Evidence map›Paper›PMID 30523055›Full record

Trial reportHaematologica2019

Impact of induction regimen and allogeneic hematopoietic cell transplantation on outcome in younger adults with acute myeloid leukemia with a monosomal karyotype.

Frédéric Baron, Marian Stevens-Kroef, Michal Kicinski, Giovanna Meloni, Petra Muus, Jean-Pierre Marie, Constantijn J M Halkes, Xavier Thomas, Radovan Vrhovac, Francesco Albano and 10 more

2 registry-linked trialsOpen access · goldAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Haematologica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 14% 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.

NCT00002549 phase3unknown statusnot on this map

Randomized phase iii study of induction (ice vs mice vs dce) and intensive consolidation (idia vs novia vs dia) followed by bone marrow transplantation in acute myelogenous leukemia: aml 10 protocol

TypeinterventionalSponsorEuropean Organisation for Research and Treatment of Cancer - EORTCRan1993Enrolled1,520ConditionsLeukemiaArmsfilgrastim, busulfan, cyclophosphamide, cytarabine, daunorubicin hydrochloride
NCT00004128 phase3unknown statusnot on this map

The Value of High Dose Versus Standard Dose ARA-C During Induction and of IL-2 After Intensive Consolidation/Autologous Stem Cell Transplantation in Patients (Age 15-60 Years) With Acute Myelogenous Leukemia. A Randomized Phase II Trial of the EORTC and the GIMEMA-ALWP

TypeinterventionalSponsorEuropean Organisation for Research and Treatment of Cancer - EORTCRan1999Enrolled2,000ConditionsLeukemiaArmsaldesleukin, filgrastim, busulfan, cyclophosphamide, cytarabine
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 13 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

20 authors at 14 institutions in 6 countries.

Frédéric BaronGroupe Interdisciplinaire de Génoprotéomique Appliquée (GIGA), Laboratory of Hematology, University of Liege, Belgium f.baron@ulg.ac.be.
Marian Stevens-KroefRadboud University Medical Center, Nijmegen, the Netherlands.
Michal KicinskiEORTC Headquarters, Brussels, Belgium.
Giovanna MeloniDepartment of Hematology, Sapienza University, Rome, Italy.
Petra MuusRadboud University Medical Center, Nijmegen, the Netherlands.
Jean-Pierre MarieDepartment of Hematology, Saint Antoine Hospital, Paris, France.
Constantijn J M HalkesLeiden University Medical Center, the Netherlands.
Xavier ThomasCHU Lyon, France.
Radovan VrhovacUniversity Hospital Center Zagreb, Croatia.
Francesco AlbanoUniversity of Bari, Italy.
François LefrèreNecker Hospital, Paris, France.
Simona SicaUniversità Cattolica Sacro Cuore, Roma, Italy.
Marco ManciniDepartment of Hematology, Sapienza University, Rome, Italy.
Adriano VendittiUniversity Tor Vergata, Roma, Italy.
Anne HagemeijerUniversity of Leuven, Belgium.
Joop H JansenRadboud University Medical Center, Nijmegen, the Netherlands.
Sergio AmadoriUniversity Tor Vergata, Roma, Italy.
Theo de WitteRadboud University Medical Center, Nijmegen, the Netherlands.
Roelof WillemzeLeiden University Medical Center, the Netherlands.
Stefan SuciuEORTC Headquarters, Brussels, Belgium.
European Organisation for Research and Treatment of Cancer · BELeiden University Medical Center · NLRadboud University Nijmegen · NLSapienza University of Rome · ITUniversity of Rome Tor Vergata · ITHôpital Necker-Enfants Malades · FRKing's College Hospital · GBKU Leuven · BERadboud University Medical Center · NLSorbonne Université · FRUniversità Cattolica del Sacro Cuore · ITUniversity Hospital Centre Zagreb · HRUniversity of Bari Aldo Moro · ITUniversity of Liège · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monosomal karyotype confers a poor prognosis in patients with acute myeloid leukemia. Here, we determined the impact of the type of remission-induction chemotherapy and the impact of having a donor in younger acute myeloid leukemia patients with a monosomal karyotype included in two phase III trials. In the first trial patients were randomized to receive either daunorubicin, mitoxantrone, or idarubicin in addition to standard-dose cytarabine and etoposide for induction chemotherapy. In the second trial patients were randomized to standard-dose cytarabine or high-dose cytarabine induction, both with daunorubicin and etoposide. In both trials, patients who achieved a complete remission with or without complete hematologic recovery underwent allogeneic hematopoietic stem cell transplantation if they had a donor; otherwise, they underwent autologous transplantation. In comparison to patients with intermediate-risk cytogenetics without a monosomal karyotype (n=1,584) and with adverse cytogenetics without a monosomal karyotype (n=218), patients with a monosomal karyotype (n=188) were more likely not to achieve a complete remission with or without count recovery [odds ratio=2.85, 95% confidence interval (95%, CI): 2.10-3.88] and had shorter overall survival [hazard ratio, (HR)=2.44, 95% CI: 2.08-2.88]. There was no impact of the type of anthracycline or of the dose of cytarabine on outcomes in patients with a monosomal karyotype. Among monosomal karyo type patients who achieved a complete remission with or without count recovery, HLA-identical related donor availability was associated with longer survival from complete remission with or without count recovery (HR=0.59, 95% CI: 0.37-0.95). ClinicalTrials.gov identifiers: AML-10: NCT00002549; AML-12: NCT00004128.

Indexed as

Abnormal KaryotypeHematopoietic Stem Cell TransplantationAdolescentAdultAge FactorsAntineoplastic Combined Chemotherapy ProtocolsCombined Modality TherapyFemaleHumansInduction ChemotherapyLeukemia, Myeloid, AcuteMaleMiddle AgedMonosomyOdds RatioPrognosis

Identifiers

PMID30523055
PMCPMC6545848
OpenAlexW2905226966

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.