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Prognostic factors and outcomes in metastatic uveal melanoma treated with programmed cell death-1 or combined PD-1/cytotoxic T-lymphocyte antigen-4 inhibition

  • Markus V. Heppt
  • , Lucie Heinzerling
  • , Katharina C. Kähler
  • , Andrea Forschner
  • , Michael C. Kirchberger
  • , Carmen Loquai
  • , Markus Meissner
  • , Friedegund Meier
  • , Patrick Terheyden
  • , Beatrice Schell
  • , Rudolf Herbst
  • , Daniela Göppner
  • , Felix Kiecker
  • , David Rafei-Shamsabadi
  • , Sebastian Haferkamp
  • , Margit A. Huber
  • , Jochen Utikal
  • , Mirjana Ziemer
  • , Irmgard Bumeder
  • , Christiane Pfeiffer
  • Susanne G. Schäd, Christoph Schmid-Tannwald, Julia K. Tietze, Thomas K. Eigentler, Carola Berking*
*Corresponding author for this work
  • Ludwig-Maximilians-Universität
  • University of Erlangen–Nuremberg
  • University of Kiel
  • University of Tubingen
  • Johannes Gutenberg University Mainz
  • Johann Wolfgang Goethe-University
  • Universitätsklinikum Carl Gustav Carus
  • SRH Wald-Klinikum Gera
  • HELIOS Klinikum Erfurt
  • University of Giessen
  • Charite - Universitatsmedizin Berlin
  • University of Freiburg
  • University of Regensburg
  • University of Ulm
  • University of Mannheim
  • University of Leipzig
  • Klinikum Augsburg
  • University of Rostock

Abstract

Background Uveal melanoma (UM) is an ocular malignancy with high potential for metastatic spread. In contrast to cutaneous melanoma, immunotherapy has not yet shown convincing efficacy in patients with UM. Combined immune checkpoint blockade with checkpoint programmed cell death-1 (PD-1) and checkpoint cytotoxic T-lymphocyte antigen-4 (CTLA-4) inhibition has not been systematically assessed for UM to date. Patients and methods Patients with metastatic UM treated with either PD-1 inhibitor monotherapy or combined PD-1 inhibitor and ipilimumab (an anti-CTLA-4 monoclonal antibody) were included from 20 German skin cancer centres. Records from 96 cases were analysed for treatment outcomes. Clinical and blood parameters associated with overall survival (OS) or treatment response were identified with multivariate Cox regression and binary logistic regression. Results Eighty-six patients were treated with PD-1 inhibitors only (n = 54 for pembrolizumab, n = 32 for nivolumab) with a centrally confirmed response rate of 4.7%. Median OS was 14 months for pembrolizumab-treated and 10 months for nivolumab-treated patients (p = 0.765). Fifteen patients were treated with combined immune checkpoint blockade with partial response observed in two cases. Median OS was not reached in this group. Multivariate Cox regression identified Eastern Cooperative Oncology Group (ECOG) performance status (p = 0.002), elevated serum levels of lactate dehydrogenase (LDH) (p = 0.002) and C-reactive protein (CRP) (p = 0.001), and a relative eosinophil count (REC) <1.5% (p = 0.002) as independent risk factors for poor survival. Patients with elevated CRP and LDH and a REC <1.5% were at highest risk for disease progression and death (p = 0.001). Conclusions Blood markers predict survival in metastatic UM treated with immune checkpoint blockade. Normal serum levels of LDH and CRP and a high REC may help identify patients with better prognosis.

Original languageEnglish
JournalEuropean Journal of Cancer
Volume82
Pages (from-to)56-65
Number of pages10
ISSN0959-8049
DOIs
Publication statusPublished - 01.09.2017

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Research Areas and Centers

  • Academic Focus: Center for Infection and Inflammation Research (ZIEL)

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