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PD-L1 免疫组织化学表达作为预测卡介苗疗效的生物标志物在难治性高危非肌肉浸润性膀胱癌(NMIBC)中的临床意义。

Clinical interest of PD-L1 immuno-histochemistry expression as a predictive factor of Bacillus Calmette Guerin (BCG) efficacy in refractory high-risk non-muscle-invasive bladder cancer (NMIBC).

机构信息

Department of Urology, Charles Nicolle Rouen University Hospital, 1 rue de Germont, 76031, Rouen Cedex, France.

Department of Pathology, Rouen University Hospital, Rouen, France.

出版信息

World J Urol. 2020 Jun;38(6):1517-1524. doi: 10.1007/s00345-019-02896-3. Epub 2019 Sep 5.

Abstract

OBJECTIVE

To assess PD-L1 expression in tumor (TC) and tumor infiltrating immune cells (IC) as a predictive factor of BCG therapy failure in high-risk NMIBC.

MATERIALS AND METHODS

Patients treated with complete resection followed by bladder BCG instillation for high-risk NMIBC were included. Early recurrence (ER) was defined as tumor recurrence after BCG induction course. The association between ER and immuno-histochemistry PD-L1 (E1L3N clone) expression by tumors cells (TC) and tumor infiltrating immune cells (IC) was investigated using an exact Fisher test variant.

RESULTS

A total of 186 patients were included, of whom 38 (20.4%) were ER, 35 (18.8%) were positive for TC PD-L1 expression and 60 (32.3%) were positive for IC PD-L1. ER was not significantly (p = 0.97) more frequent in the TC PD-L1 ≥ 1% group (n = 7, 20.0%) than in the TC PD-L1-negative group (n = 31, 20.5%). Patients with IC PD-L1 negative had ER in 15 (19.2%) cases and patients with IC PD-L1 ≥ 1% had ER in 23 (21.3%) cases. PD-L1-positive expression for IC (threshold > 1%) was correlated with immune infiltrate density (95.2% dense immune infiltrate vs 47.2% low immune infiltrate, p < 0.05), with increased expression of PD-L1 by IC after BCG therapy (p = 0.006).

CONCLUSION

No association was observed between immuno-histochemistry PD-L1 positivity and ER after BCG therapy. Nevertheless, the relationship between immune infiltrate and PD-L1 positivity confirmed the interest of assessing the immune infiltrate density to define tumor's profile.

摘要

目的

评估肿瘤(TC)和肿瘤浸润免疫细胞(IC)中 PD-L1 的表达,作为高危非肌层浸润性膀胱癌(NMIBC)BCG 治疗失败的预测因子。

材料与方法

纳入接受完全切除术联合膀胱 BCG 灌注治疗高危 NMIBC 的患者。早期复发(ER)定义为 BCG 诱导疗程后肿瘤复发。使用确切 Fisher 检验变体研究 ER 与肿瘤细胞(TC)和肿瘤浸润免疫细胞(IC)的免疫组织化学 PD-L1(E1L3N 克隆)表达之间的关系。

结果

共纳入 186 例患者,其中 38 例(20.4%)发生 ER,35 例(18.8%)TC PD-L1 表达阳性,60 例(32.3%)IC PD-L1 阳性。TC PD-L1≥1%组(n=7,20.0%)的 ER 发生率与 TC PD-L1 阴性组(n=31,20.5%)相比无显著差异(p=0.97)。IC PD-L1 阴性患者中 ER 有 15 例(19.2%),IC PD-L1≥1%患者中 ER 有 23 例(21.3%)。IC 的 PD-L1 阳性表达(阈值>1%)与免疫浸润密度相关(密集免疫浸润 95.2%,低免疫浸润 47.2%,p<0.05),BCG 治疗后 IC 的 PD-L1 表达增加(p=0.006)。

结论

免疫组织化学 PD-L1 阳性与 BCG 治疗后 ER 之间未观察到相关性。然而,免疫浸润与 PD-L1 阳性之间的关系证实了评估免疫浸润密度以定义肿瘤特征的重要性。

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