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PD-L1 expression in gastroenteropancreatic neuroendocrine neoplasms grade 3

Gastroenteropancreatic neuroendocrine neoplasms grade 3 (GEP-NENs G3) are rare tumors. These highly aggressive neoplasms are traditionally treated with platinum-based chemotherapy in combination with etoposide. Immune checkpoint proteins such as programmed cell death ligand (PD-L1) may have a role i...

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Detalles Bibliográficos
Autores principales: Ali, Abir Salwa, Langer, Seppo W., Federspiel, Birgitte, Hjortland, Geir Olav, Grønbæk, Henning, Ladekarl, Morten, Welin, Staffan, Weber Vestermark, Lene, Arola, Johanna, Osterlund, Pia, Knigge, Ulrich, Sørbye, Halfdan, Micke, Patrick, Grimelius, Lars, Grönberg, Malin, Tiensuu Janson, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735636/
https://www.ncbi.nlm.nih.gov/pubmed/33315908
http://dx.doi.org/10.1371/journal.pone.0243900
Descripción
Sumario:Gastroenteropancreatic neuroendocrine neoplasms grade 3 (GEP-NENs G3) are rare tumors. These highly aggressive neoplasms are traditionally treated with platinum-based chemotherapy in combination with etoposide. Immune checkpoint proteins such as programmed cell death ligand (PD-L1) may have a role in different cancers allowing them escape the immune system and hence, progress. We aimed to investigate the immunohistochemical expression of PD-L1 in GEP-NEN G3 and evaluate its correlation to clinical parameters. In a cohort of 136 patients, 14 (10%) expressed PD-L1 immunoreactivity; four (3%) patients in the tumor cells and 10 (7%) had immunoreactive immune cells. PD-L1 expression did not correlate to clinical parameters, progression-free survival or overall survival. We conclude that PD-L1 expression is present only in a subset of GEP-NEN G3 patients. Further studies are needed to fully understand the role of PD-L1 in patients with GEP-NEN G3, including the future possibility for treatment with immune checkpoint inhibitors.