Table 3.
Yttrium-90 radioembolization in combination with second- or third-line chemotherapy.
Author | No. of patients | Trial design | Treatment | Response | Survival | Complications |
---|---|---|---|---|---|---|
Van Hazel et al. (34) | 25 | Prospective, dose escalation study | Irinotecan at 50, 75, or 100 mg/m2 on days 1 and 8 of a 3-week cycle for the first two cycles, and full irinotecan doses (i.e., 100 mg/m2) during cycles 3–9. Radioembolization during the first chemotherapy cycle | PR in 11 (48%) of 23, and SD in 9 (39%) | Median PFS: 6.0 months; Median OS: 12.2 months | Grades 3–4 events in three of six patients at 50 mg/m2 (obstructive jaundice, thrombocytopenia, and diarrhea), in five of 13 patients at 75 mg/m2 (neutropenia, leukopenia, thrombocytopenia, elevated alkaline phosphatase, abdominal pain, ascites, and fatigue) and in four of six patients at 100 mg/m2 (diarrhea, deep vein thrombosis, constipation, and leukopenia) |
Lim et al. (35) | 30 | Prospective; all patients who failed initial 5-FU chemotherapy, 22 failed oxaliplatin or irinotecan also. EHD in 7 | Radioembolization; concurrent 5FU in 21 | PR in 10 (33%); SD in 8 (27%); no response in patients with poor performance status or with extra hepatic disease | TTP: 5.3 months | Duodenal/gastric ulcer in 13%. One death related to radiation hepatitis |
CR, complete response; PR, partial response; SD, stable disease; PD, progressive disease; PFS, progression free survival; EHD, extra-hepatic disease; ORR, objective response rate; OS, overall survival; CEA, carcinoembryonic antigen; TTP, time to progression; HAC, hepatic arterial chemoinfusion.