Evidence map›Paper›PMID 33562668›Full record

ReviewCells2021

Genetic Abnormalities in Multiple Myeloma: Prognostic and Therapeutic Implications.

Ignacio J Cardona-Benavides, Cristina de Ramón, Norma C Gutiérrez

Abstract readReview
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
–field-weighted citation impact
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

69 citing papers in PubMed.

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9 more citing papers are in PubMed but not listed here.

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

3 authors.

Ignacio J Cardona-BenavidesHematology Department, University Hospital, Institute of Biomedical Research of Salamanca (IBSAL), University Hospital of Salamanca, 37007 Salamanca, Spain.ORCID 0000-0001-6772-6859
Cristina de RamónHematology Department, University Hospital, Institute of Biomedical Research of Salamanca (IBSAL), University Hospital of Salamanca, 37007 Salamanca, Spain.
Norma C GutiérrezHematology Department, University Hospital, Institute of Biomedical Research of Salamanca (IBSAL), University Hospital of Salamanca, 37007 Salamanca, Spain.ORCID 0000-0001-5834-9510

Funding

Fundación Científica Asociación Española Contra el Cáncer PROYE20047GUTIGerencia Regional de Salud, Junta de Castilla y León GRS1654/A/17Gerencia Regional de Salud, Junta de Castilla y León GRS1849/A/18Gerencia Regional de Salud, Junta de Castilla y León GRS 2058/A/19Instituto de Salud Carlos III PI16/01074Instituto de Salud Carlos III PI19/00674
6 · The paper itself

Abstract

Some genetic abnormalities of multiple myeloma (MM) detected more than two decades ago remain major prognostic factors. In recent years, the introduction of cutting-edge genomic methodologies has enabled the extensive deciphering of genomic events in MM. Although none of the alterations newly discovered have significantly improved the stratification of the outcome of patients with MM, some of them, point mutations in particular, are promising targets for the development of personalized medicine. This review summarizes the main genetic abnormalities described in MM together with their prognostic impact, and the therapeutic approaches potentially aimed at abrogating the undesirable pathogenic effect of each alteration.

Indexed as

DNA Copy Number VariationsGenomicsHumansMultiple MyelomaPoint MutationPrognosischromosomal translocationscopy number changesmultiple myelomapoint mutationsprognosistargeted therapy

Identifiers

PMID33562668
PMCPMC7914805

What OpenQuestion holds

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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.