This randomized phase II trial studies how well embolization therapy with or without chemotherapy works in controlling liver metastases in patients with neuroendocrine tumors which have spread to the liver and cannot be removed by surgery. Embolization therapy injects tiny particles with or without chemotherapy drugs into the arteries feeding tumors to cut off their blood supply. Embolization with chemotherapy, such as doxorubicin hydrochloride and mitomycin or doxorubicin-eluting beads, may kill more tumor cells by allowing a higher concentration of the drug to reach the tumor for a longer period of time. It is not yet known if there are differences in quality of life, side effects, or safety among these types of embolization therapy or if any one type will provide longer-lasting control of tumors in the liver.
Additional locations may be listed on ClinicalTrials.gov for NCT02724540.
See trial information on ClinicalTrials.gov for a list of participating sites.
PRIMARY OBJECTIVES:
I. To estimate the duration of hepatic progression-free survival (HPFS) in participants treated with bland embolization (BE), transcatheter arterial lipiodol chemoembolization (TACE), and embolization by drug-eluting beads (DEB).
SECONDARY OBJECTIVES:
I. To compare the interval between cycles of embolotherapy among the arms.
II. To estimate the symptom-free interval for patients with tumor-related symptoms among the arms using the Carcinoid Symptom Severity Scale.
III. To compare patient-reported outcomes (European Organization for Research and Treatment of Cancer [EORTC] Quality of Life Questionnaire Core 30 [QLQ30] & Gastrointestinal Neuroendocrine Tumors 21 [GINET21]) among the arms.
IV. To compare toxicities and adverse events among the arms.
V. To compare progression-free survival and duration of symptom control in patients with carcinoid versus islet-cell sub types and for grade (G)1 vs. G2 histology.
VI. To identify biomarkers (imaging, serum and symptom) of treatment effect in all arms.
OUTLINE: Patients are randomized to 1 of 3 arms.
ARM I: Patients undergo 1-3 lobar or segmental bland embolizations with tris-acryl gelatin microspheres depending upon the number and location of tumors every 4-8 weeks.
ARM II: Patients undergo 1-3 lobar or segmental transcatheter arterial lipiodol chemoembolizations with doxorubicin hydrochloride depending upon the number and location of tumors every 4 weeks.
ARM III: Patients undergo 1-3 lobar or segmental hepatic chemoembolizations with drug-eluting beads (DEB) loaded with doxorubicin depending upon the number and location of tumors every 4-8 weeks.
In all arms, treatment repeats every 4-8 weeks for up to 4 cycles in the absence of disease progression or unacceptable toxicity. Patients with intrahepatic progression may receive additional embolization therapy for another cycle or switch to another therapy.
After completion of study treatment, patients are followed up every 3 months for 2 years.
Lead OrganizationUniversity of Pennsylvania/Abramson Cancer Center
Principal InvestigatorMichael C. Soulen