Levofloxacin-containing versus Clarithromycin-containing Therapy for Helicobacter pylori Eradication: A Prospective Randomized Controlled Clinical Trial
Vahid Sebghatollahi1, Maryam Soheilipour1, Mahsa Khodadoostan1, Alireza Shavakhi2, Ahmad Shavakhi1
1 Department of Internal Medicine, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
2 Department of Internal Medicine, Shahrekord University of Medical Sciences, Shahrekord, Iran
|Date of Web Publication||27-Mar-2018|
Dr. Maryam Soheilipour
Department of Internal Medicine, School of Medicine, Isfahan University of Medical Sciences, Isfahan
Source of Support: None, Conflict of Interest: None
Background: This study evaluated the clinical efficacy and tolerability of a 14-day course of bismuth-based quadruple therapy including tinidazole and levofloxacin in compare to a 14-day bismuth-based quadruple therapy including clarithromycin as first-line treatment for Helicobacter pylori infection in Iranian adults. Materials and Methods: The study was a prospective, parallel group, randomized controlled, clinical trial that conducted on 150 patients with H. pylori infection. Patients were randomly assigned to the two groups as follows: first group received pantoprazole 40 mg, bismuth subcitrate 240 mg, amoxicillin 1 g, and clarithromycin 500 mg (PBAC group), and other group received pantoprazole 40 mg, bismuth subcitrate 240 mg, amoxicillin 1 g, tinidazole 500 mg for 7 days, followed by levofloxacin 500 mg for the second 7 days (PBATL group). Main outcomes were eradication rate, tolerance of treatment, and dyspepsia severity. Results: The eradication rates for PBAC regimen was 81.1% (95% confidence interval [CI]: 71.9–90.2) and for PBATL regimen was 70.8% (95% CI: 60.1–81.6), which was not significantly different (P = 0.147). Tolerance of treatment was similar between groups. The median of severity of dyspeptic after treatment in PBAC group was 10 [9–14.75], which was similar to PBATL group 10 [9–13.5] (P = 0.690). Conclusion: There is no significant difference between PBAC and PBATL regimen, and efficacy was similar in both groups. The overall rate of treatment failure suggests that up to 18%–30% of patients will fail bismuth-based quadruple therapy and require retreatment for the infection.
Keywords: Clarithromycin, Helicobacter pylori, levofloxacin, tinidazole
|How to cite this article:|
Sebghatollahi V, Soheilipour M, Khodadoostan M, Shavakhi A, Shavakhi A. Levofloxacin-containing versus Clarithromycin-containing Therapy for Helicobacter pylori Eradication: A Prospective Randomized Controlled Clinical Trial. Adv Biomed Res 2018;7:55
|How to cite this URL:|
Sebghatollahi V, Soheilipour M, Khodadoostan M, Shavakhi A, Shavakhi A. Levofloxacin-containing versus Clarithromycin-containing Therapy for Helicobacter pylori Eradication: A Prospective Randomized Controlled Clinical Trial. Adv Biomed Res [serial online] 2018 [cited 2020 Jun 4];7:55. Available from: http://www.advbiores.net/text.asp?2018/7/1/55/228618
| Introduction|| |
Helicobacter pylorus has been linked conclusively to various disorders of the upper gastrointestinal tract, including peptic ulcer, gastric mucosa-associated lymphoid tissue lymphoma, and gastric cancer., Approximately over half of the world's population is reported to have H. pylori infection and depending on the population studied, infects 7% to 87% of adults., A global systematic review shows that approximately 4.4 billion people in the world were estimated to be infected with for H. pylori in 2015. This infection is more common in developing countries, and in Asia, 54.7% reported to be positive for H. pylori. In Iran, analyses of reports show that 59% of people were infected by H. pylori.
Choosing a treatment for H. pylori eradication depends on different factors, such as the local availability of antimicrobial agents, the pattern of primary antibiotic resistance, and the therapeutic cost. The most commonly recommended for first-line treatment of H. pylori included 7- to 14-day triple therapy with a proton-pump inhibitor (PPI), amoxicillin, and clarithromycin with cure rates of 80%–90%., These rates were reported for many years ago, and studies from different parts of the world have raised some important concerns about the current success of this regimen, especially with regard to increasing clarithromycin resistance., Thus, bismuth-containing quadruple therapy is recommended as first-line treatment for the eradication of H. pylori infection in regions with a high clarithromycin resistance rate. In Iran with increasing in clarithromycin resistance rate, bismuth-containing quadruple therapy has been strongly recommended.
