Cakar B, Karaoglanoglu M, Sayici Y, Gonullu Demirag G, Yucel I
Ege University Medical Faculty, Tulay Aktas Oncology Hospital, Department of Medical Oncology, Izmir, Turkey.
J BUON. 2011 Oct-Dec;16(4):677-81.
The importance of thrombocyte count as a prognostic factor has not been adequately investigated in patients with lung cancer. We retrospectively examined the value of thrombocytosis as a prognostic factor and investigated its relationship with other clinicopathologic factors and survival.
The medical records of 260 patients with lung cancer were reviewed. Pretreatment thrombocyte count, histopathological diagnosis, disease stage, gender, age, performance status (PS), thrombotic episodes, weight loss and paraneoplastic syndromes were recorded. Overall survival (OS), progression-free survival (PFS) and disease-free survival (DFS) were evaluated in all patient subgroups. Thrombocytosis was defined as platelet count >400,000/μl. We assessed statistically the possible correlation between thrombocytosis, other clinicopathologic factors and survival parameters. A two-sided p value < 0.05 was considered significant.
There were no statistically significant differences between histological subgroups (small cell/SCLC and non-small cell/NSCLC) according to age, disease stage and gender. Sixty-six (25.38%) patients had thrombocytosis before starting treatment. We found no relationship between thrombocytosis and disease stage, gender, age, PS and thrombotic episodes. Thrombocytosis was significantly correlated only with weight loss (p=0.011) and paraneoplastic syndromes (p=0.027). OS was shorter in the thrombocytosis group, but without statistical significance. PFS and DFS did not differ between thrombocytemic and non-thrombocytemic patients.
Pretreatment thrombocytosis is not an independent prognostic factor of survival in lung cancer patients and is related with paraneoplastic syndromes.
血小板计数作为肺癌患者预后因素的重要性尚未得到充分研究。我们回顾性地研究了血小板增多作为预后因素的价值,并探讨了其与其他临床病理因素及生存率的关系。
回顾了260例肺癌患者的病历。记录了治疗前的血小板计数、组织病理学诊断、疾病分期、性别、年龄、体能状态(PS)、血栓形成事件、体重减轻和副肿瘤综合征。对所有患者亚组评估总生存期(OS)、无进展生存期(PFS)和无病生存期(DFS)。血小板增多定义为血小板计数>400,000/μl。我们对血小板增多、其他临床病理因素和生存参数之间的可能相关性进行了统计学评估。双侧p值<0.05被认为具有显著性。
根据年龄、疾病分期和性别,组织学亚组(小细胞/SCLC和非小细胞/NSCLC)之间无统计学显著差异。66例(25.38%)患者在开始治疗前有血小板增多。我们发现血小板增多与疾病分期、性别、年龄、PS和血栓形成事件之间无关联。血小板增多仅与体重减轻(p=0.011)和副肿瘤综合征(p=