Evidence map›Paper›PMID 36614248›Full record

ArticleInternational journal of molecular sciences2023

Sorting Transcriptomics Immune Information from Tumor Molecular Features Allows Prediction of Response to Anti-PD1 Therapy in Patients with Advanced Melanoma.

Lucía Trilla-Fuertes, Angelo Gámez-Pozo, Guillermo Prado-Vázquez, Rocío López-Vacas, Andrea Zapater-Moros, Elena López-Camacho, María I Lumbreras-Herrera, Virtudes Soriano, Fernando Garicano, Mª José Lecumberri and 13 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
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

23 authors at 15 institutions in 1 country.

Lucía Trilla-FuertesMolecular Oncology Lab, Hospital Universitario La Paz-IdiPAZ, 28046 Madrid, Spain.ORCID 0000-0002-4452-3474
Angelo Gámez-PozoMolecular Oncology Lab, Hospital Universitario La Paz-IdiPAZ, 28046 Madrid, Spain.
Guillermo Prado-VázquezMolecular Oncology Lab, Hospital Universitario La Paz-IdiPAZ, 28046 Madrid, Spain.
Rocío López-VacasMolecular Oncology Lab, Hospital Universitario La Paz-IdiPAZ, 28046 Madrid, Spain.
Andrea Zapater-MorosMolecular Oncology Lab, Hospital Universitario La Paz-IdiPAZ, 28046 Madrid, Spain.
Elena López-CamachoBiomedica Molecular Medicine SL, 28049 Madrid, Spain.
María I Lumbreras-HerreraMolecular Oncology Lab, Hospital Universitario La Paz-IdiPAZ, 28046 Madrid, Spain.
Virtudes SorianoInstituto Valenciano de Oncología, 46009 Valencia, Spain.
Fernando GaricanoSpanish Melanoma Group (GEM), 08024 Barcelona, Spain.
Mª José LecumberriSpanish Melanoma Group (GEM), 08024 Barcelona, Spain.
María Rodríguez de la BorbollaSpanish Melanoma Group (GEM), 08024 Barcelona, Spain.
Margarita MajemSpanish Melanoma Group (GEM), 08024 Barcelona, Spain.ORCID 0000-0002-9919-7485
Elisabeth Pérez-RuizSpanish Melanoma Group (GEM), 08024 Barcelona, Spain.ORCID 0000-0001-7204-0800
María González-CaoSpanish Melanoma Group (GEM), 08024 Barcelona, Spain.ORCID 0000-0003-3791-540X
Juana OramasSpanish Melanoma Group (GEM), 08024 Barcelona, Spain.
Alejandra MagdalenoSpanish Melanoma Group (GEM), 08024 Barcelona, Spain.
Joaquín FraSpanish Melanoma Group (GEM), 08024 Barcelona, Spain.ORCID 0000-0003-4436-1572
Alfonso Martín-CarniceroSpanish Melanoma Group (GEM), 08024 Barcelona, Spain.ORCID 0000-0002-8564-2875
Mónica CorralSpanish Melanoma Group (GEM), 08024 Barcelona, Spain.
Teresa PuértolasSpanish Melanoma Group (GEM), 08024 Barcelona, Spain.
Ricardo RamosGenomics Unit, Parque Científico de Madrid, 28049 Madrid, Spain.ORCID 0000-0002-6331-9786
Juan Ángel Fresno VaraMolecular Oncology Lab, Hospital Universitario La Paz-IdiPAZ, 28046 Madrid, Spain.ORCID 0000-0003-1527-1252
Enrique EspinosaSpanish Melanoma Group (GEM), 08024 Barcelona, Spain.
Hospital Universitario La Paz · ESComplejo Hospitalario de Navarra · ESFundación Instituto Valenciano de Oncología · ESHospital Clínico Universitario Lozano Blesa · ESHospital Costa del Sol · ESHospital de Galdakao · ESHospital de Sant Pau · ESHospital General Universitario de Elche · ESHospital San Pedro · ESHospital Universitario de Canarias · ESHospital Universitario de Valme · ESHospital Universitario Dexeus · ESHospital Universitario Miguel Servet · ESHospital Universitario Río Hortega · ESUnidades Centrales Científico-Técnicas · ES

Funding

Translational MR Imaging in Cocaine Pharmacotherapy DevelopmentP50DA009262 · NIDA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MOELLER, FREDERICK GERARD · 1994 to 2014
$26.9M
SMALL INSTRUMENTATION GRANTS15DA007783 · NIDA · LOUISIANA STATE UNIV HSC SHREVEPORT · PI MUSLOW, IKE · 1991 to 1991
–
Consejeria de Educacion e Investigacion of Comunidad de Madrid IND2017/BMD7783Consejería de Educación e Investigación of Comunidad de Madrid IND2018/BMD-9262Ministry of Economy, Industry and Competitiveness PTQ2018-009760
6 · The paper itself

Abstract

Immunotherapy based on anti-PD1 antibodies has improved the outcome of advanced melanoma. However, prediction of response to immunotherapy remains an unmet need in the field. Tumor PD-L1 expression, mutational burden, gene profiles and microbiome profiles have been proposed as potential markers but are not used in clinical practice. Probabilistic graphical models and classificatory algorithms were used to classify melanoma tumor samples from a TCGA cohort. A cohort of patients with advanced melanoma treated with PD-1 inhibitors was also analyzed. We established that gene expression data can be grouped in two different layers of information: immune and molecular. In the TCGA, the molecular classification provided information on processes such as epidermis development and keratinization, melanogenesis, and extracellular space and membrane. The immune layer classification was able to distinguish between responders and non-responders to immunotherapy in an independent series of patients with advanced melanoma treated with PD-1 inhibitors. We established that the immune information is independent than molecular features of the tumors in melanoma TCGA cohort, and an immune classification of these tumors was established. This immune classification was capable to determine what patients are going to respond to immunotherapy in a new cohort of patients with advanced melanoma treated with PD-1 inhibitors Therefore, this immune signature could be useful to the clinicians to identify those patients who will respond to immunotherapy.

Indexed as

MelanomaSkin NeoplasmsHumansImmune Checkpoint InhibitorsImmunotherapyTranscriptomeImmune Checkpoint Inhibitorscomputational analysisimmunotherapymelanomapersonalized medicineprediction of response

Identifiers

PMID36614248
PMCPMC9821399
OpenAlexW4313515419

What Socratic 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 Socratic graph.