Stereotactic Body Radiation Therapy and Transarterial Chemoembolization in Treating Patients With Liver Cancer That Cannot Be Removed by Surgery

Stage IIIA Hepatocellular Carcinoma Clinical Trial

Official title:

A Pilot Trial of Stereotactic Body Radiation Therapy (SBRT) to Induce Tumor Hyperemia in Combination With Transarterial Chemoembolization (TACE) for Unresectable Hepatocellular Carcinoma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02507765
• Other study ID #: OSU-15032
• Secondary ID: NCI-2015-00894
• Status: Completed
• Phase: Phase 1
• Start date: July 2015
• Est. completion date: January 5, 2021

Study information

• Verified date: October 2021
• Source: Ohio State University Comprehensive Cancer Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This pilot clinical trial studies stereotactic body radiation therapy (SBRT) and transarterial chemoembolization (TACE) in treating patients with liver cancer that cannot be removed by surgery. SBRT is a specialized radiation therapy that delivers a high dose of radiation directly to the tumor and may kill more tumor cells and cause less damage to normal tissue. Chemoembolization kills tumor cells by carrying drugs directly into blood vessels near the tumors and then blocking the blood flow to allow a higher concentration of the drug to reach the tumor for a longer period of time. SBRT may make TACE more beneficial by increasing blood flow to the tumor, which may allow more of the TACE chemotherapy to enter the tumor. Giving SBRT with TACE may work better in treating patients with liver cancer that cannot be removed by surgery.

Description:

PRIMARY OBJECTIVES:

I. To establish the feasibility of completing SBRT followed by TACE in a 2 day time period.

SECONDARY OBJECTIVES:

I. To determine acute tumor perfusion changes after SBRT using functional magnetic resonance imaging (MRI) (magnetic resonance [MR]-dynamic contrast enhanced [DCE]/perfusion weighted imaging [PWI], MR-diffusion, blood oxygen level dependent [BOLD] sequences).

II. To establish safety and tolerability of this regimen. III. To determine overall response rates (using modified Response Evaluation Criteria in Solid Tumors [RECIST] criteria), including objective response rate (partial response [PR] + complete response [CR]) and clinical benefit rate (stable disease [SD] + PR + CR) at 1, 3, and 6 months after TACE.

IV. To evaluate local control, progression-free survival, and overall survival at 1, 3, 6, 9, and 12 months after a single-dose of SBRT followed by TACE.

V. To correlate micro ribonucleic acid (miRNA) biomarkers with response and toxicity.

OUTLINE: This is a dose-escalation study of SBRT.

Patients undergo SBRT on day 1 and TACE on day 2.

After completion of study treatment, patients are followed up at 1-2 weeks and at 1, 3, 6, 9, 12, 18, and 24 months.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 16
• Est. completion date: January 5, 2021
• Est. primary completion date: January 18, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients must have a diagnosis of hepatocellular carcinoma by at least one criterion listed below:

• Histologically confirmed

• Magnetic resonance imaging (MRI) or computerized tomography (CT) findings consistent with hepatocellular carcinoma

• Alpha fetoprotein (AFP) > 400 ng/mL AND evidence of at least one solid liver lesion > 2 cm regardless of specific imaging characteristics on CT or MRI

• Patients must be non-transplantable, unresectable, or medically inoperable and eligible for TACE as determined by a multi-disciplinary team

• Absolute neutrophil count >= 1.5 × 10^9/L

• Hemoglobin >= 9 g/dl

• Platelets >= 50,000/mm^3

• Prothrombin time (PT)/international normalized ratio (INR) and activated partial thromboplastin time (PTTa) =< 1.5

• Albumin >= 2.5 g/dL

• Alkaline phosphatase < 5 x upper limit of normal (ULN)

• Total bilirubin =< 2.0 mg/dL

• Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) < 5 x ULN

• Creatinine =< 1.5 mg/dL and calculated creatinine clearance >= 60 mL/min or 24-hour urine creatinine clearance >= 60 mL/min

• Must have Childs-Pugh A or B liver disease

• Patients must have no clinical signs of heart failure and meet New York Heart Association functional classification I or II defined as:

• Class I - patients with no limitation of activities; they suffer no symptoms from ordinary activities

• Class II - patients with slight, mild limitation of activity; they are comfortable with rest or with mild exertion

• Must have 1-3 liver lesions amenable to SBRT with tumor size < 15 cm (single lesion or sum)

• Must be able to undergo two MRI scans, one before study treatment begins and another shortly after SBRT

• Patients with extrahepatic disease, portal hypertension, or bilobar disease are allowed

• Normal renal function (creatinine < 1.5 mg/dL)

• Within 2 weeks of registration: patients must have vital signs, history/physical examination, laboratory studies (complete blood count [CBC] with differential, chemistries including liver function tests, AFP, creatinine clearance [CrCl] assessment, pregnancy test if needed)

• Life expectancy of at least 12 weeks in the opinion of investigator

• Patient has an Eastern Cooperative Oncology Group (ECOG) performance status of 0-2

• Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed

• Women of child-bearing potential (WOCBP) must have a negative pregnancy test within 14 days of the first administration of study treatment; urine human chorionic gonadotropin (HCG) is an acceptable pregnancy assessment

• Women/men of reproductive potential must be counseled on contraception/abstinence while receiving the study treatment

Exclusion Criteria:

