Table 4. Summary of Technique.
Preparatory imaging |
Tri-phasic dynamic CT or MRI |
Periprocedural medication |
Analgesics |
Antibiotics for patients with increased risk of infection |
Loading of chemotherapeutic drug |
Microspheres are mixed with chemotherapeutic drug for at least 2 hours |
After loading, 5–10 mL of nonionic contrast should be per 1 mL of DC Bead® (BTG) |
Doses of chemotherapeutic drugs |
Each single treatment for patients within Milan criteria consists of 50–75 mg of doxorubicin loaded into one vial containing 2 mL of microspheres |
Each single treatment for patients who exceed Milan criteria consists of up to 150 mg of doxorubicin loaded into two vials of microspheres |
Treatment of patients with large tumors or tumors involving both lobes usually requires two separate sessions 2–4 weeks apart |
Super-selection of HCC tumors |
Following initial diagnostic visceral arteriography of superior mesenteric artery, celiac trunk, and common hepatic artery, vascular anatomy, possible feeding arteries and any variants are assessed, as are portal vein status |
Microsphere injection |
Proper positioning of microcatheter in which it should not be wedged |
Microspheres are injected slowly until endpoint near stasis is attained |
If endpoint near stasis is not reached after complete injection of all loaded microspheres, another session should be scheduled to repeat treatment |
Follow-up and repeat procedures |
CT or MRI is done at 1, 3, and 6 months after procedure and at 3 month intervals thereafter |
If viable tumors are observed, repeated cycles of DEM-TACE are recommended at 2–3-month intervals |
Criteria for stopping treatment include disease progression, failure to achieve targeted objective response, patient deterioration, and persistent hepatic decompensation |
CT = computed tomography, MRI = magnetic resonance imaging