Evidence map›Paper›PMID 28685218›Full record

ArticlePathology oncology research : POR2018

Influence of CYP2C19 Genotypes on the Occurrence of Adverse Drug Reactions of Voriconazole among Hematological Patients after Allo-HSCT.

Beata Sienkiewicz, Donata Urbaniak-Kujda, Jarosław Dybko, Andrzej Dryś, Magdalena Hurkacz, Tomasz Wróbel, Anna Wiela-Hojeńska

Open access · hybridAbstract read
In one paragraph

Article in Pathology oncology research : POR, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 32% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Observational
  3. Article
  4. Article
  5. Optimizing antifungal prophylaxis in allogeneic stem cell transplantation: A cohort study of two different approaches.Transplant infectious disease : an official journal of the Transplantation Society · 2022
    Observational
  6. Article
  7. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Beata SienkiewiczDepartment of Clinical Pharmacology, Faculty of Pharmacy, Wrocław Medical University, 211a Borowska St, 50-556, Wrocław, Poland. beata.sienkiewicz@gmail.com.
Donata Urbaniak-KujdaDepartment and Clinic of Haematology, Blood Neoplasms, and Bone Marrow Transplantation, Wrocław Medical University, 4 Wybrzeże Pasteura St, 50-367, Wrocław, Poland.
Jarosław DybkoDepartment and Clinic of Haematology, Blood Neoplasms, and Bone Marrow Transplantation, Wrocław Medical University, 4 Wybrzeże Pasteura St, 50-367, Wrocław, Poland.
Andrzej DryśDepartment of Physical Chemistry, Wrocław Medical University, 211a Borowska St, 50-556, Wrocław, Poland.
Magdalena HurkaczDepartment of Clinical Pharmacology, Faculty of Pharmacy, Wrocław Medical University, 211a Borowska St, 50-556, Wrocław, Poland.
Tomasz WróbelDepartment and Clinic of Haematology, Blood Neoplasms, and Bone Marrow Transplantation, Wrocław Medical University, 4 Wybrzeże Pasteura St, 50-367, Wrocław, Poland.
Anna Wiela-HojeńskaDepartment of Clinical Pharmacology, Faculty of Pharmacy, Wrocław Medical University, 211a Borowska St, 50-556, Wrocław, Poland.
Wroclaw Medical University · PL

Funding

Ministry of Science and Higher Education, Republic of Poland ST-774
6 · The paper itself

Abstract

The aim of this study was to determine the influence of different CYP2C19 genotypes on selected liver function parameters, and ADR occurrence during VCZ prophylaxis in adult patients after allo-HSCT (allogeneic hematopoietic stem cell transplantation). CYP2C19 mutations were determined in a cohort of 30 adults using PCR-RFLP methods established by Sim et al. and Goldstein and Blaisdell. The patients' protocol included biometrical and biochemical data, information on the underlying disease, chemotherapy, molds infections occurring during VCZ treatment, adverse drug reactions typical for the use of voriconazole, and probable drug - drug interactions. The observation and reporting of ADR took place from the -1 until the +20th day of VCZ therapy. For statistical analysis the χ2 test was used (p < 0.05). Among the examined patients 23 suffered from at least one side effect during VCZ therapy. Most frequent ADR were gastrointestinal disturbances (n = 15), nervous system (n = 11) and skin (n = 7) disorders. Patients with at least one loss of function allele (*2) were more likely to experience adverse drug reactions than those, with different genotypes. Due to the limited number of patients the result could not be proven with a statistical significance. Previous determination of CYP2C19 genotype may be a useful tool for prevention of adverse drug reactions during VCZ prophylaxis among patients after allo-HSCT.

Indexed as

Polymorphism, GeneticBiomarkers, TumorCohort StudiesCytochrome P-450 CYP2C19Cytochrome P-450 CYP3A InhibitorsDrug-Related Side Effects and Adverse ReactionsFemaleFollow-Up StudiesGenotypeHematologic DiseasesHematopoietic Stem Cell TransplantationHumansMaleMiddle AgedPrognosisTransplantation, HomologousBiomarkers, TumorCYP2C19 protein, humanCytochrome P-450 CYP2C19Cytochrome P-450 CYP3A InhibitorsVoriconazoleAdverse drug reactionsCYP2C19GenotypingHematologyVoriconazole

Identifiers

PMID28685218
PMCPMC5972163
OpenAlexW2728893184

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.