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霍奇金病

霍奇金病的相关文献在1991年到2021年内共计210篇,主要集中在肿瘤学、内科学、临床医学 等领域,其中期刊论文205篇、会议论文3篇、专利文献54006篇;相关期刊114种,包括中华病理学杂志、中华血液学杂志、实用医学杂志等; 相关会议3种,包括中国抗癌协会临床肿瘤协作中心(CSCO)第七届学术年会、循证医学与临床实践-肿瘤治疗新进展论坛、中国抗癌协会临床肿瘤学协作中心第五届学术年会等;霍奇金病的相关文献由615位作者贡献,包括宋玉琴、赵彤、余子豪等。

霍奇金病—发文量

期刊论文>

论文:205 占比:0.38%

会议论文>

论文:3 占比:0.01%

专利文献>

论文:54006 占比:99.62%

总计:54214篇

霍奇金病—发文趋势图

霍奇金病

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  • 宋玉琴
  • 赵彤
  • 余子豪
  • 克晓燕
  • 周立强
  • 时云飞
  • 朱军
  • 刘翠苓
  • 周新华
  • 周春菊
  • 期刊论文
  • 会议论文
  • 专利文献

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    • 陶云霞; 石远凯
    • 摘要: 霍奇金淋巴瘤(HL)是一类可治愈性肿瘤.HL的治疗策略建立在分期及复发风险基础上.随着综合治疗模式不断优化,HL的预后得到极大改善.目前HL广泛使用的预后模型预测价值较前降低.因此,探索新的预后因素及丰富现有预后模型,为患者提供精准化及个体化治疗是HL重要的研究方向.文章就近年来HL预后因素研究进展进行综述.
    • 郭昆典; 林静芳; 洪桢
    • 摘要: cqvip:抗代谢型谷氨酸受体5 (metabotropic glutamate receptor 5,m GluR5)脑炎是一种罕见的自身免疫性脑炎,自LANCASTER等[1]2011年首次报告至今,国外仅报告了12例[2-5]。目前国内尚无抗mGluR5脑炎相关报告,本研究首次报告1例我国抗mGluR5脑炎并对其深入分析,以期提高临床医生对该病的认识。
    • 张蓉; 李国辉; 罗红香; 刘赞; 刘静; 徐静; 梁英民
    • 摘要: Objective To investigate the clinical value of mean platelet volume (MPV) in predicting sympomatic venous thromboembolism (VTE) in patients with newly diagnosed Hodgkin lymphoma (HL).Methods From January 2011 to December 2014,a number of 67 patients in the Department of Hematology,Xi'an High-tech Hospital and 100 patients in Department of Hematology,Tangdu Hospital,Air Force Military Medical Universityhwith who were newly diagnosed HL and treated with first-line chemotherapy were enrolled in this study.There were 77 male patients and 90 females,with the age of (42±15) years old.According to the diagnosis of symptomatic VTE within 1 year after discharging from hospital,the 167 patients were divided into VTE group (n=12) and non-VTE group (n=155).According to the cut-off value (MPV=6.8 fl) of pre-chemotherapy MPV in predicting risk of symptomatic VTE,the patients were divided into MPV<6.8 fl group (n =21) and MPV≥6.8 fl group (n=146).All patients were treated with standard first-line chemotherapy regimen of ABVD (doxorubicin +bleomycin + vincristine + dacarbazine).A retrospective method was performed to collect general clinical data and disease-related data from all HL patients,including Lugano classification,symptoms and signs,mediastinal involvement,international prognostic score (IPS),and Khorana risk score (KRS),as well as laboratory-related examination results,including hemoglobin (Hb) value,platelet count,and white blood cell count (WBC) before chemotherapy.All HL patients in this study were followed up by clinic or telephone,and the incidences of sympomatic VTE in the first year after discharging from hospital were recorded.The normal distributed data,such as age,was present as Mean± SD,and compared by independent-samples