Journal Article (Review Article) DKFZ-2026-00104

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Merkel cell carcinoma immunotherapy: key questions in the era of immune checkpoint blockade.

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2026
BioMed Central London

Journal for ImmunoTherapy of Cancer 14(1), e014090 () [10.1136/jitc-2025-014090]
 GO

Abstract: Merkel cell carcinoma (MCC) exemplifies the paradigm of immunogenic tumors that nonetheless develop sophisticated immune evasion mechanisms. This is in line with the observation that MCC exhibits remarkable susceptibility to immune checkpoint inhibitors (ICIs), with responses in approximately half of patients with advanced disease in the first-line setting. However, 40-50% of patients show primary ICI resistance, while 20-30% of patients develop acquired ICI resistance on initial disease control. Still, the advent of ICI therapy represents a revolutionary rather than evolutionary advance in MCC management, fundamentally transforming outcomes from the dismal prognosis associated with conventional chemotherapy to durable responses extending substantially beyond 2 years. Still, important questions remain: (1) Is programmed cell death protein-1 or programmed death-ligand 1 inhibition more effective? (2) How long should ICI treatment continue? (3) What is the best choice of salvage therapy for patients with primary or acquired ICI resistance? (4) Which combination regimens can increase the share of patients benefiting from ICI? (5) Which patient/tumor characteristics predict response and its duration? Finally, (6) which timing of ICI therapy, that is, the neoadjuvant, adjuvant or therapeutic setting, offers the optimal overall outcomes for patients with MCC? A number of recent studies provide initial, but unfortunately not yet definitive answers.

Keyword(s): Humans (MeSH) ; Carcinoma, Merkel Cell: drug therapy (MeSH) ; Carcinoma, Merkel Cell: immunology (MeSH) ; Immune Checkpoint Inhibitors: therapeutic use (MeSH) ; Immune Checkpoint Inhibitors: pharmacology (MeSH) ; Immunotherapy: methods (MeSH) ; Skin Neoplasms: drug therapy (MeSH) ; Skin Neoplasms: immunology (MeSH) ; Adjuvant ; Biomarker ; Immune Checkpoint Inhibitor ; Immunotherapy ; Neoadjuvant ; Immune Checkpoint Inhibitors

Classification:

Note: #DKTKZFB26#

Contributing Institute(s):
  1. DKTK Koordinierungsstelle Essen/Düsseldorf (ED01)
Research Program(s):
  1. 899 - ohne Topic (POF4-899) (POF4-899)

Appears in the scientific report 2026
Database coverage:
Medline ; DOAJ ; Article Processing Charges ; Clarivate Analytics Master Journal List ; DOAJ Seal ; Ebsco Academic Search ; Essential Science Indicators ; Fees ; IF >= 10 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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 Record created 2026-01-14, last modified 2026-01-15



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