Evidence map›Paper›PMID 42564088›Full record

ArticleFrontiers in immunology2026

Real-world treatment patterns in stage III and IV melanoma patients: insights from a global multi-center chart review study.

Miso Kim, Elizabeth M Gaughan, Agueda Azpeitia, Aparna Rao, Maria L Wei, Alexandra So, Xiaochen Zhong, Carola Berking, Ruixuan Jiang, Stéphane Dalle and 28 more

Abstract readMulticenter Study
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

38 authors.

Miso KimSeoul National University Hospital, Seoul, Republic of Korea.
Elizabeth M GaughanUniversity of Virginia Cancer Center, Charlottesville, VA, United States.
Agueda AzpeitiaOXON Epidemiology, Madrid, Spain.
Aparna RaoDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Maria L WeiUniversity of California, San Francisco, San Francisco, CA, United States.
Alexandra SoUniversity of California, San Francisco, San Francisco, CA, United States.
Xiaochen ZhongUniversity of California, San Francisco, San Francisco, CA, United States.
Carola BerkingDepartment of Dermatology, Deutsches Zentrum Immuntherapie, Universitätsklinikum Erlangen, CCC Erlangen-EMN, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Ruixuan JiangMerck Sharp & Dohme LLC (MSD), a subsidiary of Merck & Co., Inc., Rahway, NJ, United States.
Stéphane DalleCentre Hospitalier Lyon-Sud, Pierre-Benite Cedex, France.
Caroline RobertInstitut Gustave Roussy, Villejuif, France.
Salma AlamMount Vernon Cancer Centre, Northwood, United Kingdom.
Tessa DaviesVelindre University NHS Trust, Cardiff, United Kingdom.
Dirk DebusDepartment of Dermatology, Nuremberg Hospital, Paracelsus Medical University, Nuremberg, Germany.
Marcin DzienisGold Coast University Hospital, Southport, QLD, Australia.
Sarah DansonWeston Park Cancer Centre, University of Sheffield and Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, United Kingdom.
Ricky FrazerVelindre University NHS Trust, Cardiff, United Kingdom.
Christoffer GebhardtDepartment of Dermatology and Venereology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Glenn GeidelDepartment of Dermatology and Venereology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Jessica C HasselHeidelberg University, Medical Faculty Heidelberg, Department of Dermatology and National Center for Tumor Diseases (NCT), NCT Heidelberg, a partnership between DKFZ and University Hospital Heidelberg, Heidelberg, Germany.
Inga HansenDepartment of Dermatology and Venereology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Markus V HepptDepartment of Dermatology, Deutsches Zentrum Immuntherapie, Universitätsklinikum Erlangen, CCC Erlangen-EMN, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Lina HildebrandtDepartment of Dermatology and Venereology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
James IsaacsCleveland Clinic, Cleveland, OH, United States.
Koung Jin SuhSeoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Republic of Korea.
Bhumsuk KeamSeoul National University Hospital, Seoul, Republic of Korea.
Yu Jung KimSeoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Republic of Korea.
Thierry LesimpleCentre Eugéne Marquis, Rennes, France.
Phillipe SaiagDepartment of General and Oncologic Dermatology, Ambroise Paré hospital, APHP, & EA 4340 "Biomarkers in cancerology and hemato-oncology", UVSQ, Université Paris-Saclay, Boulogne-Billancourt, France.
Ryan WeightThe Melanoma and Skin Cancer Institute, Englewood, CO, United States.
Alicia DelibesOXON Epidemiology, Madrid, Spain.
Rosemarie BarnettOXON Epidemiology, Madrid, Spain.
Clemens KreplerMerck Sharp & Dohme LLC (MSD), a subsidiary of Merck & Co., Inc., Rahway, NJ, United States.
Kavita GandhiOXON Epidemiology, Madrid, Spain.
Nawab QizilbashOXON Epidemiology, Madrid, Spain.
Irene ShuiMerck Sharp & Dohme LLC (MSD), a subsidiary of Merck & Co., Inc., Rahway, NJ, United States.
Xiang-Lin TanMerck Sharp & Dohme LLC (MSD), a subsidiary of Merck & Co., Inc., Rahway, NJ, United States.
Ryan J SullivanMass General Brigham Cancer Institute, Boston, MA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Anti-PD-1 immune checkpoint inhibitors have substantially changed melanoma management in both the adjuvant and advanced settings. This study aimed to estimate the percentage of stage III and IV melanoma patients exposed to different therapies and describe treatment patterns among anti-PD-1-treated patients. Methods: We performed a retrospective chart review across 22 centers in Australia, France, Germany, South Korea, the United Kingdom, and the United States. Two patient populations were analyzed: (1) an aggregate cohort with stage III/IV melanoma (2018-2021), and (2) patients who received anti-PD-1 therapy in adjuvant or advanced settings from January 2018-12 months before data collection. Treatment patterns were evaluated. Results: In the aggregate cohort (N = 16,260), observation/watchful waiting predominated in stage III patients (56.8%) in the adjuvant setting, whereas systemic therapy was most common for stage IV disease in the advanced setting. In the anti-PD-1 cohort (N = 738), anti-PD-1 monotherapy predominated in the adjuvant setting (97.5%), while both anti-PD-1 monotherapy (63.1%) and anti-PD-1 plus anti-CTLA-4 (36.9%) were commonly used in the advanced setting. Across successive lines of therapy, anti-PD-1-based regimens remained frequently used despite substantial attrition between treatment lines. Disease progression was the leading cause of treatment discontinuation in advanced disease. Discussion: This real-world study highlights the central role of anti-PD-1 therapy across disease stages. Anti-PD-1 retreatment and reuse of anti-PD-1-based regimens were frequently observed across treatment lines, highlighting the limited availability of established post-anti-PD-1 treatment options. Novel strategies are urgently needed for patients progressing after anti-PD-1 therapy.

Indexed as

Immune Checkpoint InhibitorsMelanomaSkin NeoplasmsAgedFemaleHumansMaleMiddle AgedNeoplasm StagingProgrammed Cell Death 1 ReceptorRetrospective StudiesImmune Checkpoint InhibitorsPDCD1 protein, humanProgrammed Cell Death 1 Receptoradjuvant settingadvancedanti-PD-1melanomareal-world datatreatment patterns

Identifiers

PMID42564088
PMCPMC13442371

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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.