Oligometastasis Hepatocellular Carcinoma
Conditions
Brief summary
Oligometastasis is a definition that has been described in the past in the 1990s, and in some patients, metastases are not extensive and are limited to a small number of metastases. The local ablative treatment for oligometastasis is not a new concept. In case of liver metastasis from colorectal cancer, long-term survival can be expected if the liver resection is performed. Effectiveness has been demonstrated in studies of adrenal and brain metastasis from lung cancer as well as lung metastasis from sarcoma. A recent non-randomized study reported that patients with oligometastasis improved treatment outcomes with aggressive treatment. This study demonstrated that local ablative treatment for oligometastasis showed better treatment outcomes than expected. Also, the long-term outcomes in SABR-COMET trial showed that the overall survival were increased by 22 months. So far, the standard treatment for metastatic disease is systemic chemotherapy. However, based on these results from studies, active local treatment for patients with oligometastasis is currently being performed in the clinic. In this study, we aimed to apply this concept to patients with hepatocellular carcinoma. To confirm the efficacy and safety of stereotactic radiotherapy in patients with oligometastasis hepatocellular carcinoma
Interventions
RADIATIONRadiation: Stereotactic body radiotherapy (SBRT)
Patients will be treated with stereotactic body radiotherapy (SBRT) for oligometastasis from hepatocellular carcinoma. 1. Target delineation The GTV is set using diagnostic CT, MRI, PET-CT, etc. CTV is delineated including the microscopic range in GTV and internal margin using 4D-CT. The PTV is expanded by considering the uncertainty of the daily patient posture setting and placement. 2. Radiotherapy All patients are treated using 3D-CRT, IMRT, or VMAT. Total dose and fractionations will be determined depending on the location and character of the metastasized tumor. Detailed radiation prescriptions is summarized in the following paragraph. i. Liver: 48-60 Gy in 4 fractions ii. Lung: 45-60 Gy in 3-4 fractions iii. Brain: 27-30 Gy in 3-5 fractions iv. bone: 24-40 Gy in 3-5 fractions v. adrenal gland: 30-60 Gy in 3-8 fractions vi. other organ: depending on the clinicians' decision
Sponsors
Yonsei University
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No
Inclusion criteria
i. 19 years or older ii. Patients who signed the informed consent form iii. The clinical trial protocol can be complied with at the discretion of the investigator iv. Performance status (based on ECOG) less than 2 (0, 1) v. Patients with life expectancy greater than 3 months vi. Condition in which primary cancer is controlled • Definition: A condition that has not progressed at the time of review of clinical trials after curative treatment of primary cancer 3 months ago vii. Number of metastatic lesions up to 5 viii. 3 or less metastatic lesions in one metastatic organ ix. Those who are undergoing targeted therapy or chemotherapy can also be included (during radiation therapy, drug treatment is stopped)
Exclusion criteria
i. Serious medical complications that cannot proceed with radiation therapy ii. Previous radiation therapy history at the location where radiation therapy is to be performed iii. malignant pleural effusion iv. When the spinal cord and the tumor are close (the tumor is located within 3 mm) v. In case of brain metastasis requiring surgical intervention
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Treatment efficacy (Overall survival) | 2 year | The overall survival of patients from the start date of SBRT to either date of death or date of last follow up is evaluated |
| Treatment efficacy (Disease free survival) | 2 year | The disease free survival from the start date of SBRT to date of disease progression or date of death or date of last follow up is evaluated |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of participants with treatment-related adverse events (acute and late toxicity) as assessed by CTCAE v4.0 | 2 year | The acute and late treatment-related toxicity are evaluated. |
Countries
South Korea
Contacts
Primary ContactJinsil Seong
Outcome results
None listed