An antibody-cytotoxic conjugate, BIIB015, is a new targeted therapy for Cripto positive tumours

Rebecca K Kelly1, Dian L Olson, Yaping Sun

  • 1Biogen Idec, Inc, Discovery Oncology, 14 Cambridge Center, Cambridge, MA 02142, USA.

European Journal of Cancer (Oxford, England : 1990)
|April 5, 2011
PubMed

Insights

BIIB015, an antibody-drug conjugate targeting the Cripto oncogene, effectively inhibits solid tumor growth. This novel immunoconjugate shows promise in preclinical models, including triple-negative breast cancer.

Area of Science:

  • Oncology
  • Immunotherapy
  • Drug Development

Background:

  • Cripto is an oncogene re-expressed in various solid tumors, including breast, lung, and colorectal cancers.
  • Targeting Cripto presents a potential therapeutic strategy for cancers with high Cripto expression.
  • Current treatments for triple-negative breast cancer are limited.

Purpose of the Study:

  • To evaluate the efficacy of BIIB015, an anti-Cripto immunoconjugate, in treating solid tumors.
  • To compare the activity of BIIB015 with different linker systems.
  • To assess the potential of BIIB015 in combination therapy.

Main Methods:

  • BIIB015 is an immunoconjugate comprising a humanized anti-Cripto antibody linked to DM4 maytansinoid.
  • In vitro and in vivo studies were conducted using human xenograft models (lung, colon, testicular, breast).
  • Comparative analysis of BIIB015 with different linker systems (cleavable vs. non-cleavable).

Main Results:

  • BIIB015 demonstrated specific binding to Cripto and potent anti-tumor activity in preclinical models.
  • Significant tumor inhibition and complete regression were observed in xenograft models.
  • BIIB015 with a cleavable linker showed superior activity compared to non-cleavable linker conjugates.
  • Remarkable efficacy was noted in the MDA-MB-231 triple-negative breast cancer model.

Conclusions:

  • Targeting cell surface Cripto protein with BIIB015 is an effective strategy for inhibiting or regressing Cripto-positive solid tumors.
  • BIIB015 exhibits robust anti-tumor activity and specificity in preclinical settings.
  • BIIB015 holds promise as a therapeutic agent, particularly for triple-negative breast cancer, and can be combined with chemotherapy.

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