Evidence map›Paper›PMID 30941573›Full record

ArticleJournal of cancer research and clinical oncology2019

Results of the European survey on the assessment of deep molecular response in chronic phase CML patients during tyrosine kinase inhibitor therapy (EUREKA registry).

Susanne Möbius, Thomas Schenk, Danny Himsel, Jacqueline Maier, Georg-Nikolaus Franke, Susanne Saussele, Christiane Pott, Hajnalka Andrikovics, Nora Meggyesi, Katerina Machova-Polakova and 10 more

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. MolecularInternational journal of molecular sciences · 2023
    Article
  3. Review
  4. Review
  5. Article
  6. 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

20 authors at 12 institutions in 8 countries.

Susanne MöbiusAbteilung Hämatologie und Internistische Onkologie, Klinik für Innere Medizin II, Universitätsklinikum Jena, Am Klinikum 1, 07740, Jena, Germany.
Thomas SchenkAbteilung Hämatologie und Internistische Onkologie, Klinik für Innere Medizin II, Universitätsklinikum Jena, Am Klinikum 1, 07740, Jena, Germany.
Danny HimselAbteilung Hämatologie und Internistische Onkologie, Klinik für Innere Medizin II, Universitätsklinikum Jena, Am Klinikum 1, 07740, Jena, Germany.
Jacqueline MaierAbteilung für Hämatologie und internistische Onkologie, Universität Leipzig, Leipzig, Germany.
Georg-Nikolaus FrankeAbteilung für Hämatologie und internistische Onkologie, Universität Leipzig, Leipzig, Germany.
Susanne SausseleIII. Medizinische Klinik, Universitätsmedizin Mannheim, Universität Heidelberg, Mannheim, Germany.
Christiane PottSecond Medical Department, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Hajnalka AndrikovicsNational Blood Service, Budapest, Hungary.
Nora MeggyesiNational Blood Service, Budapest, Hungary.
Katerina Machova-PolakovaDepartment of Molecular Genetics, Institute of Hematology and Blood Transfusion, Prague, Czech Republic.
Hana ZizkovaDepartment of Molecular Genetics, Institute of Hematology and Blood Transfusion, Prague, Czech Republic.
Tomáš JurcekDepartment of Internal Medicine, Hematology and Oncology, University Hospital Brno, Brno, Czech Republic.
Semir MesanovicPathology Department, University Clinical Center Tuzla, Tuzla, Bosnia and Herzegovina.
Renata ZadroUniversity Hospital Center Zagreb, University of Zagreb, Faculty of Pharmacy and Biochemistry, Zagreb, Croatia.
Enrico GottardiDivision of Internal Medicine and Hematology, University of Turin, Orbassano, Italy.
Jens HaenigNovartis Oncology, Global Medical Affairs, Basel, Switzerland.
Peter SchuldNovartis Oncology, Global Medical Affairs, Basel, Switzerland.
Nicholas C P CrossWessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury, UK.
Andreas HochhausAbteilung Hämatologie und Internistische Onkologie, Klinik für Innere Medizin II, Universitätsklinikum Jena, Am Klinikum 1, 07740, Jena, Germany.
Thomas ErnstAbteilung Hämatologie und Internistische Onkologie, Klinik für Innere Medizin II, Universitätsklinikum Jena, Am Klinikum 1, 07740, Jena, Germany. thomas.ernst@med.uni-jena.de.ORCID http://orcid.org/0000-0003-2147-489X
Klinikum Magdeburg · DEHungarian National Blood Transfusion Service · HUInstitute of Haematology and Blood Transfusion · CZLeipzig University · DENovartis (Switzerland) · CHHeidelberg University · DEMasaryk University · CZUniversity Clinical Center Tuzla · BAUniversity Hospital Centre Zagreb · HRUniversity Hospital Schleswig-Holstein · DEUniversity of Turin · ITWessex Regional Genetics Laboratory · GB

Funding

Novartis Oncology EUTOS 2016
6 · The paper itself

Abstract

purposeThe advent of tyrosine kinase inhibitor (TKI) therapies has revolutionized the treatment of chronic myeloid leukemia (CML). The European LeukemiaNet (ELN) recommends quantification of BCR-ABL1 transcripts by real-time quantitative PCR every 3 months during TKI treatment. Since a proportion of patients in deep molecular response (DMR: MR

methodsData were collected on the standardized assessment of molecular response in the context of real-life practice. BCR-ABL1 transcript levels after > 2 years of TKI therapy were evaluated for DMR by local laboratories as well as standardized EUTOS laboratories. Since standardized molecular monitoring is a prerequisite for treatment discontinuation, central surveillance of the performance of the participating laboratories was carried out.

resultsBetween 2014 and 2017, 3377 peripheral blood samples from 1117 CML patients were shipped to 11 standardized reference laboratories in six European countries. BCR-ABL1 transcript types were b3a2 (41.63%), b2a2 (29.99%), b2a2/b3a2 (3.58%) and atypical (0.54%). For 23.72% of the patients, the initial transcript type had not been reported. Response levels (EUTOS laboratory) were: no MMR, n = 197 (6.51%); MMR, n = 496 (16.40%); MR

conclusionsMulticenter DMR assessment is feasible in the context of real-life clinical practice in Europe. Information on the BCR-ABL1 transcript type at diagnosis is crucial to accurately monitor patients' molecular response during or after TKI therapy.

Indexed as

AdultAgedAged, 80 and overCohort StudiesEuropeHumansLaboratoriesLeukemia, Myelogenous, Chronic, BCR-ABL PositiveLeukemia, Myeloid, Chronic-PhaseMiddle AgedProtein Kinase InhibitorsRegistriesYoung AdultProtein Kinase InhibitorsBCR–ABLChronic myeloid leukemiaCMLDeep molecular remissionEurekaMolecular monitoringStandardizationTFRTreatment-free remission

Identifiers

PMID30941573
PMCPMC11810353
OpenAlexW2926466404

What OpenQuestion holds

Textmetadata
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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.