Evidence map›Paper›PMID 28539671›Full record

ArticleLeukemia2017

Age-related clinical and biological features of PTEN abnormalities in T-cell acute lymphoblastic leukaemia.

M Tesio, A Trinquand, P Ballerini, G Hypolite, L Lhermitte, A Petit, N Ifrah, A Baruchel, H Dombret, E Macintyre and 1 more

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07281716 (A Phase 1b/2 Study of Combination Immunotherapy for the Treatment of Chemotherapy-refractory Metastatic Microsatellite Stable), which is not on this map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.7field-weighted citation impact, top 7% 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.

NCT07281716 phase1 / phase2recruitingnot on this mapstarted 2025, after this paper: background citation

A Phase 1b/2 Study of Combination Immunotherapy for the Treatment of Chemotherapy-refractory Metastatic Microsatellite Stable (MSS) Colorectal Cancer (CRC)

TypeinterventionalSponsorDan FengRan2025 to 2028Enrolled24ConditionsMetastatic Microsatellite Stable Colorectal CarcinomaArmsNadunolimab, Toripalimab
3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 35 citations in OpenAlex.

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  9. Clinico-Hematological Profile and Copy Number Abnormalities in a Cohort ofIndian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2021
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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

11 authors at 5 institutions in 1 country.

M TesioInstitut Necker-Enfants Malades (INEM), Institut national de recherche médicale (INSERM) U1151, Hôpital Necker-Enfants Malades, Paris, France.
A TrinquandInstitut Necker-Enfants Malades (INEM), Institut national de recherche médicale (INSERM) U1151, Hôpital Necker-Enfants Malades, Paris, France.
P BalleriniINSERM, U967, Fontenay-aux-Roses, France.
G HypoliteInstitut Necker-Enfants Malades (INEM), Institut national de recherche médicale (INSERM) U1151, Hôpital Necker-Enfants Malades, Paris, France.
L LhermitteInstitut Necker-Enfants Malades (INEM), Institut national de recherche médicale (INSERM) U1151, Hôpital Necker-Enfants Malades, Paris, France.
A PetitService d'hématologie pédiatrique, AP-HP, Hôpital Trousseau, Paris, France.ORCID 0000-0001-8363-1622
N IfrahPôle de Recherche et d'Enseignement Supérieur L'Université Nantes Angers Le Mans, Centre Hospitalier Universitaire Angers Service des Maladies du Sang et L'Institut National de la Santé et de la Recherche Médicale (INSERM) U892, Angers, France.
A BaruchelService d'hématologie pédiatrique, AP-HP, Hôpital Robert Debré, Paris, France.
H DombretUniversité Paris 7, Hôpital Saint-Louis, AP-HP, and Institut Universitaire d'Hématologie, Paris, France.
E MacintyreInstitut Necker-Enfants Malades (INEM), Institut national de recherche médicale (INSERM) U1151, Hôpital Necker-Enfants Malades, Paris, France.
V AsnafiInstitut Necker-Enfants Malades (INEM), Institut national de recherche médicale (INSERM) U1151, Hôpital Necker-Enfants Malades, Paris, France.
Hôpital Necker-Enfants Malades · FRInserm · FRAssistance Publique – Hôpitaux de Paris · FRSorbonne Université · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumour suppressor gene PTEN is commonly altered in T-cell acute lymphoblastic leukaemia but its prognostic impact is still debated. We screened a cohort of 573 fully characterised adult and paediatric T-cell acute lymphoblastic leukaemia (T-ALL) patients for genomic PTEN abnormalities. PTEN-inactivating mutations and/or deletions were identified in 91 cases (16%), including 18% of paediatric (49/277) and 14% of adult cases (42/296). Thirty-four patients harboured only mutations, 12 cases demonstrated only large deletions and 9 only microdeletions. About 36 patients had combined alterations. Different mechanisms of PTEN inactivation predicted differences in the clinical outcome for both adult and paediatric patients treated according to the GRAALL03/05 and FRALLE2000 protocols. Whereas large deletions predicted lower 5-year overall survival (P=0.0053 in adults, P=0.001 in children) and disease-free survival (P=0.0009 in adults, P=0.0002 in children), mutations were not associated with a worse prognosis. The prognostic impact of PTEN loss is therefore linked to the underlying type of genomic abnormality, both in adult and paediatric T-ALLs, demonstrating that detailed analysis of the type of abnormality type would be useful to refine risk stratification.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseGenetic VariationAdolescentAdultAge FactorsAllelesBiomarkers, TumorChildChild, PreschoolComparative Genomic HybridizationExonsFemaleHigh-Throughput Nucleotide SequencingHumansImmunophenotypingBiomarkers, TumorOncogene Proteins, FusionPTEN PhosphohydrolasePTEN protein, humanSIL-TAL1 fusion protein, human

Identifiers

PMID28539671
OpenAlexW2619060565

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.