The Systemic Treatment of Melanoma: The Place of Immune Checkpoint Inhibitors and the Suppression of Intracellular Signal Transduction

Patrick Terheyden*, Angela Krackhardt, Thomas Eigentler

*Corresponding author for this work
6 Citations (Scopus)


Background: The systemic treatment of metastatic melanoma has improved considerably with the introduction of new, targeted substances and immune checkpoint inhibitors. This article presents treatment options for advanced inoperable melanoma and in the setting of adjuvant treatment after complete metastasectomy. Methods: The data for analysis were derived from a selective literature search in PubMed and a search for systematic reviews in the Cochrane Library. Results: Immune checkpoint inhibitors, which target the cytotoxic T-lymphocyte antigen or the “programmed death” (PD) receptor, activate T-cells and other immune cells, so that the body’s own immune system attacks the melanoma. In unselected patients, immune checkpoint inhibition using nivolumab improved overall survival compared with dacarbazine (hazard ratio [HR]: 0.42; P<0.001). The antibody pembrolizumab also led to better overall survival than ipilimumab (HR 0.68; P<0.001). Combination treatment with anti-CTLA-4 and anti-PD-1 antibodies improved overall survival even more than ipilimumab monotherapy, albeit at the cost of greater toxicity (HR 0.55; P<0.001). Another treatment approach aims to inhibit intracellular signal transduction in the melanoma cells. For patients with a BRAF-V66 mutation, combination treatments with BRAF/MEK inhibitors led to a rapid response in most cases (64–75%). In principle, the novel treatments are also effective in patients with cerebral metastases. In the adjuvant setting, both immune checkpoint inhibitors and BRAF/MEK inhibitors reduced the risk of recurrence by about 50%. Conclusions: High-quality studies show that the new substances are clinically effective in the palliative and adjuvant treatment of melanoma.
Original languageEnglish
JournalDeutsches Arzteblatt International
Issue number29-30
Pages (from-to)497-504
Number of pages8
Publication statusPublished - 22.07.2019

Research Areas and Centers

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


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