Evidence map›Paper›PMID 40866998›Full record

ArticleJournal of translational medicine2025

Identification of prognostic liquid biopsy biomarkers in patients with cutaneous squamous cell carcinoma treated with cemiplimab.

I Vanni, M Croce, L Pastorino, E Allavena, F Barbero, S Coco, S Santamaria, A G Bosio, A Boutros, A Rosa and 4 more

Abstract read
In one paragraph

Article in Journal of translational medicine, 2025. 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
–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

2 citing papers in PubMed.

  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

14 authors.

I VanniIRCCS Ospedale Policlinico San Martino, Genetica Oncologica, Genoa, Italy. irene.vanni@hsanmartino.it.ORCID 0000-0001-5900-4880
M CroceIRCCS Ospedale Policlinico San Martino, Bioterapie, Genoa, Italy.
L PastorinoIRCCS Ospedale Policlinico San Martino, Genetica Oncologica, Genoa, Italy.
E AllavenaIRCCS Ospedale Policlinico San Martino, Genetica Oncologica, Genoa, Italy.
F BarberoIRCCS Ospedale Policlinico San Martino, Genetica Oncologica, Genoa, Italy.
S CocoIRCCS Ospedale Policlinico San Martino, U.O. Oncologia Medica 2, Genoa, Italy.
S SantamariaIRCCS Ospedale Policlinico San Martino, U.O. Clinica di Oncologia Medica, Genoa, Italy.
A G BosioIRCCS Ospedale Policlinico San Martino, U.O. Oncologia Medica 2, Genoa, Italy.
A BoutrosIRCCS Ospedale Policlinico San Martino, U.O. Clinica di Oncologia Medica, Genoa, Italy.
A RosaIRCCS Ospedale Policlinico San Martino, U.O. Epidemiologia Clinica, Genoa, Italy.
V FontanaDepartment of Mathematics, University of Genoa, Genoa, Italy.
F SpagnoloIRCCS Ospedale Policlinico San Martino, U.O. Oncologia Medica 2, Genoa, Italy.
P GhiorzoIRCCS Ospedale Policlinico San Martino, Genetica Oncologica, Genoa, Italy.
E T TandaDepartment of Internal Medicine and Medical Specialties, University of Genoa, Genoa, Italy.

Funding

Ministero della Salute Ricerca Corrente 2023Ministero della Salute Ricerca Corrente 2025
6 · The paper itself

Abstract

backgroundThe treatment of Cutaneous Squamous Cell Carcinoma (CSCC) has undergone significant changes with the introduction of Immune Checkpoint Inhibitors (ICIs). While promising results have been observed, their efficacy remains limited to a subset of patients. Soluble immune checkpoint molecules, Interferon-gamma (IFN-γ), and cell-free DNA (cfDNA) could serve as potential biomarkers, particularly in ICI-based therapies.

methodsIn this study, we assessed the prognostic role of serum PD-L1, LAG-3, TIM-3, CTLA-4, IFN-γ, and plasma cfDNA in a cohort of 41 advanced (locally-advanced or metastatic) CSCC patients treated with the anti-PD-1 inhibitor cemiplimab.

resultsOur findings indicate that elevated baseline serum levels of IFN-γ are significantly associated with poorer treatment response and shorter Progression-Free Survival (PFS) in patients receiving cemiplimab. Moreover, patients with worse outcomes in terms of response and PFS exhibited a post-treatment decrease in IFN-γ levels. Higher baseline levels of plasma cfDNA and serum CTLA-4 demonstrated a trend toward association with unfavourable clinical outcomes.

conclusionsThese results highlight the potential of baseline and post-treatment IFN-γ levels as significant prognostic indicators for advanced CSCC patients undergoing cemiplimab therapy.

Indexed as

Antibodies, Monoclonal, HumanizedBiomarkers, TumorCarcinoma, Squamous CellSkin NeoplasmsAgedAged, 80 and overCell-Free Nucleic AcidsFemaleHumansInterferon-gammaLiquid BiopsyMaleMiddle AgedPrognosisProgression-Free SurvivalTreatment OutcomeAntibodies, Monoclonal, HumanizedBiomarkers, TumorCell-Free Nucleic AcidscemiplimabInterferon-gammaCemiplimabcfDNACSCCCTLA-4IFN-γLAG-3PD-L1Soluble biomarkersTIM-3

Identifiers

PMID40866998
PMCPMC12382013

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Registered trials

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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.