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
Department of Medical Sciences, Section of Endocrine Oncology, Uppsala University, Uppsala, Sweden.
Department of Oncology, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
PLoS One. 2020 Dec 14;15(12):e0243900. doi: 10.1371/journal.pone.0243900. eCollection 2020.
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.
胃肠胰神经内分泌瘤3级(GEP-NENs G3)是罕见肿瘤。这些侵袭性很强的肿瘤传统上采用铂类化疗联合依托泊苷进行治疗。免疫检查点蛋白,如程序性细胞死亡配体(PD-L1),可能在不同癌症中发挥作用,使癌细胞能够逃避免疫系统从而进展。我们旨在研究PD-L1在GEP-NEN G3中的免疫组化表达,并评估其与临床参数的相关性。在一个136例患者的队列中,14例(10%)表达PD-L1免疫反应性;4例(3%)患者的肿瘤细胞中有免疫反应性,10例(7%)有免疫反应性免疫细胞。PD-L1表达与临床参数、无进展生存期或总生存期均无相关性。我们得出结论,PD-L1表达仅存在于一部分GEP-NEN G3患者中。需要进一步研究以全面了解PD-L1在GEP-NEN G3患者中的作用,包括未来使用免疫检查点抑制剂进行治疗的可能性。