Levofloxacin and tinidazole have been shown to be effective for the treatment of H. pylori infection, and some studies have also shown that these drugs are effective as the first-line treatment for H. pylori eradication.,, The optimal duration for H. pylori eradication therapy is controversial, with recommendations ranging from 7 to 14 days whereas the duration of therapy with the pattern of H. pylori antibiotic resistance, and the patients' compliance is known as the main factors in the success rate of eradication regimens. In regard to the high resistance to metronidazole and clarithromycin in patients infected by H. pylori in Iran and controversial findings on the therapy, the present study was designed to investigate effective treatment duration for 14-day bismuth-based quadruple therapy including tinidazole (for 7 days), followed by levofloxacin (for 7 days) in compare to 14-day bismuth-based quadruple therapy including clarithromycin by comparing eradication rate, compliance, and adverse event rate between the regimens as first-line treatment for H. pylori eradication.
| Materials and Methods|| |
The study was a prospective, parallel group, randomized controlled, clinical trial that conducted on 150 patients, referrals to the gastroenterology clinics of Isfahan University of Medical Sciences (IUMS) from February to November 2016. Ethical approval was obtained from the Research Ethics Committee of IUMS before recruitment.
One hundred fifty consecutive patients were included in the study according to the following inclusion criteria: (1) patients in both genders with age 18 and over and (2) patients with peptic ulcer disease. H. pylori infection was confirmed by serologic and gastric tissue. The participants with known gastrointestinal malignancy, MALT lymphoma, Zollinger–Ellison syndrome, immunodeficiency disorders, liver or renal diseases, clinical conditions that need antibiotic therapy, history of gastric surgery, and history of H. pylori eradication or using PPI, antibiotic, or probiotics within 4 weeks before the study and pregnant women were not included in the study. The exclusion criteria were serious side effects that require immediate discontinuation of therapy. Furthermore, patients who did not use their study medications regularly were excluded from the study.
All eligible patients were voluntary and gave written informed consent to participate in the study. The sampling method was consecutive, and randomization was performed by generating a random list of patient allocations before the start of intervention, by Random Allocation Software.
Enrolled patients were randomly assigned to one of the two equal groups. Group I (PBAC) had 75 patients who received treatment regimen included pantoprazole 40 mg, bismuth subcitrate 240 mg, amoxicillin 1 g, and clarithromycin 500 mg; all given twice daily (q12 h) for 14 days. Group II (PBATL) had 75 patients who received treatment regimen included pantoprazole 40 mg, bismuth subcitrate 240 mg, amoxicillin 1 g, twice/day for 14 days, tinidazole 500 mg twice daily for the first 7 days, followed by levofloxacin 500 mg daily for the second 7 days.
Collected data included age, sex, dyspepsia symptoms, medicinal effects of each regimen (bad taste, nausea, bloating, diarrhea, constipation, skin rash, and epigastric pain); intolerance of treatment which was assessed at the end of treatment as none, mild, moderate, and severe; and eradication rate. To assess the eradication rate of H. pylori in studied patients, 13C urea breath test with 94% of sensitivity and 95% of specificity, respectively, was use 1 month after the end of treatments. Dyspepsia severity was evaluated by the short-form leeds dyspepsia questionnaire (SFLDQ), which evaluates frequency and interference of four symptoms including epigastric pain/discomfort, retrosternal burning, regurgitation, and nausea. The total score of the SFLDQ ranges from 0 to 32 and was completed by patients in both groups at baseline and after treatment.
Statistical analyses were done using SPSS software for Windows (SPSS, Inc., Chicago, IL, USA, version 24). Descriptive data are reported as mean ± standard deviation, median (IQR), or number (percent) as appropriate. Independent sample t-test, Chi-square test, Mann–Whitney U-test, Wilcoxon signed-rank test, and analysis of covariance (ANCOVA) were used as appropriate. All hypothesis testing was two tailed, and level of significance was considered to be <0.05 in all tests.
| Results|| |
One hundred sixty patients were reviewed to selected eligible patients; ten patients did not enter (nine refused informed consent and one was not eligible). One hundred fifty eligible patients randomly allocated into two intervention groups. Four patients were lost during follow-up period. Finally, 74 patients in PBAC group and 72 patients in PBATL group completed the study and analyzed [Figure 1].
The mean age of studied participants was 47.3 ± 12.8 years; 44.5% (65 patients) were male and 55.5% (81 patients) were female. Other demographics and clinical characteristics of the participants by treatment regimens are shown in [Table 1].
|Table 1: Demographic and clinical characteristics of studied population by intervention groups|
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As shown in [Table 2], there has been significant reduction in the LDQ score in both regimens. The result of ANCOVA was not found any difference between groups.
|Table 2: The summary results of both frequency and severity of dyspeptic symptoms based on Leeds dyspepsia questionnaire score according to treatment regimens|
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There was no significant difference of H. pylori eradication rates between the studied regimens. The eradication rate for PBAC regimen was 81.1% (95% confidence interval [CI]: 71.9–90.2) and for PBATL regimen was 70.8% (95% CI: 60.1–81.6) (P = 0.147).
