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Infiltrating pattern and prognostic value of tertiary lymphoid structures in resected non-functional pancreatic neuroendocrine tumors - PubMed

Infiltrating pattern and prognostic value of tertiary lymphoid structures in resected non-functional pancreatic neuroendocrine tumors

Wu-Hu Zhang et al. J Immunother Cancer. 2020 Oct.

Abstract

Background: Tertiary lymphoid structures (TLS) are associated with favorable survival and play a critical role in most solid tumors. However, investigations of TLS are lacking in patients with grade 1 or grade 2 (G1/G2) non-functional pancreatic neuroendocrine tumors (NF-PanNETs). This study aimed to investigate the presence, cellular composition, association with tumor-infiltrating immune cells, and prognostic value of TLS in G1/G2 NF-PanNETs.

Methods: Tumor tissues from a 182-patient Fudan cohort and a 125-patient external validation set were assessed by H&E staining, immunohistochemistry, and/or multispectral fluorescent immunohistochemistry.

Results: TLS were identified in more than one-third of patients with G1/G2 NF-PanNETs and were located peritumorally, either just outside the tumor tissue or in the stromal area. TLS were mainly composed of B-cell follicles with germinal centers and T-cell zones with dendritic cells. Kaplan-Meier analyses showed that the presence of TLS correlated with both longer recurrence-free survival (RFS, p<0.001) and overall survival (OS, p=0.001), but the number of TLS had no prognostic significance. Multivariate Cox-regression analyses demonstrated that the presence of TLS, WHO classification, and 8th edition American Joint Committee on Cancer (AJCC8th) tumor-node-metastasis (TNM) stage were independent prognostic factors for RFS (p=0.004, p=0.001, and p<0.001, respectively) and OS (p=0.009, p=0.008, and p=0.019, respectively). These results were confirmed using an external validation set. Finally, a nomogram incorporating the presence of TLS was constructed to predict the probability of 5-year RFS of resected G1/G2 NF-PanNETs, which improved on the current WHO classification and AJCC8th TNM stage.

Conclusions: The presence of TLS is an independent and favorable predictor of resected G1/G2 NF-PanNETs, which may play a role in cancer immunobiology.

Keywords: gastrointestinal neoplasms; immunotherapy; tumor biomarkers; tumor microenvironment.

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

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Conflict of interest statement

Competing interests: There are no competing interests.

Figures

Figure 1
Figure 1

Immunohistochemistry and histology of tertiary lymphoid structures (TLS). (A–H) Cellular composition of TLS. (A) CD4+ T cells. (B) CD8+ T cells. (C) CD20+ B cells. (D) CD11c+ dendritic cells. (E) CD45RO+ memory T cells. (F) anti-NCR1+ natural killer cells. (G) FOXP3+ regulatory T cells. (H) CD68+ tumor-associated macrophages. Magnification: 100×. (I–K) TLS stained with H&E. The presence of TLS in NF-PanNETs (I), functional PanNETs (J), and PanNECs (K). Top row, magnification: 100×. Bottom row, magnification: 400×. NF-PanNETs, non-functional PanNETs; PanNECs, pancreatic neuroendocrine carcinomas; PanNETs, pancreatic neuroendocrine tumors.

Figure 2
Figure 2

Multispectral fluorescent immunohistochemistry on G1/G2 non-functional pancreatic neuroendocrine tumors (NF-PanNETs). (A) A schematic of the sequential antibody staining approach used for multispectral immunohistochemistry indicating the color used for each protein of interest: CD45RO, green; CD20, yellow; CD4, violet; CD8, red. Cell nuclei were stained with DAPI (blue). (B–E) G1/G2 NF-PanNET tissues showing the localization of each of CD45RO, CD20, CD4, CD8. Magnification: 100×. (F) Merged image showing the colocalizations of DAPI, CD45RO, CD20, CD4 and CD8. Magnification: 100×. (G) Quantification of the numbers of cells positive for each of CD45RO, CD20, CD4, and CD8. The histogram displays the average number of each kind of cell counted in the five TLS shown in figure 2F and online supplemental figure S1. Error bars represent SD of the mean. (H) Pie chart displaying the percentages of each kind of cell counted in (G) to describe the immune cell composition of the TLS. G1/G2, grade 1/grade 2; HRP, horseradish peroxidase; TLS, tertiary lymphoid structures.

Figure 3
Figure 3

Kaplan-Meier curves depicting recurrence-free survival (RFS) and overall survival (OS) for patients with and without tertiary lymphoid structures (TLS). Association of the presence of TLS with RFS and OS in the Fudan cohort (A, B) and external validation set (C, D).

Figure 4
Figure 4

Nomogram predicting the probability of 5-year recurrence-free survival (RFS) and calibration plots. (A) A nomogram incorporating the presence of TLS, WHO classification and AJCC8th TNM stage. (B) Calibration curve for predicting the probability of 5-year RFS using the nomogram (A) on the Fudan cohort. (C) Calibration curve for predicting the probability of 5-year RFS using the nomogram (A) on the external validation set. (D) The MSKCC-based nomogram incorporating number of positive lymph nodes, Ki67 index, tumor diameter, and the presence of vascular or perineural invasion. (E) Calibration curve for predicting the probability of 5-year RFS by the MSKCC-based nomogram on the Fudan cohort. (F) Calibration curve for predicting the probability of 5-year RFS by the MSKCC-based nomogram on the external validation set. AJCC8th, 8th edition American Joint Committee on Cancer; MSKCC, Memorial Sloan-Kettering Cancer Center; TLS, tertiary lymphoid structures; TNM, tumor-node-metastasis.

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