Evidence map›Paper›PMID 31699794›Full record

ReviewHaematologica2019

MYD88 in the driver's seat of B-cell lymphomagenesis: from molecular mechanisms to clinical implications.

Ruben A L de Groen, Anne M R Schrader, Marie José Kersten, Steven T Pals, Joost S P Vermaat

Open access · goldAbstract readReview
In one paragraph

Review in Haematologica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

49 citing papers in PubMed, 86 citations in OpenAlex.

  1. Review
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  8. Novel Therapies in Primary Central Nervous System Lymphoma.Clinical pharmacology : advances and applications · 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

5 authors at 3 institutions in 2 countries.

Ruben A L de GroenDepartment of Hematology, Leiden University Medical Center, Leiden.
Anne M R SchraderDepartment of Pathology, Leiden University Medical Center, Leiden.
Marie José KerstenDepartment of Hematology, Amsterdam University Medical Center, University of Amsterdam, Amsterdam.
Steven T PalsDepartment of Hematology, Amsterdam University Medical Center, University of Amsterdam, Amsterdam.
Joost S P VermaatDepartment of Hematology, Leiden University Medical Center, Leiden j.s.p.vermaat@lumc.nl.
Leiden University Medical Center · NLAmsterdam University Medical Centers · NLUniversity of Amsterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

More than 50 subtypes of B-cell non-Hodgkin lymphoma (B-NHL) are recognized in the most recent World Health Organization classification of 2016. The current treatment paradigm, however, is largely based on 'one-size-fits-all' immune-chemotherapy. Unfortunately, this therapeutic strategy is inadequate for a significant number of patients. As such, there is an indisputable need for novel, preferably targeted, therapies based on a biologically driven classification and risk stratification. Sequencing studies identified mutations in the

Indexed as

Gene Expression Regulation, NeoplasticMutationHumansLeukemia, B-CellLymphoma, B-CellMyeloid Differentiation Factor 88PrognosisMYD88 protein, humanMyeloid Differentiation Factor 88

Identifiers

PMID31699794
PMCPMC6959184
OpenAlexW2984776263

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.