t test between 2 groups.The non-normal distributed data,such as pre-chemotherapy MPV,platelet count and WBC were presented as M (P25-P75),and compared by Mann-Whitney U test between 2 groups.The ratio of patient with different gender,extranodal organ involvement,systemic symptoms,mediastinal lymph node diameter≥ 10 cm,3-7 scores of IPS,3-4 scores of KRS,Hb value< 100 g/L,pre-chemotherapy platelet count>350 × 109/L,pre-chemotherapy WBC> 11 × 109/L were presented as percentage (%),and compared by chi-square test or continuous correction chi-square test between 2 groups.Predict value of pre-chemotherapy MPV for the risk of symptomatic VTE in patients with newly diagnosed HL within 1 year after receiving chemotherapy was assessed by the receiver operating characteristic (ROC) curve,ROC-area under curve (AUC) was calculated,and the optimal threshold was determined when the Youden index reaching the maximum value.The Kaplan-Meier method and Log-rank test were used to compare the non-symptomatic VTE survival rate and overall survival (OS) rate of all patients in different MPV groups.Multivariate Cox proportional hazard regression model was used to analyze the risk factors (exceptional organ involvement and pre-chemotherapy MPV) affecting the incidence of symptomatic VTE in patients with newly diagnosed HL.The procedure of this study was accordance with the requirement of the revised World Medical Association Declaration of Helsinki in 2013.And the informed consent form of the clinical study was signed by the patient or its guardian.Results ① Among 167 patients with newly diagnosed HL,the incidence of symptomatic VTE was 7.2% (12/167) within the first year of follow-up.In the VTE group,the proportion of patients with extranodal involvement (stage Lugano stage Ⅳ) was 66.7% (8/12),which was higher than that of 27.7% (43/155) in the non-VTE group,and the difference was statistically significant (x2 =7.955,P=0.005).Median MPV was 6.7 fl (6.3-7.0 fl) in VTE group,which was lower than that of 7.4 fl (7.1-7.8 fl) in non-VTE group,and the difference was statistically significant (U=3.489,P =0.001).② ROC curve analysis results showed that pre-chemotherapy MPV had predictive value for the risk of symptomatic VTE in patients with newly diagnosed HL,and its ROC-AUC was 0.697 (95%CI:0.476-0.884,P=0.022),and the optimal cut-off value of pre-chemotherapy MPV for symptomatic VTE risk in patients with newly diagnosed HL was 6.8 fl,with specificity of 91.6% and sensitivity of 66.7%.③ The incidence of symptomatic VTE in the MPV<6.8 fl group was 38.1% (8/21),which was higher than that of 2.7% (4/146) in the MPV≥6.8 fl group,and the difference was statistically significant (x2 =38.757,P<0.001).