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A Study of Individualized Radiotherapy Based on a Prediction Model of Lymph Node Metastasis in Hepatocellular Carcinoma

Prediction of Lymph Node Metastasis in Hepatocellular Carcinoma and the Study of Individualized Radiotherapy

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03416803
Enrollment
150
Registered
2018-01-31
Start date
2018-02-28
Completion date
2020-06-30
Last updated
2018-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatocellular Carcinoma, Lymph Node Metastasis, Radiotherapy

Brief summary

Objectives: 1. To further validate the predictive efficacy of our established microRNA prediction model of HCC lymph node metastasis. 2. To establish a precise therapeutic mode of prophylactic radiation therapy in high-risk patients with HCC with lymph node metastasis under the guidance of a microRNA prediction model.

Detailed description

First, screening out patients who underwent hepatic tumor resection and pathologically diagnosed as HCC . Then,performing the detection of miR-145, miR-31 and miR-92a by using the HCC lymph node metastasis microRNA correlation prediction model established in our previous study. The patients are judged as high risk of lymph node metastasis and low risk Patients, then high-risk patients under the condition of informed consent into the group, randomized into treatment group and control groups. Last, Patients enrolled in the treatment group were treated with radiotherapy and followed up.

Interventions

RADIATIONRadiotherapy

Radiotherapy

Sponsors

Shanghai Zhongshan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. patients underwent liver tumor resection and pathological diagnosis of HCC in our hospital. 2. The tumor samples of these HCC patients were detected by in situ hybridization with miR-145, miR-31 and miR-92a. We used the previously established HCC lymph node metastasis microRNA prediction model to determine the patients with high-risk lymph node metastasis and low-risk patients at high risk Patients were randomly assigned into treatment group and control group with informed consent. 3. HCC patients were not receive other anti-cancer treatment. 4. Blood routine examination was normal. 5. Child-Pugh grade A, normal liver and kidney function in the normal range (including ALT or ASL within 2.5 times the normal), WBC\> 3 × 109 / L, Hb\> 90g / L, PLT\> 50 × 109 / 6. HCC patients were not receive the history of upper abdominal radiotherapy. 7. sign the informed consent. 8. age 18-75 years old. 9. KPS score 80-100 points.

Exclusion criteria

1. accepted other anti-cancer treatment. 2. Patients was determined to be low-risk lymph node metastasis by the pre-established HCC lymph node metastasis microRNA prediction model. 3. blood and liver and kidney dysfunction. 4. can not control the infection. 5. at the same time the merger of other malignant tumors. 6. while using other experimental drugs or to participate in other clinical trials. 7. serious heart, lung, kidney disease. 8. pregnant or lactating women. 9. serious nervous system disease, can not clearly tell the treatment

Design outcomes

Primary

MeasureTime frameDescription
2-year overall survivalThe outcome measures are assessed up to 2 years.The therapeutic effects are mainly evaluated by the 2-year overall survival.

Countries

China

Contacts

Primary ContactZhaochong Zeng, Phd
zeng.zhaochong@zs-hospital.sh.cn13817076800
Backup ContactZuolin Xiang, Phd
xiangzuolinmd@hotmail.com13701816716

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026