Evidence map›Paper›PMID 25786252›Full record

ArticlePloS one2015

Insulin growth factor 1 receptor expression is associated with NOTCH1 mutation, trisomy 12 and aggressive clinical course in chronic lymphocytic leukaemia.

Francesco Maura, Laura Mosca, Sonia Fabris, Giovanna Cutrona, Serena Matis, Marta Lionetti, Luca Agnelli, Marzia Barbieri, Marianna D'Anca, Martina Manzoni and 13 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00917540 (Prospective Collection of Biological Data of Prognostic Relevance in Patients), which is not on this map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 21% 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.

NCT00917540 unknown statusnot on this map

Prospective Collection of Biological Data of Prognostic Relevance in Patients

TypeobservationalSponsorGruppo Italiano Studio LinfomiRan2007 to 2013Enrolled495ConditionsChronic Lymphocytic Leukemia Stage A(0), Chronic Lymphocytic Leukemia Stage A(I), Chronic Lymphocytic Leukemia Stage A(II)
3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 18 citations in OpenAlex.

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  9. Common nonmutationalProceedings of the National Academy of Sciences of the United States of America · 2017
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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

23 authors at 8 institutions in 1 country.

Francesco MauraDepartment of Clinical Sciences and Community Health, University of Milano and Hematology 1 CTMO, Foundation IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milano, Italy.
Laura MoscaDepartment of Clinical Sciences and Community Health, University of Milano and Hematology 1 CTMO, Foundation IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milano, Italy.
Sonia FabrisDepartment of Clinical Sciences and Community Health, University of Milano and Hematology 1 CTMO, Foundation IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milano, Italy.
Giovanna CutronaSS Molecular Diagnostics, IRCCS S. Martino-IST, Genova, Italy.
Serena MatisScientific Direction IRCCS S. Martino-IST, Genova, Italy.
Marta LionettiDepartment of Clinical Sciences and Community Health, University of Milano and Hematology 1 CTMO, Foundation IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milano, Italy.
Luca AgnelliDepartment of Clinical Sciences and Community Health, University of Milano and Hematology 1 CTMO, Foundation IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milano, Italy.
Marzia BarbieriDepartment of Clinical Sciences and Community Health, University of Milano and Hematology 1 CTMO, Foundation IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milano, Italy.
Marianna D'AncaDepartment of Clinical Sciences and Community Health, University of Milano and Hematology 1 CTMO, Foundation IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milano, Italy.
Martina ManzoniDepartment of Clinical Sciences and Community Health, University of Milano and Hematology 1 CTMO, Foundation IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milano, Italy.
Monica ColomboScientific Direction IRCCS S. Martino-IST, Genova, Italy.
Carlotta MassuccoScientific Direction IRCCS S. Martino-IST, Genova, Italy.
Daniele ReverberiDepartment of Pathology IRCCS S. Martino-IST, Genova, Italy.
Massimo GentileU.O.C. di Ematologia, Azienda Ospedaliera di Cosenza, Cosenza, Italy.
Anna Grazia RecchiaU.O.C. di Ematologia, Azienda Ospedaliera di Cosenza, Cosenza, Italy.
Sabrina BossioU.O.C. di Ematologia, Azienda Ospedaliera di Cosenza, Cosenza, Italy.
Fiorella IlariucciDivision of Hematology, A.O. Arcispedale Santa Maria Nuova-IRCCS, Reggio Emilia, Italy.
Caterina MusolinoDivision of Haematology, University of Messina, Messina, Italy.
Francesco Di RaimondoDepartment of Biomedical Sciences, Division of Hematology, University of Catania and Ferrarotto Hospital, Catania, Italy.
Agostino CortelezziDepartment of Clinical Sciences and Community Health, University of Milano and Hematology 1 CTMO, Foundation IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milano, Italy.
Fortunato MorabitoDepartment of Pathology IRCCS S. Martino-IST, Genova, Italy.
Manlio FerrariniScientific Direction IRCCS S. Martino-IST, Genova, Italy.
Antonino NeriDepartment of Clinical Sciences and Community Health, University of Milano and Hematology 1 CTMO, Foundation IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milano, Italy.
Ospedale Policlinico San Martino · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITAzienda Ospedaliera di Cosenza · ITOspedale Maggiore · ITUniversity of Milan · ITOspedale Santa Maria · ITUniversity of Catania · ITUniversity of Messina · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IGF1R is emerging as an important gene in the pathogenesis of many solid and haematological cancers and its over-expression has been reported as frequently associated with aggressive disease and chemotherapy resistance. In this study we performed an investigation of the role of IGF1R expression in a large and representative prospective series of 217 chronic lymphocytic leukaemia (CLL) patients enrolled in the multicentre O-CLL1 protocol (clinicaltrial.gov #NCT00917540). High IGF1R gene expression was significantly associated with IGHV unmutated (IGHV-UM) status (p<0.0001), high CD38 expression (p<0.0001), trisomy 12 (p<0.0001), and del(11)(q23) (p=0.014). Interestingly, higher IGF1R expression (p=0.002) characterized patients with NOTCH1 mutation (c.7541_7542delCT), identified in 15.5% of cases of our series by next generation sequencing and ARMS-PCR. Furthermore, IGF1R expression has been proven as an independent prognostic factor associated with time to first treatment in our CLL prospective cohort. These data suggest that IGF1R may play an important role in CLL biology, in particular in aggressive CLL clones characterized by IGHV-UM, trisomy 12 and NOTCH1 mutation.

Indexed as

Gene Expression Regulation, NeoplasticMutationChromosomes, Human, Pair 12Clinical Trials as TopicHumansLeukemia, Lymphocytic, Chronic, B-CellNeoplasm StagingPrognosisReceptor, IGF Type 1Receptor, Notch1Receptors, SomatomedinRNA, MessengerTrisomyIGF1R protein, humanReceptor, IGF Type 1Receptor, Notch1Receptors, SomatomedinRNA, Messenger

Identifiers

PMID25786252
PMCPMC4365018
OpenAlexW2059544514

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.