| Literature DB >> 32804246 |
Omar Hasan Ali1,2,3, Fiamma Berner3, Christoph Jakob Ackermann4, Sandra Stephanie Ring3, Alexandre Moulin5, Joachim Müller6, Eva Markert7, Oltin Tiberiu Pop3, Stefanie Müller8, Stefan Diem9,10, Thomas Hundsberger8, Lukas Flatz11,12,13,14,15.
Abstract
Immune checkpoint inhibitors (ICIs) are emerging as the new standard of care for treating various metastatic cancers. It is known that effective anti-tumor immune responses are associated with a stronger presence of tumor-infiltrating lymphocytes (TILs) in solid tumor tissue. Cancer patients with relapsing-remitting multiple sclerosis (RRMS) are often under continuous treatment with fingolimod, an immune-modulating drug that inhibits lymphocyte egress from secondary lymphatic organs. Little is known about the effect of fingolimod on ICI cancer therapy, as fingolimod may limit the number of TILs. Here we present three patients with RRMS, who developed various cancers during fingolimod treatment. Histology of all tumors consistently showed low numbers of TILs. A second biopsy taken from one of the tumors, a melanoma, revealed a significant increase of TILs after stopping fingolimod and starting pembrolizumab, indicating a surge in the number and re-invigoration of T cells. Our study suggests that fingolimod limits the number of TILs in solid tumors and may, thus, inhibit anti-cancer immune responses.Entities:
Keywords: Cancer; Fingolimod; Immune checkpoint inhibitors; Multiple sclerosis; Oncology; Tumor immunology
Year: 2020 PMID: 32804246 DOI: 10.1007/s00262-020-02693-7
Source DB: PubMed Journal: Cancer Immunol Immunother ISSN: 0340-7004 Impact factor: 6.968