Sultana Asma, Cox Trevor, Ghaneh Paula, Neoptolemos John P
Department of Molecular and Clinical Cancer Medicine Centre, University of Liverpool, Liverpool, L69 3GA, UK.
Recent Results Cancer Res. 2012;196:65-88. doi: 10.1007/978-3-642-31629-6_5.
Pancreatic cancer is a challenging malignancy to treat, as less than one-fifth of diagnosed cases are resectable, surgery is complex and postoperative recovery slow, treated patients tend to relapse and overall survival rates are low. It is one of the leading causes of cancer-related mortality. Adjuvant therapy has been employed in resectable disease, to target micrometastases and improve prognosis. Chemotherapy, chemoradiotherapy (chemoRT) and chemoradiotherapy (chemoRT) followed on by chemotherapy have been evaluated in randomised controlled trials. The European Study Group for Pancreatic Cancer (ESPAC)-1 and CONKO-001 trials clearly established the survival advantage of adjuvant chemotherapy with 5 fluorouracil (5FU) plus folinic acid and gemcitabine respectively over no chemotherapy. The ESPAC-3 (version 2) trial demonstrated equivalence between 5FU plus folinic acid and gemcitabine in terms of survival parameters, though gemcitabine had a better toxicity profile. The results of these key studies, together with smaller ones have been subjected to meta-analyses, with confirmation of improved survival with adjuvant systemic chemotherapy. The EORTC-40891 and ESPAC-1 trials found no survival advantage with adjuvant chemoRT compared to observation, and this has been reflected in a subsequent meta-analysis. The popularisation of chemoRT, with follow on chemotherapy (versus observation) was based on the small underpowered GITSG trial. The ESPAC-1 trial was unable to find a survival benefit for chemoRT, with follow on chemotherapy compared to observation. The RTOG-9704 trial assessed chemoRT with follow on chemotherapy in both arms and found no difference between survival in the gemcitabine and 5FU arms. There has never been a published head-to-head randomised comparison of adjuvant chemotherapy to chemoRT, with follow on chemotherapy. Ongoing randomised trials are looking into adjuvant combination chemotherapy, chemotherapy with follow on chemoRT, and neoadjuvant therapy. Novel agents continue to be assessed in early phase trials with a major emphasis on predictive and prognostic biomarkers. Based on the available evidence, adjuvant chemotherapy with gemcitabine or 5FU/folinic acid is the current recommended gold standard in the management of resected pancreatic cancer.
胰腺癌是一种难以治疗的恶性肿瘤,因为不到五分之一的确诊病例可切除,手术复杂且术后恢复缓慢,接受治疗的患者容易复发且总体生存率较低。它是癌症相关死亡的主要原因之一。辅助治疗已用于可切除疾病,以针对微转移并改善预后。化疗、放化疗(chemoRT)以及放化疗后序贯化疗已在随机对照试验中进行了评估。欧洲胰腺癌研究组(ESPAC)-1和CONKO-001试验明确证实,分别使用5-氟尿嘧啶(5FU)加亚叶酸和吉西他滨进行辅助化疗比不进行化疗具有生存优势。ESPAC-3(第2版)试验表明,就生存参数而言,5FU加亚叶酸与吉西他滨相当,尽管吉西他滨的毒性特征更好。这些关键研究以及较小规模研究的结果已进行荟萃分析,证实辅助全身化疗可提高生存率。EORTC-40891和ESPAC-1试验发现,与观察相比,辅助放化疗没有生存优势,这在随后的荟萃分析中也得到了体现。放化疗并序贯化疗(与观察相比)的推广是基于规模小、效能不足的胃肠道肿瘤研究组(GITSG)试验。ESPAC-1试验未能发现放化疗并序贯化疗与观察相比有生存获益。RTOG-9704试验评估了双臂均采用放化疗并序贯化疗的情况,发现吉西他滨组和5FU组的生存率没有差异。辅助化疗与放化疗并序贯化疗从未有过公开的直接随机对照比较。正在进行的随机试验正在研究辅助联合化疗、化疗后序贯放化疗以及新辅助治疗。新型药物仍在早期试验中进行评估,主要侧重于预测性和预后生物标志物。基于现有证据,吉西他滨或5FU/亚叶酸辅助化疗是目前推荐的可切除胰腺癌管理的金标准。