④ Kaplan-Meier survival curve analysis results showed that the non-symptomatic VTE survival rate of patients in MPV<6.8 fl group was significantly lower than that of patients with MPV≥ 6.8 fl (x2 =40.220,P<0.001),and the OS rate was significantly lower than that of MPV≥6.8 fl group (x2 =44.443,P<0.001).⑤ Multivariate Cox proportional hazard regression model analysis results showed that MPV<6.8 fl was an independent risk factor for the incidence of symptomatic VTE in patients with newly diagnosed HL (OR=1.673,95%CI:1.434-3.218,P=0.012).Conclusions The decrease MPV could effectively predict the increased risk of symptomatic VTE in patients with newly diagnosed HL,and provide effective guidance for clinical prevention and treatment of symptomatic VTE in patients with newly diagnosed HL.%目的 探讨平均血小板体积(MPV)预测初发霍奇金淋巴瘤(HL)患者发生症状性静脉血栓栓塞(VTE)的临床价值.方法 选择2011年1月至2014年12月,67例于西安高新医院血液科和100例于空军军医大学唐都医院血液科接受一线化疗方案治疗的初发HL患者为研究对象.其中,男性患者为77例,女性为90例;年龄为(42±15)岁.根据患者出院后随访1年内是否发生症状性VTE,将本研究167患者分为VTE组(n=12)和未发生VTE组(n=155);根据患者化疗前MPV预测发生症状性VTE风险的临界值(MPV=6.8 fl),将其分为MPV<6.8 fl组(n=21)和MPV≥6.8 fl组(n=146).所有患者均接受标准一线化疗方案ABVD(多柔比星+博莱霉素+长春新碱+达卡巴嗪)方案治疗.采用回顾性研究方法收集本研究167例初发HL患者的一般临床资料和疾病相关资料,包括Lugano分级、症状体征、纵隔受累、国际预后评分(IPS)和Khorana风险评分(KRS),以及实验室相关检查结果,包括化疗前血红蛋白(Hb)值、血小板计数及白细胞计数(WBC)等.本研究所有初发HL患者均通过门诊或电话进行随访,并且记录患者出院后第1年内症状性VTE发生情况.呈正态分布的计量资料年龄,采用x±s表示,2组比较采用成组t检验;呈非正态分布的计量资料,如化疗前MPV、血小板计数和WBC等,采用M(P25~P75)表示,2组比较采用Mann-Whitney U检验.患者性别、结外器官累及、全身症状、纵隔淋巴结直径≥10 cm、IPS为3~7分、KRS为3~4分、Hb值<100 g/L、化疗前血小板计数>350×109/L和化疗前WBC> 11×109/L的患者所占比例等计数资料,采用率(%)表示,2组比较采用x 2检验或连续性校正x 2检验.患者化疗前MPV预测初发HL患者接受化疗后1年内发生症状性VTE的风险,采用受试者工作特征(ROC)曲线法,计算ROC-曲线下面积(AUC),并且通过约登指数最大原则确定最佳临界值.采用Kaplan-Meier法及Log-rank检验,对不同MPV分组初发HL患者的无症状性VTE生存率和总体生存(OS)率分别进行比较.采用多因素Cox比例风险回归模型分析影响初发HL患者症状性VTE发生率的影响因素(结外器官累及情况和化疗前MPV).本研究遵循的程序符合2013年修订的《世界医学会赫尔辛基宣言》要求,并由患者本人或其家属签署临床研究知情同意书.结果 ①本研究167例初发HL患者在第1年随访期内,症状性VTE发生率为7.2% (12/167).VTE组患者中,结外器官累及(Lugano分期为Ⅳ期)的患者比例为66.7%(8/12),高于未发生VTE组的27.7%(43/155),并且差异有统计学意义(x2 =7.955,P=0.005);VTE组患者的中位MPV为6.7 f1(6.3~7.0 fl),低于未发生VTE组的7.4 fl(7.1~7.8 fl),并且差异亦有统计学意义(U=3.489,P=0.001).②ROC曲线分析结果显示,化疗前MPV对初发HL患者发生症状性VTE的风险具有预测价值,其ROC-AUC为0.697(95 %CI:0.476~0.884,P=0.022),化疗前MPV预测初发HL患者发生VTE风险的最佳临界值为6.8 fl,特异度为91.6%,灵敏度为66.7%.③本研究MPV<6.8 fl组患者症状性VTE发生率为38.1% (8/21),高于MPV≥6.8 fl组的2.7% (4/146),并且差异有统计学意义(x 2 =38.757,P<0.001).④Kaplan-Meicr生存曲线分析结果显示,MPV<6.8 fl组患者的无症状性VTE生存率低于MPV≥6.8 fl组患者,OS率亦低于MPV≥6.8 fl组患者,并且差异均有统计学意义(x 2 =40.220、44.443,P<0.001).⑤多因素Cox比例风险回归模型分析结果显示,MPV<6.8 fl为影响初发HL患者症状性VTE发生的独立危险因素(OR=1.673,95% CI:1.434~3.218,P=0.012).结论 MPV降低能够有效预测初发HL患者的症状性VTE发生风险增加,为临床预防、治疗初发HL患者的VTE提供有效指导.
    • 贾茜婷; 贾韬
    • 摘要: 使用18-氟标记的氟脱氧葡萄糖(18F-fluorodeoxyglucose,18 F-FDG)正电子发射断层扫描结合计算机断层扫描(PET/CT)的功能显像在霍奇金淋巴瘤(Hodgkin lymphoma,HL)的分期中具有明确的作用,现已成为HL的主要显像模式.其作为一种预测治疗工具,通过反应适应疗法的应用而不断发展.已有大量临床研究表明18 F-FDG PET/CT对HL具有非常高的预后诊断价值,可以提高分期的准确性,鉴别残留肿瘤和纤维化组织.HL中的反应适应性治疗方法既可以通过减低剂量来降低对低风险患者的毒性,同时还通过增加对高风险患者的治疗强度以改善预后.本综述介绍了18 F-FDG PET/CT在HL中的诊断分期、治疗期间和治疗结束时的应用进展,并对总肿瘤代谢体积这一新的功能预后因素进行了探讨.