In this study, overall HP eradication rate was significantly associated with age. The whole observations indicate that younger patients had a significantly better response [Table 3] and [Figure 2]. However, there was no significant difference between the regimens by age for the H. pylori eradication rates (P > 0.05).
|Table 3: Helicobacter pylori eradication in studied population by age group|
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|Figure 2: Overall Helicobacter pylori eradication in studied population by age group|
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| Discussion|| |
In this study, PBAC regimen included 14-day treatment with bismuth, amoxicillin, clarithromycin, and pantoprazole which was associated with higher rates of H. pylori eradication in compare to PBATL regimen included 14-day treatment with bismuth, amoxicillin, tinidazole (followed by levofloxacin in the second 7 days), and pantoprazole. Eradication rate for PBAC regimen was 81.1% and for PBATL regimen was 70.8%, which did not significantly differ between groups. There is no significantly different for adverse event between groups, and both studied regimens were well tolerated based on patients' reports in two studied groups. The rates of eradication in our studied regimens were low, and according to Graham classified efficacy of H. pylori treatment,, success rate in PBATL regimen is poor and for PBAC regimen is unacceptable. The lower rate of eradication in our study might be related to the prevalence of antibiotic resistant of H. pylori strains in our studied patients, where we did not assess pretreatment antibiotic resistant in these patients.
In a meta-analysis, it is reported that sequential therapy was superior to a 7-day standard triple therapy regimen, but when compared with a longer duration of standard triple therapy, the difference disappeared. In the other studies, the duration of sequential therapy has been assessed to determine whether longer therapy will help improve the eradication rates of H. pylori infection. In Warrington et al. study, it is shown that regardless of the treatment duration, sequential regimens are not better than standard triple therapy. In this study, the eradication rate was 83.7% in the standard triple therapy, 80.0% in the 10-day sequential therapy, and 79.1% in the 14-day sequential therapy regimen. In a large study by Liou et al., it is suggested that longer therapy with a sequential regimen would provide better eradication rates. In these study for 10- and 14-day of sequential therapy, the eradication rate of 90.7% and 87.0% is reported, respectively, and in a 14-day standard triple therapy group, the eradication rate was 82.3%. In Ergül et al.'s study, eradication rate of 90.7% is reported for a 14-day bismuth-containing quadruple therapy as first-line therapy. Su et al. in their study showed an eradication rate of 80.2% and 89.7% for 1-week two regimens of bismuth-based quadruple-containing clarithromycin or levofloxacin, respectively. One study in Iranian patients reported 82.3% of eradication rate of H. pylori for quadruple therapy after 2 weeks. In another report from Iran, after 10-day quadruple therapy, eradication rate was 84.0%. In the Mousavi et al. study, 14 days of bismuth-based quadruple regimen had eradication rate of 75.7%. Aminian et al. reported 85.7% of H. pylori eradication rate after 4 days of bismuth-based quadruple with metronidazole. In a randomized clinical trial, Metanat et al. evaluated 10- and 14-day nonbismuth-based quadruple regimen for H. pylori treatment and reported eradication rate 83.5% and 92.8% for studied regimens, respectively. In the present study, in both bismuth-based quadruple therapy, eradication rates were lower than reported previously (81.1% for PBAC regimen and 70.8% for PBATL regimen). The prevalence of antibiotic resistance, differences in the studied regimens, and does of drugs might be explain the differences between study findings.
In the present study, the eradication rate was decreased with increase in age group; patients in older age group had a lower rate of eradication though this difference was not statistically significant. In other study, in Iran, it is reported that patients' age and gender are associated with H. pylori eradication rate. Another study reported that occupation, gender, and protocol compliance were positively associated with H. pylori eradication rate. Silva et al. report a significant association between age and H. pylori eradication rate but did not report a significant difference between patients' characteristics and eradication rate.
The present study has some limitations. First is the lack of any analysis of antibiotic resistance relative to the eradication rates and treatment regimens, whereas antibiotic resistance is known as the most important cause of treatment failure. Second, this trial was not a double-blind placebo-controlled trial in which the detection bias was minimized. Third, this study was a single-center study and its results need to be externally validated.
| Conclusion|| |
This randomized trial showed that a 14-day bismuth-based quadruple regimen-containing amoxicillin, tinidazole (followed by levofloxacin in the second 7 days), and pantoprazole is statistically effective as well as 14-day bismuth-based quadruple regimen-containing amoxicillin, clarithromycin, and pantoprazole in the eradication of H. pylori infection, and there is no significant difference between PBAC and PBATL regimens. The overall rate of treatment failure suggests that up to 18%–30% of patients will fail bismuth-based quadruple therapy and require retreatment for the infection. More studies are needed to draw meaningful conclusions for optimal duration of H. pylori eradication regimens.
This study was supported by a grant from Isfahan University of Medical Sciences.
Financial support and sponsorship
This study was supported by a grant from Isfahan University of Medical Sciences.
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3]
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