CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Prognostic value of CD103(+) tumor-infiltrating lymphocytes and programmed death ligand-1 (PD-L1) combined positive score in recurrent laryngeal squamous cell carcinoma.
Prognostic value of CD103(+) tumor-infiltrating lymphocytes and programmed death ligand-1 (PD-L1) combined positive score in recurrent laryngeal squamous cell carcinoma.
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在持续性或复发性 LSCC 患者中,CD103 + TILs 仅与 PD-L1 CPS 呈轻度相关。
在持续性或复发性喉鳞状细胞癌(LSCC)免疫治疗选择不断发展的背景下,需要更好的生物标志物来预测治疗应答和生存,以指导最佳治疗选择和预后判断。本研究主要目的为探究TIL(肿瘤浸润淋巴细胞)与PD-L1联合阳性评分(CPS)的相关性;次要目的为探究二者联合与接受挽救手术的持续性或复发性LSCC患者生存结局之间的关联。
这是一项单一学术医疗中心的回顾性队列研究。对持续性或复发性LSCC病理标本组织芯片进行TIL和PD-L1免疫组化染色。采用Pearson相关系数分析TIL亚群与PD-L1 CPS的相关性;采用Kaplan-Meier法和log-rank检验分析生存结局。
仅CD103+ TIL与PD-L1 CPS呈统计学显著的弱正相关(r²=0.264,p<0.015)。队列中其他TIL亚群均与PD-L1 CPS无相关性。病理N0且CD103+ TIL浸润高和/或PD-L1 CPS染色高的患者生存结局最佳。
在持续性或复发性LSCC患者中,CD103+ TIL与PD-L1 CPS仅呈轻度相关。纳入CD103+ TIL和PD-L1 CPS的联合生物标志物评分显著提高了生存区分能力。未来,该模型可能有助于预测免疫疗法用于持续性或复发性LSCC的临床获益。
In an evolving era of immunotherapeutic options for persistent or recurrent laryngeal squamous cell carcinoma (LSCC), there is a need for improved biomarkers of treatment response and survival to inform optimal treatment selection and prognostication. Herein, our primary objective was to explore correlations between tumor infiltrating lymphocytes (TILs) and PD-L1 Combined Positive Score (CPS). Secondarily, we sought to explore their combined association with survival outcomes in patients with persistent or recurrent LSCC treated with salvage surgery.
This was a retrospective cohort study at a single academic medical center. Immunohistochemistry staining for TILs and PD-L1 was performed on a tissue microarray of persistent or recurrent LSCC pathologic specimens. Correlations between TIL subsets and PD-L1 CPS were examined using Pearson's correlation coefficient and survival outcomes were analyzed with the Kaplan-Meier method and log-rank tests.
Only CD103 + TILs showed a statistically significant, weakly-positive correlation with PD-L1 CPS (r 2 = 0.264, p < 0.015). No other TIL subsets correlated with PD-L1 CPS in our cohort. The most favorable survival outcomes were seen in patients with pathologic N0 tumors showing high CD103 + TILs and/or high PD-L1 CPS staining.
Among patients with persistent or recurrent LSCC, CD103 + TILs only modestly correlated with PD-L1 CPS. A combined biomarker score incorporating CD103 + TILs and PD-L1 CPS greatly enhanced survival discrimination. This model may have additional utility in predicting the clinical benefit of immunotherapies in persistent or recurrent LSCC in the future.
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