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Factors that predict chemotherapy-induced myelosuppression in lymphoma patients: role of the tumor necrosis factor ligand-receptor system.

机译:预测化疗诱导的淋巴瘤患者骨髓抑制的因素:肿瘤坏死因子配体-受体系统的作用。

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PURPOSE: To analyze factors that predict the occurrence of chemotherapy-induced myelosuppression and, in particular, the role of the tumor necrosis factor (TNF) ligand-receptor system in lymphoma patients at the beginning of their treatment. PATIENTS AND METHODS: We investigated the predictive factors for myelosuppression after the first course of chemotherapy in a cohort of 101 consecutive, previously untreated lymphoma patients receiving regimens that include doxorubicin and cyclophosphamide. Plasma samples were tested at baseline by enzyme-linked immunosorbent assay for TNF and its soluble receptors. Univariate and multivariate analyses were performed with a forward regression procedure that included all of the parameters that were found to be significant in the univariate analysis. The dose of chemotherapy and the prophylactic treatment with granulocyte colony-stimulating factor were deliberately included in this model. RESULTS: Sixty-seven patients experienced World Health Organization (WHO) grade 4 neutropenia, and 37 patients experienced febrile neutropenia, which was responsible for WHO grade 2 through 4 infections in 23 patients. In multiparametric regression analysis, the occurrence of grade 4 neutropenia was associated with high doses of cyclophosphamide (odds ratio OR, 19.8; P =.008) and high levels of soluble p75-R-TNF (OR, 8.52; P =.001). The duration of grade 4 neutropenia for more than 5 days was associated with the lack of hematopoietic growth factor administration (OR, 6.76; P =.004) and high levels of soluble p75-R-TNF (OR, 5.84; P =.0023). The occurrence of febrile neutropenia was associated with high doses of cyclophosphamide (OR, 4.7; P =.007), altered performance status (OR, 18.8; P <.0001) and high levels of soluble p75-R-TNF (OR, 3.49; P =.029). CONCLUSION: This study indicates that in addition to the dose of chemotherapy and the administration of hematopoietic growth factors, poor performance status and high p75-R-TNF levels can predict the occurrence of chemotherapy-induced myelosuppression in lymphoma patients. This model may help in selecting patients for prophylactic growth factor administration.
机译:目的:分析预测化疗诱导的骨髓抑制发生的因素,尤其是在治疗开始时淋巴瘤患者中肿瘤坏死因子(TNF)配体-受体系统的作用。病人和方法:我们在接受化疗(包括阿霉素和环磷酰胺)的101例连续未接受治疗的淋巴瘤患者队列中,研究了化疗首个疗程后骨髓抑制的预测因素。通过酶联免疫吸附测定法在血浆中检测血浆样品中的TNF及其可溶性受体。单变量和多变量分析使用正向回归程序执行,该程序包括在单变量分析中被认为重要的所有参数。该模型中刻意包括化疗剂量和粒细胞集落刺激因子的预防性治疗。结果:67名患者经历了世界卫生组织(WHO)的4级中性粒细胞减少症,37名患者经历了发热性中性粒细胞减少症,这是23名患者中2至4级WHO感染的原因。在多参数回归分析中,4级中性粒细胞减少症的发生与高剂量的环磷酰胺(比值比,OR,19.8; P = .008)和高水平的可溶性p75-R-TNF(OR,8.52; P = .001)相关。 。 4级中性粒细胞减少症持续时间超过5天与缺乏造血生长因子给药(OR,6.76; P = .004)和高水平的可溶性p75-R-TNF(OR,5.84; P = .0023)有关)。高热中性粒细胞减少症的发生与高剂量的环磷酰胺(OR,4.7; P = .007),行为状态改变(OR,18.8; P <.0001)和高水平的可溶性p75-R-TNF(OR,3.49)有关。 ; P = .029)。结论:这项研究表明,除了化学疗法的剂量和造血生长因子的使用外,不良的工作状态和高的p75-R-TNF水平还可以预测化学疗法引起的淋巴瘤患者骨髓抑制的发生。该模型可能有助于选择要预防性生长因子给药的患者。

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