Roberta Angelico, Silvia Trapani, Tommaso Maria Manzia, Ilaria Lenci, Paolo Grossi, Andrea Ricci, Patrizia Burra, Enzo Andorno, Salvatore Agnes, Sherrie Bhoori, Umberto Baccarani, Luca S Belli, Paola Carrai, Lucio Caccamo, Amedeo Carraro, Matteo Cescon, Michele Colledan, Umberto Cillo, Luciano De Carlis, Nicola De Maria, Paolo De Simone, Fabrizio di Benedetto, Maria Francesca Donato, Giuseppe Maria Ettorre, Flaminia Ferri, Alfonso Galeota Lanza, Davide Ghinolfi, Antonio Grieco, Salvatore Gruttadauria, Simona Marenco, Silvia Martini, Vincenzo Mazzaferro, Adriano Pellicelli, Domenico Pinelli, Maria Rendina, Mario Rizzetto, Renato Romagnoli, Massimo Rossi, Francesco Paolo Russo, Laura Schiadà, Francesco Tandoi, Pierluigi Toniutto, Laura Turco, Giovanni Vennarecci, Mauro Viganò, Marco Vivarelli, Giuseppe Tisone, Giuseppe Feltrin, Alessandra Nardi, Mario Angelico
{"title":"Liver Transplantation For HDV/HBV Coinfection In Italy: An Intention-To-Treat Analysis Of Long-Term Outcomes.","authors":"Roberta Angelico, Silvia Trapani, Tommaso Maria Manzia, Ilaria Lenci, Paolo Grossi, Andrea Ricci, Patrizia Burra, Enzo Andorno, Salvatore Agnes, Sherrie Bhoori, Umberto Baccarani, Luca S Belli, Paola Carrai, Lucio Caccamo, Amedeo Carraro, Matteo Cescon, Michele Colledan, Umberto Cillo, Luciano De Carlis, Nicola De Maria, Paolo De Simone, Fabrizio di Benedetto, Maria Francesca Donato, Giuseppe Maria Ettorre, Flaminia Ferri, Alfonso Galeota Lanza, Davide Ghinolfi, Antonio Grieco, Salvatore Gruttadauria, Simona Marenco, Silvia Martini, Vincenzo Mazzaferro, Adriano Pellicelli, Domenico Pinelli, Maria Rendina, Mario Rizzetto, Renato Romagnoli, Massimo Rossi, Francesco Paolo Russo, Laura Schiadà, Francesco Tandoi, Pierluigi Toniutto, Laura Turco, Giovanni Vennarecci, Mauro Viganò, Marco Vivarelli, Giuseppe Tisone, Giuseppe Feltrin, Alessandra Nardi, Mario Angelico","doi":"10.1016/j.ajt.2025.03.003","DOIUrl":null,"url":null,"abstract":"<p><p>Patients with HDV/HBV-related end-stage liver disease candidates for liver transplantation(LT) have traditionally been regarded as a special population, although their outcomes are controversial. A intention-to-treat(ITT) analysis of long-term outcomes of HDV/HBV-coinfected patients waitlisted for LT in Italy, between 2011-2020, was performed and compared to HBV-monoinfected LT candidates. Out of 1,731 HBV-infected LT candidates, 1,237(71.5%) had HBV-monoinfection and 494(28.5%) HDV/HBV-coinfection. At listing, HDV/HBV-coinfected patients were significantly younger, listed mainly for decompensated cirrhosis, and with less hepatocellular carcinoma (HCC:26% vs 65.8%,P<0.0001) compared to HBV-monoinfected patients. HDV/HBV-coinfected patients showed better 5-year ITT-survival (83.2%,95%CI:79.4-83.4% vs 71.6%,95%CI:68.8-74.2%;P<0.0001). ITT-multivariable analysis identified the presence of HCC, advanced recipient age, and high-MELD-Na scores as mortality risk factors. Five-years after LT, 99.1% of HDV/HBV-coinfected patients received oral nucleos(t)ide analogues, with immunoglobulins against HBsAg(HBIg) in 91.8% of cases. HBV and HDV viral recurrences were 1.1% and 0.2%, respectively, whereas recurrent or de novo HCC were 8.9% and 0.3%, respectively. In Italy, HDV/HBV-coinfected patients waitlisted for LT showed more favourable outcomes compared to HBV-monoinfected patients, both before and after LT. These excellent results, from the largest cohort reported so far, suggest that HDV/HBV-coinfected LT recipients don't represent a risky population and may be considered for simpler long-term antiviral prophylactic strategies.</p>","PeriodicalId":123,"journal":{"name":"American Journal of Transplantation","volume":" ","pages":""},"PeriodicalIF":8.9000,"publicationDate":"2025-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Transplantation","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.ajt.2025.03.003","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"SURGERY","Score":null,"Total":0}
引用次数: 0
Abstract
Patients with HDV/HBV-related end-stage liver disease candidates for liver transplantation(LT) have traditionally been regarded as a special population, although their outcomes are controversial. A intention-to-treat(ITT) analysis of long-term outcomes of HDV/HBV-coinfected patients waitlisted for LT in Italy, between 2011-2020, was performed and compared to HBV-monoinfected LT candidates. Out of 1,731 HBV-infected LT candidates, 1,237(71.5%) had HBV-monoinfection and 494(28.5%) HDV/HBV-coinfection. At listing, HDV/HBV-coinfected patients were significantly younger, listed mainly for decompensated cirrhosis, and with less hepatocellular carcinoma (HCC:26% vs 65.8%,P<0.0001) compared to HBV-monoinfected patients. HDV/HBV-coinfected patients showed better 5-year ITT-survival (83.2%,95%CI:79.4-83.4% vs 71.6%,95%CI:68.8-74.2%;P<0.0001). ITT-multivariable analysis identified the presence of HCC, advanced recipient age, and high-MELD-Na scores as mortality risk factors. Five-years after LT, 99.1% of HDV/HBV-coinfected patients received oral nucleos(t)ide analogues, with immunoglobulins against HBsAg(HBIg) in 91.8% of cases. HBV and HDV viral recurrences were 1.1% and 0.2%, respectively, whereas recurrent or de novo HCC were 8.9% and 0.3%, respectively. In Italy, HDV/HBV-coinfected patients waitlisted for LT showed more favourable outcomes compared to HBV-monoinfected patients, both before and after LT. These excellent results, from the largest cohort reported so far, suggest that HDV/HBV-coinfected LT recipients don't represent a risky population and may be considered for simpler long-term antiviral prophylactic strategies.
期刊介绍:
The American Journal of Transplantation is a leading journal in the field of transplantation. It serves as a forum for debate and reassessment, an agent of change, and a major platform for promoting understanding, improving results, and advancing science. Published monthly, it provides an essential resource for researchers and clinicians worldwide.
The journal publishes original articles, case reports, invited reviews, letters to the editor, critical reviews, news features, consensus documents, and guidelines over 12 issues a year. It covers all major subject areas in transplantation, including thoracic (heart, lung), abdominal (kidney, liver, pancreas, islets), tissue and stem cell transplantation, organ and tissue donation and preservation, tissue injury, repair, inflammation, and aging, histocompatibility, drugs and pharmacology, graft survival, and prevention of graft dysfunction and failure. It also explores ethical and social issues in the field.