Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Int J Radiat Oncol Biol Phys. 2014 Aug 1;89(5):1084-1091. doi: 10.1016/j.ijrobp.2014.04.025. Epub 2014 Jul 8.
Radiation therapy (RT) can both suppress and stimulate the immune system. We sought to investigate the mechanisms underlying radiation-induced lymphopenia and its associations with patient outcomes in non-small cell lung cancer (NSCLC).
Subjects consisted of 711 patients who had received definitive RT for NSCLC. A lymphocyte nadir was calculated as the minimum lymphocyte value measured during definitive RT. Associations between gross tumor volumes (GTVs) and lung dose-volume histogram (DVH) parameters with lymphocyte nadirs were assessed with Spearman correlation coefficients. Relationships between lymphocyte nadirs with overall survival (OS) and event free survival (EFS) were evaluated with Kaplan-Meier analysis and compared with log-rank test results. Multivariate regressions were conducted with linear and Cox regression analyses. All variables were analyzed as continuous if possible.
Larger GTVs were correlated with lower lymphocyte nadirs regardless of concurrent chemotherapy receipt (with concurrent: r = -0.26, P<.0001; without: r = -0.48, P<.0001). Analyses of lung DVH parameters revealed significant correlations at lower doses (lung V5-V10: P<.0001) that incrementally decreased and became nonsignificant at higher doses (lung V60-V70: P>.05). Of note, no significant associations were detected between GTV and lung DVH parameters with total leukocyte, neutrophil, or monocyte nadirs during RT or with lymphocyte count prior to RT. Multivariate analysis revealed larger GTV (P<.0001), receipt of concurrent chemotherapy (P<.0001), twice-daily radiation fractionation (P=.02), and stage III disease (P=.05) to be associated with lower lymphocyte nadirs. On univariate analysis, patients with higher lymphocyte nadirs exhibited significantly improved OS (hazard ratio [HR] = 0.51 per 10(3) lymphocytes/μL, P=.01) and EFS (HR = 0.46 per 10(3) lymphocytes/μL, P<.0001). These differences held on multivariate analyses, controlling for common disease and treatment characteristics including GTV.
Lower lymphocyte nadirs during definitive RT were associated with larger GTVs and worse patient outcomes.
放射治疗(RT)既能抑制又能刺激免疫系统。我们试图研究放射诱导性淋巴细胞减少的机制及其与非小细胞肺癌(NSCLC)患者结局的关系。
本研究共纳入 711 例接受 NSCLC 根治性放疗的患者。淋巴细胞最低点定义为根治性放疗期间测量的最低淋巴细胞值。采用 Spearman 相关系数评估大体肿瘤体积(GTV)和肺剂量-体积直方图(DVH)参数与淋巴细胞最低点之间的相关性。采用 Kaplan-Meier 分析和对数秩检验结果评估淋巴细胞最低点与总生存期(OS)和无事件生存期(EFS)的关系。采用线性和 Cox 回归分析进行多变量回归。如果可能,所有变量均作为连续变量进行分析。
无论是否同步接受化疗,较大的 GTV 与较低的淋巴细胞最低点相关(同步化疗:r=-0.26,P<.0001;无同步化疗:r=-0.48,P<.0001)。肺 DVH 参数分析显示,在较低剂量(肺 V5-V10:P<.0001)下存在显著相关性,随着剂量增加,相关性逐渐降低,在较高剂量(肺 V60-V70:P>.05)下不再显著。值得注意的是,在放疗期间或放疗前,GTV 与肺 DVH 参数之间与总白细胞、中性粒细胞或单核细胞最低点或淋巴细胞计数之间均无显著相关性。多变量分析显示,较大的 GTV(P<.0001)、同步化疗(P<.0001)、每日两次放疗分割(P=.02)和 III 期疾病(P=.05)与较低的淋巴细胞最低点相关。单变量分析显示,淋巴细胞计数较高的患者具有显著改善的 OS(危险比[HR]每 103 个淋巴细胞/μL 降低 0.51,P=.01)和 EFS(HR 每 103 个淋巴细胞/μL 降低 0.46,P<.0001)。这些差异在多变量分析中仍然存在,控制了包括 GTV 在内的常见疾病和治疗特征。
根治性放疗期间较低的淋巴细胞最低点与较大的 GTV 相关,并与患者预后不良相关。