Recurrent Hepatocellular Carcinoma
Conditions
Keywords
Primary liver cancer, Hepatocellular carcinoma, CyberKnife, Accuray, TACE, Transarterial chemoembolization
Brief summary
To compare the efficacy of Transarterial Chemoembolization (TACE) to CyberKnife stereotactic body radiotherapy in the treatment of patients with locally recurrent hepatocellular carcinoma (HCC) after TACE.
Detailed description
Hepatocellular carcinoma (HCC) is the third most deadly cancer in the world. It is primarily seen in areas where hepatitis is endemic, such as Asia, but other risk factors include alcoholic cirrhosis. Surgical resection and/or transplantation remain the only curative options. However, more than 80% of patients present with unresectable disease. For these patients with unresectable tumors, a variety of treatment options are available, including transarterial chemoembolization (TACE), radiofrequency ablation (RFA), radioactive microspheres, microwave coagulation, laser-induced thermotherapy, and percutaneous alcohol injection, all of which have similar survival rates. Stereotactic body radiotherapy (SBRT) for unresectable HCC is a relatively new treatment option made available because of significant improvements in diagnostic imaging and radiation delivery techniques. Although follow-up is limited, results show encouraging local control rates. Some investigators have combined TACE with fractionated conventional radiotherapy as a means of intensifying local therapy, with evidence of efficacy. TACE remains the dominant mode of local therapy for unresectable HCC. However, recurrence rates are high. Because SBRT is rapidly becoming an accepted local therapy for hepatic lesions, its role in treating HCC needs to be further defined. Moreover, once patients have recurred after initial TACE, it is unclear if additional TACE will be as effective or if another mode of local therapy such as SBRT would be preferable. We propose to conduct a multicenter randomized study comparing TACE vs. SBRT using CyberKnife for locally recurrent HCC. Locally recurrent HCC will include lesions that persist, progress or recur minimum 3 months after initial TACE.
Interventions
PROCEDURETransarterial Chemoembolization
Transarterial Chemoembolization will be given within 12 weeks and up to 3 staged procedures, depending on the architecture of the tumor vasculature.
RADIATIONCyberKnife SBRT
Dose is 45 Gy (15 Gy in 3 fractions) or 36 Gy(12 Gy in 3 fractions). Tumors should receive the higher dose unless normal tissue constraints cannot be met.
Sponsors
Stanford University
Accuray Incorporated
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Confirmed hepatocellular carcinoma by one of the following: 1. Histopathology 2. One radiographic technique that confirms a lesion \>2 cm with arterial enhancement with washout on delayed phase. * Hepatic lesion in patients for whom surgical resection is not possible or would not result in an opportunity for cure. * Radiographic evidence of persistent, progressive or recurrent disease in an area previously treated with TACE. This evaluation should be determined after 6 weeks of initial TACE. * Multi-specialty evaluation whereby the recurrent liver lesion was deemed by both the attending radiation oncologist and interventional radiologist amenable to treatment by the respective modality 1. Eligible patients must undergo an IV contrast CT scan of the liver within 6 weeks of enrollment onto the study; a contrast enhanced liver MRI may be substituted for the contrast liver CT 2. A recent serum AFP must be obtained within 4 weeks of enrollment. * Unifocal liver tumors not to exceed 7.5 cm in greatest axial dimension. Multifocal lesions will be restricted to lesions that can be treated within a single target volume within the same liver segment and to an aggregate of 7.5 cm as long as the dose constraints to normal tissue can be met. * Eastern Clinical Oncology Group performance status 0, 1 or 2 (Appendix I). * Patients with liver disease classified as Child Pugh class A/B, if Child's class B, score must be 8 or less. * Life expectancy \>= 6 months * Age \>= 18 years old * Albumin \>= 2.5 g/dL * Total Bilirubin \<= 3 mg/dL * INR \<= 1.5 * Creatinine \<= 2.0 mg/dL * Both men and women and members of all races and ethnic groups are eligible for this study * Ability of the research subject or authorized legal representative to understand and the willingness to sign a written informed consent document.
Exclusion criteria
* Prior radiation for the recurrent liver tumor * Prior radiotherapy to the upper abdomen * Prior RFA to index lesion * Liver transplant * Tumors greater than 7.5 cm in greatest axial dimension * Portal vein thrombus * Large varices within 2 cm of index lesion (seen on cross section imaging) * Contraindication to receiving radiotherapy * Active gastrointestinal bleed within 2 weeks of study enrollment * Ascites refractory to medical therapy * Women who are pregnant * Administration of chemotherapy within the last 1 month * Presence of multifocal lesions located in different lobes of the liver or extrahepatic metastases * Participation in another concurrent systemic treatment protocol * Prior history of malignancy other than HCC
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Freedom from local progression | 12 months | Freedom from local progression at time T is defined as lack of local progression in the treated liver lesion in the set of patients alive and on study at time T and without distant progression up to time T. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Progression-free survival | 6, 12 and 18 months | Progression-free survival will be defined as subject alive and free from local progression, disease recurrence elsewhere in the liver, extrahepatic progression, or clinical deterioration unattributable to another underlying medical condition in the absence of clear radiographic findings of progressive disease. |
| Overall survival | Up to three years following therapy | Overall survival will be determined as a measure of time from diagnosis of initial recurrence until death from any cause. |
| Serum AFP levels | 3, 6, 12 and 18 months | Serum AFP levels will be measured at specific points during the study. The 2 endpoints to be analyzed are: * Initial AFP levels * AFP response - the percent decrease in serum AFP levels from the initial result to the eventual nadir after therapy These endpoints will be correlated to the clinical endpoints (freedom from local progression, progression free-survival, and overall survival). |
| Freedom from local progression | 6 and 18 months | Freedom from local progression at time T is defined as lack of local progression in the treated liver lesion in the set of patients alive and on study at time T and without distant progression up to time T. |
Countries
United States
Outcome results
None listed