Improved Survival After Liver Transplantation for Patients With Human Immunodeficiency Virus (HIV) and HIV/Hepatitis C Virus Coinfection in the Integrase Strand Transfer Inhibitor and Direct-Acting Antiviral Eras

Author:

Jacob Jake Sheraj1,Shaikh Anjiya2,Goli Karthik1,Rich Nicole E3,Benhammou Jihane N4,Ahmed Aijaz5,Kim Donghee5,Rana Abbas6,Goss John A6,Naggie Susanna7,Lee Tzu-Hao16,Kanwal Fasiha1,Cholankeril George16

Affiliation:

1. Department of Internal Medicine, Section of Gastroenterology and Hepatology, Baylor College of Medicine , Houston, Texas , USA

2. Department of Internal Medicine, University of Connecticut , Mansfield, Connecticut , USA

3. Division of Digestive and Liver Diseases, University of Texas Southwestern Medical Center , Dallas, Texas , USA

4. Division of Gastroenterology and Hepatology, University of California , Los Angeles, California , USA

5. Division of Gastroenterology and Hepatology, Stanford University School of Medicine , Stanford, California , USA

6. Hepatology Program, Division of Abdominal Transplantation, Baylor College of Medicine , Houston, Texas , USA

7. Division of Infectious Diseases, Department of Medicine, Duke University School of Medicine , Durham, North Carolina , USA

Abstract

Abstract Background People with human immunodeficiency virus (HIV) with and without hepatitis C virus (HCV) coinfection had poor outcomes after liver transplant (LT). Integrase strand transfer inhibitors (INSTIs) and direct-acting antivirals (DAAs) have changed the treatment landscape for HIV and HCV, respectively, but their impact on LT outcomes remains unclear. Methods This retrospective analysis of adults with HIV monoinfection (n = 246) and HIV/HCV coinfection (n = 286) who received LT compared mortality in patients with HIV who received LT before versus after approval of INSTIs and in patients with HIV/HCV coinfection who received LT before versus after approval of DAAs. In secondary analysis, we compared the outcomes in the different eras with those of propensity score–matched control cohorts of LT recipients without HIV or HCV infection. Results LT recipients with HIV monoinfection did not experience a significant improvement in survival between the pre-INSTI and INSTI recipients with HIV (adjusted hazard ratio [aHR], 0.70 [95% confidence interval {CI}, .36–1.34]). However, recipients with HIV/HCV coinfection in the DAA era had a 47% reduction (aHR, 0.53 [95% CI, .31–9.2] in 1-year mortality compared with coinfected recipients in the pre-DAA era. Compared to recipients without HIV or HCV, HIV-monoinfected recipients had higher mortality during the pre-INSTI era, but survival was comparable between groups during the INSTI era. HIV/HCV-coinfected recipients also experienced comparable survival during the DAA era compared to recipients without HCV or HIV. Conclusions Post-LT survival for people with HIV monoinfection and HIV/HCV coinfection has improved with the introduction of INSTI and DAA therapy, suggesting that LT has become safer in these populations.

Funder

Cancer Prevention and Research Institute of Texas

National Cancer Institute

NIH

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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