Evidence map›Paper›PMID 28514758›Full record

ArticleOncotarget2017

BCL2L10 positive cells in bone marrow are an independent prognostic factor of azacitidine outcome in myelodysplastic syndrome and acute myeloid leukemia.

Valérie Vidal, Guillaume Robert, Laure Goursaud, Laetitia Durand, Clemence Ginet, Jean Michel Karsenti, Frederic Luciano, Lauris Gastaud, Georges Garnier, Thorsten Braun and 11 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. 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

21 authors at 10 institutions in 2 countries.

Valérie VidalINSERM U1131, Institut Universitaire d'hématologie, Paris, France.
Guillaume RobertINSERM U1065, Centre Méditerranéen de Médecine Moléculaire, Nice, France.
Laure GoursaudINSERM U1131, Institut Universitaire d'hématologie, Paris, France.
Laetitia DurandINSERM U1131, Institut Universitaire d'hématologie, Paris, France.
Clemence GinetINSERM U1065, Centre Méditerranéen de Médecine Moléculaire, Nice, France.
Jean Michel KarsentiCote d'azur University, Nice Sophia Antipolis University, CHU of Nice, Nice, France.
Frederic LucianoINSERM U1065, Centre Méditerranéen de Médecine Moléculaire, Nice, France.
Lauris GastaudCentre Antoine Lacassagne, Service d'oncologie, Nice, France.
Georges GarnierCH Princesse Grace, Service de Médecine Interne, Monaco, Monaco.
Thorsten BraunHôpital Avicenne, Paris 13 University, APHP, Bobigny, France.
Pierre HirschHôpital Saint Antoine, Service d'Hématologie Clinique et de Thérapie Cellulaire, Paris, France.
Emmanuel RaffouxHôpital Saint Louis, Paris 7 University, Service d'Hématologie Adulte, APHP, Paris, France.
Anne Marie NlogaHôpital Saint Louis, Paris 7 University, Service d'Hématologie Sénior, APHP, Paris, France.
Rose Ann PaduaINSERM U1131, Institut Universitaire d'hématologie, Paris, France.
Hervé DombretHôpital Saint Louis, Paris 7 University, Service d'Hématologie Adulte, APHP, Paris, France.
Pierre RohrlichCote d'azur University, Nice Sophia Antipolis University, CHU of Nice, Nice, France.
Lionel AdesINSERM U1131, Institut Universitaire d'hématologie, Paris, France.
Christine ChomienneINSERM U1131, Institut Universitaire d'hématologie, Paris, France.
Patrick AubergerINSERM U1065, Centre Méditerranéen de Médecine Moléculaire, Nice, France.
Pierre FenauxINSERM U1131, Institut Universitaire d'hématologie, Paris, France.
Thomas CluzeauINSERM U1131, Institut Universitaire d'hématologie, Paris, France.
Inserm · FRInstitut Universitaire de France · FRCentre Méditerranéen de Médecine Moléculaire · FRUniversité Côte d'Azur · FRUniversité Paris Cité · FRCentre Antoine Lacassagne · FRHôpital Avicenne · FRHôpital Saint-Louis · FRPrincess Grace Hospital Centre · MCSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Azacitidine (AZA), the reference treatment for most higher-risk myelodysplastic (MDS) patients can also improve overall survival (OS) in elderly acute myeloid leukemia (AML) patients ineligible for intensive chemotherapy, but reliable biological markers predicting response and OS in patients treated with AZA are lacking. In a preliminary study, we found that an increase of the percentage of BCL2L10, an anti-apoptotic member of the bcl-2 family, was correlated with AZA resistance. In this study, we assessed prospectively by flow cytometry the prognostic value of BCL2L10 positive bone marrow mononuclear cells in 70 patients (42 MDS and 28 AML), prior to AZA treatment.In patients with baseline marrow blasts below 30%, the baseline percentage of bone marrow BCL2L10 positive cells inversely correlated with response to AZA and OS independently of the International Prognostic Scoring System (IPSS) and IPSS-revised (IPSS-R). Specifically, OS was significantly lower in patients with more than 10% BCL2L10 positive cells (median 8.3 vs 22.9 months in patients with less than 10% positivity, p = 0,001). In summary, marrow BCL2L10 positive cells may be a biomarker for azacitidine response and OS, with a potential impact in clinical practice.

Indexed as

AdultAgedAged, 80 and overAntimetabolites, AntineoplasticAzacitidineBiomarkersBone Marrow CellsFemaleGene ExpressionHumansLeukemia, Myeloid, AcuteMaleMiddle AgedMyelodysplastic SyndromesNeoplasm StagingPrognosisAntimetabolites, AntineoplasticAzacitidineBCL2-like 10 proteinBiomarkersProto-Oncogene Proteins c-bcl-2AMLBCL2L10IPSSIPSS-RMDS

Identifiers

PMID28514758
PMCPMC5564547
OpenAlexW2609607471

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.