首页> 外文期刊>The lancet oncology >Targeting tumour-associated macrophages with CCR2 inhibition in combination with FOLFIRINOX in patients with borderline resectable and locally advanced pancreatic cancer: a single-centre, open-label, dose-finding, non-randomised, phase 1b trial
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Targeting tumour-associated macrophages with CCR2 inhibition in combination with FOLFIRINOX in patients with borderline resectable and locally advanced pancreatic cancer: a single-centre, open-label, dose-finding, non-randomised, phase 1b trial

机译:靶向CCR2抑制联合FOLFIRINOX的肿瘤相关巨噬细胞在边缘可切除和局部晚期胰腺癌患者中的研究:一项单中心,开放标签,剂量确定,非随机,1b期临床试验

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摘要

Background In pancreatic ductal adenocarcinoma, the CCL2-CCR2 chemokine axis is used to recruit tumour-associated macrophages for construction of an immunosuppressive tumour microenvironment. This pathway has prognostic implications in pancreatic cancer, and blockade of CCR2 restores anti-tumour immunity in preclinical models. We aimed to establish the safety, tolerability, and recommended phase 2 oral dose of the CCR2 inhibitor PF-04136309 in combination with FOLFIRINOX chemotherapy (oxaliplatin and irinotecan plus leucovorin and fluorouracil).
机译:背景技术在胰腺导管腺癌中,CCL2-CCR2趋化因子轴用于募集与肿瘤相关的巨噬细胞,以构建免疫抑制性肿瘤微环境。该途径在胰腺癌中具有预后意义,而CCR2的阻断可恢复临床前模型中的抗肿瘤免疫力。我们旨在确定CCR2抑制剂PF-04136309与FOLFIRINOX化疗(奥沙利铂和伊立替康加亚叶酸和氟尿嘧啶)联合使用的安全性,耐受性和推荐的2期口服剂量。

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