A snapshot of virological presentation and outcome of immunosuppression-driven HBV reactivation from real clinical practice: Evidence of a relevant risk of death and evolution from silent to chronic infection.


Journal

Journal of viral hepatitis
ISSN: 1365-2893
Titre abrégé: J Viral Hepat
Pays: England
ID NLM: 9435672

Informations de publication

Date de publication:
07 2019
Historique:
received: 10 12 2018
revised: 26 02 2019
accepted: 26 02 2019
pubmed: 12 4 2019
medline: 14 7 2020
entrez: 12 4 2019
Statut: ppublish

Résumé

The study was undertaken in order to provide a snapshot from real clinical practice of virological presentation and outcome of patients developing immunosuppression-driven HBV reactivation. Seventy patients with HBV reactivation were included (66.2% treated with rituximab, 10% with corticosteroids and 23.8% with other immunosuppressive drugs). Following HBV reactivation, patients received anti-HBV treatment for a median (IQR) follow-up of 31(13-47) months. At baseline-screening, 72.9% of patients were HBsAg-negative and 27.1% HBsAg-positive. About 71.4% had a diagnosis of biochemical reactivation [median (IQR) HBV DNA and ALT: 6.9 (5.4-7.8) log IU/mL and 359 (102-775) U/L]. Moreover, 10% of patients died from hepatic failure. Antiviral prophylaxis was documented in 57.9% and 15.7% of HBsAg-positive and HBsAg-negative patients at baseline-screening (median [IQR] prophylaxis duration: 24[15-33] and 25[17-36] months, respectively). Notably, HBV reactivation occurred 2-24 months after completing the recommended course of anti-HBV prophylaxis in 35.3% of patients. By analysing treatment outcome, the cumulative probability of ALT normalization and of virological suppression was 97% and 69%, respectively. Nevertheless, in patients negative to HBsAg at baseline-screening, only 27% returned to HBsAg-negative status during prolonged follow-up, suggesting the establishment of chronic infection. In conclusion, most patients received a diagnosis of HBV reactivation accompanied by high ALT and 10% died for hepatic failure, supporting the importance of strict monitoring for an early HBV reactivation diagnosis. Furthermore, HBV reactivation correlates with high risk of HBV chronicity in patients negative for HBsAg at baseline-screening, converting a silent into a chronic infection, requiring long-term antiviral treatment. Finally, a relevant proportion of patients experienced HBV reactivation after completing the recommended course of anti-HBV prophylaxis, suggesting the need to reconsider proper duration of prophylaxis particularly in profound immunosuppression.

Identifiants

pubmed: 30974483
doi: 10.1111/jvh.13101
doi:

Substances chimiques

Hepatitis B Surface Antigens 0
Immunosuppressive Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

846-855

Informations de copyright

© 2019 John Wiley & Sons Ltd.

Auteurs

Romina Salpini (R)

Department of Experimental Medicine, Tor Vergata University, Rome, Italy.

Arianna Battisti (A)

Department of Experimental Medicine, Tor Vergata University, Rome, Italy.

Luna Colagrossi (L)

Department of Experimental Medicine, Tor Vergata University, Rome, Italy.
Department of Microbiology and Virology, University of Milan, Milan, Italy.

Domenico Di Carlo (D)

Department of Experimental Medicine, Tor Vergata University, Rome, Italy.
Pediatric Clinical Research Center 'Romeo and Erica Invernizzi', University of Milan, Milan, Italy.
Department of Biology and Biotechnology, University of Pavia, Pavia, Italy.

Lavinia Fabeni (L)

Department of Experimental Medicine, Tor Vergata University, Rome, Italy.

Lorenzo Piermatteo (L)

Department of Experimental Medicine, Tor Vergata University, Rome, Italy.

Carlotta Cerva (C)

Infectious Diseases Unit, Tor Vergata University Hospital, Rome, Italy.

Miriam Lichtner (M)

Department of Public Health and Infectious Disease, Sapienza University, Rome, Italy.

Claudio Mastroianni (C)

Department of Public Health and Infectious Disease, Sapienza University, Rome, Italy.

Massimo Marignani (M)

Department of Digestive and Liver Disease, S.Andrea Hospital, Rome, Italy.

Sarah Maylin (S)

Laboratoire de Virologie, AP-HP Hopital Saint-Louis, Paris, France.

Constance Delaugerre (C)

Laboratoire de Virologie, AP-HP Hopital Saint-Louis, Paris, France.

Filomena Morisco (F)

Section of Infectious Diseases, Department of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.

Nicola Coppola (N)

Section of Infectious Diseases, Department of Mental Health and Public Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.

Aldo Marrone (A)

Department of Medical, Surgical, Neurological, Metabolic and Geriatric Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.

Mario Angelico (M)

Hepatology Unit, Tor Vergata University Hospital, Rome, Italy.

Loredana Sarmati (L)

Infectious Diseases Unit, Tor Vergata University Hospital, Rome, Italy.

Massimo Andreoni (M)

Infectious Diseases Unit, Tor Vergata University Hospital, Rome, Italy.

Carlo-Federico Perno (CF)

Department of Experimental Medicine, Tor Vergata University, Rome, Italy.
Department of Oncology and Oncohematology, Università degli Studi di Milano, Milan, Italy.

Francesca Ceccherini-Silberstein (F)

Department of Experimental Medicine, Tor Vergata University, Rome, Italy.

Valentina Svicher (V)

Department of Experimental Medicine, Tor Vergata University, Rome, Italy.

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