Evidence map›Paper›PMID 26963909›Full record

Trial reportPloS one2016

Inter-Reader Reliability of Early FDG-PET/CT Response Assessment Using the Deauville Scale after 2 Cycles of Intensive Chemotherapy (OEPA) in Hodgkin's Lymphoma.

Regine Kluge, Lidia Chavdarova, Martha Hoffmann, Carsten Kobe, Bogdan Malkowski, Françoise Montravers, Lars Kurch, Thomas Georgi, Markus Dietlein, W Hamish Wallace and 9 more

Registry-linked trialOpen access · goldAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03500133 (Non Randomized, Multicenter, Prospective Pediatric Hodgkin Lymphoma Treatment Trial Stratified According to Initial Risk Factors and Response to Chemotherapy, Reduced Cumulative Doses of Antineoplastic Agents and Radiotherapy.), which is not on this map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 3% 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.

NCT03500133 phase4recruitingnot on this mapstarted 2017, after this paper: background citation

Non Randomized, Multicenter, Prospective Pediatric Hodgkin Lymphoma Treatment Trial Stratified According to Initial Risk Factors and Response to Chemotherapy, Reduced Cumulative Doses of Antineoplastic Agents and Radiotherapy.

TypeinterventionalSponsorHospital JP GarrahanRan2017 to 2032Enrolled500ConditionsPediatric Hodgkin's DiseaseArmsNo radiotherapy if CR at the end of chemotherapy., Low risk with complete early response after two cycles of ABVD chemotherapy schedule. Only one more ABVD course is delivered., Low risk with partial remisssion after 4 cycles of ABVD chemotherapy schedule. Two ESHAP courses are delivered., IN 30Gy RT in case of PR at the end of chemotherapy, Intermediate risk with complete early response after two cycles of ABVD chemotherapy schedule. Three more ABVD courses are delivered.
3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Performance of Deauville Criteria inDiagnostics (Basel, Switzerland) · 2023
    Article
  9. Article
  10. Semi-automatedComputational and structural biotechnology journal · 2023
    Article
  11. Article
  12. Influences on PET Quantification and Interpretation.Diagnostics (Basel, Switzerland) · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. The British journal of radiology · 2019
    Review
  19. FDG PET for therapy monitoring in Hodgkin and non-Hodgkin lymphomas.European journal of nuclear medicine and molecular imaging · 2017
    Review
  20. 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

19 authors at 13 institutions in 11 countries.

Regine KlugeDepartment of Nuclear Medicine, University of Leipzig, Leipzig, Germany.
Lidia ChavdarovaClinic of Nuclear Medicine, National Hospital for Active Treatment in Oncology, Sofia, Bulgaria.
Martha HoffmannDepartment of Biomedical Imaging and Image-guided Therapy, Division of Nuclear Medicine, Medical University of Vienna, Vienna, Austria.
Carsten KobeDepartment of Nuclear Medicine, University Hospital of Cologne, Cologne, Germany.
Bogdan MalkowskiDept. of PET and Molecular Imaging, Nicolaus Copernicus University, Collegium MedicumBydgoszcz, Poland.
Françoise MontraversDepartment of Nuclear Medicine, Hopital Tenon, Assistance Publique Hôpitaux de Paris, Faculté de médecine Pierre et Marie Curie, Paris, France.
Lars KurchDepartment of Nuclear Medicine, University of Leipzig, Leipzig, Germany.
Thomas GeorgiDepartment of Nuclear Medicine, University of Leipzig, Leipzig, Germany.
Markus DietleinDepartment of Nuclear Medicine, University Hospital of Cologne, Cologne, Germany.
W Hamish WallaceDepartment of Paediatric Oncology, Royal Hospital for Sick Children, University of Edinburgh, Edinburgh, United Kingdom.
Jonas KarlenKarolinska University Hospital, Astrid Lindgrens Childrens Hospital, Stockholm, Sweden.
Ana Fernández-TeijeiroPediatric Oncology Unit, Hospitales Universitarios Virgen Macarena y Virgen del Rocio, Sevilla, Spain.
Michaela CepelovaDepartment of Pediatric Hematology and Oncology, University Hospital Motol and 2nd Medical Faculty of Charles University, Prague, Czech Republic.
Lorrain WilsonDepartment of Nuclear Medicine, Blackrock Clinic, Dublin, Ireland.
Eva BergstraesserDepartment of Paediatric Oncology, University Children's Hospital Zurich, Switzerland.
Osama SabriDepartment of Nuclear Medicine, University of Leipzig, Leipzig, Germany.
Christine Mauz-KörholzDepartment of Pediatric Oncology, University of Halle, Halle/Saale, Germany.
Dieter KörholzDepartment of Pediatric Oncology, University of Halle, Halle/Saale, Germany.
Dirk HasencleverInstitute for Medical Informatics, Statistics and Epidemiology (IMISE), University of Leipzig, Leipzig, Germany.
Leipzig University · DEMartin Luther University Halle-Wittenberg · DEUniversity Hospital Cologne · DECharles University · CZHôpital Tenon · FRHospital Universitario Virgen Macarena · ESKarolinska University Hospital · SEMedical University of Vienna · ATNational Hospital for Neurology and Neurosurgery · GBNicolaus Copernicus University · PLRoyal Hospital for Sick Children · GBStone Clinic · USUniwersytecki Szpital Dziecięcy · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe five point Deauville (D) scale is widely used to assess interim PET metabolic response to chemotherapy in Hodgkin lymphoma (HL) patients. An International Validation Study reported good concordance among reviewers in ABVD treated advanced stage HL patients for the binary discrimination between score D1,2,3 and score D4,5. Inter-reader reliability of the whole scale is not well characterised.

methodsFive international expert readers scored 100 interim PET/CT scans from paediatric HL patients. Scans were acquired in 51 European hospitals after two courses of OEPA chemotherapy (according to the EuroNet-PHL-C1 study). Images were interpreted in direct comparison with staging PET/CTs.

resultsThe probability that two random readers concord on the five point D score of a random case is only 42% (global kappa = 0.24). Aggregating to a three point scale D1,2 vs. D3 vs. D4,5 improves concordance to 60% (kappa = 0.34). Concordance if one of two readers assigns a given score is 70% for score D1,2 only 36% for score D3 and 64% for D4,5. Concordance for the binary decisions D1,2 vs. D3,4,5 is 67% and 86% for D1,2,3 vs D4,5 (kappa = 0.36 resp. 0.56). If one reader assigns D1,2,3 concordance probability is 92%, but only 64% if D4,5 is called. Discrepancies occur mainly in mediastinum, neck and skeleton.

conclusionInter-reader reliability of the five point D-scale is poor in this interobserver analysis of paediatric patients who underwent OEPA. Inter-reader variability is maximal in cases assigned to D2 or D3. The binary distinction D1,2,3 versus D4,5 is the most reliable criterion for clinical decision making.

Indexed as

Positron-Emission TomographyTomography, X-Ray ComputedAdolescentAntineoplastic Combined Chemotherapy ProtocolsChildChild, PreschoolDoxorubicinEtoposideFemaleGlucose-6-PhosphateHodgkin DiseaseHumansMalePrednisoneVincristine2-fluoro-2-deoxyglucose-6-phosphateDoxorubicinEtoposideGlucose-6-PhosphatePrednisoneVincristine

Identifiers

PMID26963909
PMCPMC4786307
OpenAlexW2294000995

What OpenQuestion holds

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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.