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临床试验/NCT03614546
NCT03614546Unknown不适用

Clinical Trial of Radiotherapy in Treating Primary Hepatocellular Carcinoma

The Third Xiangya Hospital of Central South University1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2018年10月10日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
200
试验地点
1
主要终点
Overall Survival(OS)

研究概览

简要总结

The subjects of primary hepatocellular carcinoma diagnosed pathologically or clinically will be grouped according to the size, location, number and function of the liver, and respectively received Intensity-modulated Radiation Therapy (IMRT), Stereotactic Body Radiation Therapy (SBRT), Transarterial chemoembolization (TACE) or surgery.

详细描述

Primary hepatocellular carcinoma (HCC) is the sixth most malignant tumor in the world. In 2015, 466,000 people had been diagnosed as HCC in China, accounting more than half of the total incidence in the world; and 422,000 people died, making the HCC as the second reason for cancer related deaths in this country. Although many advances have been made in recent years in treatments such as Radiofrequency Ablation (RFA) and transarterial chemoembolization (TACE), the prognosis of patients with HCC is still poor. As a result, the prevention and treatments of HCC in China are still urgently needed to improve.

Being one of the three major treatments of cancer, radiotherapy has been used for HCC in very early times. In the pioneering days, however; whole-liver radiation was impossible to give lethal dose for cancer tissue due to the high risk of radiation induced liver disease (RILD) and even liver failure, which might lead to death of patients. Consequently, radiotherapy has long failed to play a major role in the treatment of liver cancer. But things are likely to be changed. In recent years, many research teams have applied precise external radiotherapy, such as intensity modulated radiation therapy (IMRT) and stereotactic body radiation therapy (SBRT), to the treatment of liver cancer, and has achieved good results. Despite of this, many guidelines still do not recommend radiotherapy as a first-line treatment for early and mid-term liver cancer due to the lack of high level of evidence from good clinical trials proving the effectiveness of SBRT/IMRT and other new radiotherapy techniques in the treatment of HCC.

In the investigator's previous clinical work, the investigators found that precise external radiotherapy such as SBRT and IMRT is effective in treating primary liver cancer. For example, patients with early stage HCC could achieve complete response (CR) after SBRT, and patients with local advanced HCC could be observed a significant reduction in the size of lesions and obvious improvement in the symptoms. Considering the poor prognosis of HCC and the shortcomings of surgery, RFA and TACE, the investigators then decided to carry out this multi-centered clinical trial of radiotherapy in HCC with the purpose of obtaining true and reliable clinical data and evidence, and focused on the following two questions: (1) whether radiotherapy, combined or not combined with TACE, could be a radical and first-line treatment for inoperable patients with early stage HCC; (2) what is the optimal sequence and timing of the combination of radiotherapy and TACE for patients with lesions adjacent to organs at risk and radical doses cannot be given. It is foreseeable that this clinical trial will change clinicians' understanding of the value of radiotherapy in the treatment of liver cancer, improve its status and even lead to revision of related guidelines/norms, and exert a far-reaching impact on the prognosis of patients with HCC.

The subjects who were pathologically or clinically diagnosed as primary liver cancer were grouped according to physical status, size/location/number of tumor, vascular invasion, extrahepatic metastasis, the relationship with organ at risk (OAR), and liver function. Then the subjects received IMRT, SBRT, TACE or surgery, and were followed up until the completion of treatment, the emergence of intolerance of toxicity, or the withdrawal of the trial.

Treatment methods:

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Meeting the diagnosis criteria of primary hepatocellular carcinoma: (1) primary hepatocellular carcinoma diagnosed by histology or cytology; (2) primary hepatocellular carcinoma diagnosed clinically (referring to the standard of diagnosis and treatment of primary hepatocellular carcinoma, version 2017);
  • Stage Ia-IIIa disease (referring to the standard of diagnosis and treatment of primary hepatocellular carcinoma, version 2017).
  • Child-Pugh score class A or B without encephalopathy;
  • Age between 18-80 years old;
  • At least one measurable lesion according to the 1.1 version of response evaluation criteria in solid tumors (RECIST).
  • ECOG(Eastern Cooperative Oncology Group) performance status of 0-2 at enrollment(subjects with ECOG performance status of 2 did not deteriorate in the last 2 weeks).
  • Written informed consent for the trial.
  • Be Willing and able to comply with planned visits, treatment plans, laboratory tests and other test procedures.
  • Have a life expectancy greater than 3 months judged by investigators;

