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首页> 外文期刊>Japanese journal of clinical oncology. >Impact of inflammatory marker levels one month after the first-line targeted therapy initiation on progression-free survival prediction in patients with metastatic clear cell renal cell carcinoma
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Impact of inflammatory marker levels one month after the first-line targeted therapy initiation on progression-free survival prediction in patients with metastatic clear cell renal cell carcinoma

机译:炎症标志物水平的影响在第一线靶向治疗后1个月在转移透明细胞肾细胞癌患者的无进展生存预测中

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Objectives: Progression-free survival of first-line targeted therapy greatly influences the survival of patients with metastatic renal cell carcinoma. We evaluated whether post-treatment inflammatory markers and lactate dehydrogenase levels had impacts on progression-free survival prediction in addition to those of conventional predictors. Methods: Two hundred and fifteen patients whose tumors were clear cell type and in whom first-line targeted therapies could be continued for >1 month were evaluated. Pretreatment clinical factors, pathological factors and laboratory data 1 month after targeted therapy initiation -including inflammatory markers (neutrophil count, neutrophil-to-lymphocyte ratio and C-reactive protein) and lactate dehydrogenase-were reviewed. To identify progression-free survival predictors, multivariate analyses were done. Results: The 1-year progression-free survival rate was 47%. Female gender, Karnofsky performance status <80%, time from diagnosis to systemic treatment <12 months, pretreatment C-reactive protein >3.0mg/dl and post-treatment neutrophil-to-lymphocyte ratio >3.0 were independent predictors for progression-free survival. In contrast, neither C-reactive protein increase nor neutrophil-to-lymphocyte ratio increase after targeted therapy initiation were independent predictors. Pretreatment lactate dehydrogenase, post-treatment lactate dehydrogenase and lactate dehydrogenase decline were not independent predictors. When all patients were stratified by these independent factors into three groups (0 risk vs. 1 or 2 risks vs. 3 or more risks), there were significant differences in progression-free survival rates between the groups (P < 0.0001). Furthermore, there were also significant differences in overall survival rates between the groups (P< 0.0001). Conclusions: Integration of post-treatment neutrophil-to-lymphocyte ratio value with pretreatment factors may lead to the establishment of effective predictive model for disease progression in patients with metastatic clear cell renal cell carcinoma who received first-line targeted therapies.
机译:目标:一线靶向治疗的无进展生存率极大地影响转移性肾细胞癌的患者的存活。除了传统预测因子之外,我们评估了治疗后炎症标记和乳酸脱氢酶水平是否对无进展的存活预测产生影响。方法:两百五十例患者,肿瘤是透明细胞类型,其持续持续的一线靶向疗法> 1个月。预处理临床因素,病理因素和实验室数据在靶向治疗开始后1个月 - 综述了炎症标志物(中性粒细胞计数,中性粒细胞对淋巴细胞比和C反应蛋白)和乳酸脱氢酶 - 综述。为了识别无进展的存活率,进行多变量分析。结果:1年的无进展生存率为47%。女性性别,Karnofsky性能状态<80%,从诊断到全身治疗<12个月,预处理C-反应蛋白> 3.0mg / d1和后治疗中性粒细胞到淋巴细胞比例> 3.0是无流动存活的独立预测因子。相反,在靶向治疗开始后,C反应性蛋白质增加也不是中性粒细胞对淋巴细胞比率增加。预处理乳酸脱氢酶,治疗后乳酸脱氢酶和乳酸脱氢酶下降不是独立的预测因子。当所有患者通过这些独立因素分层分为三组(0风险与1或2次风险,风险3或更多风险),组之间的无进展存活率存在显着差异(P <0.0001)。此外,在组之间的总存活率存在显着差异(P <0.0001)。结论:治疗后的中性粒细胞与淋巴细胞比例的融合因素可能导致在接受一线靶向疗法的转移细胞肾细胞癌患者中建立有效的疾病进展预测模型。

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