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Serum cytokine profiles and metabolic tumor burden in patients with non-small cell lung cancer undergoing palliative thoracic radiation therapy

机译:血清细胞因子分布和非小细胞肺癌患者进行姑息胸部放射治疗患者的代谢肿瘤负担

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摘要

Purpose: Radiation therapy effectively kills cancer cells and elicits local effects in the irradiated tissue. The aim of this study was to investigate the kinetics of cytokines in the serum of patients with lung cancer undergoing radiation therapy and to identify associations with metabolic tumor burden as determined by 2-deoxy-2-fluoro-D-glucose (18F-FDG) positron emission tomography (PET). Methods and materials: Forty-five patients with advanced non-small cell lung cancer were included in a phase 2 clinical trial and randomized between fractionated thoracic radiation therapy alone or concurrent with an epidermal growth factor receptor inhibitor. Blood was sampled at 4 different time points: prior to treatment, midtherapy, at the end of therapy, and 6 to 8 weeks after the start of treatment. The serum concentrations of 48 cytokines and 9 matrix metalloproteinases were measured with multiplex immunoassays. A subset of patients was examined by 18F-FDG PET/computed tomography before, during, and after radiation therapy. The maximum standardized uptake values (SUVmax) of the primary lung tumor, whole-body metabolic tumor volume, and total lesion glycolysis were calculated, and correlations between the PET parameters and cytokines were investigated. Results: The SUVmax decreased from baseline through midtherapy to posttherapy 18F-FDG PET/computed tomography (P = .018). The serum levels of C-C motif chemokine ligand (CCL) 23, CCL24, C-X3-C motif chemokine ligand 1, and interleukin-8 (C-X-C motif ligand [CXCL]8) were significantly correlated to SUVmax, metabolic tumor volume, and total lesion glycolysis before, during, and after radiation therapy. CXCL2 (P = .030) and CXCL6 (P = .010) decreased after the start of therapy and changed significantly across the sample time points. Serum concentrations of CCL15 (P = .031), CXCL2 (P = .028), and interleukin-6 (P = .007) were positively correlated to the irradiated volume during the second week of treatment. Conclusions: Cytokine serum levels vary and correlate with metabolic tumor burden in patients with advanced non-small cell lung cancer undergoing palliative thoracic radiation therapy.
机译:目的:放射治疗有效杀死癌细胞,并引发在被照射的组织局部效应。本研究的目的是调查的肺癌患者的血清中的细胞因子进行放射治疗的动力学和由2-脱氧-2-氟 - d-葡萄糖测定,以识别与代谢肿瘤负荷协会(18F-FDG)正电子发射断层扫描(PET)。方法和材料:45只患有晚期非小细胞肺癌患者包括在2期临床试验和单独分馏胸部放射治疗或同时表皮生长因子受体抑制剂之间随机化。血液在4个不同的时间点进行取样:在治疗之前,midtherapy,在治疗结束时,和6至8周的治疗开始后。 48种细胞因子和9个基质金属蛋白酶的血清浓度与多重免疫测定。的患者的子集是通过18F-FDG PET /之前,计算机断层扫描期间,和放射治疗后检查。主肺肿瘤,全身代谢的肿瘤体积,和总损伤糖酵解的最大标准化摄取值(SUVmax值)进行了计算,并进行了调查的PET参数和细胞因子之间的相关性。结果:从SUVmax的基线降低通过midtherapy到足堪18F-FDG PET /计算机断层扫描(P = 0.018)。 CC基序趋化因子配体(CCL)23,CCL24的血清水平,C-X3-C基序趋化因子配体1,和白细胞介素-8(CXC基序配体[CXCL] 8)显著相关SUVmax的,代谢的肿瘤体积和总病变之前糖酵解,期间,和放射治疗后。 CXCL2(P = 0.030)和CXCL6(P = 0.010)治疗开始后减少,在样品的时间点显著改变。 CCL15(P = 0.031),CXCL2(P = 0.028)的血清浓度,和白细胞介素6(P = 0.007)在治疗的第二周呈正相关,使辐照体积。结论:细胞因子的血清水平变化,并与在晚期非小细胞肺癌发生姑息胸部放射治疗代谢肿瘤负荷相关联。

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