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目的探讨D-二聚体水平在弥漫大B细胞淋巴瘤(DLBCL)患者中的预后意义。方法回顾性分析2015年1月至2019年6月天津市人民医院收治的70例初诊DLBCL患者的临床资料,根据受试者工作特征(ROC)曲线确定D-二聚体判断患者生存的最佳截断值,并将患者分组。比较不同D-二聚体水平患者间凝血相关指标及临床病理特征差异;采用Kaplan-Meier法对总生存(OS)进行单因素分析,采用Cox回归模型进行OS多因素分析。结果根据ROC曲线,D-二聚体判断患者生存的最佳截断值为0.75 mg/L。D-二聚体≥0.75 mg/L组(36例)和<0.75 mg/L组(34例)中不同临床分期、国际预后指数评分、乳酸脱氢酶水平的患者比例比较,差异均有统计学意义(均P<0.05);血浆凝血酶原时间分别为(13.5±0.9)s和(13.0±0.8)s,活化部分凝血活酶时间分别为(37±5)s和(34±6)s,差异均有统计学意义(均P<0.05)。单因素生存分析显示,Ann Arbor分期Ⅲ~Ⅳ期、国际预后指数评分>2分、乳酸脱氢酶水平>240 U/L、有B症状、D-二聚体水平≥0.75 mg/L DLBCL患者5年OS率均降低(均P<0.05)。多因素Cox回归分析显示,D-二聚体≥0.75 mg/L为DLBCL患者OS独立危险因素(HR=0.368,95%CI 0.144~0.944,P=0.038)。结论D-二聚体水平可作为判断DLBCL患者预后的临床指标,D-二聚体水平高患者预后不良。 相似文献
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Background
Diffuse large B-cell lymphoma (DLBCL) comprises 31% of lymphomas in the United States. Although it is an aggressive type of lymphoma, 40% to 50% of patients are cured with treatment. The study objectives were to identify patient factors associated with treatment and survival in DLBCL. 相似文献4.
目的 探讨细胞因子在弥漫大B细胞淋巴瘤(DLBCL)患者外周血中的水平及其临床意义.方法 采用免疫荧光法检测2013年4月至2017年1月安庆市立医院38例初诊DLBCL患者及20名健康体检者(对照组)外周血白细胞介素(IL)-1β、IL-2R、IL-6、IL-8、肿瘤坏死因子(TNF)及IL-10的表达水平.结果 DLBCL组IL-2R、IL-6、IL-8、TNF及IL-10水平均高于对照组,差异均有统计学意义(均P<0.05).DLBCL患者中,临床分期Ⅲ~Ⅳ期组IL-2R及TNF水平为(5985±26)U/ml、(42.2±5.8)pg/ml,高于Ⅰ~Ⅱ期组的(3672±28)U/ml、(30.4±2.6)pg/ml(t值分别为34.861、28.451,P值分别为0.023、0.038);高危组[国际预后指数(IPI)评分4~5分]IL-2R及IL-10水平为(6322±36)U/ml、(77±7)pg/ml,高于低危组(IPI 0~1分)的(2567±32)U/ml、(50±5)pg/ml(t值分别为58.327、24.264,P值分别为0.001、0.041);有B症状组IL-2R、IL-6及IL-10水平为(6234±26)U/ml、(38.1±2.3)pg/ml、(90±10)pg/ml,高于无B症状组的(3588±33)U/ml、(25.3±1.5)pg/ml、(54±5)pg/ml(t值分别为32.263、24.321、36.529,P值分别为0.027、0.043、0.020).结论 DLBCL患者IL-2R、IL-6、IL-8、TNF及IL-10水平均高于健康体检者,并且细胞因子的水平与DLBCL患者临床特征存在一定的相关性. 相似文献
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目的:分析初诊时伴有大肿块的弥漫性大B细胞淋巴瘤(diffuse large B-cell lymphoma,DLBCL)患者的临床特征与预后因素。方法:回顾性分析2018年1月至2021年9月郑州大学第一附属医院收治的194例大肿块DLBCL患者的临床资料,其中大肿块定义为肿瘤最大直径(maximum tumor diameter,MTD)≥7.5 cm,根据大肿块所在部位将患者分为:腹盆腔组、胸腔组、头颈部组。结果:194例大肿块DLBCL患者中位总生存(median overall survival,mOS)期为16(0~50)个月,患者1、3年总生存(overall survival,OS)率分别为75.6%、66.2%。1、3年无进展生存(progression-free survival,PFS)率分别为55.9%和44.1%。患者一线治疗后达到完全缓解(complete response, CR)、部分缓解(partial response,PR)、疾病稳定(stable disease,SD)、疾病进展(progressive disease,PD)分别为45例(23.... 相似文献
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目的 探讨原发性乳腺弥漫性大B细胞淋巴瘤(PB-DLBCL)的临床特征、诊断和治疗。方法 回顾性分析2010年1月至2015年11月13例PB-DLBCL患者的临床资料。13例均接受手术治疗,其中4例行乳腺癌改良根治术,1例行单侧乳腺切除术,8例行乳腺肿块切除术。结果 13例均为女性,6例发生于右乳,6例发生于左乳,1例发生于双乳。肿块大小1.5 cm~8.0 cm。术前2例诊断为乳腺纤维腺瘤,1例诊断为巨纤维瘤,10例诊断为乳腺癌。13例患者均经免疫组化检测确诊为PB-DLBCL。Ann Arbor分期:Ⅰ期10例,Ⅱ期3例。12例术后给予CHOP或R-CHOP方案化疗,1例放弃治疗。随访1个月~5年,2例复发,2例死亡,其余病例均无复发生存。结论 PB-DLBCL临床少见,多见于女性。术前检查、术中冰冻病理检查易误诊,免疫组化检查可明确诊断。治疗采用以化疗为主的综合治疗。 相似文献
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Min Zhou Jing Wang Jian Ouyang Jing-yan Xu Bing Chen Qi-guo Zhang Rong-fu Zhou Yong-gong Yang Xiao-yan Shao Yong Xu Ya-mei Chen Xiang-shan Fan Hong-yan Wu 《Tumour biology》2014,35(7):6757-6762
