pSTAT3、pAKT1表达与弥漫性大b细胞淋巴瘤患者生存的关系

E. Vaneeva, Ванеева Елена Викторовна, V. Rosin, Росин Виталий Анатольевич, D. Dyakonov, Дьяконов Дмитрий Андреевич, S. Samarina, Самарина Светлана Валерьевна
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摘要

的目标。评估肿瘤细胞中pSTAT3、pACT1的分离表达和联合表达与弥漫大b细胞淋巴瘤(DLBCL)患者生存的关系。方法。该研究包括100名首次诊断为弥漫性大b细胞淋巴瘤的患者,这些患者于2010年至2018年期间在该研究所的诊所观察到,接受了标准的一线R-CHOP(利妥昔单抗+环磷酰胺、阿霉素、长春新碱和泼尼松)化疗。通过免疫组织化学和形态计量学方法测定表达pSTAT3和pAKT1 -肿瘤细胞的相对数量。通过受试者工作特征(ROC)曲线分析,pSTAT3在肿瘤细胞上的最佳表达截止水平为68%,pACT1 - 70%。根据这些值,将所有DLBCL患者分为生物标志物高表达度组和低表达度组。结果,53例患者被纳入pSTAT3高表达组(≥68%肿瘤细胞),47例患者被纳入pSTAT3低表达组(<68%肿瘤细胞)。Spearman相关系数用于检验相关关系。用Kaplan-Meier曲线估计总生存期和无事件生存期。组间比较采用log-rank检验。结果。pSTAT3高表达组的5年总生存率为55%,低表达组为87%,p=0.015。pSTAT3高表达组无事件生存率为43%,低表达组为66%,p=0.011。高水平的pACT1表达对5年总生存率和无事件生存率有统计学意义(p <0.001和p=0.003)。pACT1低表达组和高表达组的总生存率分别为81%和43%,无事件生存率分别为64%和41%。此外,与рАКТ1 - / stat3 -(低水平)组相比,рАКТ1+/ stat3 +(高水平)共表达的患者的总体生存率和无事件生存率极低(p=0.001;p < 0.001)。结论。pSTAT3和pAKT1生物标志物可作为弥漫性大b细胞淋巴瘤的附加预后标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of expression of pSTAT3, pAKT1 with the survival of patients with diffuse large B-cell lymphoma
Aim. To assess the relationship between isolated and combined expression of pSTAT3, pACT1 in tumor cells with the survival of patients with diffuse large B-cell lymphoma (DLBCL). Methods. The study included 100 patients with the first diagnosed diffuse large B-cell lymphoma, observed in the institute's clinic between 2010 and 2018 who received standard first-line R-CHOP (rituximab + cyclophosphamide, doxorubicin, vincristine and prednisone) chemotherapy. The relative number of expressing pSTAT3 and pAKT1 ­tumor cells was determined by using immunohistochemical and morphometric methods. The optimal cut-off level of expression on tumor cells estimated by using receiver operating characteristic (ROC) curve analysis for pSTAT3 was 68% and for pACT1 — 70%. Given these values, all patients with DLBCL were divided into groups with a high and low degree of expression of the biomarkers. As a result, 53 patients were enrolled in the pSTAT3 high expression group (≥68% tumor cells) and 47 patients to the pSTAT3 low expression group (<68% tumor cells). Spearman’s correlation coefficient was used to examine relationships. Overall survival and event-free survival were estimated by Kaplan–Meier curves. The log-rank test was used for groups comparison. Results. The five-year overall survival rate in the pSTAT3 high expression group was 55% versus 87% in the low expression group, p=0.015. A significant difference was found in the assessment of event-free survival: 43% for the group of pSTAT3 high expression, 66% for the group of low expression, p=0.011. A statistically significant value of a high level of pACT1 expression was revealed for 5-year overall and event-free survival (p <0.001 and p=0.003). Overall survival rate was 81% for the pACT1 low expression group and 43% for the high expression group while event-free survival rate was 64 and 41%, respectively. Also, patients with рАКТ1+/рSTAT3+ (high level) co-expression had extremely low rates of overall and event-free survival rates compared with the рАКТ1–/рSTAT3– (low ­level) group (p=0.001; p <0.001). Conclusion. The pSTAT3 and pAKT1 biomarkers can be used as additional prognosis criteria for diffuse large B-cell lymphoma.
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