Boddu Prajwal, Villlines Dana, Aklilu Mebea
Department of Internal Medicine, Advocate Illinois Masonic Medical Center, Chicago, IL 60657, USA.
Department of Clinical Research, Advocate Illinois Masonic Hospital, Chicago, IL 60657, USA.
Zhongguo Fei Ai Za Zhi. 2016 Nov 20;19(11):725-730. doi: 10.3779/j.issn.1009-3419.2016.11.02.
Search for inexpensive laboratory markers have identified associations between blood counts and lung cancer outcomes. In this study, we evaluated the prognostic value of paraneoplastic leukocytosis (p-Leukocytosis) and paraneoplastic thrombocytosis (p-Thrombocytosis) in patients with non-small cell lung cancer (NSCLC). We also studied their relation to the expression of commonly detected molecular markers.
We conducted a retrospective chart review on 571 consecutive NSCLC patients over a 10 year period. Blood counts were recorded at the time of cancer diagnosis. survival curves were used to compare overall survival (OS) between patients with and without p-Leukocytosis (or) p-Thrombocytosis (p-Leuko/Thrombocytosis). regression was used to determine if leukocytosis/thrombocytosis was a predictor of OS in NSCLC.
Patients with p-Leukocytosis and p-Thrombocytosis had a significantly poorer survival compared patients with normal blood counts ( < 0.001). In a multivariate survival analysis, both continued to correlate even when adjusted for histology, gender, stage and chemotherapy ( < 0.01, 0.03 respectively). Stage Ⅰ and Ⅱ NSCLC with p-Leuko/Thrombocytosis did not perform poorly compared to stage Ⅰ/Ⅱ NSCLC patients without paraneoplasia. Patients with the combined leukothrombocytosis syndrome did not have worse outcomes compared to those with either paraneoplastic syndrome alone.
p-Leuko/Thrombocytosis is an accessible laboratory parameter of prognostic value in NSCLC. Evidence of p-Leuko/Thrombocytosis portends poor survival. The role of various cytokines in tumor pathobiology provides a rationale for identifying cytokine factors responsible for the paraneoplasia and administering anti-cytokine therapies alongside traditional chemotherapy in an attempt to improve survival outcomes in these subset of patients.
寻找廉价的实验室标志物已确定血细胞计数与肺癌预后之间的关联。在本研究中,我们评估了副肿瘤性白细胞增多(p - 白细胞增多)和副肿瘤性血小板增多(p - 血小板增多)在非小细胞肺癌(NSCLC)患者中的预后价值。我们还研究了它们与常见检测分子标志物表达的关系。
我们对连续10年的571例NSCLC患者进行了回顾性病历审查。在癌症诊断时记录血细胞计数。生存曲线用于比较有和无p - 白细胞增多(或)p - 血小板增多(p - 白细胞/血小板增多)患者的总生存期(OS)。回归分析用于确定白细胞增多/血小板增多是否为NSCLC患者OS的预测指标。
与血细胞计数正常的患者相比,p - 白细胞增多和p - 血小板增多的患者生存期明显更差(P < 0.001)。在多因素生存分析中,即使在调整了组织学、性别、分期和化疗后,两者仍具有相关性(分别为P < 0.01,P < 0.03)。与无副肿瘤的Ⅰ/Ⅱ期NSCLC患者相比,伴有p - 白细胞/血小板增多的Ⅰ期和Ⅱ期NSCLC患者预后并不差。合并白细胞血小板增多综合征的患者与单独患有任一副肿瘤综合征的患者相比,预后并无更差。
p - 白细胞/血小板增多是NSCLC中具有预后价值的可获取实验室参数。p - 白细胞/血小板增多的证据预示着生存期较差。各种细胞因子在肿瘤病理生物学中的作用为识别导致副肿瘤的细胞因子以及在传统化疗的同时给予抗细胞因子治疗以改善这些患者亚组的生存结局提供了理论依据。