This study aims to investigate the prognostic significance of the MYC protein expression in diffuse large B cell lymphoma (DLBCL) patients treated with RCHOP (rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone). A total of 60 patients with DLBCL from 2008 to 2013 were included. Formalin-fixed, paraffin-embedded DLBCL samples were analyzed for MYC protein expression and divided into high or low MYC group. The MYC protein expression and the international prognostic variables were evaluated. The high MYC protein expression predicted a shorter 3-year estimated overall survival (OS) and progression-free survival (PFS) versus the low MYC protein expression (57 % vs. 96 %, P?<?0.001 and 50 % vs. 96 %, P?=?0.001, respectively). Multivariate analysis confirmed the prognostic significance of the MYC protein expression for both OS (HR, 11.862; 95 % CI, 1.462–96.218; P?=?0.021) and PFS (HR, 6.073; 95 % CI, 1.082–34.085; P?=?0.040). MYC protein expression with International Prognostic Index (IPI) score distinguished patients into three risk groups with different 3-year OS rates (χ 2 23.079; P?<?0.001) and distinct 3-year PFS rates (χ 2 15.862; P?<?0.001). This study suggests that the MYC protein expression is an important inferior prognostic factor for survival in patients with DLBCL treated with RCHOP. The combinative model with IPI score and MYC protein expression could stratify DLBCL patients into prognostically relevant subgroups more effectively than either the IPI or the MYC alone. 相似文献
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Gascoyne RD 《Current opinion in oncology》2004,16(5):436-441
PURPOSE OF REVIEW: Diffuse large B cell lymphoma (DLBCL) is the most common lymphoma subtype, characterized by marked clinical and biologic heterogeneity. Gene expression studies together with new monoclonal antibody production are playing an increasing role in determining important prognostic factors/biomarkers predictive of outcome. Despite these technical advances, much confusion exists in the literature as to what constitutes the important biomarkers for determining patient outcome. The purpose of this review is to highlight recent advances in our understanding of novel biomarkers in DLBCL and how these might be incorporated into current risk-adjustment models for prognosis. RECENT FINDINGS: Microarray gene expression analyses have revolutionized our approach to biomarkers in non-Hodgkin lymphomas. Thousands of genes can now be simultaneously analyzed for individual patients, creating a wealth of new data. This has resulted in an improved understanding of the basic biology, as well as the development of new outcome predictors. Monoclonal antibody reagents for some of these biomarkers already exist, allowing for their rapid validation at the level of protein expression and potential clinical translation. SUMMARY: A molecular classification of DLBCL is a current reality, and together with routine morphology, immunophenotype, and molecular cytogenetics, has allowed us to more accurately subclassify DLBCL and determine clinically relevant subgroups. The time is right to begin to consider how these novel biomarkers should be incorporated into current prognostic models to move beyond the clinically based International Prognostic Index 相似文献
