Medical Oncology, Curie Institute, Versailles Saint-Quentin University, Saint-Cloud, France; Medical Oncology, Henri Mondor University Hospital, AP-HP, Créteil, France.
Division of Medical Oncology, Department of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena, Italy.
Eur J Cancer. 2019 Apr;111:94-106. doi: 10.1016/j.ejca.2019.01.019. Epub 2019 Mar 1.
The benefit of second-line chemotherapy (L2) over standard first-line (L1) gemcitabine plus cisplatin (GEMCIS) or oxaliplatin (GEMOX) chemotherapy in advanced biliary tract cancer (aBTC) is unclear. Our aim was to identify and validate prognostic factors for overall survival (OS) with L2 in aBTC to guide clinical decisions in this setting.
We performed a retrospective analysis of four prospective patient cohorts: a development cohort (28 French centres) and three validation cohorts from Italy, UK and France. All consecutive patients with aBTC receiving L2 after GEMCIS/GEMOX L1 between 2003 and 2016 were included. The association of clinicobiological data with OS was investigated in univariate and multivariate Cox analyses. A simple score was derived from the multivariate model.
The development cohort included 405 patients treated with L1 GEMOX (91%) or GEMCIS. Of them, 55.3% were men, and median age was 64.8 years. Prior surgical resection was observed in 26.7%, and 94.8% had metastatic disease. Performance status (PS) was 0, 1 and 2 in 17.8%, 52.4% and 29.7%, respectively. Among 22 clinical parameters, eight were associated with OS in univariate analysis. In multivariate analysis, four were independent prognostic factors (p < 0.05): PS, reason for L1 discontinuation, prior resection of primary tumour and peritoneal carcinomatosis. The model had the Harrell's concordance index of 0.655, a good calibration and was validated in the three external cohorts (N = 392).
We validated previously reported predictive factors of OS with L2 and identified peritoneal carcinomatosis as a new pejorative factor in nearly 800 patients. Our model and score may be useful in daily practice and for future clinical trial design.
二线化疗(L2)相对于标准一线(L1)吉西他滨联合顺铂(GEMCIS)或奥沙利铂(GEMOX)化疗在晚期胆道癌(aBTC)中的优势尚不清楚。我们的目的是确定并验证 L2 治疗 aBTC 患者总生存期(OS)的预后因素,以指导该人群的临床决策。
我们对四个前瞻性患者队列进行了回顾性分析:一个开发队列(28 个法国中心)和来自意大利、英国和法国的三个验证队列。所有在 2003 年至 2016 年期间接受 L1 GEMCIS/GEMOX 治疗后接受 L2 治疗的 aBTC 连续患者均被纳入本研究。采用单因素和多因素 Cox 分析研究临床生物学数据与 OS 的相关性。从多因素模型中得出一个简单的评分。
开发队列包括 405 例接受 L1 GEMOX(91%)或 GEMCIS 治疗的患者。其中,55.3%为男性,中位年龄为 64.8 岁。26.7%的患者接受过手术切除,94.8%的患者为转移性疾病。17.8%、52.4%和 29.7%的患者的体能状态(PS)分别为 0、1 和 2。在 22 个临床参数中,8 个与 OS 相关(单因素分析)。多因素分析中,有 4 个是独立的预后因素(p<0.05):PS、L1 停药原因、原发肿瘤切除和腹膜转移。该模型的 Harrell 一致性指数为 0.655,具有良好的校准度,并在三个外部队列(N=392)中得到验证。
我们验证了以前报道的与 L2 治疗 OS 相关的预测因素,并发现腹膜转移是近 800 例患者中一个新的预后不良因素。我们的模型和评分可能在日常实践和未来的临床试验设计中有用。