Evidence map›Paper›PMID 41277783›Full record

ArticleJournal of the European Academy of Dermatology and Venereology : JEADV2026

Benefit of immune checkpoint inhibitors as adjuvant treatment for acral melanomas.

Damien Sanogo, Romain Levard, Julie Cassecuel, Amir Khammari, Gaelle Quereux, Florent Grange, Henri Montaudié, Florence Brunet-Possenti, Justine Lavaud, Marie-Thérèse Leccia and 4 more

Abstract read
In one paragraph

Article in Journal of the European Academy of Dermatology and Venereology : JEADV, 2026. 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. Benefit of immune checkpoint inhibitors as adjuvant treatment for acral melanomas.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
    Article
  2. Adjuvant treatment for acral melanoma.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
    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.

Damien SanogoUNICAEN, INSERM U1086 ANTICIPE, Biology Research Building, Normandy University, Caen, France.
Romain LevardDermatology Unit, Caen-Normandie University Hospital, Caen, France.ORCID https://orcid.org/0009-0006-6349-8952
Julie CassecuelDermatology Unit, Nantes University Hospital, Nantes, France.
Amir KhammariDermatology Unit, Nantes University Hospital, Nantes, France.
Gaelle QuereuxDermatology Unit, Nantes University Hospital, Nantes, France.
Florent GrangeDermatology Unit, Valence Hospital, Valence, France.
Henri MontaudiéDermatology Unit, Nice University Hospital, Nice, France.ORCID https://orcid.org/0000-0002-0528-4829
Florence Brunet-PossentiDermatology Unit, Bichat Hospital, Paris, France.ORCID https://orcid.org/0000-0003-2100-2913
Justine LavaudDermatology Unit, Limoges University Hospital, Limoges, France.
Marie-Thérèse LecciaDermatology Unit, Grenoble University Hospital, Grenoble, France.
Géraldine JeudyDermatology Unit, Dijon University Hospital, Dijon, France.
Anne DompmartinDermatology Unit, Caen-Normandie University Hospital, Caen, France.
Brigitte DrenoNantes University, Nantes, France.ORCID https://orcid.org/0000-0001-5574-5825
Jean-Matthieu L'OrphelinUNICAEN, INSERM U1086 ANTICIPE, Biology Research Building, Normandy University, Caen, France.ORCID https://orcid.org/0000-0002-5680-7888

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSolar factors play no role in the development of acral melanoma (AM). AM is characterized by low cumulative solar damage (low CSD). Responses to immunotherapy are correlated with mutational load, which, in turn, is correlated with high cumulative sun damage (CSD). This suggests that AM patients may have poor responses to immunotherapy. The clinical benefit and safety profile of adjuvant immunotherapies in AM treatment have not been fully investigated.

objectivesTo investigate whether the use of adjuvant immunotherapy for treating patients with AM in Stages IIb, IIc, III and IV NED (no evidence of disease) improves distant metastasis-free survival.

methodsAmong the 1005 AM patients in the RIC-Mel melanoma database, 64 AM patients who were treated with adjuvant immunotherapy were included in this study. We then calculated a propensity score to make the adjuvant immunotherapy-treated (n = 64) group and the untreated group (n = 64) comparable in all respects.

resultsThe use of adjuvant immunotherapy for treating AM offers no clear benefit in terms of relapse-free survival or distant metastasis-free survival (RFS: HR = 0.84 [0.534, 1.324, 95% CI] and DMFS: HR = 0.94 [0.565, 1.562, 95% CI]). Among the AM patients who received adjuvant immune checkpoint inhibitors (ICI), 18.8% experienced severe (Grades 3-4) immune-related adverse events.

conclusionsThe benefit-risk balance must be carefully weighed, including the relapse-free survival (RFS), distant metastasis-free survival (DMFS) and rate of severe immune-related adverse events (irAE) occurrence. Other therapeutic strategies should be investigated in larger studies to confirm the potential limited clinical benefit of this treatment strategy.

Indexed as

Immune Checkpoint InhibitorsMelanomaSkin NeoplasmsAdultAgedChemotherapy, AdjuvantFemaleHumansImmunotherapyMaleMiddle AgedRetrospective StudiesImmune Checkpoint Inhibitorsadjuvant drug therapyfoothandimmune checkpoint inhibitorsmelanomanivolumabpembrolizumabrecurrence

Identifiers

PMID41277783
PMCPMC13206508

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.