Evidence map›Paper›PMID 27056923›Full record

Trial reportHaematologica2016

Are somatic mutations predictive of response to erythropoiesis stimulating agents in lower risk myelodysplastic syndromes?

Olivier Kosmider, Marie Passet, Valeria Santini, Uwe Platzbecker, Valérie Andrieu, Gina Zini, Odile Beyne-Rauzy, Agnès Guerci, Erico Masala, Enrico Balleari and 6 more

Open access · goldAbstract readClinical TrialLetterMulticenter Study
In one paragraph

Trial report in Haematologica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

15 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
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  14. Article
  15. Treatment of low-risk myelodysplastic syndromes.Hematology. American Society of Hematology. Education Program · 2016
    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

16 authors at 12 institutions in 3 countries.

Olivier KosmiderHématologie Biologique, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris (AP-HP), France.
Marie PassetHématologie Biologique, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris (AP-HP), France.
Valeria SantiniUniversity of Florence, AOU Careggi, Hematology, Italy.
Uwe PlatzbeckerUniversity Hospital Carl Gustav Carus Dresden, Germany.
Valérie AndrieuHématologie Biologique, Hôpital Bichat, Assistance Publique-Hôpitaux de Paris (AP-HP), France.
Gina ZiniUniversità Cattolica Sacro Cuore, Roma, Italy.
Odile Beyne-RauzyIUCT, Oncopole, Toulouse, France.
Agnès GuerciHôpital de Brabois, Nancy, France.
Erico MasalaUniversita degli Studi di Firenze, Italy.
Enrico BalleariIRCCS AOU San Martino-IST di Genova, Italy.
Ekaterina BulychevaUniversity Hospital Carl Gustav Carus Dresden, Germany.
François DreyfusHôpital Cochin, Service d'hématologie, Paris, France.
Pierre FenauxHôpital Saint Louis, Service d'hématologie séniors, Paris, France.
Michaela FontenayHématologie Biologique, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris (AP-HP), France.
Sophie ParkCHU de Grenoble Alpes, Université Grenoble Alpes, Clinique Universitaire d'hématologie, Grenoble, France spark@chu-grenoble.fr.
GFM, FISM AND D-MDS
Assistance Publique – Hôpitaux de Paris · FRUniversity Hospital Carl Gustav Carus · DEAzienda Ospedaliero-Universitaria Careggi · ITCentre Hospitalier Régional et Universitaire de Nancy · FRHôpital Bichat-Claude-Bernard · FRHôpital Cochin · FRHôpital Saint-Louis · FRInstitut universitaire du cancer de Toulouse Oncopole · FROspedale Policlinico San Martino · ITUniversità Cattolica del Sacro Cuore · ITUniversité Grenoble Alpes · FRUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

MutationMyelodysplastic SyndromesDisease-Free SurvivalFemaleHematinicsHumansMaleRisk FactorsSurvival RateHematinicscytogenetics and molecular geneticsmyelodysplastic syndromesred cells

Identifiers

PMID27056923
PMCPMC5004472
OpenAlexW2320702474

What OpenQuestion holds

Textmetadata
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.