Evidence map›Paper›PMID 28522576›Full record

Trial reportHaematologica2017

Natural killer-cell counts are associated with molecular relapse-free survival after imatinib discontinuation in chronic myeloid leukemia: the IMMUNOSTIM study.

Delphine Rea, Guylaine Henry, Zena Khaznadar, Gabriel Etienne, François Guilhot, Franck Nicolini, Joelle Guilhot, Philippe Rousselot, Françoise Huguet, Laurence Legros and 11 more

Abstract readClinical Trial
In one paragraph

Trial report in Haematologica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed
–field-weighted citation impact
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

98 citing papers in PubMed.

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  10. Road to treatment-free remission in chronic myeloid leukemia.International journal of hematology · 2026
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38 more citing papers are in PubMed but not listed here.

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

21 authors.

Delphine ReaINSERM UMRS-1160, Paris, France delphine.rea@aphp.fr nicolas.dulphy@univ-paris-diderot.fr.
Guylaine HenryLaboratoire d'Immunologie et Histocompatibilité, Hôpital Saint-Louis, Paris, France.
Zena KhaznadarINSERM UMRS-1160, Paris, France.
Gabriel EtienneFrance Intergroupe des Leucémies Myéloïdes Chroniques (Fi-LMC), Institut Bergonié, Bordeaux, France.
François GuilhotFrance Intergroupe des Leucémies Myéloïdes Chroniques (Fi-LMC), Institut Bergonié, Bordeaux, France.
Franck NicoliniFrance Intergroupe des Leucémies Myéloïdes Chroniques (Fi-LMC), Institut Bergonié, Bordeaux, France.
Joelle GuilhotFrance Intergroupe des Leucémies Myéloïdes Chroniques (Fi-LMC), Institut Bergonié, Bordeaux, France.
Philippe RousselotFrance Intergroupe des Leucémies Myéloïdes Chroniques (Fi-LMC), Institut Bergonié, Bordeaux, France.
Françoise HuguetFrance Intergroupe des Leucémies Myéloïdes Chroniques (Fi-LMC), Institut Bergonié, Bordeaux, France.
Laurence LegrosFrance Intergroupe des Leucémies Myéloïdes Chroniques (Fi-LMC), Institut Bergonié, Bordeaux, France.
Martine GardembasFrance Intergroupe des Leucémies Myéloïdes Chroniques (Fi-LMC), Institut Bergonié, Bordeaux, France.
Viviane DubruilleFrance Intergroupe des Leucémies Myéloïdes Chroniques (Fi-LMC), Institut Bergonié, Bordeaux, France.
Agnès Guerci-BreslerFrance Intergroupe des Leucémies Myéloïdes Chroniques (Fi-LMC), Institut Bergonié, Bordeaux, France.
Aude CharbonnierFrance Intergroupe des Leucémies Myéloïdes Chroniques (Fi-LMC), Institut Bergonié, Bordeaux, France.
Frédéric MaloiselGroupe Oncologie-Maladies du Sang, Clinique Sainte Anne, Strasbourg, France.
Jean-Christophe IanottoService Hématologie Clinique, Hôpital Morvan, CHRU de Brest, France.
Bruno VillemagneService Médecine Onco-hématologie, CH de la Roche sur Yon, France.
François-Xavier MahonFrance Intergroupe des Leucémies Myéloïdes Chroniques (Fi-LMC), Institut Bergonié, Bordeaux, France.
Hélène Moins-TeisserencINSERM UMRS-1160, Paris, France.
Nicolas DulphyINSERM UMRS-1160, Paris, France delphine.rea@aphp.fr nicolas.dulphy@univ-paris-diderot.fr.
Antoine ToubertINSERM UMRS-1160, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite persistence of leukemic stem cells, patients with chronic myeloid leukemia who achieve and maintain deep molecular responses may successfully stop the tyrosine kinase inhibitor imatinib. However, questions remain unanswered regarding the biological basis of molecular relapse after imatinib cessation. In IMMUNOSTIM, we monitored 51 patients from the French Stop IMatinib trial for peripheral blood T cells and natural killer cells. Molecular relapse-free survival at 24 months was 45.1% (95% CI: 31.44%-58.75%). At the time of imatinib discontinuation, non-relapsing patients had significantly higher numbers of natural killer cells of the cytotoxic CD56

Indexed as

Cell CountDisease-Free SurvivalHumansImatinib MesylateInterferon-gammaKiller Cells, NaturalLeukemia, Myelogenous, Chronic, BCR-ABL PositiveProtein Kinase InhibitorsReceptors, Natural Killer CellRecurrenceImatinib MesylateInterferon-gammaProtein Kinase InhibitorsReceptors, Natural Killer Cell

Identifiers

PMID28522576
PMCPMC6643734

What OpenQuestion holds

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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.