Abstract
Aim: To investigate orthotopic targeted alpha-radioimmunotherapy for the control of early-stage PC3 prostate cancer nude mouse xenografts using the radiolabeled bevacizumab (BZ) immunoconjugate (Bi-213-BZ), which emits short-range alpha-radiation. Materials & methods: 10(6) PC3 human prostate cancer cells were injected into the lower capsule of the mouse prostate gland 1 week prior to alpha-radioimmunotherapy. Mice were euthanized and assessed for tumour growth at 2 (two mice), 4 (two mice) and 6 weeks (three mice) post-therapy. The no-therapy control mice received a saline injection in equal volume to each BZ administration. Results: Bi-213-BZ is significantly more efficacious in inhibiting xenograft progression in the prostate gland compared with BZ alone (p = 0.009) and when compared with the 'no therapy' protocol (p < 0.0001). Conclusion: Orthotopic administration of Bi-213-BZ greatly improves the early control of organ-confined prostate cancer compared with BZ alone (p < 0.01).
| Original language | English |
|---|---|
| Pages (from-to) | 549-554 |
| Number of pages | 6 |
| Journal | Immunotherapy |
| Volume | 4 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - 2012 |
Keywords
- PC3 xenografts
- alpha-radioimmunotherapy
- bevacizumab-213
- bismuth
- breast cancer
- cytotoxicity
- prostate cancer