Steele Laboratories of Tumor Biology, Department of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts.
Clin Cancer Res. 2023 Apr 14;29(8):1605-1619. doi: 10.1158/1078-0432.CCR-22-1630.
Adding losartan (LOS) to FOLFIRINOX (FFX) chemotherapy followed by chemoradiation (CRT) resulted in 61% R0 surgical resection in our phase II trial in patients with locally advanced pancreatic cancer (LAPC). Here we identify potential mechanisms of benefit by assessing the effects of neoadjuvant LOS on the tumor microenvironment.
We performed a gene expression and immunofluorescence (IF) analysis using archived surgical samples from patients treated with LOS+FFX+CRT (NCT01821729), FFX+CRT (NCT01591733), or surgery upfront, without any neoadjuvant therapy. We also conducted a longitudinal analysis of multiple biomarkers in the plasma of treated patients.
In comparison with FFX+CRT, LOS+FFX+CRT downregulated immunosuppression and pro-invasion genes. Overall survival (OS) was associated with dendritic cell (DC) and antigen presentation genes for patients treated with FFX+CRT, and with immunosuppression and invasion genes or DC- and blood vessel-related genes for those treated with LOS+FFX+CRT. Furthermore, LOS induced specific changes in circulating levels of IL-8, sTie2, and TGF-β. IF revealed significantly less residual disease in lesions treated with LOS+FFX+CRT. Finally, patients with a complete/near complete pathologic response in the LOS+FFX+CRT-treated group had reduced CD4+FOXP3+ regulatory T cells (Tregs), fewer immunosuppressive FOXP3+ cancer cells (C-FOXP3), and increased CD8+ T cells in pancreatic ductal adenocarcinoma lesions.
Adding LOS to FFX+CRT reduced pro-invasion and immunosuppression-related genes, which were associated with improved OS in patients with LAPC. Lesions from responders in the LOS+FFX+CRT-treated group had reduced Tregs, decreased C-FOXP3 and increased CD8+ T cells. These findings suggest that LOS may potentiate the benefit of FFX+CRT by reducing immunosuppression.
在局部晚期胰腺癌(LAPC)患者的 II 期试验中,我们发现洛沙坦(LOS)联合 FOLFIRINOX(FFX)化疗后再进行放化疗(CRT)可使 61%的患者达到 R0 手术切除。在此,我们通过评估新辅助 LOS 对肿瘤微环境的影响,来确定其获益的潜在机制。
我们对接受洛沙坦+FFX+CRT(NCT01821729)、FFX+CRT(NCT01591733)或直接手术治疗、无新辅助治疗的患者的手术标本进行了基因表达和免疫荧光(IF)分析。我们还对接受治疗的患者的多个生物标志物进行了纵向分析。
与 FFX+CRT 相比,LOS+FFX+CRT 下调了免疫抑制和促侵袭基因。对于接受 FFX+CRT 治疗的患者,总体生存(OS)与树突状细胞(DC)和抗原呈递基因相关,而对于接受 LOS+FFX+CRT 治疗的患者,OS 与免疫抑制和侵袭基因或 DC 和血管相关基因相关。此外,LOS 诱导了循环 IL-8、sTie2 和 TGF-β水平的特异性变化。IF 显示 LOS+FFX+CRT 治疗的病变中残留疾病明显减少。最后,在 LOS+FFX+CRT 治疗组中完全/近乎完全病理缓解的患者,其 CD4+FOXP3+调节性 T 细胞(Tregs)减少,FOXP3+免疫抑制性癌细胞(C-FOXP3)减少,胰腺导管腺癌病变中的 CD8+T 细胞增加。
在 FFX+CRT 中加入 LOS 可降低促侵袭和免疫抑制相关基因,从而改善 LAPC 患者的 OS。LOS+FFX+CRT 治疗组中应答者的病变中 Tregs 减少,C-FOXP3 减少,CD8+T 细胞增加。这些发现表明,LOS 可能通过减少免疫抑制来增强 FFX+CRT 的疗效。