Table 2.
List of studies combining antiangiogenic agents with oncolytic viruses.
| Oncolytic Virus used | Type of virus | Tumor model | Treatment strategy | Efficacy | Reference | |
|---|---|---|---|---|---|---|
| Avastin | ||||||
| 1 | Dl922-947 | E1A deleted Adenovirus | Anaplastic thyroid carcinomas in athymic nude mice | Avastin (i.p.) every 5th day and OV twice a week for 4 weeks | Co-treatment group enhanced efficacy over single agent alone | Libertini et al. Clin Cancer Res 2008;14:6505–14 |
| 2 | Ad5/3-Δ24 | Ad5 virus with E1 gene with 24 bp deltion, and serotype 3 knob | Peritoneal disseminated Renal Cell cancer in SCID mice | Avastin: i.p. once a week for 5 weeks and OV: i.p. on days 7, 14, and 21 post tumor implant. | No enhancement over OV alone | Guse et al. Mol Cancer Ther 2007;6:2728–32 |
| 3 | Ad5-Δ24RGD | Ad5 virus with E1 gene with 24 bp deltion, RGD motif in H1 loop of knob protein | Peritoneal disseminated Renal Cell cancer in SCID mice | Avastin: i.p. once a week for 5 weeks and OV: i.p. on days 7, 14, and 21 post tumor implant. | No enhancement over OV alone | Guse et al. Mol Cancer Ther 2007;6:2728–32 |
| 4 | Ad5.pk7-Δ24 | Ad5 virus with E1 gene with 24 bp deltion, and 7 lysine residues at C terminus of fiber | Peritoneal disseminated Renal Cell cancer in SCID mice | Avastin: i.p. once a week for 5 weeks and OV: i.p. on days 7, 14, and 21 post tumor implant. | No enhancement over OV alone | Guse et al. Mol Cancer Ther 2007;6:2728–32 |
| 5 | GLV-1h68 | Renilla luciferase, GFP, and fusion, β-galactosidase, and β-glucuronidase expressing VV | s.c Pancreatic cancer cells in mice | Avastin: twice a week for 5 weeks 13 days post OV treatment; OV: single dose i.v | Co treatment group enhanced efficacy over single agent alone. | Frentzen et al. Proc Natl Acad Sci USA 2009;106:12915–20 |
| Thrombospondin 1 peptide | ||||||
| 5 | G207 | HSV-1 deleted for ICP34.5 and disrupted for ICP6 | s.c glioma in nude mice | TSR peptide: i.p. daily days 1–27. OV: on days 2 and 5. | Co treatment group enhanced efficacy over single agent alone. | Aghi et al. Cancer Res 2007;67:440–4 |
| 6 | G47Δ | HSV-1 deleted for ICP34.5 and disrupted for ICP6, and deted for α47. | s.c glioma in nude mice | TSR peptide: i.p. daily days 1–27. OV: on days 2 and 5. | No enhancement over OV alone | Aghi et al. Cancer Res 2007;67:440–4 |
| Trichostatin A | ||||||
| 7 | G47Δ | HSV-1 deleted for ICP34.5 and disrupted for ICP6, and deted for α47. | s.c glioma in nude mice | TSA:i.p. daily for twelve days; OV: i.t on days 1, and 4. | Co treatment group enhanced efficacy over single agent alone. | Liu et al. Mol Ther 2008;16:1041–7 |
| Cilengitide | ||||||
| 8 | hrR3 | HSV-1 deleted for ICP34.5 and disrupted for ICP6, and deted for α47. | i.c rat glioma in rats | Cilengitide: i.t on day 3; OV: i.t day 7 | Co treatment group enhanced efficacy over single agent alone. | Kurozumi et al. J Natl Cancer Inst. 2007;99:1768–81 |
| Thalidomide | ||||||
| 9 | HSV-1 +/− forICP34.5 and mutant gB and gK. | s.c 4T1 tumors in mice | Thalidomide: orally in chow from day 4; OV: i.t three times | Co treatment group enhanced efficacy over single agent alone. | Israyelyan et al. Cancer Chemother Pharmacol 2009;64:1201–10 | |
Abbreviations; i.v: intra venous; s.c: sub cutaneous; i.p: intra peritoneal; i.c: intra cranial; Ad: Adenovirus; VV: Vaccinia virus