The Christie NHS Foundation Trust, 550 Wilmslow Road, Manchester M20 4BX, UK.
Division of Cancer Sciences, University of Manchester, Oxford Road, Manchester M13 9PL, UK.
Curr Oncol. 2024 Sep 4;31(9):5206-5223. doi: 10.3390/curroncol31090385.
Pancreatic ductal adenocarcinoma (PDAC) is a significant cause of cancer-associated mortality, with a rising global incidence. A paucity of strong predictive risk factors mean screening programmes are difficult to implement. Historically, a lack of identifiable and actionable driver mutations, coupled with a relatively immunosuppressed tumour microenvironment, has led to a reliance on cytotoxic chemotherapy. The NAPOLI-3 trial has reported data supporting consideration of NALIRIFOX as a new first-line standard of care. Kirsten Rat Sarcoma Virus (KRAS) G12D mutations are present in >90% of all PDAC's; exciting breakthroughs in small molecule inhibitors targeting KRAS G12D may open new modalities of treatment, and therapies targeting multiple KRAS mutations are also in early clinical trials. Although immunotherapy strategies to date have been disappointing, combination with chemotherapy and/or small molecule inhibitors hold promise and warrant further exploration.
胰腺导管腺癌(PDAC)是癌症相关死亡的重要原因,其全球发病率呈上升趋势。由于缺乏强有力的预测风险因素,因此难以实施筛查计划。从历史上看,由于缺乏可识别和可操作的驱动突变,加上相对免疫抑制的肿瘤微环境,导致人们依赖细胞毒性化疗。NAPOLI-3 试验报告的数据支持将 NALIRIFOX 作为新的一线标准治疗药物。Kirsten Rat Sarcoma Virus (KRAS) G12D 突变存在于所有 PDAC 的 >90%中;针对 KRAS G12D 的小分子抑制剂的令人兴奋的突破可能开辟新的治疗方式,并且针对多种 KRAS 突变的治疗方法也处于早期临床试验阶段。尽管迄今为止免疫疗法策略令人失望,但与化疗和/或小分子抑制剂联合使用具有前景,值得进一步探索。