Fingolimod and tumor-infiltrating lymphocytes in checkpoint-inhibitor treated cancer patients.
Cancer
Fingolimod
Immune checkpoint inhibitors
Multiple sclerosis
Oncology
Tumor immunology
Journal
Cancer immunology, immunotherapy : CII
ISSN: 1432-0851
Titre abrégé: Cancer Immunol Immunother
Pays: Germany
ID NLM: 8605732
Informations de publication
Date de publication:
Feb 2021
Feb 2021
Historique:
received:
05
03
2020
accepted:
04
08
2020
pubmed:
18
8
2020
medline:
12
3
2021
entrez:
18
8
2020
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 32804246
doi: 10.1007/s00262-020-02693-7
pii: 10.1007/s00262-020-02693-7
pmc: PMC7889549
doi:
Substances chimiques
Immune Checkpoint Inhibitors
0
Immunosuppressive Agents
0
Fingolimod Hydrochloride
G926EC510T
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
563-568Subventions
Organisme : Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
ID : PP00P3_157448
Références
Nat Rev Neurol. 2017 Dec;13(12):755-763
pubmed: 29104289
Blood. 2012 Mar 1;119(9):2176-7
pubmed: 22383793
Nat Rev Immunol. 2015 Sep 15;15(9):545-58
pubmed: 26250739
Nat Rev Drug Discov. 2010 Nov;9(11):883-97
pubmed: 21031003
BMC Cancer. 2019 Oct 24;19(1):998
pubmed: 31651263
Nature. 2014 Nov 27;515(7528):568-71
pubmed: 25428505
BMJ Case Rep. 2019 Apr 29;12(4):
pubmed: 31036735
Mol Cancer Ther. 2016 Oct;15(10):2465-2474
pubmed: 27507852
N Engl J Med. 2017 Oct 5;377(14):1345-1356
pubmed: 28889792
Cancer Res. 2010 Nov 1;70(21):8651-61
pubmed: 20959468
N Engl J Med. 2015 Jul 9;373(2):123-35
pubmed: 26028407
J Clin Invest. 2016 Sep 1;126(9):3447-52
pubmed: 27525433
Mult Scler Relat Disord. 2018 Jan;19:115-117
pubmed: 29190574
Eur J Cancer. 2020 Mar;127:240-250
pubmed: 31956037
CNS Drugs. 2018 Oct;32(10):939-949
pubmed: 30143945
Clin Transl Oncol. 2019 Oct;21(10):1336-1342
pubmed: 30788836
Ther Adv Neurol Disord. 2016 Mar;9(2):130-47
pubmed: 27006700
J Immunol. 2000 Jun 1;164(11):5761-70
pubmed: 10820254
Nature. 2017 May 4;545(7652):60-65
pubmed: 28397821
Eur J Cancer. 2019 May;113:75-77
pubmed: 30986706