Evidence map›Paper›PMID 32748433›Full record

ArticleBritish journal of haematology2020

p53 is associated with high-risk and pinpoints TP53 missense mutations in mantle cell lymphoma.

Joana M Rodrigues, May Hassan, Catja Freiburghaus, Christian W Eskelund, Christian Geisler, Riikka Räty, Arne Kolstad, Christer Sundström, Ingrid Glimelius, Kirsten Grønbaek and 4 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of haematology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

36 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
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  13. Your chemo is no good here: management of high-risk MCL.Hematology. American Society of Hematology. Education Program · 2024
    Review
  14. To consolidate or not to consolidate: the role of autologous stem cell transplantation in MCL.Hematology. American Society of Hematology. Education Program · 2024
    Review
  15. Article
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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

14 authors at 7 institutions in 4 countries.

Joana M RodriguesDepartment of Immunotechnology, Lund University, Lund, Sweden.ORCID 0000-0003-1806-331X
May HassanDepartment of Immunotechnology, Lund University, Lund, Sweden.
Catja FreiburghausDepartment of Immunotechnology, Lund University, Lund, Sweden.
Christian W EskelundDepartment of Haematology, Rigshospitalet, Copenhagen, Denmark.
Christian GeislerDepartment of Haematology, Rigshospitalet, Copenhagen, Denmark.
Riikka RätyDepartment of Haematology, Helsinki University Hospital, Helsinki, Finland.
Arne KolstadDepartment of Oncology, Oslo University Hospital, Oslo, Norway.
Christer SundströmDepartment of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Ingrid GlimeliusDepartment of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.ORCID 0000-0001-6158-3041
Kirsten GrønbaekDepartment of Haematology, Rigshospitalet, Copenhagen, Denmark.
Anna KwiecinskaDepartment of Pathology-Oncology, Karolinska Institute, Stockholm, Sweden.
Anna PorwitDepartment of Pathology, Lund University, Lund, Sweden.
Mats JerkemanDepartment of Oncology, Lund University, Lund, Sweden.
Sara EkDepartment of Immunotechnology, Lund University, Lund, Sweden.ORCID 0000-0002-1388-4912
Lund University · SEUniversity of Copenhagen · DKUppsala University · SEHelsinki University Hospital · FIKarolinska Institutet · SEOslo University Hospital · NORigshospitalet · DK

Funding

Cancerfonden 2016/465Cancerfonden 2019/0309European Community's Horizon 2020 Framework Programme for Research and Innovation EU-H2020-MSCA-COFUND-2016-754299Fru Berta Kamprads Stiftelse FBKS-2018-7-(149)
6 · The paper itself

Abstract

Survival for patients diagnosed with mantle cell lymphoma (MCL) has improved drastically in recent years. However, patients carrying mutations in tumour protein p53 (TP53) do not benefit from modern chemotherapy-based treatments and have poor prognosis. Thus, there is a clinical need to identify missense mutations through routine analysis to enable patient stratification. Sequencing is not widely implemented in clinical practice for MCL, and immunohistochemistry (IHC) is a feasible alternative to identify high-risk patients. The aim of the present study was to investigate the accuracy of p53 as a tool to identify patients with TP53 missense mutations and the prognostic impact of overexpression and mutations in a Swedish population-based cohort. In total, 317 cases were investigated using IHC and 255 cases were sequenced, enabling analysis of p53 and TP53 status among 137 cases divided over the two-cohort investigated. The accuracy of predicting missense mutations from protein expression was 82%, with sensitivity at 82% and specificity at 100% in paired samples. We further show the impact of p53 expression and TP53 mutations on survival (hazard ratio of 3·1 in univariate analysis for both), and the association to risk factors, such as high MCL International Prognostic Index, blastoid morphology and proliferation, in a population-based setting.

Indexed as

Cell ProliferationDatabases, FactualGene Expression Regulation, NeoplasticLymphoma, Mantle-CellMutation, MissenseTumor Suppressor Protein p53FemaleHumansMaleRisk FactorsSwedenTP53 protein, humanTumor Suppressor Protein p53digital pathologyimmunohistochemistrymantle cell lymphomap53targeted sequencingTP53

Identifiers

PMID32748433
PMCPMC7754513
OpenAlexW3047197230

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.