NIHR Liverpool Pancreas Biomedical Research Unit, Institute of Translational Medicine, Royal Liverpool University Hospital, United Kingdom.
Department of Medicine A, University Medicine Greifswald, Greifswald, Germany; Medical Department II, University Hospital, LMU, Munich, Germany.
Pancreatology. 2019 Jan;19(1):97-104. doi: 10.1016/j.pan.2018.10.003. Epub 2018 Oct 15.
Pancreatic ductal adenocarcinoma (PDAC) is associated with poor prognosis. Gemcitabine is the standard chemotherapy for patients with metastatic pancreatic adenocarcinoma (MPA). Randomized clinical trials evaluating intensified chemotherapies including FOLFIRINOX and nab-paclitaxel plus gemcitabine (NAB+GEM) have shown improvement in survival. Here, we have evaluated the efficacy of intensified chemotherapy versus gemcitabine monotherapy in real-life settings across Europe.
A retrospective multi-center study including 1056 MPA patients, between 2012 and 2015, from nine centers in UK, Germany, Italy, Hungary and the Swedish registry was performed. Follow-up was at least 12 months. Cox proportional Harzards regression was used for uni- and multivariable evaluation of prognostic factors.
Of 1056 MPA patients, 1030 (98.7%) were assessable for survival analysis. Gemcitabine monotherapy was the most commonly used regimen (41.3%), compared to FOLFIRINOX (n = 204, 19.3%), NAB+GEM (n = 81, 7.7%) and other gemcitabine- or 5-FU-based regimens (n = 335, 31.7%). The median overall survival (OS) was: FOLFIRINOX 9.9 months (95%CI 8.4-12.6), NAB+GEM 7.9 months (95%CI 6.2-10.0), other combinations 8.5 months (95%CI 7.7-9.3) and gemcitabine monotherapy 4.9 months (95%CI 4.4-5.6). Compared to gemcitabine monotherapy, any combination of chemotherapeutics improved the survival with no significant difference between the intensified regimens. Multivariable analysis showed an association between treatment center, male gender, inoperability at diagnosis and performance status (ECOG 1-3) with poor prognosis.
Gemcitabine monotherapy was predominantly used in 2012-2015. Intensified chemotherapy improved OS in comparison to gemcitabine monotherapy. In real-life settings, the OS rates of different treatment approaches are lower than shown in randomized phase III trials.
胰腺导管腺癌(PDAC)预后不良。吉西他滨是转移性胰腺腺癌(MPA)患者的标准化疗药物。随机临床试验评估了包括 FOLFIRINOX 和 nab-紫杉醇联合吉西他滨(NAB+GEM)在内的强化化疗的疗效,显示了生存的改善。在这里,我们评估了强化化疗与吉西他滨单药治疗在欧洲真实环境中的疗效。
这是一项回顾性多中心研究,纳入了 2012 年至 2015 年间来自英国、德国、意大利、匈牙利和瑞典登记处的 9 个中心的 1056 例 MPA 患者。随访时间至少 12 个月。Cox 比例风险回归用于单变量和多变量评估预后因素。
在 1056 例 MPA 患者中,有 1030 例(98.7%)可进行生存分析。吉西他滨单药治疗是最常用的方案(41.3%),其次是 FOLFIRINOX(n=204,19.3%)、NAB+GEM(n=81,7.7%)和其他吉西他滨或 5-FU 为基础的方案(n=335,31.7%)。中位总生存期(OS)为:FOLFIRINOX 9.9 个月(95%CI 8.4-12.6),NAB+GEM 7.9 个月(95%CI 6.2-10.0),其他联合方案 8.5 个月(95%CI 7.7-9.3),吉西他滨单药治疗 4.9 个月(95%CI 4.4-5.6)。与吉西他滨单药治疗相比,任何化疗联合方案均改善了生存,强化方案之间无显著差异。多变量分析显示,治疗中心、男性、诊断时无法手术和体能状态(ECOG 1-3)与预后不良相关。
2012-2015 年期间,吉西他滨单药治疗主要用于转移性胰腺腺癌(MPA)患者。强化化疗与吉西他滨单药治疗相比,可改善总生存期(OS)。在真实环境中,不同治疗方法的 OS 率低于随机 III 期试验结果。