The Jefferson Pancreas, Biliary and Related Cancer Center, Department of Surgery, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107, United States.
Department of Pharmaceutical Sciences, Jefferson College of Pharmacy, Thomas Jefferson University, Philadelphia, PA 19107, United States.
World J Gastroenterol. 2021 Oct 21;27(39):6527-6550. doi: 10.3748/wjg.v27.i39.6527.
Pancreatic ductal adenocarcinoma (PDAC) is the third leading cause of cancer-related deaths in the United States. Although chemotherapeutic regimens such as gemcitabine+ nab-paclitaxel and FOLFIRINOX (FOLinic acid, 5-Fluroruracil, IRINotecan, and Oxaliplatin) significantly improve patient survival, the prevalence of therapy resistance remains a major roadblock in the success of these agents. This review discusses the molecular mechanisms that play a crucial role in PDAC therapy resistance and how a better understanding of these mechanisms has shaped clinical trials for pancreatic cancer chemotherapy. Specifically, we have discussed the metabolic alterations and DNA repair mechanisms observed in PDAC and current approaches in targeting these mechanisms. Our discussion also includes the lessons learned following the failure of immunotherapy in PDAC and current approaches underway to improve tumor's immunological response.
胰腺导管腺癌(PDAC)是美国癌症相关死亡的第三大主要原因。尽管吉西他滨+ nab-紫杉醇和 FOLFIRINOX(亚叶酸、5-氟尿嘧啶、伊立替康和奥沙利铂)等化疗方案显著提高了患者的生存率,但治疗耐药性的普遍存在仍然是这些药物成功的主要障碍。这篇综述讨论了在 PDAC 治疗耐药性中起关键作用的分子机制,以及对这些机制的更好理解如何为胰腺癌化疗临床试验提供了指导。具体来说,我们讨论了在 PDAC 中观察到的代谢改变和 DNA 修复机制,以及目前针对这些机制的方法。我们的讨论还包括免疫疗法在 PDAC 中失败的教训,以及目前正在进行的提高肿瘤免疫反应的方法。