Table 2.
Selected clinical studies of oncolytic NDV in patients with cancer
| NDV strain | Cancer type | Route | Outcome | Trial ID & Reference |
|---|---|---|---|---|
| 73-T | Melanoma | Subcutaneous |
55% 15-year overall survival; single-arm cohort |
No trial ID [15] |
| ATV-NDV | Solid tumors | Intradermal | High disease control rates, with 2-year survival improvements of 20–36% |
No trial ID [16] |
| MTH-68 | High-grade glioblastomas | Intravenous |
Long-term (> 5 years) survival and near-complete tumor regression in 4/4 terminal GBM patients, with no toxicity |
No trial ID [96] |
| PV701 | Advanced or recurrent tumors | Intravenous | 20% ORR |
[93] |
| NDV-HUJ | Recurrent glioblastoma | Intravenous | One transient CR lasting > 3 months |
[97] |
|
MEDI5395 (rNDV-GM-CSF) |
Advanced solid tumors | Intravenous | 10.3% ORR (PR) with manageable toxicity |
[50] |
|
MEDI9253 (rNDV-IL 12) |
Solid tumors | Intravenous |
No efficacy data (ORR, PFS, OS) disclosed yet |
No reference yet |
| NDV-GT | Multiple advanced cancers |
Intravenous ± intraperitoneal |
90% disease control (1 CR + 6 PR + 11 SD) with durable responses and no serious adverse events |
ChiCTR2000031980 [14] |
ATV-NDV, NDV-modified autologous tumor vaccine; ORR, objective response rate; PFS, progression-free survival; OS, overall survival; PR, partial response; CR, complete response; SD, stable disease