Evidence map›Paper›PMID 27821812›Full record

ArticleOncotarget2016

Karyotypic complexity rather than chromosome 8 abnormalities aggravates the outcome of chronic lymphocytic leukemia patients with TP53 aberrations.

Gonzalo Blanco, Anna Puiggros, Panagiotis Baliakas, Anastasia Athanasiadou, MªDolores García-Malo, Rosa Collado, Aliki Xochelli, María Rodríguez-Rivera, Margarita Ortega, Mª José Calasanz and 20 more

Open access · diamondAbstract readMulticenter Study
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Chromoanagenesis Detection in Chronic Lymphocytic Leukemia.Methods in molecular biology (Clifton, N.J.) · 2025
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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

30 authors at 17 institutions in 3 countries.

Gonzalo BlancoLaboratori de Citogenètica Molecular, Laboratori de Citologia Hematològica, Servei de Patologia, Hospital del Mar, Barcelona, Spain.
Anna PuiggrosLaboratori de Citogenètica Molecular, Laboratori de Citologia Hematològica, Servei de Patologia, Hospital del Mar, Barcelona, Spain.
Panagiotis BaliakasDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Anastasia AthanasiadouHematology Department and HCT Unit, G. Papanicolaou Hospital, Thessaloniki, Greece.
MªDolores García-MaloServicio de Hematología, Hospital Universitario Morales Meseguer, Murcia, Spain.
Rosa ColladoServicio de Hematología, Consorcio Hospital General Universitario, Valencia, Spain.
Aliki XochelliDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
María Rodríguez-RiveraLaboratori de Citogenètica Molecular, Laboratori de Citologia Hematològica, Servei de Patologia, Hospital del Mar, Barcelona, Spain.
Margarita OrtegaLaboratorio de Citogenética y Servicio de Hematología, Hospital Vall d'Hebron, Barcelona, Spain.
Mª José CalasanzServicio de Citogenética, Departamento de Genética, Universidad de Navarra, Pamplona, Spain.
Elisa LuñoServicio de Hematología, Hospital Universitario Central de Asturias, Oviedo, Spain.
MªTeresa VargasUGC de Hematología, Hospital Universitario Virgen del Rocío, Instituto de Biomedicina de Sevilla (IBIS), Sevilla, Spain.
Javier GrauServei d'Hematologia, ICO-Hospital Germans Trias i Pujol, Institut de Recerca Contra la Leucèmia Josep Carreras (IJC), Universitat Autònoma de Barcelona, Badalona, Spain.
Carolina Martínez-LapercheLaboratorio de Genética Hematológica, Servicio de Hematología, Hospital G.U. Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, Madrid, Spain.
Alberto ValienteServicios de Genética y Hematología, Complejo Hospitalario de Navarra, Pamplona, Spain.
José CerveraUnidad de Genética, Hospital Universitario La Fe, Valencia, Spain.
Achilles AnagnostopoulosHematology Department and HCT Unit, G. Papanicolaou Hospital, Thessaloniki, Greece.
Eva GimenoServei d'Hematologia, Hospital del Mar, Barcelona, Spain.
Eugènia AbellaServei d'Hematologia, Hospital del Mar, Barcelona, Spain.
Evangelia StalikaInstitute of Applied Biosciences, CERTH, Thessaloniki, Greece.
Jesús Mª Hernández-RivasServicio de Hematología, Hospital Universitario de Salamanca, IBSAL, IBMCC, Centro de Investigación del Cáncer, Universidad de Salamanca, CSIC, Salamanca, Spain.
Francisco José OrtuñoServicio de Hematología, Hospital Universitario Morales Meseguer, Murcia, Spain.
Diego RoblesServicio de Hematología, Hospital Txagorritxu, Vitoria, Spain.
Ana FerrerLaboratori de Citogenètica Molecular, Laboratori de Citologia Hematològica, Servei de Patologia, Hospital del Mar, Barcelona, Spain.
David IvarsServicio de Hematología, Consorcio Hospital General Universitario, Valencia, Spain.
Marcos GonzálezServicio de Hematología, Hospital Universitario de Salamanca, IBSAL, IBMCC, Centro de Investigación del Cáncer, Universidad de Salamanca, CSIC, Salamanca, Spain.
Francesc BoschLaboratorio de Citogenética y Servicio de Hematología, Hospital Vall d'Hebron, Barcelona, Spain.
Pau AbrisquetaLaboratorio de Citogenética y Servicio de Hematología, Hospital Vall d'Hebron, Barcelona, Spain.
Kostas StamatopoulosDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Blanca EspinetLaboratori de Citogenètica Molecular, Laboratori de Citologia Hematològica, Servei de Patologia, Hospital del Mar, Barcelona, Spain.
Hospital Del Mar · ESMunicipal Institute for Medical Research · ESUppsala University · SEVall d'Hebron Hospital Universitari · ESCentro de Investigación del Cáncer · ESG. Papanikolaou General Hospital · GRHospital General Universitario De Valencia · ESHospital General Universitario Morales Meseguer · ESCentre for Research and Technology Hellas · GRComplejo Hospitalario de Navarra · ESHospital General Universitario Gregorio Marañón · ESHospital Txagorritxu · ESHospital Universitari i Politècnic La Fe · ESHospital Universitario Central de Asturias · ESInstituto de Biomedicina de Sevilla · ESUniversidad de Navarra · ESUniversitat Autònoma de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with chronic lymphocytic leukemia (CLL) harboring TP53 aberrations (TP53abs; chromosome 17p deletion and/or TP53 mutation) exhibit an unfavorable clinical outcome. Chromosome 8 abnormalities, namely losses of 8p (8p-) and gains of 8q (8q+) have been suggested to aggravate the outcome of patients with TP53abs. However, the reported series were small, thus hindering definitive conclusions. To gain insight into this issue, we assessed a series of 101 CLL patients harboring TP53 disruption. The frequency of 8p- and 8q+ was 14.7% and 17.8% respectively. Both were associated with a significantly (P < 0.05) higher incidence of a complex karyotype (CK, ≥3 abnormalities) detected by chromosome banding analysis (CBA) compared to cases with normal 8p (N-8p) and 8q (N-8q), respectively. In univariate analysis for 10-year overall survival (OS), 8p- (P = 0.002), 8q+ (P = 0.012) and CK (P = 0.009) were associated with shorter OS. However, in multivariate analysis only CK (HR = 2.47, P = 0.027) maintained independent significance, being associated with a dismal outcome regardless of chromosome 8 abnormalities. In conclusion, our results highlight the association of chromosome 8 abnormalities with CK amongst CLL patients with TP53abs, while also revealing that CK can further aggravate the prognosis of this aggressive subgroup.

Indexed as

Chromosome DeletionChromosomes, Human, Pair 8KaryotypeAdultAgedAged, 80 and overBiomarkers, TumorChi-Square DistributionFemaleGenetic Predisposition to DiseaseHumansKaplan-Meier EstimateLeukemia, Lymphocytic, Chronic, B-CellMaleMiddle AgedMultivariate AnalysisBiomarkers, TumorTP53 protein, humanTumor Suppressor Protein p53chromosome 8 abnormalitiesCLLcomplex karyotypeprognosisTP53 aberrations

Identifiers

PMID27821812
PMCPMC5348364
OpenAlexW2547215453

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LicenceCC BY
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Registered trials

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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.