摘要:血管紧张素系统抑制剂的使用与胰腺导管腺癌患者的免疫激活和更长的生存期有关

Nilesh P. Talele, Hao Liu, K. Naxerova, M. Pinter, J. Incio, Hang Lee, Kohei Shigeta, William W. Ho, T. Michelakos, T. Hong, Jeffrey W. Clark, Janet E. Murphy, D. Ryan, V. Deshpande, K. Lillemoe, C. F. Castillo, M. Downes, R. Evans, J. Michaelson, D. Duda, C. Ferrone, Yves Bouches, R. Jain
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引用次数: 0

摘要

目的:血管紧张素系统抑制剂(ASIs)可以改善多种癌症类型的预后,包括胰腺导管腺癌(PDAC)。然而,目前还没有研究考察ASIs单独或联合辅助化疗对PDAC切除患者的影响。实验设计:我们对2006年1月至2010年12月在马萨诸塞州总医院(Massachusetts General Hospital)就诊的ASI使用者和非ASI使用者PDAC患者的记录进行了分析。为了确定ASIs在PDAC中的机制,我们对切除的原发病变进行了rna测序。在一项前瞻性试验(NCT01821729)中,我们调查了氯沙坦活性的循环生物标志物。结果:连续纳入794例患者。在299例手术切除的患者中,单因素(中位生存期:36.3个月vs. 19.3个月,p=0.011)和调整多因素(HR, 0.505;95%ci, 0.339 - 0.750;p = 0.001)分析。倾向评分调整分析也显示慢性ASI使用者的中位OS更长。在未切除的患者中,ASIs的有益效果在局部晚期患者中显着,而在转移患者中则不明显。RNA-Seq分析显示,在asi使用者(赖诺普利)的肿瘤中,细胞外基质正常化,参与PDAC进展的基因表达减少(例如,WNT和Notch信号),与t细胞和抗原呈递细胞活性相关的基因表达增加。最后,在独立验证队列中,长期使用ASI与预测生存的基因表达特征相关。将在会议上介绍流行的生物标志物数据。结论:在非转移性PDAC患者中,慢性ASI使用与化疗无关的更长的生存期相关。我们的RNA-Seq分析表明,ASI降低了癌细胞的恶性潜能,并刺激了原发性PDAC的免疫微环境。引文格式:Nilesh P. Talele, Hao Liu, Kamila Naxerova, Matthias Pinter, Joao Incio, Hang Lee, Kohei Shigeta, William W. Ho, Theodoros Michelakos, Theodore S. Hong, Jeffrey W. Clark, Janet E. Murphy, David P. Ryan, Vikram Deshpande, Kieth D. Lillemoe, Carlos Fernandez-del Castillo, Michael Downes, Ronald M. Evans, James Michaelson, Dan G. Duda, Cristina R. Ferrone, Yves Bouches, Rakesh Jain。血管紧张素系统抑制剂的使用与胰腺导管腺癌患者的免疫激活和更长的生存期有关[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫,2019;7(2增刊):摘要nr A115。
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Abstract A115: Use of angiotensin system inhibitors is associated with immune activation and longer survival in pancreatic ductal adenocarcinoma patients
Purpose: Angiotensin system inhibitors (ASIs) can improve prognosis in multiple cancer types, including pancreatic ductal adenocarcinoma (PDAC). However, no study has examined the effect of ASIs alone or combined with adjuvant chemotherapy in resected PDAC patients. Experimental Design: We performed an analysis of the records of ASI users and non-user patients with PDAC seen at Massachusetts General Hospital between January 2006 and December 2010. To identify mechanisms of ASIs in PDAC, we performed RNA-Seq of resected primary lesions. In a prospective trial (NCT01821729), we investigated circulating biomarkers of losartan activity. Results: 794 consecutive patients were included. In 299 resected patients, ASI-users experienced longer overall survival (OS) in both univariate (median OS: 36.3 vs. 19.3 months, p=0.011) and adjusted multivariate (HR, 0.505; 95%CI, 0.339 - 0.750; p=0.001) analyses. Propensity score adjusted analysis also showed a longer median OS for chronic ASI users. In unresected patients, the beneficial effect of ASIs was significant in patients with locally advanced disease, but not in metastatic patients. RNA-Seq analysis revealed in tumors of ASI-users (lisinopril) a normalized extracellular matrix, a reduced expression of genes involved in PDAC progression (e.g., WNT and Notch signaling) and an increased expression of genes linked with the activity of T-cells and antigen-presenting cells. Finally, chronic use of ASI was associated with a gene expression signature that is predictive of survival in independent validation cohorts. Circulating biomarker data will be presented at the meeting. Conclusions: In patients with non-metastatic PDAC, chronic ASI use is associated with longer OS independently of chemotherapy. Our RNA-Seq analysis suggests that ASI reduce the malignant potential of cancer cells and stimulate the immune microenvironment in primary PDAC. Citation Format: Nilesh P. Talele, Hao Liu, Kamila Naxerova, Matthias Pinter, Joao Incio, Hang Lee, Kohei Shigeta, William W. Ho, Theodoros Michelakos, Theodore S. Hong, Jeffrey W. Clark, Janet E. Murphy, David P. Ryan, Vikram Deshpande, Kieth D. Lillemoe, Carlos Fernandez-del Castillo, Michael Downes, Ronald M. Evans, James Michaelson, Dan G. Duda, Cristina R. Ferrone, Yves Bouches, Rakesh Jain. Use of angiotensin system inhibitors is associated with immune activation and longer survival in pancreatic ductal adenocarcinoma patients [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr A115.
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