Department of Hepato-gastroenterology, Groupe Hospitalier Pitié Salpêtrière, Paris.
Department of Digestive Surgery, Rouen University Hospital.
Curr Opin Oncol. 2020 Jul;32(4):356-363. doi: 10.1097/CCO.0000000000000639.
The modalities of management of resectable pancreatic ductal adenocarcinoma (PDAC) have evolved in recent years with new practice guidelines on adjuvant chemotherapy and results of randomized phase III trials. The aim of this review is to describe the state of the art in this setting and to highlight future possible perspectives.
Resectable PDAC is the tumor without vascular contact or a limited venous contact without vein irregularity. Several pathologic and biologic robust prognostic factors such as an R0 resection defined by a margin at least 1 mm have been validated. In phase III trials, the doublet gemcitabine-capecitabine provided a statistically significant, albeit modest overall survival benefit, but failed to show an improvement in relapse-free survival. Similarly, gemcitabine plus nab-paclitaxel did not increase disease-free survival. Modified FOLFIRINOX led to improved disease-free survival, overall survival, and metastasis-free survival, with acceptable toxicity. In the future, prognostic and/or predictive biomarkers could lead the optimization of therapeutic strategies and neoadjuvant treatment could become a standard of care in PDAC.
After curative intent resection, modified FOLFIRINOX is the standard of care in adjuvant in fit patients with PDAC. Others regimens (monotherapy or gemcitabine-based) are an option in unfit patients.
近年来,随着新的辅助化疗实践指南和随机 III 期试验结果的出现,可切除胰腺导管腺癌(PDAC)的治疗模式发生了变化。本综述的目的是描述这一领域的最新进展,并强调未来可能的前景。
可切除 PDAC 是指没有血管接触或仅有有限静脉接触且静脉无不规则的肿瘤。已经验证了几种病理和生物学上强有力的预后因素,如至少 1 毫米的边缘定义的 R0 切除。在 III 期试验中,吉西他滨-卡培他滨联合治疗方案提供了统计学上显著但适度的总生存获益,但未能显示无复发生存的改善。同样,吉西他滨加 nab-紫杉醇也不能提高无病生存期。改良 FOLFIRINOX 方案可改善无病生存期、总生存期和无转移生存期,且毒性可接受。在未来,预后和/或预测生物标志物可能会优化治疗策略,新辅助治疗可能成为 PDAC 的标准治疗方法。
在有治愈意图的手术后,改良 FOLFIRINOX 是适合患者的辅助治疗标准方案。其他方案(单药治疗或吉西他滨为基础的方案)是不适合患者的选择。