Turpin Anthony, Neuzillet Cindy, Colle Elise, Dusetti Nelson, Nicolle Rémy, Cros Jérôme, de Mestier Louis, Bachet Jean-Baptiste, Hammel Pascal
Department of Medical Oncology, CNRS UMR9020, Inserm UMR-S 1277-Canther-Cancer Heterogeneity, Plasticity and Resistance to Therapies, University Lille, CHU Lille, Lille, France.
Department of Medical Oncology, Curie Institute, Versailles Saint-Quentin University, Paris-Saclay University, Saint-Cloud, France.
Ther Adv Med Oncol. 2022 Sep 6;14:17588359221118019. doi: 10.1177/17588359221118019. eCollection 2022.
Mortality from pancreatic ductal adenocarcinoma (PDAC) is increasing worldwide and effective new treatments are urgently needed. The current treatment of metastatic PDAC in fit patients is based on two chemotherapy combinations (FOLFIRINOX and gemcitabine plus nab-paclitaxel) which were validated more than 8 years ago. Although almost all treatments targeting specific molecular alterations have failed so far when administered to unselected patients, encouraging results were observed in the small subpopulations of patients with germline mutations, and somatic gene fusions ( 1, which are enriched in KRAS wild-type PDAC), G12C mutations, or microsatellite instability. While targeted tumor metabolism therapies and immunotherapy have been disappointing, they are still under investigation in combination with other drugs. Optimizing pharmacokinetics and adapting available chemotherapies based on molecular signatures are other promising avenues of research. This review evaluates the current expectations and limits of available treatments and analyses the existing trials. A permanent search for actionable vulnerabilities in PDAC tumor cells and microenvironments will probably result in a more personalized therapeutic approach, keeping in mind that supportive care must also play a major role if real clinical efficacy is to be achieved in these patients.
在全球范围内,胰腺导管腺癌(PDAC)导致的死亡率正在上升,因此迫切需要有效的新治疗方法。目前,对于身体状况良好的转移性PDAC患者,治疗方案基于两种化疗联合方案(FOLFIRINOX和吉西他滨联合纳米白蛋白结合型紫杉醇),这两种方案在8年多以前就已得到验证。尽管迄今为止,几乎所有针对特定分子改变的治疗方法在应用于未经筛选的患者时均告失败,但在携带种系突变、体细胞基因融合(在KRAS野生型PDAC中富集)、G12C突变或微卫星不稳定性的小部分患者中观察到了令人鼓舞的结果。虽然靶向肿瘤代谢疗法和免疫疗法令人失望,但它们仍在与其他药物联合进行研究。优化药代动力学并根据分子特征调整现有化疗方案是其他有前景的研究途径。本综述评估了现有治疗方法的当前期望和局限性,并分析了现有试验。持续寻找PDAC肿瘤细胞和微环境中可操作的脆弱点可能会带来更个性化的治疗方法,同时要记住,如果要在这些患者中取得真正的临床疗效,支持性护理也必须发挥重要作用。