CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Concordance, Correlation, and Clinical Impact of Standardized PD-L1 and TIL Scoring in SCCHN.
Concordance, Correlation, and Clinical Impact of Standardized PD-L1 and TIL Scoring in SCCHN.
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在配对组织样本上测定 PD-L1 CPS 和 TIL 计数时,瘤间异质性、尤其是瘤内异质性是混杂因素,提示在具代表性的组织材料上评估这两种生物标志物的必要性日益增加。
头颈部鳞状细胞癌(SCCHN)中TIL(肿瘤浸润淋巴细胞)和程序性细胞死亡配体 1(PD-L1)的表达已得到充分研究。为明确这些生物标志物的瘤内及瘤间异质性影响,我们评估了不同配对组织样本中 PD-L1 综合阳性评分(CPS)和间质 TIL 的一致性,并分析其相互关系及预后影响。
对 80 例 SCCHN 患者的 165 个组织蜡块进行 TIL 和 PD-L1 CPS 评估。评估配对组织样本间的一致性,并分析其与多项临床病理变量、总生存期(OS)和无病生存期(DFS)的关联。
活检与配对切除标本在 CPS 和 TIL 计数上的严重不一致率分别为 39% 和 34%;其中 27% 的活检低估了 CPS。配对原发肿瘤与转移灶的 CPS 差异较低(19%),但 TIL 计数差异仍为 44%。按取材时点计算的 PD-L1 CPS 与 OS 延长相关;TIL 密度高则与 OS 和 DFS 延长相关。
瘤间、尤其是瘤内异质性会干扰配对组织样本中 PD-L1 CPS 和 TIL 计数的判定,提示有必要使用具有代表性的组织材料评估这两种标志物。尽管 TIL 在 SCCHN 中具有重要预后信息,PD-L1 作为 SCCHN 生物标志物的可靠性仍不明确。
The clinical significance of tumor-infiltrating lymphocytes (TILs) and programmed cell death-ligand 1 (PD-L1) expression has been thoroughly researched in squamous cell carcinoma of the head and neck (SCCHN). To address the impact of intra- and intertumoral heterogeneity in these biomarkers, we explored the concordance of PD-L1 combined positive score (CPS) and stromal TILs in different paired tissue sample types, while evaluating their internal relationship and prognostic impact.
A total of 165 tissue blocks from 80 SCCHN patients were reviewed for TILs and PD-L1 CPS. Concordance between paired tissue samples was evaluated, and their association with several clinicopathological variables, overall survival (OS), and disease-free survival (DFS) was determined.
Biopsies and paired resection material were severely discordant in 39% and 34% of samples for CPS and TIL count, respectively, of which CPS was underscored in 27% of biopsies. In paired primary tumor-metastatic lesions, the disagreement was lower for CPS (19%) but not for TIL count (44%). PD-L1 CPS was correlated with prolonged OS when calculated from tissue acquirement, while extended OS and DFS were observed for high TIL density.
Intertumoral and, especially, intratumoral heterogeneity were confounding factors when determining PD-L1 CPS and TIL count on paired tissue samples, indicating the increasing necessity of assessing both biomarkers on representative tissue material. Although TILs hold valuable prognostic information in SCCHN, the robustness of PD-L1 as a biomarker in SCCHN remains ambiguous.
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