排除标准

  • History of upper abdominal radiotherapy;
  • History of liver transplantation;
  • Abnormal laboratory results as follows:
  • abnormal hematology results, including hemoglobin less than 8.5 g/dL (no blood transfusion within 14 days before); neutrophils less than 1.5×109 /L or platelets less than 60×109 /L (no blood transfusion or growth factor was used within 7 days before);
  • abnormal liver function: total bilirubin >3×upper limit of normal (ULN); aspartate aminotransferase (AST) / alanine aminotransferase (ALT) > 5×ULN;
  • abnormal renal function: serum creatinine >1.5×ULN, or creatinine clearance rate (CrCl) < 60 mL/min according to Cockcroft-Gault formula.
  • international normalized ratio (INR) > 2.3 (according to the revised Child-Pugh grading Guide);
  • the calibration values of potassium, sodium, magnesium or calcium not within the normal range, and have clinical significance according to the judgment of the primary investigator.
  • History of other cancers besides primary hepatocellular carcinoma, with the exception of cured non-melanoma skin cancer, in situ cervical cancer, or other cancers received cured treatment and showed no signs of disease in at least 3 years.
  • Metastases to central nervous system (CNS) or brain;
  • Significant gastrointestinal bleeding occurred within 4 weeks before entering the trial.
  • Cardiac dysfunction as demonstrated by any of the following conditions:
  • recent echocardiography revealed a left ventricular ejection fraction < 45%.
  • severe arrhythmia;
  • unstable angina pectoris;
  • New York Heart Association III and IV congestive heart failure;
  • myocardial infarction occurred in the last 12 months before admission.
  • pericardial effusion;
  • Uncontrolled hypertension after standard treatment (blood pressure not stably below 150/90 mmHg)
  • Known human immunodeficiency virus (HIV) infection;
  • Pregnant or during lactation period, or is fertile male and female who is not willing or unable to take birth control/contraception to prevent pregnancy during the period between 2 weeks before radiation and 1 month after radiation;
  • Substance abuse, other acute or chronic physical or mental illness or abnormal laboratory examination that might increase the risk of participation judged by investigator.
  • Previous cancer treatment related toxicities that did not return to baseline or grade 0-1 (except for hair loss and peripheral neuropathy).
  • Any physical condition or illness that might increase the risk of participation judged by investigator.

研究组 & 干预措施

C2a(TACE+ IMRT ) group

Experimental

First,treat with intensity modulated radiation therapy (IMRT),50Gy/25F/5W, 4 weeks after IMRT,treat with transcatheter arterial chemoembolization(TACE) 2-4 times

干预措施: TACE (Procedure)

A(surgery) group

Other

Hepatectomy

干预措施: Hepatectomy (Procedure)

B1(SBRT) group

Experimental

Stereotactic Body Radiation Therapy(SBRT), 40-55Gy/5-6F

干预措施: SBRT (Radiation)

B2a(TACE+ IMRT ) group

Experimental

First,treat with intensity modulated radiation therapy (IMRT),50Gy/25F/5W, 4 weeks after IMRT,treat with transcatheter arterial chemoembolization(TACE) 2-4 times

干预措施: IMRT (Radiation)

B2b(TACE+ IMRT ) group

Experimental

First,treat with transcatheter arterial chemoembolization(TACE) 2-4 times,4 weeks after TACE,treat with intensity modulated radiation therapy (IMRT),50Gy/25F/5W

干预措施: IMRT (Radiation)

C1(SBRT) group

Experimental

Stereotactic Body Radiation Therapy, 40-55Gy/5-6F

干预措施: SBRT (Radiation)

C2a(TACE+ IMRT ) group

Experimental

First,treat with intensity modulated radiation therapy (IMRT),50Gy/25F/5W, 4 weeks after IMRT,treat with transcatheter arterial chemoembolization(TACE) 2-4 times

干预措施: IMRT (Radiation)

C2b(TACE+ IMRT ) group

Experimental

First,treat with transcatheter arterial chemoembolization(TACE) 2-4 times,4 weeks after TACE,treat with intensity modulated radiation therapy (IMRT),50Gy/25F/5W

干预措施: IMRT (Radiation)

B2a(TACE+ IMRT ) group

Experimental

First,treat with intensity modulated radiation therapy (IMRT),50Gy/25F/5W, 4 weeks after IMRT,treat with transcatheter arterial chemoembolization(TACE) 2-4 times

干预措施: TACE (Procedure)

C2b(TACE+ IMRT ) group

Experimental

First,treat with transcatheter arterial chemoembolization(TACE) 2-4 times,4 weeks after TACE,treat with intensity modulated radiation therapy (IMRT),50Gy/25F/5W

干预措施: TACE (Procedure)

B2b(TACE+ IMRT ) group

Experimental

First,treat with transcatheter arterial chemoembolization(TACE) 2-4 times,4 weeks after TACE,treat with intensity modulated radiation therapy (IMRT),50Gy/25F/5W

干预措施: TACE (Procedure)

结局指标

主要结局

Overall Survival(OS)

时间窗: up to 5 years

The time of patients from randomization to death caused by any cause.

次要结局

  • Disease control rate(DCR)(up to 5 years)
  • Progression free survival (PFS)(up to 5 years)
  • Incidence of adverse events(up to 5 years)
  • Minimal volume of liver free from radiation(up to 5 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Department of oncology

Director of oncology department

The Third Xiangya Hospital of Central South University

研究点 (1)

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