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

Sponsor
Shanghai Zhongshan Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT03416803
Collaborator
(none)
150
1
2
28.9
5.2

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Radiation: Radiotherapy
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Prevention
Official Title:
Prediction of Lymph Node Metastasis in Hepatocellular Carcinoma and the Study of Individualized Radiotherapy
Anticipated Study Start Date :
Feb 1, 2018
Anticipated Primary Completion Date :
Dec 31, 2019
Anticipated Study Completion Date :
Jun 30, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Radiotherapy

Patients in the experimental group, who were at high risk for lymph node metastasis, underwent radiotherapy in the lymphatic drainage area. Radiotherapy was started in lymphatic drainage areas about 1 month after HCC surgery. The range of radiotherapy was hepatic portal area, pancreas circumference, celiac trunk and abdomen Around the aortic lymph drainage area, the dose of radiation 45Gy, conventional segmentation.

Radiation: Radiotherapy
Radiotherapy

No Intervention: Blank control

Patients in the control group , who were at high risk for lymph node metastasis,were followed up.

Outcome Measures

Primary Outcome Measures

  1. 2-year overall survival [The outcome measures are assessed up to 2 years.]

    The therapeutic effects are mainly evaluated by the 2-year overall survival.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 180 Fenglin Road Shanghai China 200032

Sponsors and Collaborators

  • Shanghai Zhongshan Hospital

Investigators

  • Principal Investigator: Zhongshan Hospital, PhD, Fudan University, Shanghai,China

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Shanghai Zhongshan Hospital
ClinicalTrials.gov Identifier:
NCT03416803
Other Study ID Numbers:
  • ZS-LNM-2017
First Posted:
Jan 31, 2018
Last Update Posted:
Feb 5, 2018
Last Verified:
Jan 1, 2018
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 5, 2018