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免疫生物标志物在黑色素瘤局部区域转移中的预后价值。

Prognostic value of immune biomarkers in melanoma loco-regional metastases.

作者信息

Hugdahl Emilia, Aziz Sura, Klingen Tor A, Akslen Lars A

机构信息

Department of Clinical Medicine, Centre for Cancer Biomarkers CCBIO, University of Bergen, Bergen, Norway.

Department of Pathology, Haukeland University Hospital, Bergen, Norway.

出版信息

PLoS One. 2025 Jan 30;20(1):e0315284. doi: 10.1371/journal.pone.0315284. eCollection 2025.

DOI:10.1371/journal.pone.0315284
PMID:39883679
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11781691/
Abstract

The prognosis for patients with melanoma loco-regional metastases is very heterogenous. Adjuvant PD-L1-inhibitors have improved clinical outcome for this patient group, but the prognostic impact of tumour PD-L1 expression and number of tumour infiltrating lymphocytes (TILs) is still largely unknown. Here, we investigated the impact on survival for CD3, CD8, FOXP3 and PD-L1 TIL counts and tumour PD-L1 expression in melanoma loco-regional metastases. In a patient series of loco-regional metastases from nodular melanomas (n = 78; n = 26 skin metastases, n = 52 lymph node metastases), expression of PD-L1 in tumour cells and the number of CD3, CD8, FOXP3 and PD-L1 positive TILs were determined by immunohistochemistry on tissue microarray (TMA) slides. Due to limited tumour tissue in the paraffin blocks, 67 of the 78 cases were included for tissue microarrays. Low FOXP3 TIL count and negative tumour PD-L1 expression (cut off 1%) were both significantly associated with reduced survival in lymph node metastases. Low FOXP3 TIL count was significantly associated with low CD8, CD3 and PD-L1 TIL counts. Negative tumour PD-L1 expression was significantly associated with low CD8 and PD-L1 TIL count, large lymph node metastasis tumour size and presence of necrosis in lymph node metastases. Our findings demonstrate for the first time the negative prognostic value of low FOXP3 TIL count and confirm a negative prognostic value of negative tumour PD-L1 expression in melanoma lymph node metastases.

摘要

黑色素瘤局部区域转移患者的预后差异很大。辅助性PD-L1抑制剂改善了该患者群体的临床结局,但肿瘤PD-L1表达和肿瘤浸润淋巴细胞(TILs)数量的预后影响仍大多未知。在此,我们研究了黑色素瘤局部区域转移中CD3、CD8、FOXP3和PD-L1 TIL计数以及肿瘤PD-L1表达对生存的影响。在一个来自结节性黑色素瘤的局部区域转移患者系列中(n = 78;n = 26例皮肤转移,n = 52例淋巴结转移),通过组织微阵列(TMA)载玻片上的免疫组织化学测定肿瘤细胞中PD-L1的表达以及CD3、CD8、FOXP3和PD-L1阳性TILs的数量。由于石蜡块中的肿瘤组织有限,78例病例中有67例被纳入组织微阵列研究。低FOXP3 TIL计数和肿瘤PD-L1阴性表达(截断值为1%)均与淋巴结转移患者生存率降低显著相关。低FOXP3 TIL计数与低CD8、CD3和PD-L1 TIL计数显著相关。肿瘤PD-L1阴性表达与低CD8和PD-L1 TIL计数、大的淋巴结转移肿瘤大小以及淋巴结转移中存在坏死显著相关。我们的研究结果首次证明了低FOXP3 TIL计数的负面预后价值,并证实了黑色素瘤淋巴结转移中肿瘤PD-L1阴性表达的负面预后价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f8f/11781691/33f74879d17f/pone.0315284.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f8f/11781691/56ec339bb051/pone.0315284.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f8f/11781691/33f74879d17f/pone.0315284.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f8f/11781691/56ec339bb051/pone.0315284.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f8f/11781691/33f74879d17f/pone.0315284.g002.jpg

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本文引用的文献

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EBioMedicine. 2023 Oct;96:104774. doi: 10.1016/j.ebiom.2023.104774. Epub 2023 Sep 4.
2
Appraisal of clinicopathological prognosticators in advanced acral lentiginous melanoma with characterization of PD-L1 and CD8/CD4 immunoprofiles.评估晚期肢端雀斑样黑素瘤的临床病理预后因子,并对 PD-L1 和 CD8/CD4 免疫组化特征进行分析。
Jpn J Clin Oncol. 2022 Sep 18;52(9):975-981. doi: 10.1093/jjco/hyac093.
3
Novel adjuvant options for cutaneous melanoma.
皮肤黑色素瘤的新型辅助治疗选择。
Ann Oncol. 2021 Jul;32(7):854-865. doi: 10.1016/j.annonc.2021.03.198. Epub 2021 Mar 24.
4
PD-L1 Expression in 65 Conjunctival Melanomas and Its Association with Clinical Outcome.65例结膜黑色素瘤中程序性死亡受体配体1(PD-L1)的表达及其与临床结局的关联
Int J Mol Sci. 2020 Nov 30;21(23):9147. doi: 10.3390/ijms21239147.
5
Peritumoral Immune Infiltrate as a Prognostic Biomarker in Thin Melanoma.肿瘤周围免疫浸润作为薄型黑色素瘤的预后生物标志物。
Front Immunol. 2020 Sep 29;11:561390. doi: 10.3389/fimmu.2020.561390. eCollection 2020.
6
Tumor-Infiltrating Lymphocytes and Their Prognostic Value in Cutaneous Melanoma.肿瘤浸润淋巴细胞及其在皮肤黑色素瘤中的预后价值。
Front Immunol. 2020 Sep 10;11:2105. doi: 10.3389/fimmu.2020.02105. eCollection 2020.
7
Association of combined PD-L1 expression and tumour-infiltrating lymphocyte features with survival and treatment outcomes in patients with metastatic melanoma.转移性黑色素瘤患者中PD-L1联合表达与肿瘤浸润淋巴细胞特征与生存及治疗结果的关联
J Eur Acad Dermatol Venereol. 2020 May;34(5):984-994. doi: 10.1111/jdv.16016. Epub 2019 Nov 24.
8
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J Cancer. 2019 Jun 2;10(13):3070-3078. doi: 10.7150/jca.30573. eCollection 2019.
9
Prognostic value of tumor-infiltrating lymphocytes in melanoma: a systematic review and meta-analysis.肿瘤浸润淋巴细胞在黑色素瘤中的预后价值:一项系统评价和荟萃分析。
Oncoimmunology. 2019 Apr 3;8(7):1593806. doi: 10.1080/2162402X.2019.1593806. eCollection 2019.
10
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PLoS One. 2019 Jan 14;14(1):e0210399. doi: 10.1371/journal.pone.0210399. eCollection 2019.