Kos Mehmet, Hocazade Cemil, Kos F Tugba, Uncu Dogan, Karakas Esra, Dogan Mutlu, Uncu Hikmet Gulsen, Yildirim Nuriye, Zengin Nurullah
Department of Internal Medicine, Faculty of Medicine, Duzce University, Duzce, Turkey.
Department of Medical Oncology, Ankara Numune Education and Research Hospital, Ankara, Turkey.
Wien Klin Wochenschr. 2016 Sep;128(17-18):635-40. doi: 10.1007/s00508-015-0724-8. Epub 2015 Feb 27.
It was reported that hematological markers of systemic inflammatory response might be prognostic in various cancer types. We aimed to evaluate the platelet/lymphocyte ratio (PLR) as a prognostic factor and its effect on overall survival in non-small cell lung cancer (NSCLC).
Clinicopathological characteristics and basal (pretreatment) PLR of 145 patients with NSCLC were evaluated retrospectively. The preoperative or pretreatment blood count data were obtained from the recorded computerized database. PLR was defined as the absolute platelet count divided by the absolute lymphocyte count.
A total of 145 patients were enrolled. Median age was 57 years(range 26-83). Receiver operating characteristic curves for overall survival prediction were plotted to verify the optimum cut-off point for PLR. The recommended cut-off values for PLR was 198.2 with a sensitivity of 65.0 % and a specificity of 71.4 %. Median overall survival was 34.0 (95 % confidence interval (CI) 14.7-53.3) months in the group with low PLR (< 198.2), while it was 11.0 (95 % CI 5.6-16.3) months in the group with high PLR (≥ 198.2). The difference between the groups was statistically significant (p < 0.0001).
Our study supports the view that a high basal PLR is a poor prognostic factor in NSCLC. However, the validity of the cut-off values for PLR identified in our study needs further prospective trials.
据报道,全身炎症反应的血液学标志物可能对多种癌症类型具有预后价值。我们旨在评估血小板/淋巴细胞比值(PLR)作为非小细胞肺癌(NSCLC)预后因素及其对总生存期的影响。
回顾性评估145例NSCLC患者的临床病理特征和基础(治疗前)PLR。术前或治疗前血常规数据来自记录的计算机数据库。PLR定义为绝对血小板计数除以绝对淋巴细胞计数。
共纳入145例患者。中位年龄为57岁(范围26 - 83岁)。绘制总生存期预测的受试者工作特征曲线以验证PLR的最佳截断点。PLR的推荐截断值为198.2,敏感性为65.0%,特异性为71.4%。低PLR(<198.2)组的中位总生存期为34.0(95%置信区间(CI)14.7 - 53.3)个月,而高PLR(≥198.2)组为11.0(95%CI 5.6 - 16.3)个月。两组之间的差异具有统计学意义(p < 0.0001)。
我们的研究支持高基础PLR是NSCLC不良预后因素的观点。然而,我们研究中确定的PLR截断值的有效性需要进一步的前瞻性试验。