Department of Radiation Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Sun Yat-sen University Cancer Center, Guangzhou 510060, Guangdong Province, China.; Department of Radiation Oncology, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, Guangdong Province 519001, China..
Department of Radiation Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Sun Yat-sen University Cancer Center, Guangzhou 510060, Guangdong Province, China.
Clin Chim Acta. 2018 Sep;484:314-319. doi: 10.1016/j.cca.2018.05.058. Epub 2018 May 31.
We evaluated the prognostic value of serum bilirubin in advanced nasopharyngeal carcinoma (NPC) patients.
Seven-hundred fifty-nine advanced NPC patients treated with definitive chemoradiotherapy were retrospectively analyzed. Serum indirect bilirubin (IBIL) and direct bilirubin (DBIL) were measured before treatment. To evaluate different cutoff points for serum bilirubin, we utilized ROC curves. The Kaplan-Meier method and log-rank test were adopted to calculate and compare survival outcomes. Cox proportional hazard models were used to perform univariate and multivariate analyses.
At 5 y, IBIL >7.15 μmol/l were significantly associated with superior progression-free survival (PFS, 83.6% vs 70.3%; P < .001), overall survival (OS, 88.6% vs 80.5%; P = .012), distant metastasis-free survival (DMFS, 90.3% vs 82.8%; P = .006), and locoregional relapse-free survival (LRFS, 92.1% vs 86.4%; P = .048) than IBIL ≤7.15 μmol/l. Similarly, patients with DBIL >2.65 μmol/l had better prognosis across all outcomes than those of patients with DBIL ≤2.65 μmol/l (all P < .05), except no difference was observed in LRFS (90.5% vs. 87.3%, P = .195). Multivariate analyses showed that IBIL >7.15 μmol/l was an independent protective prognostic factor for PFS (HR, 0.57; 95% CI, 0.40-0.81; P = .002), OS (HR, 0.67; 95% CI, 0.43-0.92; P = .041), and DMFS (HR, 0.63; 95% CI, 0.40-0.98; P = .034); while serum DBIL only remained significant for PFS (HR, 0.63; 95% CI, 0.44-0.89; P = .009).
Pretreatment IBIL and DBIL are potentially independent prognostic factors for patients with advanced NPC.
我们评估了血清胆红素在晚期鼻咽癌(NPC)患者中的预后价值。
回顾性分析了 759 例接受根治性放化疗的晚期 NPC 患者。治疗前检测血清间接胆红素(IBIL)和直接胆红素(DBIL)。为了评估血清胆红素的不同截断值,我们利用 ROC 曲线。采用 Kaplan-Meier 方法和对数秩检验计算和比较生存结果。采用 Cox 比例风险模型进行单因素和多因素分析。
5 年时,IBIL>7.15μmol/L 与无进展生存(PFS,83.6%比 70.3%;P<.001)、总生存(OS,88.6%比 80.5%;P=.012)、无远处转移生存(DMFS,90.3%比 82.8%;P=.006)和无局部区域复发生存(LRFS,92.1%比 86.4%;P=.048)显著相关。同样,DBIL>2.65μmol/L 的患者在所有结局方面的预后均优于 DBIL≤2.65μmol/L 的患者(所有 P<.05),但在 LRFS 方面无差异(90.5%比 87.3%,P=.195)。多因素分析显示,IBIL>7.15μmol/L 是 PFS(HR,0.57;95%CI,0.40-0.81;P=.002)、OS(HR,0.67;95%CI,0.43-0.92;P=.041)和 DMFS(HR,0.63;95%CI,0.40-0.98;P=.034)的独立保护预后因素;而血清 DBIL 仅对 PFS 有显著意义(HR,0.63;95%CI,0.44-0.89;P=.009)。
治疗前 IBIL 和 DBIL 可能是晚期 NPC 患者的独立预后因素。