Evidence map›Paper›PMID 37297002›Full record

ArticleCancers2023

Cytogenetic Assessment and Risk Stratification in Myelofibrosis with Optical Genome Mapping.

Álvaro Díaz-González, Elvira Mora, Gayane Avetisyan, Santiago Furió, Rosalía De la Puerta, José Vicente Gil, Alessandro Liquori, Eva Villamón, Carmen García-Hernández, Marta Santiago and 15 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

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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

25 authors at 8 institutions in 1 country.

Álvaro Díaz-GonzálezHematology Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.
Elvira MoraHematology Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.
Gayane AvetisyanHematology Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.
Santiago FurióHematology Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.
Rosalía De la PuertaDepartment of Hematology, Hospital Arnau de Vilanova, 46015 Valencia, Spain.
José Vicente GilHematology Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.
Alessandro LiquoriHematology Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.ORCID 0000-0002-4842-5986
Eva VillamónDepartment of Hematology, Hospital Clínico Universitario-INCLIVA, 46010 Valencia, Spain.
Carmen García-HernándezDepartment of Hematology, Hospital General Universitario de Alicante, 03010 Alicante, Spain.
Marta SantiagoHematology Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.
Cristian García-RuizHematology Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.ORCID 0000-0003-2914-7914
Marta LlopCentro de Investigación Biomédica en Red de Cáncer (CIBERONC), 28029 Madrid, Spain.
Blanca Ferrer-LoresDepartment of Hematology, Hospital Clínico Universitario-INCLIVA, 46010 Valencia, Spain.
Eva BarragánCentro de Investigación Biomédica en Red de Cáncer (CIBERONC), 28029 Madrid, Spain.
Silvia García-PalomaresHematology Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.
Empar MayordomoPathology Department, Hospital Universitario y Politécnico La Fe, 46026 Valencia, Spain.
Irene LunaHematology Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.
Ana VicenteHematology Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.
Lourdes CordónHematology Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.
Leonor SenentHematology Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.
Alberto Álvarez-LarránDepartment of Hematology, Hospital Clínic, 08036 Barcelona, Spain.
José CerveraHematology Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.ORCID 0000-0001-8252-1106
Javier De la RubiaHematology Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.ORCID 0000-0002-8354-768X
Juan Carlos Hernández-BoludaDepartment of Hematology, Hospital Clínico Universitario-INCLIVA, 46010 Valencia, Spain.ORCID 0000-0002-4289-3113
Esperanza SuchHematology Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.
Hospital Universitari i Politècnic La Fe · ESInstituto de Investigación Sanitaria La Fe · ESHospital Clínico Universitario de Valencia · ESCentro de Investigación Biomédica en Red de Cáncer · ESHospital Arnau de Vilanova · ESHospital Clínic de Barcelona · ESHospital General Universitario de Alicante Doctor Balmis · ESUniversitat de València · ES

Funding

Generalitat Valenciana APOSTD2021/212Instituto de Investigación Sanitaria La Fe 2021-487-1SPANISH MINISTRY OF SCIENCE AND INNOVATION PID2021-126138OB-I00
6 · The paper itself

Abstract

Cytogenetic assessment in myelofibrosis is essential for risk stratification and patient management. However, an informative karyotype is unavailable in a significant proportion of patients. Optical genome mapping (OGM) is a promising technique that allows for a high-resolution assessment of chromosomal aberrations (structural variants, copy number variants, and loss of heterozygosity) in a single workflow. In this study, peripheral blood samples from a series of 21 myelofibrosis patients were analyzed via OGM. We assessed the clinical impact of the application of OGM for disease risk stratification using the DIPSS-plus, GIPSS, and MIPSS70+v2 prognostic scores compared with the standard-of-care approach. OGM, in combination with NGS, allowed for risk classification in all cases, compared to only 52% when conventional techniques were used. Cases with unsuccessful karyotypes (

Indexed as

chromosome banding analysismyelofibrosisoptical genome mappingprognosis

Identifiers

PMID37297002
PMCPMC10252182
OpenAlexW4379473671

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.