Evidence map›Paper›PMID 31965270›Full record

ArticleAnnals of hematology2020

Identification of CD318 (CDCP1) as novel prognostic marker in AML.

Jonas S Heitmann, Ilona Hagelstein, Clemens Hinterleitner, Malte Roerden, Gundram Jung, Helmut R Salih, Melanie Märklin, Joseph Kauer

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Annals of hematology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04708444 (Prognostic Value of CD318 in Acute Myeloid Leukemia Patients at Assiut University Hospital), which is not on this map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 13% 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.

NCT04708444 unknown statusnot on this mapstarted 2021, after this paper: background citation

Prognostic Value of CD318 in Acute Myeloid Leukemia Patients at Assiut University Hospital

TypeobservationalSponsorShimaa Arafa IbrahimRan2021 to 2023Enrolled100ConditionsAcute Myeloid LeukemiaArmsCD318
3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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 4 institutions in 1 country.

Jonas S HeitmannClinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Department of Internal Medicine, University Hospital Tübingen, Tübingen, Germany.
Ilona HagelsteinClinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Department of Internal Medicine, University Hospital Tübingen, Tübingen, Germany.
Clemens HinterleitnerDFG Cluster of Excellence 2180 'Image-guided and Functional Instructed Tumor Therapy' (IFIT), University of Tübingen, Tübingen, Germany.
Malte RoerdenUniversity Hospital Tübingen, Department of Oncology, Haematology and Immunology, Tübingen, Germany.
Gundram JungDepartment of Immunology, German Cancer Consortium (DKTK) and German Cancer Research Center (DKFZ), Interfaculty Institute for Cell Biology, University of Tübingen, Partner Site Tübingen, Tübingen, Germany.
Helmut R SalihClinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Department of Internal Medicine, University Hospital Tübingen, Tübingen, Germany.
Melanie MärklinClinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Department of Internal Medicine, University Hospital Tübingen, Tübingen, Germany. melanie.maerklin@med.uni-tuebingen.de.ORCID http://orcid.org/0000-0002-2920-3894
Joseph KauerDepartment of Immunology, German Cancer Consortium (DKTK) and German Cancer Research Center (DKFZ), Interfaculty Institute for Cell Biology, University of Tübingen, Partner Site Tübingen, Tübingen, Germany.
Deutschen Konsortium für Translationale Krebsforschung · DEGerman Cancer Research Center · DEUniversity Children's Hospital Tübingen · DEUniversity of Tübingen · DE

Funding

Deutsche Forschungsgemeinschaft SA1360/7-3Deutsche Forschungsgemeinschaft SA1360/9-1Deutsche Krebshilfe 111828Deutsche Krebshilfe 70113496Deutsche Krebshilfe (DE) 70112914Germany's Excellence Strategy EXC 2180/1Wilhelm Sander-Stiftung 2007.115.3
6 · The paper itself

Abstract

Genetic and morphological markers are well-established prognostic factors in acute myeloid leukemia (AML). However, further reliable markers are urgently needed to improve risk stratification in AML. CD318 (CDCP1) is a transmembrane protein which in solid tumors promotes formation of metastasis and correlates with poor survival. Despite its broad expression on hematological precursor cells, its prognostic significance in hematological malignancies so far remains unclear. Here, we evaluated the role of CD318 as novel prognostic marker in AML by immunophenotyping of leukemic blasts. Flow cytometric evaluation of CD318 on leukemic cells in 70 AML patients revealed a substantial expression in 40/70 (57%) of all cases. CD318 surface levels were significantly correlated with overall survival in patients receiving anthracycline-based induction therapy or best available alternative therapy. Using receiver-operating characteristics, we established a cut-off value to define CD318

Indexed as

Blast CrisisGene Expression Regulation, LeukemicLeukemia, Myeloid, AcuteAdultAgedAged, 80 and overAntigens, NeoplasmBiomarkers, TumorCell Adhesion MoleculesDisease-Free SurvivalFemaleHumansMaleMiddle AgedSurvival RateAntigens, NeoplasmBiomarkers, TumorCDCP1 protein, humanCell Adhesion MoleculesAMLCD318CDCP1PrognosisRisk stratification

Identifiers

PMID31965270
PMCPMC7060168
OpenAlexW3001825804

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.