PD-L1 expression by tumor cell lines: A predictive marker in melanoma

被引:9
作者
Knol, Anne C. [1 ]
Nguyen, Jean-Michel [1 ,2 ]
Pandolfino, Marie-Christine [1 ,3 ]
Denis, Marc G. [1 ,4 ]
Khammari, Amir [1 ,5 ]
Dreno, Brigitte [1 ,3 ,5 ]
机构
[1] Univ Angers, Univ Nantes, CHU Nantes, CRCINA,INSERM,INSERM1232, Nantes, France
[2] CHU Nantes, St Jacques Univ Hosp, SEME, PHU11, Nantes, France
[3] CHU Nantes, UTCG, Nantes, France
[4] CHU Nantes, Lab Biochim & Plateforme Genet Canc, Nantes, France
[5] CHU Nantes, Serv Dermatocancerol, 1 Pl Alexis Ricordeau, F-44035 Nantes, France
关键词
flow cytometry; melanoma cell line; metastatic melanoma; prognostic markers; survival; STAGE-III MELANOMA; INDOLEAMINE 2,3-DIOXYGENASE; CLINICAL-SIGNIFICANCE; INFILTRATING LYMPHOCYTES; TRYPTOPHAN CATABOLISM; METASTATIC MELANOMA; MALIGNANT-MELANOMA; GENE SIGNATURE; BREAST-CANCER; BRAF MUTATION;
D O I
10.1111/exd.13526
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Prognostic biomarkers for patients with melanoma after lymph node resection are of clinical relevance and could thus enable the identification of patients who therefore would most benefit from adjuvant treatment. The aim of this work was to determine, using an in vitro model, whether immune-related biomarkers, such as MHC-class I and II, melanoma-associated antigens, IDO1 and PD-L1, could also be relevant to predict the risk of relapse of patients with stage III melanoma after lymph node resection. We established tumor cell lines from metastatic lymph nodes of 50 patients with melanoma. The expression of investigated biomarkers was determined on untreated and IFN- treated melanoma cell lines using flow cytometry. Among the selected biomarkers, the IFN--induced expression of PD-L1 and IDO1 was associated with an increased risk of relapse (P=.0001 and P=.013, respectively) and was also associated with death for IDO1 (P=.0005). In the future, this immunologic signature could permit the identification of patients at higher risk of relapse and justifying an adjuvant treatment using immunotherapy.
引用
收藏
页码:647 / 655
页数:9
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