Evidence map›Paper›PMID 29950693›Full record

Trial reportLeukemia2018

A prospective study on serum Cytokeratin (CK)-18 and CK18 fragments as biomarkers of acute hepato-intestinal GVHD.

Sandra Sauer, Johannes Hüsing, Jacek Hajda, Frank Neumann, Aleksandar Radujkovic, Anthony D Ho, Peter Dreger, Thomas Luft

Registry-linked trialAbstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Leukemia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00935324 (CK18-Fragments as Tools for Evaluating Diagnosis, Biological Activity, and Prognosis of Graft-Versus-Host Disease), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 24% 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.

NCT00935324 unknown statusnot on this map

CK18-Fragments as Tools for Evaluating Diagnosis, Biological Activity, and Prognosis of Graft-Versus-Host Disease

TypeobservationalSponsorHeidelberg UniversityRan2009 to 2011Enrolled120ConditionsAllo-SCT
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Honokiol Inhibits Melanoma Growth by Targeting Keratin 18Frontiers in cell and developmental biology · 2020
    Article
  3. Article
  4. Review
  5. Biomarkers in acute graft-Therapeutic advances in hematology · 2019
    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

8 authors at 2 institutions in 2 countries.

Sandra SauerDepartment of Hematology and Oncology, University of Heidelberg, Heidelberg, Germany.
Johannes HüsingDivision of Biostatistics, Coordination Centre for Clinical Trials, University of Heidelberg, Heidelberg, Germany.
Jacek HajdaDivision of Biostatistics, Coordination Centre for Clinical Trials, University of Heidelberg, Heidelberg, Germany.
Frank NeumannBIOAXXESS, Tewkesbury, UK.
Aleksandar RadujkovicDepartment of Hematology and Oncology, University of Heidelberg, Heidelberg, Germany.
Anthony D HoDepartment of Hematology and Oncology, University of Heidelberg, Heidelberg, Germany.
Peter DregerDepartment of Hematology and Oncology, University of Heidelberg, Heidelberg, Germany.
Thomas LuftDepartment of Hematology and Oncology, University of Heidelberg, Heidelberg, Germany. thomas.luft@med.uni-heidelberg.de.
Heidelberg University · DETewkesbury Community Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Apoptotic intestinal crypt cells are pathognomonic of acute intestinal graft versus host disease (GVHD). Serum levels of the apoptotic degradation product cytokeratin-18 fragments (CK18F) were associated with acute hepato-intestinal GVHD. Here we present a prospective clinical observational trial (NCT00935324) investigating serum levels of total CK18 (tCK18) and apoptotic CK18F to predict imminent acute hepato-intestinal GVHD and response to treatment. Total (t)CK18 and CK18F kinetics were measured before transplantation and in weekly intervals thereafter. In total 109 patients were enrolled. Acute hepato-intestinal GVHD grade I-IV was suspected in 36 patients (33%) at a median of 56 days post-transplant, 12 of these patients developed steroid-refractory GVHD. Both tCK18 and apoptotic CK18F increased at GVHD onset, and distinguished patients with suspected acute hepato-intestinal GVHD who were negative in intestinal histology. In patients with clinical acute hepato-intestinal GVHD, tCK18 significantly raised already 7-14 days before symptom onset. In receiver operator characteristics, areas under the curve at GVHD onset were 0.927 (p < 0.001) for tCK18 and 0.875 (p < 0.001) for apoptotic CK18F for patients with proven hepato-intestinal acute GVHD. This prospective study validates CK18F and highlights tCK18 as specific biomarkers suitable for improving prediction and diagnosis of suspected imminent and clinically manifest acute hepato-intestinal GVHD.

Indexed as

Acute DiseaseAdultAgedBiomarkersFemaleGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansIntestinesKeratin-18LiverMaleMiddle AgedProspective StudiesTransplantation, HomologousYoung AdultBiomarkersKeratin-18KRT18 protein, human

Identifiers

PMID29950693
OpenAlexW2809888275

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.