Optimizing immune checkpoint blockade in metastatic uveal melanoma: exploring the association of overall survival and the occurrence of adverse events

Front Immunol. 2024 Jun 10:15:1395225. doi: 10.3389/fimmu.2024.1395225. eCollection 2024.

Abstract

Introduction: Despite recent advancements in the treatment of metastatic uveal melanoma (UM), the availability of further treatment options remains limited and the prognosis continues to be poor in many cases. In addition to tebentafusp, immune checkpoint blockade (ICB, PD-1 (+/-) CTLA-4 antibodies) is commonly used for metastatic UM, in particular in HLA-A 02:01-negative patients. However, ICB comes at the cost of potentially severe immune-related adverse events (irAE). Thus, the selection of patient groups that are more likely to benefit from ICB is desirable.

Methods: In this analysis, 194 patients with metastatic UM undergoing ICB were included. Patients were recruited from German skin cancer sites and the ADOReg registry. To investigate the association of irAE occurrence with treatment response, progression-free survival (PFS), and overall survival (OS) two cohorts were compared: patients without irAE or grade 1/2 irAE (n=137) and patients with grade 3/4 irAE (n=57).

Results: In the entire population, the median OS was 16.4 months, and the median PFS was 2.8 months. Patients with grade 3/4 irAE showed more favorable survival than patients without or grade 1/2 irAE (p=0.0071). IrAE occurred in 44.7% (87/194), and severe irAE in 29.4% (57/194) of patients. Interestingly, irColitis and irHepatitis were significantly associated with longer OS (p=0.0031 and p=0.011, respectively).

Conclusions: This data may indicate an association between irAE and favorable survival outcomes in patients with metastatic UM undergoing ICB treatment and suggests that a reduced tolerance to tumor antigens could be linked to reduced tolerance to self-antigens.

Keywords: CTLA-4; PD-1; adverse events; immune checkpoint blockade; immune-related; toxicity; uveal melanoma.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Female
  • Humans
  • Immune Checkpoint Inhibitors* / adverse effects
  • Immune Checkpoint Inhibitors* / therapeutic use
  • Male
  • Melanoma* / drug therapy
  • Melanoma* / immunology
  • Melanoma* / mortality
  • Middle Aged
  • Neoplasm Metastasis
  • Uveal Neoplasms* / drug therapy
  • Uveal Neoplasms* / immunology
  • Uveal Neoplasms* / mortality
  • Uveal Neoplasms* / pathology

Substances

  • Immune Checkpoint Inhibitors

Supplementary concepts

  • Uveal melanoma

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The study was supported by the Matthias-Lackas-Stiftung and the Hiege Foundation (die Deutsche Hautkrebsstiftung). MVH was supported by an Else-Kröner Fresenius Excellence Fellowship. EATK was supported by the Clinician Scientist Programme of the IZKF (Interdisciplinary Center for Clinical Research) at the Medical Faculty of the FAU Erlangen. EATK and MVH were supported by the clinician-scientist program awarded by the German Society of Dermatology (DDG) and the Arbeitsgemeinschaft Dermatologische Forschung (ADF).