Department of Surgery, Cancer Center Amsterdam, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Department of Research and Development, Netherlands Comprehensive Cancer Organization (IKNL), Utrecht, The Netherlands.
Biomarkers. 2021 Jun;26(4):325-334. doi: 10.1080/1354750X.2021.1893814. Epub 2021 Mar 21.
Identification of metastatic pancreatic cancer (mPC) patients with the worst prognosis could help to tailor therapy. We evaluated readily available biomarkers for the prediction of 90-day mortality in a nationwide cohort of mPC patients.
Patients with synchronous mPC were included from the Netherlands Cancer Registry (2015-2017). Baseline CA19-9, albumin, CRP, LDH, CRP/albumin ratio, and (modified) Glasgow Prognostic Score ((m)GPS composed of albumin and CRP) were evaluated. Multivariable logistic regression analyses were performed to identify predictors of 90-day mortality. Prognostic value per predictor was quantified by Nagelkerke's partial R.
Overall, 4248 patients were included. Median overall survival was 2.2 months and 90-day mortality was 59.4% (n = 1629). All biomarkers predicted 90-day mortality in univariable analysis, and remained statistically significant after adjustment for clinically relevant factors and all other biomarkers (all < 0.001). The prognostic value of the biomarkers combined was similar to WHO performance status. Patients who received chemotherapy had better outcomes than those who did not, regardless of biomarker levels.
In mPC patients, albumin, CA19-9, CRP, LDH, CRP/albumin ratio, and (m)GPS are prognostic for poor survival. Biomarkers did not predict response to chemotherapy. These readily available biomarkers can be used to better inform patients and to stratify in clinical trials.
识别预后最差的转移性胰腺癌(mPC)患者有助于制定个体化治疗方案。我们评估了可用于预测全国性 mPC 患者 90 天死亡率的易于获得的生物标志物。
从荷兰癌症登记处(2015-2017 年)纳入同步性 mPC 患者。评估基线 CA19-9、白蛋白、CRP、LDH、CRP/白蛋白比值和(改良)格拉斯哥预后评分((m)GPS,由白蛋白和 CRP 组成)。采用多变量逻辑回归分析确定 90 天死亡率的预测因素。通过 Nagelkerke 的部分 R 来量化每个预测因素的预后价值。
共纳入 4248 例患者。总体中位生存时间为 2.2 个月,90 天死亡率为 59.4%(n=1629)。所有生物标志物在单变量分析中均预测 90 天死亡率,且在调整临床相关因素和所有其他生物标志物后仍具有统计学意义(均 < 0.001)。生物标志物联合的预后价值与世界卫生组织(WHO)表现状态相似。接受化疗的患者无论生物标志物水平如何,其预后均优于未接受化疗的患者。
在 mPC 患者中,白蛋白、CA19-9、CRP、LDH、CRP/白蛋白比值和(m)GPS 与生存不良相关。生物标志物不能预测化疗反应。这些易于获得的生物标志物可用于更好地告知患者,并在临床试验中进行分层。