PD-L1 expression in gastroenteropancreatic neuroendocrine neoplasms grade 3
Ali, Abir Salwa; Langer, Seppo W.; Federspiel, Birgitte; Hjortland, Geir Olav; Grønbæk, Henning; Ladekarl, Morten; Welin, Staffan; Vestermark, Lene Weber; Arola, Johanna; Österlund, Pia; Knigge, Ulrich; Sørbye, Halfdan; Micke, Patrick; Grimelius, Lars; Grönberg, Malin; Janson, Eva Tiensuu (2020)
Ali, Abir Salwa
Langer, Seppo W.
Federspiel, Birgitte
Hjortland, Geir Olav
Grønbæk, Henning
Ladekarl, Morten
Welin, Staffan
Vestermark, Lene Weber
Arola, Johanna
Österlund, Pia
Knigge, Ulrich
Sørbye, Halfdan
Micke, Patrick
Grimelius, Lars
Grönberg, Malin
Janson, Eva Tiensuu
2020
PLoS ONE
e0243900
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202101121208
https://urn.fi/URN:NBN:fi:tuni-202101121208
Kuvaus
Peer reviewed
Tiivistelmä
<p>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.</p>
Kokoelmat
- TUNICRIS-julkaisut [20027]