Literature DB >> 17215846

Pharmacogenomics-based tailored versus standard therapeutic regimen for eradication of H. pylori.

T Furuta1, N Shirai, M Kodaira, M Sugimoto, A Nogaki, S Kuriyama, M Iwaizumi, M Yamade, I Terakawa, K Ohashi, T Ishizaki, A Hishida.   

Abstract

Helicobacter pylori eradication rates by triple therapy with a proton pump inhibitor, amoxicillin, and clarithromycin at standard doses depend on bacterial susceptibility to clarithromycin and patient CYP2C19 genotypes. We examined the usefulness of a personalized therapy for H. pylori infection based on these factors as determined by genetic testing. First, optimal lansoprazole dosing schedules that would achieve sufficient acid inhibition to allow H. pylori eradication therapy in each of different CYP2C19 genotype groups were determined by a 24-h intragastric pH monitoring. Next, 300 H. pylori-positive patients were randomly assigned to the standard regimen group (lansoprazole 30 mg twice daily (b.i.d.)), clarithromycin 400 mg b.i.d., and amoxicillin 750 mg b.i.d. for 1 week) or the tailored regimen group based on CYP2C19 status and bacterial susceptibility to clarithromycin assessed by genetic testing. Patients with failure of eradication underwent the second-line regimen. The per-patient cost required for successful eradication was calculated for each of the groups. In the first-line therapy, the intention-to-treat eradication rate in the tailored regimen group was 96.0% (95% CI=91.5-98.2%, 144/150), significantly higher than that in the standard regimen group (70.0%: 95% CI=62.2-77.2%, 105/150) (P<0.001). Final costs per successful eradication in the tailored and standard regimen groups were $669 and $657, respectively. In conclusion, the pharmacogenomics-based tailored treatment for H. pylori infection allowed a higher eradication rate by the initial treatment without an increase of the final per-patient cost for successful eradication. However, the precise cost-effectiveness of this strategy remains to be determined.

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Year:  2007        PMID: 17215846     DOI: 10.1038/sj.clpt.6100043

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  56 in total

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Authors:  Takuma Kagami; Mitsushige Sugimoto; Hitomi Ichikawa; Shu Sahara; Takahiro Uotani; Mihoko Yamade; Yasushi Hamaya; Moriya Iwaizumi; Satoshi Osawa; Ken Sugimoto; Hiroaki Miyajima; Takahisa Furuta
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Review 3.  [CYP2D6-, CYP2C9- and CYP2C19-based dose adjustments: when do they make sense?].

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4.  The (R)-omeprazole hydroxylation index reflects CYP2C19 activity in healthy Japanese volunteers.

Authors:  Satoshi Yamada; Hideo Shiohira; Norio Yasui-Furukori; Tomonori Tateishi; Yumiko Akamine; Tsukasa Uno
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6.  Comparison of acid inhibition with standard dosages of proton pump inhibitors in relation to CYP2C19 genotype in Japanese.

Authors:  Mitsushige Sugimoto; Naohito Shirai; Masafumi Nishino; Chise Kodaira; Takahiro Uotani; Shu Sahara; Hitomi Ichikawa; Takuma Kagami; Ken Sugimoto; Takahisa Furuta
Journal:  Eur J Clin Pharmacol       Date:  2014-07-06       Impact factor: 2.953

7.  High-dose versus standard-dose PPI in triple therapy for Helicobacter pylori eradication.

Authors:  Mitsushige Sugimoto; David Y Graham
Journal:  Nat Clin Pract Gastroenterol Hepatol       Date:  2009-01-27

Review 8.  Clinical practice: diagnosis and evaluation of dyspepsia.

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Journal:  J Clin Gastroenterol       Date:  2010-03       Impact factor: 3.062

Review 9.  Pharmacoeconomic evaluations of pharmacogenetic and genomic screening programmes: a systematic review on content and adherence to guidelines.

Authors:  Stefan Vegter; Cornelis Boersma; Mark Rozenbaum; Bob Wilffert; Gerjan Navis; Maarten J Postma
Journal:  Pharmacoeconomics       Date:  2008       Impact factor: 4.981

Review 10.  Virulence factor genotypes of Helicobacter pylori affect cure rates of eradication therapy.

Authors:  Mitsushige Sugimoto; Yoshio Yamaoka
Journal:  Arch Immunol Ther Exp (Warsz)       Date:  2009-02-14       Impact factor: 4.291

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