Two-dimension Tailor-made Therapy: A New Salvage Therapy After Multiple Eradication Failures for

Antibiotics Susceptibility Test CYP2C19 Genotype Proton Pump Inhibitor Third-line Therapy Vonoprazan

Journal

Gastro hep advances
ISSN: 2772-5723
Titre abrégé: Gastro Hep Adv
Pays: Netherlands
ID NLM: 9918350485906676

Informations de publication

Date de publication:
2022
Historique:
received: 24 09 2021
accepted: 05 11 2021
medline: 3 2 2022
pubmed: 3 2 2022
entrez: 12 8 2024
Statut: epublish

Résumé

Vonoprazan-based eradication therapies have a higher eradication rate than usual proton pump inhibitor (PPI)-based therapies in treating Patients who failed twice or more PPI-based triple therapies were recruited. Patients underwent CYP2C19 genotype and antibiotic susceptibility tests (ASTs). PPI doses per day were decided as per the CYP2C19 genotype: twice for poor and 4 times for extensive metabolizers (dimension 1). Two antibiotics were selected as per the results of the AST in each patient (dimension 2). Regimens of 2dTMT included 2 susceptible antibiotics and a PPI. For those who could not have enough information with the AST, tailor-made PPI dosing was indicated with empirically selected 2 antibiotics (one-dimension tailor-made therapy [1dTMT]). Of 51 candidates with multiple eradication failures, 37 patients underwent the genotype test and AST, and 24 succeeded to obtain sufficient information to select 2 susceptible antibiotics. Of them, 22 patients accepted to receive 14-day 2dTMT. Of the residual patients, 12 accepted to receive 14-day 1dTMT. The mean eradication rate of 2dTMT was 86.4% (95% confidence interval [CI]: 65.1%-98.8%) in intention-to-treat and 90.5% (95% CI: 69.6%-98.8%) in per-protocol analyses, whereas that of 1dTMT was 75.0% (95% CI: 42.8%-94.5%) in intention-to-treat and 90.0% (95% CI: 55.5%-99.7%) in per-protocol analyses. Without vonoprazan, 14-day 2dTMT could be one of the salvage therapies for patients with multiple eradication failures. In cases of insufficient information with the AST, 14-day 1dTMT could be an alternative therapy. Clinical Trials Registry number, UMIN000022154 (https://www.umin.ac.jp/icdr/index.html).

Sections du résumé

Background and Aims UNASSIGNED
Vonoprazan-based eradication therapies have a higher eradication rate than usual proton pump inhibitor (PPI)-based therapies in treating
Methods UNASSIGNED
Patients who failed twice or more PPI-based triple therapies were recruited. Patients underwent CYP2C19 genotype and antibiotic susceptibility tests (ASTs). PPI doses per day were decided as per the CYP2C19 genotype: twice for poor and 4 times for extensive metabolizers (dimension 1). Two antibiotics were selected as per the results of the AST in each patient (dimension 2). Regimens of 2dTMT included 2 susceptible antibiotics and a PPI. For those who could not have enough information with the AST, tailor-made PPI dosing was indicated with empirically selected 2 antibiotics (one-dimension tailor-made therapy [1dTMT]).
Results UNASSIGNED
Of 51 candidates with multiple eradication failures, 37 patients underwent the genotype test and AST, and 24 succeeded to obtain sufficient information to select 2 susceptible antibiotics. Of them, 22 patients accepted to receive 14-day 2dTMT. Of the residual patients, 12 accepted to receive 14-day 1dTMT. The mean eradication rate of 2dTMT was 86.4% (95% confidence interval [CI]: 65.1%-98.8%) in intention-to-treat and 90.5% (95% CI: 69.6%-98.8%) in per-protocol analyses, whereas that of 1dTMT was 75.0% (95% CI: 42.8%-94.5%) in intention-to-treat and 90.0% (95% CI: 55.5%-99.7%) in per-protocol analyses.
Conclusion UNASSIGNED
Without vonoprazan, 14-day 2dTMT could be one of the salvage therapies for patients with multiple eradication failures. In cases of insufficient information with the AST, 14-day 1dTMT could be an alternative therapy. Clinical Trials Registry number, UMIN000022154 (https://www.umin.ac.jp/icdr/index.html).

Identifiants

pubmed: 39131120
doi: 10.1016/j.gastha.2021.11.006
pii: S2772-5723(21)00032-7
pmc: PMC11308230
doi:

Types de publication

Journal Article

Langues

eng

Pagination

210-222

Informations de copyright

© 2022 The Authors.

Auteurs

Shigemi Nakajima (S)

Consortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Department of General Medicine, Japan Community Healthcare Organization (JCHO) Shiga Hospital, Otsu, Shiga, Japan.
Department of Gastroenterology, Japan Community Healthcare Organization (JCHO) Shiga Hospital, Otsu, Shiga, Japan.

Hisayuki Inoue (H)

Inoue Clinic, Moriyama, Shiga, Japan.

Hiroshi Satake (H)

Satake Clinic, Kusatsu, Shiga, Japan.

Rena Chatani (R)

Consortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Department of Gastroenterology, Japan Community Healthcare Organization (JCHO) Shiga Hospital, Otsu, Shiga, Japan.

Mariko Ohara (M)

Consortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Department of Gastroenterology, Japan Community Healthcare Organization (JCHO) Shiga Hospital, Otsu, Shiga, Japan.

Yuki Tsubakimoto (Y)

Consortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Department of Gastroenterology, Japan Community Healthcare Organization (JCHO) Shiga Hospital, Otsu, Shiga, Japan.

Makoto Fujii (M)

Consortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Department of Gastroenterology, Japan Community Healthcare Organization (JCHO) Shiga Hospital, Otsu, Shiga, Japan.

Hiroshi Hasegawa (H)

Consortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Department of Gastroenterology, Japan Community Healthcare Organization (JCHO) Shiga Hospital, Otsu, Shiga, Japan.

Keiko Takahashi (K)

Consortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Department of Gastroenterology, Japan Community Healthcare Organization (JCHO) Shiga Hospital, Otsu, Shiga, Japan.

Kiyoyuki Hayafuji (K)

Consortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Department of Gastroenterology, Japan Community Healthcare Organization (JCHO) Shiga Hospital, Otsu, Shiga, Japan.

Yoshihide Fujiyama (Y)

Consortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Department of General Medicine, Japan Community Healthcare Organization (JCHO) Shiga Hospital, Otsu, Shiga, Japan.
Department of Gastroenterology, Japan Community Healthcare Organization (JCHO) Shiga Hospital, Otsu, Shiga, Japan.

Classifications MeSH