05 level of significance. The characteristics of the 221 patients are shown in Table 1 according to assigned treatment regimen. Patients were comparable across both groups with regard to age, race, HBV genotype distribution, selleck chemicals llc baseline prevalence of cirrhosis, and ALT and HBV DNA levels. Overall, 43 (19%) patients had a response at week 78, and these patients were distributed

equally across the two study arms. Baseline mean serum HBsAg was 4.4 log IU/mL in both treatment groups. Serum HBsAg was positively correlated with HBV DNA (r = 0.66, P < 0.01) and inversely correlated with age (r = −0.16, P = 0.02) but did not correlate with ALT. Variation was observed in pretreatment HBsAg levels between genotypes, with the highest baseline levels in genotypes A and D (mean = 4.5 log IU/mL for both) and lower levels in genotypes B (mean = 4.3 log IU/mL) and C (mean = 3.8 IU/mL) (P < 0.001 for genotype C versus other genotypes with Bonferroni correction). Overall, HBsAg levels decreased significantly through 52 weeks of therapy (mean decline = 1.2 log IU/mL, P < 0.001), and the decrease was sustained after 26 weeks of follow-up (mean decline compared to baseline = 0.9 IU/mL, P < 0.001). Patterns of HBsAg decline for both treatment groups are depicted in Fig. 1. Declines

were similar in both treatment arms at weeks 4, 8, and 12, but slightly more pronounced in the combination (PEG-IFN + LAM) compared to the monotherapy group (PEG-IFN + placebo) at week 24 (mean decline = 1.0 log IU/mL versus 0.6 log IU/mL, P = 0.04) and at week 52 (mean decline = Gemcitabine cell line 1.46 and 0.87 log IU/mL for combination therapy and monotherapy, respectively, P = 0.04). This difference was not sustained through

posttreatment follow-up 上海皓元医药股份有限公司 (mean decline of 0.98 and 0.86 log IU/mL for combination and monotherapy at week 78, respectively, P = 0.63). Considering the equal response rates and HBsAg levels at week 78 in the two treatment groups, we analyzed the relationship between HBsAg decline and treatment response in all 221 patients. Baseline mean HBsAg levels were comparable in the 43 patients who achieved a response at week 78 and those who did not; 4.4 versus 4.3 log IU/mL in nonresponders and responders, respectively (P = 0.19). Mean HBsAg declines from baseline for responders and nonresponders at week 78 are shown in Fig. 2. Nonresponders showed a modest decline through 52 weeks of therapy (0.69 log IU/mL, P < 0.001), and relapsed during follow-up (decline from baseline at week 78 was 0.35 log IU/mL, P < 0.001 compared to week 52). Mean decline from baseline in responders was 3.3 log IU/mL at week 52 and 3.4 at week 78 (P < 0.001 for both when compared to baseline). Responders thus showed a more vigorous decline in HBsAg starting at week 4, and this difference increased through 52 weeks of therapy and was sustained during posttreatment follow-up (P < 0.005 for week 4 and P ≤ 0.001 for all other time points compared to nonresponders).