Evidence map›Paper›PMID 36553668›Full record

ArticleGenes2022

Some New Aspects of Genetic Variability in Patients with Cutaneous T-Cell Lymphoma.

Vladimír Vašků, Jan Máchal, Filip Zlámal, Anna Vašků

Abstract read
In one paragraph

Article in Genes, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

4 authors.

Vladimír Vašků1st Department of Dermatovenereology, St. Anne's University Hospital, Faculty of Medicine, Masaryk University, 65691 Brno, Czech Republic.
Jan MáchalDepartment of Pathological Physiology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.ORCID 0000-0002-8292-3145
Filip ZlámalDepartment of Pathological Physiology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.
Anna VaškůDepartment of Pathological Physiology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.ORCID 0000-0002-9956-5823

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimCutaneous T-cell lymphoma (CTCL) is a group of T-cell malignancies that develop in the skin. Though studied intensively, the etiology and pathogenesis of CTCL remain elusive. This study evaluated the survival of CTCL patients in the 1st Department of Dermatovenereology of St. Anne's University Hospital Brno. It included analysis of 19 polymorphic gene variants based on their expected involvement in CTCL severity. MATERIAL AND

methods75 patients with CTCL, evaluated and treated at the 1st Department of Dermatovenereology of St. Anne´s University Hospital Brno, Faculty of Medicine, Masaryk University, were recruited for the study over the last 28 years (44 men and 31 women, average age 58 years, range 20-82 years). All patients were genotyped for 19 chosen gene polymorphisms by the conventional PCR method with restriction analysis. A multivariate Cox regression model was calculated to reveal genetic polymorphisms and other risk factors for survival.

resultsThe model identified MDR Ex21 2677 (rs2032582) as a significant genetic factor influencing the survival of the patients, with the T-allele playing a protective role. A multivariate stepwise Cox regression model confirmed the following as significant independent risk factors for overall survival: increased age at admission, clinical staging of the tumor, and male sex.

conclusionWe showed that the TT genotype at position 2677 of the MDR1 gene exhibited statistically significant longer survival in CTCL patients. As such, the TT genotype of MDR1 confers a significant advantage for the CTCL patients who respond to treatment.

Indexed as

Lymphoma, T-Cell, CutaneousSkin NeoplasmsAdultAgedAged, 80 and overFemaleGenotypeHumansMaleMiddle AgedPolymorphism, GeneticRisk FactorsYoung AdultCTCLmycosis fungoidespolymorphism-MDR1skin T-cell lymphoma

Identifiers

PMID36553668
PMCPMC9778129

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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.