TABLE 12.
Name of the study | Year of the study | Phase of the study | Research group | Dose | Results |
---|---|---|---|---|---|
Galanis et al. (Galanis et al., 2010) | 2021 | I | 21 | MV-CEA virus every 4 weeks for up to 6 cycles at seven different dose levels (103–109 TCID50) | Median survival was 12.15 (1.3–38.4 months), best objective response was dose-dependent disease stabilization was observed in 14 of 21 patients and with median duration of 92.5 days (54–277 days) |
Cohn et al. (Cohn et al., 2017) | 2017 | II | 108 | Paclitaxel (80 mg/m2 intravenously days 1, 8, and 15 every 4 weeks) or the combination of paclitaxel (80 mg/m2 intravenously days 1, 8, and 15) plus reovirus 3 × 1010 TCID50/day intravenously on days 1–5, both every 4 weeks until disease progression or toxicity | Median PFS was 4.3 months for paclitaxel and 4.4 months for paclitaxel plus reovirus |
ColoAd1-2001 (Moreno et al., 2021) | 2021 | I | 38 | Enadenotucirev iv. (1 × 1,012 viral particles; days 1, 3 and 5 every 28-day for two cycles) plus paclitaxel (80 mg/m2; days 9, 16 and 23 of each cycle) | 4-month PFS rate for 20 patients who received intravenous enadenotucirev plus paclitaxel was 64% (median 6.2 months) and 63% of the patients experienced treatment-emergent adverse event - first of all neutropenia (21%) |
MV-CEA, carcinoembryonic antigen-expressing oncolytic measles virus derivative; TCID, tissue culture infectious dose; PFS, progression-free survival.