Puleo Francesco, Maréchal Raphaël, Demetter Pieter, Bali Maria-Antonietta, Calomme Annabelle, Closset Jean, Bachet Jean-Baptiste, Deviere Jacques, Van Laethem Jean-Luc
Francesco Puleo, Raphaël Maréchal, Annabelle Calomme, Jean Closset, Jacques Deviere, Jean-Luc Van Laethem, Department of Gastroenterology and Digestive Oncology, Erasme Hospital, 1070 Brussels, Belgium.
World J Gastroenterol. 2015 Feb 28;21(8):2281-93. doi: 10.3748/wjg.v21.i8.2281.
Pancreatic ductal adenocarcinoma (PDAC) is the fourth leading cause of cancer-related death in the industrialized world. Despite progress in the understanding of the molecular and genetic basis of this disease, the 5-year survival rate has remained low and usually does not exceed 5%. Only 20%-25% of patients present with potentially resectable disease and surgery represents the only chance for a cure. After decades of gemcitabine hegemony and limited therapeutic options, more active chemotherapies are emerging in advanced PDAC, like 5-Fluorouracil, folinic acid, irinotecan and oxaliplatin and nab-paclitaxel plus gemcitabine, that have profoundly impacted therapeutic possibilities. PDAC is considered a systemic disease because of the high rate of relapse after curative surgery in patients with resectable disease at diagnosis. Neoadjuvant strategies in resectable, borderline resectable, or locally advanced pancreatic cancer may improve outcomes. Incorporation of tissue biomarker testing and imaging techniques into preoperative strategies should allow clinicians to identify patients who may ultimately achieve curative benefit from surgery. This review summarizes current knowledge of adjuvant and neoadjuvant treatment for PDAC and discusses the rationale for moving from adjuvant to preoperative and perioperative therapeutic strategies in the current era of more active chemotherapies and personalized medicine. We also discuss the integration of good specimen collection, tissue biomarkers, and imaging tools into newly designed preoperative and perioperative strategies.
胰腺导管腺癌(PDAC)是工业化国家癌症相关死亡的第四大主要原因。尽管在了解这种疾病的分子和遗传基础方面取得了进展,但5年生存率仍然很低,通常不超过5%。只有20%-25%的患者表现为潜在可切除疾病,而手术是唯一的治愈机会。在吉西他滨占据主导地位且治疗选择有限数十年后,晚期PDAC出现了更有效的化疗方法,如5-氟尿嘧啶、亚叶酸、伊立替康和奥沙利铂以及纳米白蛋白结合型紫杉醇加吉西他滨,这些方法深刻影响了治疗可能性。由于诊断时可切除疾病患者在根治性手术后复发率很高,PDAC被认为是一种全身性疾病。可切除、临界可切除或局部晚期胰腺癌的新辅助治疗策略可能会改善治疗效果。将组织生物标志物检测和成像技术纳入术前策略应能使临床医生识别出最终可能从手术中获得治愈益处的患者。本综述总结了目前关于PDAC辅助和新辅助治疗的知识,并讨论了在当前更有效的化疗和个性化医疗时代从辅助治疗转向术前和围手术期治疗策略的基本原理。我们还讨论了将良好的标本采集、组织生物标志物和成像工具整合到新设计的术前和围手术期策略中。