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首页> 外文期刊>Cancer science. >Supplementary granulocyte macrophage colony‐stimulating factor to chemotherapy and programmed death‐ligand 1 blockade decreases local recurrence after surgery in bladder cancer
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Supplementary granulocyte macrophage colony‐stimulating factor to chemotherapy and programmed death‐ligand 1 blockade decreases local recurrence after surgery in bladder cancer

机译:化疗中补充粒细胞巨噬细胞集落刺激因子和程序性死亡配体1阻滞减少了膀胱癌手术后的局部复发

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Despite advances and refinements in surgery and perioperative chemotherapy, there are still unmet medical needs with respect to radical cystectomy for muscle‐invasive bladder cancer (MIBC). We investigated the potential benefit of supplementary granulocyte macrophage colony‐stimulating factor (GM‐CSF) to chemoimmunotherapy with programmed cell death protein‐1 (PD‐1)/programmed death‐ligand 1 (PD‐L1) axis blockade and standard neoadjuvant chemotherapy in bladder cancer. We inoculated 2?×?10sup5/sup MBT2 cells s.c. in C3H mice to create a syngeneic animal model of local recurrence (LR). When the tumor diameter reached 12?mm, the mice were allocated randomly as follows: (i) non‐treated control?(vehicle only); (ii) anti‐mPD‐L1 monotherapy; (iii) mGM‐CSF monotherapy; (iv) anti‐mPD‐L1 plus mGM‐CSF; (v) gemcitabine and cisplatin (GC); (vi) GC plus anti‐mPD‐L1; (vii) GC plus mGM‐CSF; and (viii) GC plus anti‐mPD‐L1 plus mGM‐CSF. After completing 2‐week neoadjuvant therapy, tumors were resected for resection margin evaluation and immunohistochemical staining and blood was collected for flow cytometry and ELISA. Operative wounds were sutured, and the operative site was monitored to detect LR. Addition of anti‐mPD‐L1 and mGM‐CSF to neoadjuvant GC chemotherapy enhanced the antitumor effect and reduced positive resection margins (50% vs 12.5%). Combination of GC, anti‐mPD‐L1, and mGM‐CSF resulted in longer LR‐free survival and cancer‐specific survival compared to those in other groups. These effects involved an immunotherapy‐related decrease in oncological properties such as tumor invasion capacity and epithelial‐mesenchymal transition. mGM‐CSF significantly decreased the accumulation of myeloid‐derived suppressor cells in both the blood and tumor microenvironment and blood interleukin‐6 levels. Supplementary GM‐CSF to neoadjuvant GC plus PD‐L1 blockade could decrease LR after radical surgery by immune modulation in the blood and tumor microenvironment.
机译:尽管在外科手术和围手术期化疗方面取得了进步和改进,但针对肌肉浸润性膀胱癌(MIBC)的根治性膀胱切除术仍存在医疗需求未得到满足的情况。我们研究了通过程序性细胞死亡蛋白-1(PD-1)/程序性死亡配体1(PD-L1)轴阻断和标准新辅助化疗对补充粒细胞巨噬细胞集落刺激因子(GM-CSF)进行化学免疫治疗的潜在益处。膀胱癌。我们接种了2?×?10 5 MBT2细胞s.c。在C3H小鼠中创建局部复发(LR)的同系动物模型。当肿瘤直径达到12?mm时,按以下方式随机分配小鼠:(i)未经治疗的对照? (ii)抗mPD-L1单药治疗; (iii)mGM‐CSF单一疗法; (iv)抗mPD-L1加mGM-CSF; (v)吉西他滨和顺铂(GC); (vi)GC加抗mPD-L1; (vii)GC加mGM-CSF; (viii)GC加抗mPD-L1加mGM-CSF。在完成2周的新辅助治疗后,将肿瘤切除以进行切除边缘评估和免疫组织化学染色,并收集血液进行流式细胞术和ELISA。缝合手术伤口,并监测手术部位以检测LR。在新辅助GC化疗中添加抗mPD-L1和mGM-CSF可以增强抗肿瘤作用并降低阳性切除率(50%比12.5%)。与其他组相比,GC,抗mPD-L1和mGM-CSF的组合可导致更长的无LR生存期和癌症特异性生存期。这些影响包括与免疫疗法相关的肿瘤学特性降低,例如肿瘤侵袭能力和上皮间质转化。 mGM‐CSF显着降低了血液和肿瘤微环境以及血液白介素6水平中髓样来源的抑制细胞的积累。 GM-CSF补充新辅助GC加上PD-L1阻断剂可通过血液和肿瘤微环境中的免疫调节在根治性手术后降低LR。

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