Evidence map›Paper›PMID 33116240›Full record

Observational studyScientific reports2020

Time to first treatment and P53 dysfunction in chronic lymphocytic leukaemia: results of the O-CLL1 study in early stage patients.

Paola Monti, Marta Lionetti, Giuseppa De Luca, Paola Menichini, Anna Grazia Recchia, Serena Matis, Monica Colombo, Sonia Fabris, Andrea Speciale, Marzia Barbieri and 10 more

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Observational
  9. Article
  10. Mutant p53Frontiers in genetics · 2022
    Article
  11. Article
  12. Review
  13. Article
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

20 authors at 6 institutions in 2 countries.

Paola MontiMutagenesis and Cancer Prevention Unit, IRCCS Ospedale Policlinico San Martino, 16132, Genoa, Italy.
Marta LionettiDepartment of Oncology and Hemato-Oncology, University of Milan, 20122, Milan, Italy.
Giuseppa De LucaMolecular Diagnostic Unit, IRCCS Ospedale Policlinico San Martino, 16132, Genoa, Italy.
Paola MenichiniMutagenesis and Cancer Prevention Unit, IRCCS Ospedale Policlinico San Martino, 16132, Genoa, Italy.
Anna Grazia RecchiaBiotechnology Research Unit, Aprigliano, A.O./ASP of Cosenza, 87100, Cosenza, Italy.
Serena MatisMolecular Pathology Unit, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Monica ColomboMolecular Pathology Unit, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Sonia FabrisHematology Unit, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, 20122, Milan, Italy.
Andrea SpecialeMutagenesis and Cancer Prevention Unit, IRCCS Ospedale Policlinico San Martino, 16132, Genoa, Italy.
Marzia BarbieriHematology Unit, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, 20122, Milan, Italy.
Massimo GentileHematology Unit, Department of Onco-Hematology, A.O. of Cosenza, 87100, Cosenza, Italy.
Simonetta ZupoMolecular Diagnostic Unit, IRCCS Ospedale Policlinico San Martino, 16132, Genoa, Italy.
Mariella DonoMolecular Diagnostic Unit, IRCCS Ospedale Policlinico San Martino, 16132, Genoa, Italy.
Adalberto IbaticiHematology Unit and Bone Marrow Transplantation, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Antonino NeriDepartment of Oncology and Hemato-Oncology, University of Milan, 20122, Milan, Italy.
Manlio FerrariniDepartment of Experimental Medicine, University of Genoa, 16132, Genoa, Italy.
Franco FaisMolecular Pathology Unit, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Gilberto FronzaMutagenesis and Cancer Prevention Unit, IRCCS Ospedale Policlinico San Martino, 16132, Genoa, Italy.
Giovanna CutronaMolecular Pathology Unit, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Fortunato MorabitoBiotechnology Research Unit, Aprigliano, A.O./ASP of Cosenza, 87100, Cosenza, Italy. f.morabito53@gmail.com.
Ospedale Policlinico San Martino · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITAzienda Ospedaliera di Cosenza · ITUniversity of Genoa · ITAugusta Victoria Hospital · ILUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic lymphocytic leukaemia (CLL) is characterised by a heterogeneous clinical course. Such heterogeneity is associated with a number of markers, including TP53 gene inactivation. While TP53 gene alterations determine resistance to chemotherapy, it is not clear whether they can influence early disease progression. To clarify this issue, TP53 mutations and deletions of the corresponding locus [del(17p)] were evaluated in 469 cases from the O-CLL1 observational study that recruited a cohort of clinically and molecularly characterised Binet stage A patients. Twenty-four cases harboured somatic TP53 mutations [accompanied by del(17p) in 9 cases], 2 patients had del(17p) only, and 5 patients had TP53 germ-line variants. While del(17p) with or without TP53 mutations was capable of significantly predicting the time to first treatment, a reliable measure of disease progression, TP53 mutations were not. This was true for cases with high or low variant allele frequency. The lack of predictive ability was independent of the functional features of the mutant P53 protein in terms of transactivation and dominant negative potential. TP53 mutations alone were more frequent in patients with mutated IGHV genes, whereas del(17p) was associated with the presence of adverse prognostic factors, including CD38 positivity, unmutated-IGHV gene status, and NOTCH1 mutations.

Indexed as

Genes, p53Time-to-TreatmentFemaleHumansLeukemia, Lymphocytic, Chronic, B-CellMaleMiddle AgedMutationProspective Studies

Identifiers

PMID33116240
PMCPMC7595214
OpenAlexW3097125279

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.