Department of Internal Medicine III and Comprehensive Cancer Center, Klinikum Grosshadern, Ludwig-Maximilians-University of Munich, Marchioninistr. 15, 81377 Munich, Germany.
J Cancer Res Clin Oncol. 2013 Apr;139(4):681-9. doi: 10.1007/s00432-012-1371-3. Epub 2013 Jan 13.
CA 19-9 is the only established tumor marker in pancreatic cancer (PC); the prognostic role of other serum markers like CEA, CRP, LDH or bilirubin has not yet been defined.
We pooled pre-treatment data on CA 19-9, CEA, CRP, LDH and bilirubin levels from two German multicenter randomized phase II trials together with prospective patient data from one high-volume German Cancer Center. Marker levels were assessed locally before the start of palliative first-line therapy for advanced PC and serially during treatment (for CA 19-9 only). Clinical and biomarker data (overall 12 variables) were correlated with the efficacy endpoints time-to-progression (TTP) and overall survival (OS) by using uni- and multivariate Cox models.
Data from 291 patients were included in this pooled analysis; 253 patients (87 %) received treatment within prospective clinical trials. Median TTP in the study cohort was 5.1 months and median OS 9.0 months. In univariate analysis, pre-treatment CA 19-9 (HR 1.55), LDH (HR 2.04) and CEA (HR 1.89) levels were significantly associated with TTP. Regarding OS, baseline CA 19-9 (HR 1.46), LDH (HR 2.07), CRP (HR 1.69) and bilirubin (HR 1.62) were significant prognostic factors. Within multivariate analyses, pre-treatment log [CA 19-9] (as continuous variable for TTP) and log [bilirubin] as well as log [CRP] (for OS) had an independent prognostic value. A CA 19-9 decline of ≥25 % during the first two chemotherapy cycles was predictive for TTP and OS, independent of the applied CA 19-9 assay.
Baseline CA 19-9 and CA 19-9 kinetics during first-line chemotherapy are prognostic in advanced PC. Besides that finding other serum markers like CRP, LDH and bilirubin can also provide prognostic information on TTP and OS.
CA 19-9 是胰腺癌(PC)中唯一确立的肿瘤标志物;其他血清标志物如 CEA、CRP、LDH 或胆红素的预后作用尚未确定。
我们将来自德国两个多中心随机二期临床试验的 CA 19-9、CEA、CRP、LDH 和胆红素的预处理数据与来自德国一个大容量癌症中心的前瞻性患者数据合并。在姑息性一线治疗晚期 PC 之前,在当地评估标志物水平,并在治疗期间进行连续评估(仅针对 CA 19-9)。使用单变量和多变量 Cox 模型,将临床和生物标志物数据(共 12 个变量)与疗效终点无进展生存期(TTP)和总生存期(OS)相关联。
本汇总分析纳入了 291 例患者的数据;253 例(87%)患者在前瞻性临床试验中接受了治疗。研究队列的中位 TTP 为 5.1 个月,中位 OS 为 9.0 个月。在单变量分析中,预处理 CA 19-9(HR 1.55)、LDH(HR 2.04)和 CEA(HR 1.89)水平与 TTP 显著相关。关于 OS,基线 CA 19-9(HR 1.46)、LDH(HR 2.07)、CRP(HR 1.69)和胆红素(HR 1.62)是显著的预后因素。在多变量分析中,预处理 log [CA 19-9](作为 TTP 的连续变量)和 log [胆红素]以及 log [CRP](用于 OS)具有独立的预后价值。在头两个化疗周期中 CA 19-9 下降≥25%可预测 TTP 和 OS,与所应用的 CA 19-9 检测无关。
基线 CA 19-9 和一线化疗期间的 CA 19-9 动力学在晚期 PC 中具有预后价值。除了这一发现,其他血清标志物如 CRP、LDH 和胆红素也可以提供 TTP 和 OS 的预后信息。