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PIM1表达与弥漫大B细胞淋巴瘤患者预后的关系 总被引:2,自引:0,他引:2
背景与目的:Pim1是一种原癌基因,具有抑制肿瘤细胞凋亡、促进肿瘤细胞增殖的功能.本研究旨在探讨PIM1蛋白与原发性弥漫大B细胞淋巴瘤(diffuse large B-cell lymphoma,DLBCL)预后的关系.方法:采用免疫组化方法评估53例初治原发性DLBCL患者的PIM1表达,回顾性分析PIM1的表达与化疗反应性和总生存的关系.结果:PIM1蛋白高表达与DLBCL的负性预后相关,且它的表达与非生发中心的表型相关(r=0.404,P=0.003).PIM1蛋白高表达患者的3年总生存率和化疗完全缓解率均比低表达者低,差异有统计学意义(29.2%vs62.1%:29.2%vs 68.9%,P<0.001和P=0.006).PIM1和国际预后指数(international prognostic index,IPI)的多因素分析表明,PIM1是总生存独立的预后因素(P=0.013).单因素Logistic回归分析表明,PIM1的表达与化疗的完全缓解率呈负相关.结论:在DLBCL患者中,PIM1的高表达可以作为一个临床预后不良标志. 相似文献
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目的 探讨Y-盒结合蛋白(YB-1)在弥漫性大B细胞淋巴瘤(DLBCL)中表达及其临床意义。方法 采用Envision两步法检测50例DLBCL和10例反应性淋巴结增生(RLH)患者石蜡标本中YB-1与增生细胞核抗原(PCNA)的表达,分析YB-1表达与临床参数及PCNA表达的关系。结果 DLBCL组与RLH组的YB-1胞质阳性表达率差异无统计学意义(P>0.05),而DLBCL组的YB-1胞核阳性表达率明显高于RLH组(P<0.05);DLBCL临床Ⅲ~Ⅳ期患者的YB-1胞核阳性表达率明显高于Ⅰ~Ⅱ期(P<0.05);结外淋巴组织侵犯组的YB-1胞核阳性表达率明显高于结内病变组(P<0.05);骨髓浸润组的YB-1胞核阳性表达率显著高于无骨髓浸润组(P<0.05);YB-1的胞核阳性表达与PCNA积分呈正相关(P<0.05);化疗无效组的YB-1核阳性表达率及PCNA积分均明显高于化疗有效组(P<0.05)。结论 YB-1的核阳性表达可能参与了肿瘤的发生;YB-1核阳性表达与肿瘤的高侵袭力及肿瘤细胞的高增生能力密切相关,提示患者预后不良。 相似文献
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《Cancer cell》2021,39(10):1305-1307
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弥漫大B细胞淋巴瘤(DLBCL)是最常见的成人非霍奇金淋巴瘤。现阶段利妥昔单抗与CHOP方案的联合应用已显著改善了DLBCL的预后,约50%的DLBCL可以治愈。然而由于肿瘤的异质性,对于难治、复发的DLBCL仍然缺乏行之有效的治疗方法。随着基因表达谱(GEP)的运用以及对淋巴瘤细胞内活化信号途径的深入研究,发现了很多潜在的治疗靶点。 相似文献
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Cao Y Shi YX Chen JO Tan YT Cai YC Luo HY Qiu MZ Cai XY Jin Y Sun YL Jiang WQ 《Tumour biology》2012,33(4):1039-1044
C-reactive protein (CRP) is an acute-phase reactant that is a promising biomarker in patients with cancer of many kinds. The aim of this retrospective study was to evaluate significant changes in CRP levels as a parameter for the response effect and long-term survival of patients with diffuse large B cell lymphoma (DLBCL). Serum CRP data were collected in 94 patients with DLBCL from October 2006 to August 2009 in Cancer Center, Sun Yat-Sen University. Results were correlated with clinical data. The median CRP serum level in patients with DLBCL was 30.91 ± 53.35 in male and 22.39 ± 29.89 mg/L in female. Base line CRP levels were correlated with International Prognostic Index (IPI) scores (p = 0.03). Among the patients with an IPI score of 1-2, base line CRP levels were correlated with long-term survival (p = 0.001). Base line CRP levels were also correlated with OS (p = 0.001) and varied with different clinical stages (p = 0.03). The corresponding CRP levels in the patients with 2 cycles of chemotherapy were correlated with short-term treatment response (p = 0.003) and OS (p = 0.04) or TTP (p = 0.03). CRP serum levels can be used as additional prognostic parameter in patients with diffuse large B cell type lymphoma. 相似文献