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HBV Treatment Induced HBsAg Seroconversion to Anti-HBs in 9 Asian-American Patients: Experience in a Community Clinic
H. Lee1; K. Hu1; S. Tonthat1
1. GI/Hepatology, U.C. Irvine, Irvine, CA, United States.
Background: Although HBeAg seroconversion to anti-HBe has been a standard treatment endpoint for HBeAg+ patients, patients who achieve this endpoint have a 20-40% relapse rate over a 5 year period. HBsAg seroconversion appears to be a more durable endpoint of HBV treatment than HBeAg seroconversion, but it is difficult to achieve. Several natural history cohorts of HBV patients have shown a low incidence of spontaneous HBsAg seroconversion, approximately 0.5-1.0% per year. Registration trials of HBeAg+ patients on tenofovir DF have shown 10.8% of patients achieve HBsAg loss and 7.7% of patients seroconvert to anti-HBs over 4 years. However, HBsAg loss was not seen in Asian patients or in HBeAg-negative patients.
Aim: To assess the probability and durability of HBsAg seroconversion in Asian-American patients treated with standard of care (SOC) nucleos(t)ide analogue oral agents in a community clinic.
Methods: A retrospective chart review of patients with CHB, who received nucleos(t)ide therapy from a single Irvine, CA clinic from 2008-2010.
Results: We identified nine Asian-American patients on treatment with nucleos(t)ide analogs who achieved HBsAg seroconversion. 4/9 (44%) were male, 8/9 (89%) were HBeAg negative at baseline, and the median age was 48 y.o. 4/9 patients were started on therapy by their primary physician, and their baseline viral load and ALT were not available. For the five patients with complete data, the median starting HBV DNA level was 69,392 IU/ml, and median ALT level was 53 U/L. 6/9 patients were treated with tenofovir (one of whom had lamivudine + TDF), 2 were treated with entecavir (ETV), and 1 was treated with adefovir (ADV). All nine patients achieved a normal ALT and undetectable HBV DNA on treatment. Treatment was discontinued in one patient when he achieved a HBsAb level over 50 mIU/ml. He was treated for 27 months with entecavir before achieving this endpoint. Ten months later, this patient was found to have a viral load of 13,737 IU/ml (79,949 copies/ml). His HBsAg was detectable, and he was started on tenofovir (TDF) at the time of this abstract submission.
Conclusions: Our experience shows it is possible for HBeAg negative Asian-American patients to seroconvert to anti-HBs while on oral CHB therapy. Using a quantitative HBsAb level of >50 mIU/ml as an endpoint to discontinue therapy was difficult to achieve, and did not prevent relapse in the one patient who achieved it, despite a persistently detectable HBsAb level. Further studies are needed in larger patient populations to determine the best endpoint for stopping oral CHB therapy, to maximize durable seroconversion and viral suppression.
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