Evidence map›Paper›PMID 31705171›Full record

ArticleCancer immunology, immunotherapy : CII2019

Tumor genetic alterations and features of the immune microenvironment drive myelodysplastic syndrome escape and progression.

Paola Montes, Mónica Bernal, Laura N Campo, Amanda Rocío González-Ramírez, Pilar Jiménez, Pilar Garrido, Manuel Jurado, Federico Garrido, Francisco Ruiz-Cabello, Francisca Hernández

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2019. 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
4.9field-weighted citation impact, top 4% 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, 52 citations in OpenAlex.

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  5. Characterization and Clinical Implications of p53 Dysfunction in Patients With Myelodysplastic Syndromes.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 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

10 authors at 2 institutions in 1 country.

Paola MontesServicio de Análisis Clínicos e Inmunología, Hospital Universitario Virgen de las Nieves, Avda. Fuerzas Arnadas s/n, 18014, Granada, Spain.
Mónica BernalServicio de Hematología, Hospital Universitario Virgen de las Nieves, Granada, Spain.
Laura N CampoServicio de Análisis Clínicos e Inmunología, Hospital Universitario Virgen de las Nieves, Avda. Fuerzas Arnadas s/n, 18014, Granada, Spain.
Amanda Rocío González-RamírezHospital Universitario San Cecilio, Granada, Spain.
Pilar JiménezServicio de Análisis Clínicos e Inmunología, Hospital Universitario Virgen de las Nieves, Avda. Fuerzas Arnadas s/n, 18014, Granada, Spain.
Pilar GarridoServicio de Hematología, Hospital Universitario Virgen de las Nieves, Granada, Spain.
Manuel JuradoServicio de Hematología, Hospital Universitario Virgen de las Nieves, Granada, Spain.
Federico GarridoServicio de Análisis Clínicos e Inmunología, Hospital Universitario Virgen de las Nieves, Avda. Fuerzas Arnadas s/n, 18014, Granada, Spain.
Francisco Ruiz-CabelloServicio de Análisis Clínicos e Inmunología, Hospital Universitario Virgen de las Nieves, Avda. Fuerzas Arnadas s/n, 18014, Granada, Spain. fruiz@ugr.es.
Francisca HernándezServicio de Hematología, Hospital Universitario Virgen de las Nieves, Granada, Spain.
Hospital Universitario Virgen de las Nieves · ESInstituto de Investigación Biosanitaria de Granada · ES

Funding

Instituto de Salud Carlos III PI 16/00752Junta de Andalucía PI09/0382
6 · The paper itself

Abstract

The transformation and progression of myelodysplastic syndromes (MDS) to secondary acute myeloid leukemia (sAML) involve genetic, epigenetic, and microenvironmental factors. Driver mutations have emerged as valuable markers for defining risk groups and as candidates for targeted treatment approaches in MDS. It is also evident that the risk of transformation to sAML is increased by evasion of adaptive immune surveillance. This study was designed to explore the immune microenvironment, immunogenic tumor-intrinsic mechanisms (HLA and PD-L1 expression), and tumor genetic features (somatic mutations and altered karyotypes) in MDS patients and to determine their influence on the progression of the disease. We detected major alterations of the immune microenvironment in MDS patients, with a reduced count of CD4

Indexed as

AdultAgedAged, 80 and overB7-H1 AntigenCarcinogenesisCD4-Positive T-LymphocytesCellular SenescenceDisease ProgressionFemaleHLA-C AntigensHumansImmunologic SurveillanceKiller Cells, NaturalLeukemia, Myeloid, AcuteMaleMiddle AgedB7-H1 AntigenHLA-C AntigensHigh molecular risk (HMR) mutationsImmune-evasionImmune microenvironmentLoss of heterozygosity (LOH)Myelodysplastic syndrome (MDS)

Identifiers

PMID31705171
PMCPMC11028123
OpenAlexW2985152308

What OpenQuestion holds

Textmetadata
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.