Evidence map›Paper›PMID 40108790›Full record

Observational studyCancer medicine2025

Real-Life Cohort of Patients With Resected High-Risk Melanoma Treated by Adjuvant Anti-PD1 Therapy.

Liza Benzoni, Anaïs Eberhardt, Sarah Milley, Safa Idoudi, Camille Trefcon, Nicolas Romain-Scelle, Luc Thomas, Stéphane Dalle

Abstract readObservational Study
In one paragraph

Observational study in Cancer medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Liza BenzoniService de Dermatologie, Hospices Civils de Lyon, Hôpital Lyon Sud, Lyon, France.ORCID https://orcid.org/0009-0003-3541-5425
Anaïs EberhardtService de Dermatologie, Hospices Civils de Lyon, Hôpital Lyon Sud, Lyon, France.
Sarah MilleyService de Dermatologie, Hospices Civils de Lyon, Hôpital Lyon Sud, Lyon, France.
Safa IdoudiService de Dermatologie, Hôpital Saint Louis, Paris, France.
Camille TrefconService de Dermatologie, Hospices Civils de Lyon, Hôpital Lyon Sud, Lyon, France.
Nicolas Romain-ScelleService de Biostatistique, Hospices Civils de Lyon, Hôpital Lyon Sud, Pierre-Bénite, France.
Luc ThomasService de Dermatologie, Hospices Civils de Lyon, Hôpital Lyon Sud, Lyon, France.
Stéphane DalleService de Dermatologie, Hospices Civils de Lyon, Hôpital Lyon Sud, Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProgrammed cell death protein-1 (PD1) antibodies are currently the standard treatment for resected high-risk melanoma, yet recurrence rate remains high.

objectivesThis real-life observational study aimed to describe the outcomes of patients with resected high-risk melanoma following adjuvant anti-PD1 immunotherapy and identify factors associated with recurrence risk. MATERIALS AND

methodsA total of 235 patients with resected stage III/IV melanoma treated with adjuvant nivolumab or pembrolizumab were included. Imaging scans and cerebral imaging were performed every 12 weeks to detect recurrences. Adverse events were collected. Univariate and multivariate analyses were performed to identify predictive factors of recurrence. Overall survival (OS) and recurrence-free survival (RFS) were estimated.

resultsAmong the 235 patients, 103 experienced at least one recurrence (43%); first recurrences were predominantly locoregional (47%). The predictive factor for recurrence identified by multivariate analysis was ulceration (RR 2,03, 95% CI [1,20; 2,86]). RFS was estimated at 75% [70-81] at 12 months and at 64% [58-71] at 24 months. RFS at 12 months was significantly lower in patients with ulcerations (RFS at 83%) compared to those without ulceration (RFS at 66%), p < 0.01. Overall survival (OS) was estimated at 91% [87%-94%] at 12 months and 84% [79%-89%] at 24 months. The OS after a first recurrence was estimated at 69% [60%-80%] at 12 months and decreased to 43% [32%-57%] at 24 months. After a first locoregional recurrence, surgery with a year of adjuvant immunotherapy (40%) was the favoured therapeutic approach. For distant recurrences, clinical trial enrolment was preferred (21%). Double curative immunotherapy was the preferred strategy for cerebral recurrences (30%).

conclusionsIn this cohort, nearly half of the patients underwent recurrences and RFS at 24 months was 64%. The RFS and OS data were comparable o those reported in the pivotal study Ulceration was the only significant predictive factor for recurrence, associated with decreased RFS at 24 months.

Indexed as

Antibodies, Monoclonal, HumanizedImmune Checkpoint InhibitorsMelanomaNeoplasm Recurrence, LocalNivolumabProgrammed Cell Death 1 ReceptorSkin NeoplasmsAdultAgedAged, 80 and overChemotherapy, AdjuvantFemaleHumansMaleMiddle AgedAntibodies, Monoclonal, HumanizedImmune Checkpoint InhibitorsNivolumabPDCD1 protein, humanpembrolizumabProgrammed Cell Death 1 Receptoradjuvantanti‐PD1 therapyhigh‐risk melanoma

Identifiers

PMID40108790
PMCPMC11922813

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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.