffaele Scientific Institute, Università Vita-Salute San Raffaele, Milan, Italy

19. European AIDS Treatment Group

20. ViiV Healthcare, RTP, USA

21. Gilead Sciences, Foster City, USA

22. Merck, USA

23. University Hospital Bonn, Bonn, Germany

24. Department of Infectious Diseases 144, Hvidovre University Hospital

25. Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.

Abstract

Objectives: People with HIV and extensive antiretroviral exposure may have limited/exhausted treatment options (LExTO) due to resistance, comorbidities, or antiretroviral-related toxicity. Predictors of LExTO were investigated in the RESPOND cohort. Methods: Participants on ART for at least 5 years were defined as having LExTO when switched to at least two anchor agents and one-third antiretroviral (any class), a two-drug regimen of two anchor agents (excluding rilpivirine with dolutegravir/cabotegravir), or at least three nucleoside reverse transcriptase inhibitors. Baseline was the latest of January 1, 2012, cohort enrolment or 5 years after starting antiretrovirals. Poisson regression modeled LExTO rates and clinical events (all-cause mortality, non-AIDS malignancy, cardiovascular disease [CVD], and chronic kidney disease [CKD]). Results: Of 23 827 participants, 2164 progressed to LExTO (9.1%) during 130 061 person-years follow-up (PYFU); incidence 1.66/100 PYFU (95% CI 1.59–1.73). Predictors of LExTO were HIV duration more than 15 years (vs. 7.5–15; adjusted incidence rate ratio [aIRR] 1.32; 95% CI 1.19–1.46), development of CKD (1.84; 1.59–2.13), CVD (1.64; 1.38–1.94), AIDS (1.18; 1.07–1.30), and current CD4+ cell count of 350 cells/μl or less (vs. 351–500 cells/μl, 1.51; 1.32–1.74). Those followed between 2018 and 2021 had lower rates of LExTO (vs. 2015–2017; 0.52; 0.47–0.59), as did those with baseline viral load of 200 cp/ml or less (0.46; 0.40–0.53) and individuals under 40. Development of LExTO was not significantly associated with clinical events after adjustment for age and current CD4, except CKD (1.74; 1.48–2.05). Conclusion: Despite an aging and increasingly comorbid population, we found declining LExTO rates by 2018–2021, reflecting recent developments in contemporary ART options and clinical management. Reassuringly, LExTO was not associated with a significantly increased incidence of serious clinical events apart from CKD.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Infectious Diseases,Immunology,Immunology and Allergy

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