TAF treatment for HBV prophylaxis could lead to significant reduction in ALT and significant improvement in renal function. However, data are scarce regarding to TAF monotherapy without HBIG for HBV prophylaxis in post orthotopic liver transplant with HBV-related disease. This study is based on a real-world, multi-center, prospective study to assess the effectiveness and safety of TAF for HBV prophylaxis, which will fill in gaps with TAF monotherapy without HBIG in post liver transplant.
LT has evolved rapidly, becoming the standard therapy for acute and chronic liver failure of a variety of aetiologies, with more than 80,000 procedures performed to date \[13\]. HBV infection is a worldwide public health problem, especially in China. The need for an antiviral treatment with NAs for liver transplant recipients has two objectives: the improvement of liver function and to decrease the risk of HBV recurrence after transplant. TAF, TDF and ETV are currently the first-line therapy in patients with CHB in all CHB treatment guidelines, which have a greater potency and higher barriers to resistance. TAF treatment for HBV prophylaxis could lead to significant reduction in ALT and significant improvement in renal function. However, data are scarce regarding to TAF monotherapy without HBIG for HBV prophylaxis in post orthotopic liver transplant with HBV-related disease. This study is based on a real-world, multi-center, prospective study to assess the effectiveness and safety of TAF for HBV prophylaxis, which will fill in gaps with TAF monotherapy without HBIG in post liver transplant.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
150
After orthotopic liver transplant, all patients will receive Tenofovir Alafenamide monotherapy without HBIG for HBV Prophylaxis.
Zhongshan hospital, Fudan University
Shanghai, Shanghai Municipality, China
HBV DNA undetectable rate at week 48.
evaluate the HBV DNA undetectable rate (defined as HBV DNA \< 20 IU/mL) at week 48 after liver transplant.
Time frame: 48 weeks
HBV DNA undetectable rate at week 96
evaluate the HBV DNA undetectable rate (defined as HBV DNA \< 20 IU/mL) at week 96 after liver transplant.
Time frame: 96 weeks
HBsAg negative rate at week 48
evaluate the HBsAg negative rate at week 48 after liver transplant.
Time frame: 48 weeks
HBsAg negative rate at week 96
evaluate the HBsAg negative rate at week 96 after liver transplant.
Time frame: 96 weeks
ALT normalization rate at week 48
evaluate the ALT normalization rate at week 48 after liver transplant.
Time frame: 48 weeks
ALT normalization rate at week 96
evaluate the ALT normalization rate at week 96 after liver transplant.
Time frame: 96 weeks
Changes in Serum Creatinine at week 48
evaluate the change of Serum Creatinine at week 48 after liver transplant.
Time frame: 48 weeks
Changes in Serum Creatinine at week 96
evaluate the change of Serum Creatinine at week 96 after liver transplant.
Time frame: 96 weeks
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Changes in eGFR (MDRD) at week 48
evaluate the change of eGFR (MDRD) at week 48 after liver transplant.
Time frame: 48 weeks
Changes in eGFR (MDRD) at week 96
evaluate the change of eGFR (MDRD) at week 96 after liver transplant.
Time frame: 96 weeks
Changes in β2-MG:Cr at week 48
evaluate the change of β2-MG:Cr at week 48 after liver transplant.
Time frame: 48 weeks
Changes in β2-MG:Cr at week 96
evaluate the change of β2-MG:Cr at week 96 after liver transplant.
Time frame: 96 weeks