TY - JOUR
T1 - A randomized control trial comparing 2 levofloxacin-containing second-line therapies for helicobacter pylori eradication
AU - Chuah, S.-K.
AU - Liang, C.-M.
AU - Lee, C.-H.
AU - Chiou, S.-S.
AU - Chiu, Yi-Chen
AU - Hu, M.-L.
AU - Wu, K.-L.
AU - Lu, L.-S.
AU - Chou, Y.-P.
AU - Chang, K.-C.
AU - Kuo, C.-H.
AU - Kuo, C.-M.
AU - Hu, T.-H.
AU - Tai, W.-C.
PY - 2016
Y1 - 2016
N2 - Summary of Trial Design. Lengthy exposure to quinolone-containing triple therapy in Helicobacter pylori eradication leads to the development of drug resistance. Sequential therapy with a quinolone and metronidazole-containing regimen appears to be an effective treatment option. This randomized controlled trial aimed to compare the efficacy of 5-plus 5 days' levofloxacin and metronidazole-containing sequential therapy (EALM) with that of 10-day levofloxacin-containing triple therapy (EAL) in secondline H pylori eradication treatment. One hundred and sixty-four patients who had failed the H pylori eradication attempts using the standard triple therapy (proton pump inhibitor bid, clarithromycin 500mg bid, amoxicillin 1 g bid<7 days) were randomly assigned to either an EALM therapy group (n=82; esomeprazole 40mg bid and amoxicillin 1 g bid for 5 days, followed by esomeprazole 40mg bid, levofloxacin 500mg qd, and metronidazole 500mg tid, for 5 days) or a 10-day EAL therapy group (n=82; levofloxacin 500mg qd, amoxicillin 1 g bid, and esomeprazole 40mg bid). One patient was lost to follow-up in each group. Follow-up for H pylori status was performed 4 to 8 weeks later. Eradication rates for the EALM and EAL groups were 90.2% (74/82, 95% confidence interval [CI]=83.7%-96.8%) and 80.5% (66/82, 95% CI=71.7%-89.2%, P=0.077) in the intention-to-treat analysis; and 91.4% (74/81, 95% CI=85.1%-97.6%) and 81.5% (66/81, 95% CI=72.8%-90.1%, P=0.067) in the per-protocol analysis. The adverse events for the EALM and EAL groups were 23.5% versus 11.1%, P=0.038 but were all very mild and were well tolerated except for 1 patient with poor compliance. The compliances were 98.8% and 100%, respectively, between the 2 groups. An antibiotic resistance to levofloxacin was the clinical factor influencing the efficacy of H. pylori eradication therapy in the EAL group, and dual resistance to levofloxacin and metronidazole in the EALM group. Levofloxacin and metronidazole-containing sequential therapy achieved a >90% eradication rate as a second-line H pylori therapy. Dual antibiotic resistance to levofloxacin and metronidazole was the clinical factor influencing the efficacy of H pylori eradication therapy in the sequential therapy (ClinicalTrials.gov number: NCT02596620).
AB - Summary of Trial Design. Lengthy exposure to quinolone-containing triple therapy in Helicobacter pylori eradication leads to the development of drug resistance. Sequential therapy with a quinolone and metronidazole-containing regimen appears to be an effective treatment option. This randomized controlled trial aimed to compare the efficacy of 5-plus 5 days' levofloxacin and metronidazole-containing sequential therapy (EALM) with that of 10-day levofloxacin-containing triple therapy (EAL) in secondline H pylori eradication treatment. One hundred and sixty-four patients who had failed the H pylori eradication attempts using the standard triple therapy (proton pump inhibitor bid, clarithromycin 500mg bid, amoxicillin 1 g bid<7 days) were randomly assigned to either an EALM therapy group (n=82; esomeprazole 40mg bid and amoxicillin 1 g bid for 5 days, followed by esomeprazole 40mg bid, levofloxacin 500mg qd, and metronidazole 500mg tid, for 5 days) or a 10-day EAL therapy group (n=82; levofloxacin 500mg qd, amoxicillin 1 g bid, and esomeprazole 40mg bid). One patient was lost to follow-up in each group. Follow-up for H pylori status was performed 4 to 8 weeks later. Eradication rates for the EALM and EAL groups were 90.2% (74/82, 95% confidence interval [CI]=83.7%-96.8%) and 80.5% (66/82, 95% CI=71.7%-89.2%, P=0.077) in the intention-to-treat analysis; and 91.4% (74/81, 95% CI=85.1%-97.6%) and 81.5% (66/81, 95% CI=72.8%-90.1%, P=0.067) in the per-protocol analysis. The adverse events for the EALM and EAL groups were 23.5% versus 11.1%, P=0.038 but were all very mild and were well tolerated except for 1 patient with poor compliance. The compliances were 98.8% and 100%, respectively, between the 2 groups. An antibiotic resistance to levofloxacin was the clinical factor influencing the efficacy of H. pylori eradication therapy in the EAL group, and dual resistance to levofloxacin and metronidazole in the EALM group. Levofloxacin and metronidazole-containing sequential therapy achieved a >90% eradication rate as a second-line H pylori therapy. Dual antibiotic resistance to levofloxacin and metronidazole was the clinical factor influencing the efficacy of H pylori eradication therapy in the sequential therapy (ClinicalTrials.gov number: NCT02596620).
KW - Medicine (all)
U2 - 10.1097/MD.0000000000003586
DO - 10.1097/MD.0000000000003586
M3 - Journal Article
C2 - 27175657
SN - 0025-7974
VL - 95
JO - Medicine (United States)
JF - Medicine (United States)
IS - 19
ER -