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首页> 外文期刊>Oncoimmunology. >Combined assessment of peritumoral Th1/Th2 polarization and peripheral immunity as a new biomarker in the prediction of BCG response in patients with high-risk NMIBC
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Combined assessment of peritumoral Th1/Th2 polarization and peripheral immunity as a new biomarker in the prediction of BCG response in patients with high-risk NMIBC

机译:腹膜肿瘤术术综合评估为高风险NMIBC患者预测BCG响应中的新生物标志物

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摘要

Intravesical Bacille Calmette-Guerin (BCG) remains the most effective treatment for high-risk non-muscle-invasive bladder cancer (NMIBC), unfortunately there is no validated biomarker to predict clinical outcome. Here we tried to explore the possibility that a combination of the density of peritumoral infiltrating cells (Thi, Th2 and PD-L1) and the composition of peripheral immune cells (neutrophil and lymphocyte counts) could generate a more reliable prognostic biomarker. Twenty-two patients with high-risk NMIBC treated with BCG (10 BCG nonresponders and 12 BCG responders) were selected. BCG responders had significantly lower level of peritumoral T-bet+ cells with an associated higher GATA-3+/T-bet+ ratio (p = 0.04, p = 0.02, respectively). Furthermore, the immune polarization in tissue (GATA-3+/T-bet+ ratio) adjusted for the systemic inflammation (neutrophil-to-lymphocyte ratio) showed a significantly higher association with the BCG response (p = 0.004). A survival analysis demonstrated prolonged recurrence-free survival (RFS) in patients with a lower T-bet+/Lymphocyte ratio and higher GTR/NLR (p = 0.01). No association was observed between peritumoral PD-L1 +expression and the BCG response. In conclusion, alterations in overall immune function, both local and systemic, may influence the therapeutic response to BCG, therefore a combined analysis of tumoral (Th2/Th1 ratio) and peripheral (NLR) immune composition prior to treatment may be a promising approach to predict the BCG response in high-risk NMIBC patients.
机译:膀胱内的Bacille Calmette-guerin(BCG)仍然是高风险的非肌肉侵袭性膀胱癌(NMIBC)的最有效治疗,不幸的是没有验证的生物标志物预测临床结果。在这里,我们试图探讨腹部渗透细胞(TH1,TH2和PD-L1)的密度组合的可能性和外周免疫细胞(中性粒细胞和淋巴细胞计数)可以产生更可靠的预后生物标志物。选择了用BCG(10bcg无反应者和12bcg响应者10bcg响应者10例高危NMIBC患者。 BCG响应者的腹膜瘤+细胞水平明显较低,具有相关的较高的GATA-3 + / T-BET +比率(P = 0.04,P = 0.02)。此外,用于全身炎症(中性粒细胞对淋巴细胞比)调节的组织(GATA-3 + / T-BET +比率)的免疫偏振显示出与BCG响应显着更高的关联(p = 0.004)。生存分析在T-Bet + /淋巴细胞比和更高的GTR / NLR较高的患者中延长了无复发的存活(RFS)(P = 0.01)。腹膜PD-L1 +表达与BCG响应之间没有观察到任何关联。总之,总体免疫功能的改变,局部和全身,可能影响对BCG的治疗反应,因此治疗前的肿瘤(TH2 / TH1比率)和外周(NLR)免疫组合物的组合分析可能是一种有希望的方法预测高风险NMIBC患者的BCG响应。

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