Evidence map›Paper›PMID 40552104›Full record

ArticleJournal of extracellular biology2025

Monitoring Pseudoprogression Using Circulating Small Extracellular Vesicles Expressing PD-L1 in a Melanoma Patient Treated With Immune Checkpoint Inhibitors.

Charlée Nardin, Valentin Vautrot, Isen Naiken, Alexandre Doussot, Eve Puzenat, Célia De Girval, Carmen Garrido, François Aubin, Jessica Gobbo

Registry-linked trialAbstract read
In one paragraph

Article in Journal of extracellular biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05744076 (Analysis of Circulating Exosomes in Melanoma Patients), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

NCT05744076 unknown statusnot on this map

Analysis of Circulating Exosomes in Melanoma Patients

TypeobservationalSponsorCentre Hospitalier Universitaire de BesanconRan2019 to 2024Enrolled150ConditionsMelanoma
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

9 authors.

Charlée NardinDepartment of Dermatology University Hospital of Besançon Besançon France.
Valentin VautrotINSERM 1231, CTM, HSP-pathies, Label "Ligue National contre le Cancer" and Label d'Excellence LipSTIC Dijon France.
Isen NaikenFaculty of Medicine and Pharmacy University of Burgundy Dijon France.ORCID https://orcid.org/0009-0004-5950-5799
Alexandre DoussotDepartment of Digestive Surgical Oncology - Liver Transplant Unit University Hospital of Besançon Besançon France.
Eve PuzenatDepartment of Dermatology University Hospital of Besançon Besançon France.
Célia De GirvalINSERM 1231, CTM, HSP-pathies, Label "Ligue National contre le Cancer" and Label d'Excellence LipSTIC Dijon France.
Carmen GarridoINSERM 1231, CTM, HSP-pathies, Label "Ligue National contre le Cancer" and Label d'Excellence LipSTIC Dijon France.
François AubinDepartment of Dermatology University Hospital of Besançon Besançon France.
Jessica GobboINSERM 1231, CTM, HSP-pathies, Label "Ligue National contre le Cancer" and Label d'Excellence LipSTIC Dijon France.ORCID https://orcid.org/0000-0003-3201-9067

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICI) have revolutionized the treatment of metastatic malignancy. However, unique immune response patterns can occur, such as pseudoprogression, which corresponds to new lesion development or temporary tumour growth followed by regression. Misidentifying pseudoprogression may halt ICI therapy, due to the absence of biomarkers to distinguish progression from pseudoprogression. In 2020, our team proposed small extracellular vesicles expressing PD-L1 (sEV-PD-L1) as a predictor of melanoma treatment response. We report a case of pseudoprogression in a patient treated with nivolumab and ipilimumab for metastatic melanoma, and showing reduced circulating sEV-PD-L1. To our knowledge, this is the first report of PD-L1 monitoring in circulating sEV during pseudoprogression under ICI. A decrease in PD-L1 in circulating sEV might be an early sign of disease response to ICI, and may help to diagnose pseudoprogression. This case supports further evaluation of sEV-PD-L1 to identify responder patients to ICI, especially in case of pseudoprogression. Trial Registration: EXOMEL1 P/2018/40 1 AC-2015-2496/DC-2014-2086. NCT05744076.

Indexed as

biomarkerimmune checkpoint inhibitorimmunotherapymelanomaPD‐L1pseudoprogressionsmall extracellular vesicles

Identifiers

PMID40552104
PMCPMC12183339

What OpenQuestion holds

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Registered trials

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.