<link rel="stylesheet" href="styles.f3b1fba60ec7970c.css">

Efficacy and tolerability of tenofovir alafenamide fumarate prophylaxis in HBV-infected individuals receiving chemo/ immunosuppressive therapy

dc.contributor.authorDilber, Feyza
dc.contributor.authorDurak, Serdar
dc.contributor.authorUnsal, Yasemin
dc.contributor.authorDemir, Mehmet
dc.contributor.authorYildirim, Abdullah Emre
dc.contributor.authorEllik, Zeynep Melekoglu
dc.contributor.authorMehdiyev, Shahin
dc.contributor.authorAdanir, Haydar
dc.contributor.authorYapali, Suna
dc.contributor.authorDemirtas, Coskun Ozer
dc.contributor.authorUcbilek, Enver
dc.contributor.authorBalaban, Yasemin
dc.contributor.authorEkmen, Nergis
dc.contributor.authorGokcan, Hale
dc.contributor.authorKoc, Elif Sitre
dc.contributor.authorDincer, Dinc
dc.contributor.authorSezgin, Orhan
dc.contributor.authorSimsek, Halis
dc.contributor.authorTozun, Nurdan
dc.contributor.authorArslan, Mehmet
dc.contributor.authorIdilman, Ramazan
dc.contributor.authorEtik, Digdem Ozer
dc.contributor.authorGokcen, Pinar
dc.contributor.authorAri, Derya
dc.contributor.authorOzdil, Kamil
dc.contributor.authorAkdogan, Meral
dc.contributor.authorBoyacioglu, Sedat
dc.date.accessioned2026-11-05T11:03:47Z
dc.date.issued2026
dc.description.abstractBackground and Aim: This study aimed to determine the efficacy and safety of tenofovir alafenamide fumarate (TAF) prophylaxis in hepatitis B virus (HBV)-infected or HBV-experienced individuals with benign and malignant diseases receiving chemo/immunosuppressive or biological modifier therapy. Materials and Methods: This is a multicenter, observational study in which data from 13 centers were reviewed and entered into a standardized electronic case report form. Results: A total of 158 individuals who received TAF prophylaxis were included in the analysis. Before starting the prophylaxis, 51 individuals were hepatitis B surface antigen positive, while 107 were HBV-experienced. Thirty patients had detectable HBV DNA levels. Twelve of them had abnormal serum alanine aminotransferase levels. Forty patients were switched to TAF. Solid tumors (34%) were the most common primary disease types. The median follow-up period was 17.2 months. From baseline to the end of the follow-up period, none of the patients had clinical, biochemical, or serological evidence of HBV reactivation under TAF prophylaxis. The virological response rate was 87%. HBV suppression was well maintained after switching in the 40 patients who were switched to TAF treatment. All patients maintained their chemo/ immunosuppressive therapy without interruption. TAF prophylaxis was well tolerated. No drug discontinuation due to adverse effects was observed. No HBV-related morbidity or mortality was observed during the TAF prophylaxis. No significant differences were found in the glomerular filtration rate change or hypophosphatemia during TAF prophylaxis, but the serum triglyceride levels were significantly increased (p=0.019). Conclusion: TAF prophylaxis is effective, safe, and tolerable in preventing chemo/immunosuppressive or biological modifier-induced HBV reactivation in HBV-infected or HBV-experienced individuals.
dc.description.issue1
dc.description.volume7
dc.identifier.doi10.14744/hf.2025.62002
dc.identifier.issn1307-5888
dc.identifier.issn2757-7392
dc.identifier.urihttps://doi.org/10.14744/hf.2025.62002
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/11107
dc.identifier.wosWOS:001710328600005
dc.language.isoen
dc.publisherKARE PUBL
dc.relation.hasversion10.14744/hf.2025.62002
dc.relation.ispartofHEPATOLOGY FORUM
dc.subjectChemotherapy
dc.subjectefficacy
dc.subjectHBV infection
dc.subjectimmunosuppressive therapy
dc.subjectprophylaxis
dc.subjectsafety
dc.subjecttenofovir alafenamide fumarate
dc.subjectB-VIRUS REACTIVATION
dc.subjectCHRONIC HEPATITIS-B
dc.subjectDISOPROXIL FUMARATE
dc.subjectWEIGHT-GAIN
dc.subjectRISK
dc.subjectPREVENTION
dc.subjectMANAGEMENT
dc.subjectSWITCH
dc.subjectGastroenterology & Hepatology
dc.titleEfficacy and tolerability of tenofovir alafenamide fumarate prophylaxis in HBV-infected individuals receiving chemo/ immunosuppressive therapy
dc.typeArticle
oaire.citation.editionEmerging Sources Citation Index (ESCI)
oaire.citation.issue1
oaire.citation.volume7
person.identifier.orcid0000-0002-0004-2740
person.identifier.ridAFL-0461-2022
person.identifier.ridAAE-7637-2021
person.identifier.ridAAR-8893-2020
person.identifier.ridJEZ-5664-2023
person.identifier.ridK-4930-2019
person.identifier.ridABK-6123-2022
person.identifier.ridAAD-7378-2021
person.identifier.ridABG-7641-2021
person.identifier.ridNQF-8430-2025
person.identifier.ridJAO-1030-2023

Files

Collections