...
首页> 外文期刊>Hepatology: Official Journal of the American Association for the Study of Liver Diseases >Patients with advanced hepatocellular carcinoma need a personalized management: A lesson from clinical practice
【24h】

Patients with advanced hepatocellular carcinoma need a personalized management: A lesson from clinical practice

机译:患有晚期肝细胞癌的患者需要个性化管理:临床实践的课程

获取原文
获取原文并翻译 | 示例
           

摘要

The Barcelona Clinic Liver Cancer (BCLC) advanced stage (BCLC C) of hepatocellular carcinoma (HCC) includes a heterogeneous population, where sorafenib alone is the recommended treatment. In this study, our aim was to assess treatment and overall survival (OS) of BCLC C patients subclassified according to clinical features (performance status [PS], macrovascular invasion [MVI], extrahepatic spread [EHS] or MVI + EHS) determining their allocation to this stage. From the Italian Liver Cancer database, we analyzed 835 consecutive BCLC C patients diagnosed between 2008 and 2014. Patients were subclassified as: PS1 alone (n = 385; 46.1%), PS2 alone (n = 146; 17.5%), MVI (n = 224; 26.8%), EHS (n = 51; 6.1%), and MVI + EHS (n = 29; 3.5%). MVI, EHS, and MVI + EHS patients had larger and multifocal/massive HCCs and higher alpha‐fetoprotein (AFP) levels than PS1 and PS2 patients. Median OS significantly declined from PS1 (38.6 months) to PS2 (22.3 months), EHS (11.2 months), MVI (8.2 months), and MVI + EHS (3.1 months; P 0.001). Among MVI patients, OS was longer in those with peripheral than with central (portal trunk) MVI (11.2 vs. 7.1 months; P = 0.005). The most frequent treatments were: curative approaches in PS1 (39.7%), supportive therapy in PS2 (41.8%), sorafenib in MVI (39.3%) and EHS (37.3%), and best supportive care in MVI + EHS patients (51.7%). Independent prognostic factors were: Model for End‐stage Liver Disease score, Child‐Pugh class, ascites, platelet count, albumin, tumor size, MVI, EHS, AFP levels, and treatment type. Conclusion: BCLC C stage does not identify patients homogeneous enough to be allocated to a single stage. PS1 alone is not sufficient to include a patient into this stage. The remaining patients should be subclassified according to PS and tumor features, and new patient‐tailored therapeutic indications are needed. (H epatology 2018;67:1784‐1796).
机译:肝细胞癌(HCC)的巴塞罗那临床肝癌(BCLC)晚期(BCLC C)包括异质群体,其中Sorafenib仅是推荐的治疗方法。在这项研究中,我们的目的是评估根据临床特征(性能状态[PS],大血管侵袭[MVI],侵略性蔓延[EHS]或MVI + EHS)划分的BCLC C患者的治疗和整体存活(OS)。分配到这个阶段。从意大利肝癌数据库中,我们分析了2008年至2014年诊断的835名连续的BCLC C患者。患者被亚分类为:单独的PS1(n = 385; 46.1%),单独pS2(n = 146; 17.5%),mvi(n = 224; 26.8%),EHS(n = 51; 6.1%)和MVI + EHS(n = 29; 3.5%)。 MVI,EHS和MVI + EHS患者具有比PS1和PS2患者更大,多焦点/大规模的HCC和更高的α-胎蛋白(AFP)水平。中位数OS从PS1(38.6个月)到PS2(22.3个月),EHS(11.2个月),MVI(8.2个月)和MVI + EHS(3.1个月; P <0.001)。在MVI患者中,OS在具有外周的患者比中央(门户躯干)MVI(11.2与7.1个月; P = 0.005)。最常见的处理是:PS1(39.7%),PS2(41.8%),MVI(39.3%)和EHS(37.3%)中的支持治疗(41.8%),以及MVI + EHS患者的最佳支持护理(51.7%) )。独立的预后因素是:终末期肝病评分模型,儿童-PUGH类,腹水,血小板计数,白蛋白,肿瘤大小,MVI,EHS,AFP水平和治疗型。结论:BCLC C阶段不识别均匀的患者足以分配给单一阶段。单独的PS1不足以将患者纳入该阶段。剩余的患者应根据PS和肿瘤特征进行亚类化,需要新的患者量身定制的治疗适应症。 (2018年Hopatology; 67:1784-1796)。

著录项

  • 来源
  • 作者单位

    Department of Internal Medicine Gastroenterology Unit San Martino PolyclinicUniversity of;

    Department of Medical and Surgical SciencesSemeiotica Medica Unit Alma Mater Studiorum–University;

    Department of Medical and Surgical SciencesSemeiotica Medica Unit Alma Mater Studiorum–University;

    Department of Internal Medicine Gastroenterology Unit San Martino PolyclinicUniversity of;

    Department of Medical and Surgical SciencesSemeiotica Medica Unit Alma Mater Studiorum–University;

    Department of Medical and Surgical SciencesSemeiotica Medica Unit Alma Mater Studiorum–University;

    Operative Unit of GastroenterologyBelcolle HospitalViterbo Italy;

    Biomedical Department of Internal and Specialistic MedicineGastroenterologyPalermo Italy;

    Department of Medical and Surgical Sciences Internal Medicine UnitAlma Mater Studiorum–University;

    Biomedical Department of Internal and Specialistic Medicine Internal Medicin 2 UnitVilla Sofia;

    Gastroenterology Physiopathology and Digestive EndoscopyCentral Hospital of BolzanoBolzano Italy;

    Surgery DivisionSan Marco PolyclinicZingonia Italy;

    Department of Internal MedicineInfermi Hospital of FaenzaFaenza Italy;

    Gastroenterology and Metabolic Diseases UnitHospital‐University Agency of PisaPisa Italy;

    Department of Gastroenterology GastroenterologyPolytechnic–University of MarcheAncona Italy;

    Department of Surgical and Gastroenterological Sciences GastroenterologyUniversity of PadovaItaly;

    Department of Internal MedicineCattolica University of RomeRome Italy;

    Department of Oncohematology and Internal MedicineInfection diseases and Hepatology UnitParma Italy;

    Internal Medicine and Gastroenterology Unit‐Gemelli Department of Internal MedicineRome Italy;

    Medicine DivisionBolognini Hospital AgencySeriate Italy;

    Gastroenterology Unit Department of Clinical and Sperimental MedicineNaples Italy;

    Department of Medical and Surgical Sciences Zoli Internal MedicineAlma Mater Studiorum–University;

    GastroenterologySacro Cuore Don Calabria HospitalNegrar Italy;

    Department of Internal Medicine and HepatologyFatebenefratelli HospitalMilan Italy;

    Department of Molecular Medicine University of PadovaPadova Italy;

    Internal Medicine and Hepatology Department of Sperimental and Clinical MedicineFlorence Italy;

    Department of Medical and Surgical SciencesGastroenterology Unit Alma Mater Studiorum–University;

    Department of Clinical and Surgical Medicine‐Federico II UniversityNaples Italy;

    Department of Medical and Surgical SciencesSemeiotica Medica Unit Alma Mater Studiorum–University;

    Department of Medical and Surgical SciencesSemeiotica Medica Unit Alma Mater Studiorum–University;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 消化系及腹部疾病;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号