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Orthotopic administration of 213Bi-bevacizumab inhibits progression of PC3 xenografts in the prostate

  • S. M. A. Rizvi
  • , B. J. Allen
  • , C. S. Lee
  • , F. Bruchertseifer
  • , C. Apostolidis
  • , A. Morgenstern
  • , R. A. Clarke

Research output: Contribution to journalArticlepeer-review

5 Citations (Scopus)

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 languageEnglish
Pages (from-to)549-554
Number of pages6
JournalImmunotherapy
Volume4
Issue number5
DOIs
Publication statusPublished - 2012

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • PC3 xenografts
  • alpha-radioimmunotherapy
  • bevacizumab-213
  • bismuth
  • breast cancer
  • cytotoxicity
  • prostate cancer

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