Radiation Therapy With Protons or Photons in Treating Patients With Liver Cancer

Launched by NRG ONCOLOGY · Jun 12, 2017

Keywords

ClinConnect Summary

This clinical trial is investigating the effectiveness of two types of radiation therapy—proton therapy and photon therapy—for treating patients with liver cancer that cannot be surgically removed or has come back in the same area. Proton therapy uses protons, which are charged particles, and may be better at targeting tumors while causing less harm to nearby healthy tissues. This trial aims to find out if proton therapy leads to better outcomes for patients compared to traditional photon therapy.

To participate in this trial, patients should have liver cancer that meets certain criteria, such as having tumors that can be measured and are within specific size limits. They must also meet health requirements, including certain blood counts and liver function tests. The trial is currently recruiting participants aged 65 to 74, and both men and women can join. If eligible, participants can expect to receive either type of radiation therapy and will be closely monitored throughout the study. It’s important for potential participants to discuss this opportunity with their healthcare provider to see if it’s a good fit for them.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Pathologically (histologically or cytologically) or radiographically-proven (based on the American Association for the Study of Liver Diseases \[AALSD\] criteria) unresectable or locally recurrent hepatocellular cancer prior to registration
• * Appropriate stage for study entry based on the following diagnostic workup:
• • All patients must have computed tomography (CT) scan chest/abdomen/pelvis with multiphasic liver CT scan prior to registration; if CT contrast is contraindicated, CT chest without contrast and magnetic resonance imaging (MRI) of abdomen is permitted
• • Participants must have measurable disease at study entry, defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded) as \> 2 cm with conventional techniques or as \> 1 cm with spiral CT scan
• • Patient must have 3 or fewer single or multinodular tumors; for patients with a single lesion, lesion must be 15 cm or less in greatest dimension; for patients with two lesions, no lesion may be greater than 10 cm in greatest dimension; for patients with three lesions, no lesion may be greater than 6 cm in greatest dimension; portal vein involvement or thrombosis combined with a single lesion that is \>= 1 cm and =\< 15 cm in greatest dimension is allowed
• • Age \>= 18
• • Zubrod performance status 0-1 within 30 days prior to registration
• • Negative urine or serum pregnancy test for women of childbearing potential within 7 days prior to study entry
• • Absolute neutrophil count (ANC) \>= 1,000 cells/mm\^3
• • Platelets \>= 50,000 cells/mm\^3
• • Hemoglobin \>= 9.0 g/dl; (Note: The use of transfusion or other intervention to achieve hemoglobin \[Hgb\] \>= 9.0 g/dl is acceptable)
• • Total bilirubin \< 4 x institutional upper limit of normal (ULN)
• • Transaminases (aspartate aminotransferase \[AST\] and alanine aminotransferase \[ALT\]) \< 6 x institutional ULN
• • Albumin \>= 2.5 g/dl
• • Creatinine \< 2 mg/dl
• • Prior chemotherapy, targeted biological therapy (e.g. sorafenib), surgery, transarterial chemoembolization (TACE), ablation for present disease is acceptable
• • Must have Child-Turcotte-Pugh (CTP) A or B7
• • The patient or a legally authorized representative must provide study-specific informed consent prior to study registration
• Exclusion Criteria:
• * PRIOR TO STEP ONE REGISTRATION:
• • Definitive clinical or radiologic documentation of extrahepatic tumor, defined as extrahepatic metastases or malignant nodes (that enhance with typical features of HCC) \> 3.0 cm, in sum of maximal diameters (e.g. presence of one 3.4 cm metastatic lymph node or two 2 cm lung lesions); note that benign non-enhancing periportal lymphadenopathy is not unusual in the presence of hepatitis and is permitted, even if the sum of enlarged nodes is \> 2.0 cm
• • Uncontrolled prior invasive malignancy, excluding the current diagnosis
• • Systemic chemotherapy for the study cancer \< 2 weeks prior to registration
• • Pregnancy or women of childbearing potential and men who are sexually active and not willing/able to use medically acceptable forms of contraception; this exclusion is necessary because the treatment involved in this study may be significantly teratogenic
• • HIV positive with CD4 count \< 200 cells/microliter; note that patients who are human immunodeficiency virus (HIV) positive are eligible, provided they are under treatment with highly active antiretroviral therapy (HAART) and have a CD4 count \>= 200 cells/microliter prior to registration; note also that HIV testing is not required for eligibility for this protocol; this exclusion criterion is necessary because the treatments involved in this protocol may be significantly immunosuppressive
• • Prior radiotherapy to the region of the study cancer that would result in overlap of radiation therapy fields (to include Y90)
• • Prior liver transplant
• * PRIOR TO STEP TWO RANDOMIZATION:
• • Unable to obtain confirmation of payment coverage (insurance or other) for either possible treatment