Department of Urology, Charles Nicolle Rouen University Hospital, 1 rue de Germont, 76031, Rouen Cedex, France.
Department of Pathology, Rouen University Hospital, Rouen, France.
World J Urol. 2020 Jun;38(6):1517-1524. doi: 10.1007/s00345-019-02896-3. Epub 2019 Sep 5.
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.
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.
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).
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.
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。
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。
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)。
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。