    • 曹婷雍; 李亚茹; 吴俣; 刘霆; 贾永前
    • 摘要: 目的 探讨程序性死亡蛋白-1(PD-1)单克隆抗体在复发难治性经典型霍奇金淋巴瘤(r/r cHL)中的治疗效果及药物相关不良反应.方法 3例经多线治疗失败的r/r cHL,给于PD-1单克隆抗体单药治疗100 mg/次,3周/次,每月通过CT或超声评估治疗效果.结果 在治疗累积剂量约330 mg时,3例患者均获得部分缓解(PR),且生存状况明显改善.病例1共接受pembrolirumab或nivolumab治疗18个周期,已停药10个月,东部肿瘤协作组(ECOG)从3~4分恢复至0分,目前无进展生存时间(PFS) 21个月.病例2、3目前均接受nivolumab治疗8个周期,均无进展生存6个月.整体生存率100%.病例1和3仅出现1级药物相关不良反应:皮疹气紧、疲乏;病例2无药物相关不良反应.结论 PD-1单克隆抗体在r/r cHL中的具有较高的反应率,耐受性好,PD-1单克隆抗体可以为r/r cHL提供一种更加经济、反应率更高、不良反应更少的治疗选择.
    • 应志涛; 宋玉琴; 朱军
    • 摘要: 经典霍奇金淋巴瘤(cHL)通常预后较好,但复发/难治cHL(R/R cHL)患者仍难以获得长期缓解和生存.程序性死亡受体-1(PD-1)抗体单药及联合治疗在R/R cHL病人中显示出良好的耐受性和治疗效果.在B细胞淋巴瘤治疗领域围绕B细胞受体信号传导通路涌现出众多生物药物及小分子药物,这些药物在复发/难治B细胞淋巴瘤中取得了很好的疗效.除ALK+间变性大细胞淋巴瘤之外的外周T细胞淋巴瘤(PTCL)患者预后均不佳,新型化疗药物,如普拉曲沙、苯达莫司汀,新型靶向药物,如罗米地辛、西达本胺、Brentuximab vedotin等,在初治或复发/难治PTCL患者中取得了一定疗效.本文就近期淋巴瘤领域的治疗进展进行综述.
    • 戴滨冰; 赵婷媛; 戴辉艳
    • 摘要: 目的 为临床处理博来霉素致过敏性休克提供经验参考.方法 报道1例博来霉素致过敏性休克,结合博来霉素的药理作用和临床用药情况,针对该患者个体特点对病例进行分析.结果 该患者为霍奇金淋巴瘤,输注博来霉素过程中出现了严重的过敏性休克反应(血压下降、呼吸困难、 意识丧失、四肢湿冷、多汗等)及心律失常,经无创呼吸机辅助呼吸、升压、扩容、补液、 镇静、抗心律失常等治疗后患者生命体征逐步平稳,休克得以纠正,无其他不良反应.结论 医护人员在计划使用博来霉素时就应提高警惕,仔细阅读说明书,了解药品的注意事项和不良反应,尤其初次使用患者.
    • 王蓉; 李良; 张胜华; 甄永苏; 苗庆芳
    • 摘要: 目的 制备抗人CD30单克隆抗体并进行活性研究,为其作为抗体偶联药物的靶向运输载体提供研究依据.方法 通过基因工程技术构建真核表达载体pIZDHL-CD30-IgG,将质粒稳定转染CHO/dhFr-细胞并筛选,获得稳定表达anti-CD30-IgG抗体的细胞株并纯化抗体,通过HPLC检测其纯度.ELISA、Biacore和流式细胞术实验检测anti-CD30-IgG的亲和活性;免疫荧光共聚焦实验观察其在肿瘤细胞的内吞情况;利用小动物活体成像技术研究抗体在NOD/SCID鼠移植瘤模型中的靶向性.结果 成功构建了anti-CD30-IgG抗体的表达载体,并筛选出稳定表达的单克隆细胞株CHO-CD30-IgG,纯化后的抗体anti-CD30-IgG纯度达到98%以上.Anti-CD30-IgG与重组人CD30抗原具有很好的亲和活性,亲和常数为4.15×108 L/mol,其可通过肿瘤细胞表面CD30受体介导的内吞进入细胞.在NOD/SCID小鼠L540和Karpas299移植瘤模型中,anti-CD30-IgG可以选择性地富集并滞留在肿瘤部位.结论 Anti-CD30-IgG对抗原和肿瘤细胞具有高亲和性和特异性,并且可被内吞进入肿瘤细胞内部,在小鼠体内可选择性靶向并且长时间滞留在肿瘤部位,可作为抗体偶联药物中"弹头"部分的靶向输送载体.
    • 魏赟晨; 徐卫
    • 摘要: Hodgkin lymphoma (HL) is a curable malignancy for most patients, while the treatment of relapsed and refractory (R/R) HL is still facing severe challenges. In the 60th American Society of Hematology (ASH) Annual Meeting, many researches reported the latest development of the treatment of R/R HL. For chemosensitive patients, autologous stem cell transplantation after high-dose of salvage chemotherapy still remains the standard treatment method. The emerging of antibody drug conjugate, inhibitors of programmed death-1, chimeric antigen receptor T-cell immunotherapy and the combinations of multiple drugs have brought an increasing options for R/R HL treatment. This paper reviews the progress of R/R HL therapy.%大多数霍奇金淋巴瘤(HL)可治愈,但复发难治(R/R)HL的治疗依旧面临严峻挑战.第60届美国血液学年会上,多项研究报道了R/R HL治疗的最新进展.对化疗敏感的患者而言,高剂量挽救化疗后序贯自体造血干细胞移植仍然是标准的治疗方法.抗体药物偶联物、程序性死亡受体1抑制剂、嵌合抗原受体T细胞免疫疗法及多药联合方案的涌现也为R/R HL的治疗提供了更多的选择.现对R/R HL治疗的最新进展进行介绍.
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