• Childs-Pugh C liver function

• Major liver vascular invasion

• Prior radiation to the liver or other upper abdominal regions

• Must not have any evidence of bleeding diathesis or active gastrointestinal bleeding

• Any concurrent malignancy other than non-melanoma skin cancer, non-invasive bladder cancer, or carcinoma in situ of the cervix; patients with a previous malignancy without evidence of disease for >= 3 years will be allowed to enter the trial

• History of active connective tissue disease (scleroderma)

• Subjects who are breast-feeding, or have a positive pregnancy test will be excluded from the study; should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately

• Medical contraindication to MR imaging (e.g. pacemakers, metallic implants, aneurysm clips, known contrast allergy to gadolinium contrast, pregnancy, nursing mothers, weight greater than 350 pounds)

• Any serious and/or unstable pre-existing medical disorder (aside from malignancy exception above), psychiatric disorder, or other conditions that could interfere with subject's safety, obtaining informed consent or compliance to the study procedures, in the opinion of the investigator; this could include severe, active co-morbidities such as:

• Uncontrolled cardiac disease (hypertension, unstable angina, myocardial infarction within last 6 months, uncontrolled congestive heart failure, cardiomyopathy with decreased ejection fraction)

• Acute bacterial or fungal infection requiring intravenous antibiotics at time of registration

• Chronic obstructive pulmonary disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy within 30 days of registration

• Hepatic insufficiency resulting in jaundice and/or coagulation defects

Related Conditions & MeSH terms

• Carcinoma
• Carcinoma, Hepatocellular
• Child-Pugh Class A
• Child-Pugh Class B
• Stage IIIA Hepatocellular Carcinoma
• Stage IIIB Hepatocellular Carcinoma
• Stage IIIC Hepatocellular Carcinoma
• Stage IVA Hepatocellular Carcinoma
• Stage IVB Hepatocellular Carcinoma

Intervention

Other:
• Laboratory Biomarker Analysis
Correlative studies

Radiation:
• Stereotactic Body Radiation Therapy
Undergo SBRT

Procedure:
• Transarterial Chemoembolization
Undergo TACE

Locations

Country	Name	City	State
United States	Ohio State University Comprehensive Cancer Center	Columbus	Ohio

Sponsors (2)

Lead Sponsor	Collaborator
Ohio State University Comprehensive Cancer Center	Varian Medical Systems

Country where clinical trial is conducted

United States, 

References & Publications (1)

Sebastian NT, Miller ED, Yang X, Diaz DA, Tan Y, Dowell J, Spain J, Rikabi A, Elliott E, Knopp M, Williams TM. A Pilot Trial Evaluating Stereotactic Body Radiation Therapy to Induce Hyperemia in Combination With Transarterial Chemoembolization for Hepatoc — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Change in BOLD response to oxygen breathing based on T2 contrast induced by deoxyhemoglobin serving as an endogenous contrast agent		Baseline to day 1 post-SBRT
Other	Change in Kel (washout phase constant) values calculated from the DCE curve		Baseline to day 1 post-SBRT
Other	Change in mean apparent diffusion coefficient generated from diffusion weighted images by using the b values		Baseline to day 1 post-SBRT
Other	Change in miRNA expression		Baseline to up to 3 months
Other	Change in plateau signal intensity calculated from the DCE curve		Baseline to day 1 post-SBRT
Primary	Feasibility of SBRT in combination with TACE, measured by the number of patients able to tolerate all study procedures	Determined on the intent-to-treat principle. Any treatment delivery difficulties that arise that could impede successful delivery of this therapy sequence will be evaluated. The capability of the Ohio State University (OSU) system and communication between departments will be analyzed and deemed effective if it facilitates the successful treatment completion of all patients.	2 days
Secondary	Change in diffusion	Tested by comparing mean values pre- and post-SBRT using a paired t-test. Should there be concern for outliers, the median for each metric will be determined and compared using a corresponding non-parametric procedure.	Baseline to day 1 post-SBRT
Secondary	Change in hypoxia measurements	Tested by comparing mean values pre- and post-SBRT using a paired t-test. Should there be concern for outliers, the median for each metric will be determined and compared using a corresponding non-parametric procedure.	Baseline to day 1 post-SBRT
Secondary	Change in perfusion	Tested by comparing mean values pre- and post-SBRT using a paired t-test. Should there be concern for outliers, the median for each metric will be determined and compared using a corresponding non-parametric procedure.	Baseline to day 1 post-SBRT
Secondary	Incidence of toxicities	Includes measurement of grade 2-5 gastrointestinal symptoms, such as nausea, abdominal pain, hepatitis, enteritis, gastritis, bowel perforation, and fistula, as defined by Common Terminology Criteria for Adverse Events version 4.03.	Up to 30 days
Secondary	Local control	Calculated using standard clinical follow-up with MRI imaging and labs.	Up to 12 months
Secondary	Objective response rate (CR + PR) as measured by modified RECIST criteria version 1		Up to 6 months
Secondary	Overall survival	Calculated using standard clinical follow-up with MRI imaging and labs. Estimated using Kaplan-Meier analysis.	Up to 12 months
Secondary	Progression-free survival	Calculated using standard clinical follow-up with MRI imaging and labs. Estimated using Kaplan-Meier analysis.	Up to 12 months

External Links

•   The Jamesline