A Phase III Randomized Trial of Standard Dose Stereotactic Body Radiation Therapy (SBRT) Versus Radiobiologically-Guided Dose Selected SBRT in Primary or Secondary Liver Carcinoma (SAVIOR).

Status: Recruiting
Location: See location...
Intervention Type: Radiation
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Radiation is a standard treatment option for patients with liver cancer. Unfortunately, the tumour grows after radiation in many patients and radiation can harm normal tissues. A new treatment using a specialized radiation procedure called Stereotactic body radiotherapy (SBRT) may increase the chance to control liver cancer and reduce the chance of harm to normal tissues. SBRT allows radiation treatments to be focused more precisely, and be delivered more accurately than with older treatments. SBRT has become a routine treatment. Further research has found that specialized computer programs can possibly guide the selection of an appropriate SBRT dose. This is called radiobiological guidance. However, this has not yet been proven to improve outcomes and/or reduce toxicity. Therefore, the purpose of this study is to find out if SBRT at standard dose versus SBRT guided by radiobiological techniques is better for you and your liver cancer.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Eligible patients include patients with any of the following:

‣ Primary hepatobiliary cancer confirmed pathologically or,

⁃ Non-lymphoma liver metastases confirmed pathologically or,

⁃ Radiographic liver lesions most consistent with metastases, in a patient with known pathologically proven non-lymphoma cancer and a previously negative CT or MRI of the liver or,

⁃ Hepatocellular carcinoma diagnosed with vascular enhancement of the lesion consistent with hepatocellular carcinoma, and with an elevated AFP, in the setting of cirrhosis or chronic hepatitis.

• ≤ 5 liver lesions measurable on a contrast-enhanced liver CT or MRI performed within 90 days prior to study entry.

• Primary liver lesion or liver metastases measuring ≤ 25 cm.

• Extrahepatic cancer is permitted if liver involvement is judged to be life-limiting

• No contraindications to radiotherapy

• Patient must be judged medically or surgically unresectable

• Zubrod Performance Scale = 0-3

• Age \> 18

• Systemic treatment including multikinase inhibitors and immunotherapy are allowed.

• Multikinase inhibitors must be held 2 weeks prior to radiation and may be restarted 1 week post radiation.

⁃ Previous liver resection or ablative therapy is permitted

⁃ Chemotherapy must be completed at least 2 weeks prior to radiation therapy and not planned to be administered for at least 1 week (for anthracyclines at least 4 weeks) after completion of treatment.

⁃ Life expectancy \> 6 months.

⁃ Women of childbearing potential and male participants must practice adequate contraception.

Locations
Other Locations
Canada
London Regional Cancer Program
RECRUITING
London
Contact Information
Primary
Morgan Black
morgan.black@lhsc.on.ca
519-685-8500
Time Frame
Start Date: 2021-08-01
Estimated Completion Date: 2027-04
Participants
Target number of participants: 110
Treatments
Active_comparator: Standard Dose Radiation
Patients in the standard arm will receive a standard dose of 2000cGy in 5 fractions using simple CT planning. IMRT is allowed. Treatment will be every second day excluding weekends and holidays.
Experimental: Personalized Dose Selection Radiation
Patients in the experimental arm will receive individually selected prescription dose guided by radiobiological parameters described below, preferably delivered in 5 fractions every other day, excluding weekends and holidays. Volumetric-modulated arc therapy (VMAT) is the preferred planning technique. Typical planning uses 2 arcs, \<=10MV and FFF mode where possible as almost all liver treatments are gated). In the event of multiple lesions, multiple isocentres are allowed. Often lateral isocentre shifts are significant and therefore arc ranges should be chosen to minimize collision risk. Treatment will be every second day excluding weekends and holidays.
Related Therapeutic Areas
Sponsors
Leads: London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

This content was sourced from clinicaltrials.gov

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