BCLC, Barcelona-Clinic Liver Cancer

  • 文章类型: Journal Article
    晚期肝细胞癌是一个异质性群体,治疗选择有限。TACE最近被各种研究小组提倡。这项研究的目的是评估TACE联合索拉非尼,以及单独的TACE,治疗BCLCC期HCC安全有效。
    对78例BCLCC期HCC患者的临床数据进行回顾性评估,这些患者接受TACE-索拉非尼(TS)联合治疗或TACE单药治疗作为其首次治疗。干预后1个月比较两组肿瘤的放射学反应。比较两组患者的进展时间(TTP),总生存期(OS),和不良事件。
    疾病控制率(44.9%和25.8%,分别,治疗1个月后,TS组合组的P=0.09)高于TACE单药治疗组。TS联合组TTP和OS明显优于TACE组(TTP分别为4.6和3.1个月,分别,P=0.001),OS分别为10.1和7.8个月,分别,P<0.001)。TACE-S组在6个月时的累积生存时间更长,9个月,和1年比TACE组(97.9%,51.1%,25.7%与90.4%,51.6%,0%,分别)。
    TS联合治疗晚期(BCLC-C)HCC可显着提高疾病控制率,TTP,和操作系统与单独的TACE相比,没有任何显著增加的不良反应。
    UNASSIGNED: Advanced-stage hepatocellular carcinoma is a heterogeneous group with limited treatment options. TACE has been advocated recently by various study groups. The purpose of this study was to evaluate if TACE in combination with sorafenib, as well as TACE alone, was safe and efficacious in treating BCLC stage C HCC.
    UNASSIGNED: A retrospective evaluation of the clinical data of 78 patients with BCLC stage C HCC who received either TACE-sorafenib (TS) combination therapy or TACE monotherapy as their first treatment was done. The two groups were compared in terms of radiological tumor response 1 month after the intervention. The two groups were also compared in terms of time to progression (TTP), overall survival (OS), and adverse events.
    UNASSIGNED: The disease control rate (44.9% and 25.8%, respectively, P = 0.09) was higher in the TS combination group than in the TACE monotherapy group after 1 month of treatment. The TS combination group had significantly superior TTP and OS than the TACE group (TTP was 4.6 and 3.1 months, respectively, P = 0.001), and OS was 10.1 and 7.8 months, respectively, P < 0.001). The TACE-S group had a greater cumulative survival time at 6 months, 9 months, and 1 year than the TACE group (97.9%, 51.1%, 25.7% vs. 90.4%, 51.6%, and 0%, respectively).
    UNASSIGNED: TS combination therapy in advanced-stage (BCLC-C) HCC significantly improved disease control rate, TTP, and OS compared with TACE alone, without any significant increase in adverse reactions.
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  • 文章类型: Journal Article
    UNASSIGNED: Liver resection (LR) in patients with hepatocellular carcinoma (HCC) and clinically significant portal hypertension (CSPH) defined as a hepatic venous pressure gradient (HVPG) ≥10 mmHg is not encouraged. Here, we reappraised the outcomes of patients with cirrhosis and CSPH who underwent LR for HCC in highly specialised liver centres.
    UNASSIGNED: This was a retrospective multicentre study from 1999 to 2019. Predictors for postoperative liver decompensation and textbook outcomes were identified.
    UNASSIGNED: In total, 79 patients with a median age of 65 years were included. The Child-Pugh grade was A in 99% of patients, and the median model for end-stage liver disease (MELD) score was 8. The median HVPG was 12 mmHg. Major hepatectomies and laparoscopies were performed in 28% and 34% of patients, respectively. Ninety-day mortality and severe morbidity rates were 6% and 27%, respectively. Postoperative and persistent liver decompensation occurred in 35% and 10% of patients at 3 months. Predictors of liver decompensation included increased preoperative HVPG (p = 0.004), increased serum total bilirubin (p = 0.02), and open approach (p = 0.03). Of the patients, 34% achieved a textbook outcome, of which the laparoscopic approach was the sole predictor (p = 0.004). The 5-year overall survival and recurrence-free survival rates were 55% and 43%, respectively.
    UNASSIGNED: Patients with cirrhosis, HCC and HVPG ≥10 mmHg can undergo LR with acceptable mortality, morbidity, and liver decompensation rates. The laparoscopic approach was the sole predictor of a textbook outcome.
    UNASSIGNED: Patients with cirrhosis, hepatocellular carcinoma, and clinically significant portal hypertension (defined as a hepatic venous pressure gradient ≥10 mmHg) can undergo resection with acceptable mortality, morbidity, liver decompensation rates, and a textbook outcome. These results can be achieved in selected patients with preserved liver function, good general status, and sufficient remnant liver volume.
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  • 文章类型: Journal Article
    肝细胞癌(HCC)是其发病的主要原因之一。慢性肝病患者的死亡率和医疗支出。印度尚无关于HCC诊断和管理的共识指南。印度全国肝脏研究协会(INASL)于2011年成立了HCC工作组,其任务是制定HCC诊断和管理的共识指南。与印度的疾病模式和临床实践有关。工作队首先确定了HCC各个方面的各种有争议的问题,这些问题被分配给工作队的个别成员,他们对这些问题进行了详细的审查。工作组使用牛津循证医学中心-2009年的证据水平来开发基于证据的方法。2月9日和10日举行了为期2天的圆桌讨论会,2013年在普里,奥里萨邦,讨论,辩论,并最终确定共识声明。工作队成员在本次会议上审查并讨论了现有文献,并为每个问题制定了INASL共识声明。我们在这里介绍INASL关于预防的共识指南(Puri建议),印度肝癌的诊断和治疗。
    Hepatocellular carcinoma (HCC) is one of the major causes of morbidity, mortality and healthcare expenditure in patients with chronic liver disease. There are no consensus guidelines on diagnosis and management of HCC in India. The Indian National Association for Study of the Liver (INASL) set up a Task-Force on HCC in 2011, with a mandate to develop consensus guidelines for diagnosis and management of HCC, relevant to disease patterns and clinical practices in India. The Task-Force first identified various contentious issues on various aspects of HCC and these issues were allotted to individual members of the Task-Force who reviewed them in detail. The Task-Force used the Oxford Center for Evidence Based Medicine-Levels of Evidence of 2009 for developing an evidence-based approach. A 2-day round table discussion was held on 9th and 10th February, 2013 at Puri, Odisha, to discuss, debate, and finalize the consensus statements. The members of the Task-Force reviewed and discussed the existing literature at this meeting and formulated the INASL consensus statements for each of the issues. We present here the INASL consensus guidelines (The Puri Recommendations) on prevention, diagnosis and management of HCC in India.
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