Evidence map›Paper›PMID 26859076›Full record

Trial reportLeukemia2016

Secondary malignancies in chronic myeloid leukemia patients after imatinib-based treatment: long-term observation in CML Study IV.

M B Miranda, M Lauseker, M-P Kraus, U Proetel, B Hanfstein, A Fabarius, G M Baerlocher, D Heim, D K Hossfeld, H-J Kolb and 19 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Leukemia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
8.6field-weighted citation impact, top 2% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 87 citations in OpenAlex.

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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

29 authors at 18 institutions in 2 countries.

M B MirandaIII. Medizinische Klinik, Universitätsmedizin, Medizinische Fakultät Mannheim der Universität Heidelberg, Mannheim, Germany.
M LausekerInstitut für Medizinische Informationsverarbeitung, Biometrie und Epidemiologie, Ludwig-Maximilians-Universität, München, Germany.
M-P KrausIII. Medizinische Klinik, Universitätsmedizin, Medizinische Fakultät Mannheim der Universität Heidelberg, Mannheim, Germany.
U ProetelIII. Medizinische Klinik, Universitätsmedizin, Medizinische Fakultät Mannheim der Universität Heidelberg, Mannheim, Germany.
B HanfsteinIII. Medizinische Klinik, Universitätsmedizin, Medizinische Fakultät Mannheim der Universität Heidelberg, Mannheim, Germany.
A FabariusIII. Medizinische Klinik, Universitätsmedizin, Medizinische Fakultät Mannheim der Universität Heidelberg, Mannheim, Germany.
G M BaerlocherUniversitätsklinik für Hämatologie und Hämatologisches Zentrallabor, Inselspital, Bern, Switzerland.
D HeimKlinik für Hämatologie, Universitätsspital, Basel, Switzerland.
D K HossfeldII. Medizinische Klinik, Universitätsklinikum Eppendorf, Hamburg, Germany.
H-J KolbMedizinische Klinik und Poliklinik III, Klinikum der Ludwig-Maximilians-Universität, München, Germany.
S W KrauseMedizinische Klinik 5, Universitätsklinikum, Erlangen, Germany.
C NerlKlinik für Hämatologie, Onkologie, Immunologie, Palliativmedizin, Infektiologie und Tropenmedizin, Klinikum Schwabing, München, Germany.
T H BrümmendorfMedizinische Klinik IV, Uniklinik RWTH, Aachen Germany.
W VerbeekZentrum für ambulante Hämatologie und Onkologie, Bonn, Germany.
A A FauserKlinik für Knochenmarktransplantation und Hämatologie/Onkologie, Klinikum, Idar-Oberstein, Germany.
O PrümmerKlinik für Hämatologie, Onkologie und Palliativmedizin, Klinikum, Kempten, Germany.
K NebenMedizinische Klinik 2, Klinikum Mittelbaden, Standort Balg, Baden-Baden, Germany.
U HessKlinik für Onkologie/Hämatologie, Kantonsspital, St Gallen, Switzerland.
R MahlbergInnere Medizin 1, Klinikum Mutterhaus der Borromäerinnen, Trier, Germany.
C PlögerMannheimer Onkologie Praxis, Mannheim, Germany.
M FlasshoveMedizinische Klinik III, Krankenhaus, Düren, Germany.
B RendenbachPraxis für Innere Medizin, Nephrologie, Hämatologie und Onkologie, Trier, Germany.
W-K HofmannIII. Medizinische Klinik, Universitätsmedizin, Medizinische Fakultät Mannheim der Universität Heidelberg, Mannheim, Germany.
M C MüllerIII. Medizinische Klinik, Universitätsmedizin, Medizinische Fakultät Mannheim der Universität Heidelberg, Mannheim, Germany.
M PfirrmannInstitut für Medizinische Informationsverarbeitung, Biometrie und Epidemiologie, Ludwig-Maximilians-Universität, München, Germany.
A HochhausKlinik für Innere Medizin II, Universitätsklinikum, Jena, Germany.
J HasfordInstitut für Medizinische Informationsverarbeitung, Biometrie und Epidemiologie, Ludwig-Maximilians-Universität, München, Germany.
R HehlmannIII. Medizinische Klinik, Universitätsmedizin, Medizinische Fakultät Mannheim der Universität Heidelberg, Mannheim, Germany.
S SaußeleIII. Medizinische Klinik, Universitätsmedizin, Medizinische Fakultät Mannheim der Universität Heidelberg, Mannheim, Germany.
Medizinische Fakultät MannheimHeidelberg University · DEPraxis für Hämatologie und Onkologie · DEZimmer Biomet (Germany) · DEJena University Hospital · DEKantonsspital St. Gallen · CHKempten University of Applied Sciences · DEKlinikum Mittelbaden · DEKlinikum Mutterhaus der Borromäerinnen · DEKrankenhaus Düren · DELMU Klinikum · DELudwig-Maximilians-Universität München · DEMünchen Klinik · DEUniversitätsklinikum Aachen · DEUniversitätsklinikum Erlangen · DEUniversity Hospital of Basel · CHUniversity Hospital of Bern · CHUniversity Medical Center Hamburg-Eppendorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment of chronic myeloid leukemia (CML) has been profoundly improved by the introduction of tyrosine kinase inhibitors (TKIs). Long-term survival with imatinib is excellent with a 8-year survival rate of ∼88%. Long-term toxicity of TKI treatment, especially carcinogenicity, has become a concern. We analyzed data of the CML study IV for the development of secondary malignancies. In total, 67 secondary malignancies were found in 64 of 1525 CML patients in chronic phase treated with TKI (n=61) and interferon-α only (n=3). The most common malignancies (n⩾4) were prostate, colorectal and lung cancer, non-Hodgkin's lymphoma (NHL), malignant melanoma, non-melanoma skin tumors and breast cancer. The standardized incidence ratio (SIR) for all malignancies excluding non-melanoma skin tumors was 0.88 (95% confidence interval (0.63-1.20)) for men and 1.06 (95% CI 0.69-1.55) for women. SIRs were between 0.49 (95% CI 0.13-1.34) for colorectal cancer in men and 4.29 (95% CI 1.09-11.66) for NHL in women. The SIR for NHL was significantly increased for men and women. An increase in the incidence of secondary malignancies could not be ascertained. The increased SIR for NHL has to be considered and long-term follow-up of CML patients is warranted, as the rate of secondary malignancies may increase over time.

Indexed as

Imatinib MesylateLeukemia, Myelogenous, Chronic, BCR-ABL PositiveNeoplasms, Second PrimaryProtein Kinase InhibitorsAdultAgedAged, 80 and overColorectal NeoplasmsFemaleFollow-Up StudiesHumansIncidenceInterferon-alphaLymphoma, Non-HodgkinMaleMiddle AgedImatinib MesylateInterferon-alphaProtein Kinase Inhibitors

Identifiers

PMID26859076
PMCPMC4895174
OpenAlexW2261255074

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.