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. Author manuscript; available in PMC: 2012 Dec 27.
Published in final edited form as: Curr Pharm Des. 2012;18(17):2472–2481. doi: 10.2174/13816128112092472

Table 1.

Completed Clinical Trials Evaluating Mucin Vaccines in PC Patients

Year Phase Mucin Formulation Adjuvant Major Outcomes References
1996 I MUC1 105 AA BCG
  • Vaccine well tolerated

  • No partial/complete response

Goydos et al. [39]
2002 II Adoptive transfer of autologous DCs transfected with MUC1
  • Vaccine well tolerated

  • PC patients presented higher frequencies of IFNγ-secreting CD8+ T cells compared to other patients after immunization

  • Nine out of 10 patients presented progressive disease

Pecher et al. [45]
2005 I MUC1 100 AA SB-AS2
  • Vaccine well tolerated even at 3000 μg MUC1 peptide dose

Ramanathan et al. [41]
2005 I MUC1 100 AA Incomplete Freund's
  • Seven out of eight patients had progressive disease

Yamamoto et al. [43]
2007 I Vaccinia and Fowlpox viral vectors expressing CEA and MUC1 TRICOM + GM-CSF
  • Antigen-specific T cell immune responses

Kaufman et al. [86]
2008 I/II Adoptive transfer of MUCl-peptide pulsed DCs
  • No increase in anti-MUCl antibodies

  • High non-specific T cell activation

Lepisto et al. [40]
2008 I Adoptive transfer of in vitro activated CTLs with MUC1-expressing cell line
  • Vaccine well tolerated

  • No improvement in survival

Kawaoka et al. [46, 47]
2008 I Adoptive transfer of MUC1 peptide pulsed DCs + activated CTLs
  • Vaccine well tolerated

  • Mean survival of 9.8 months

  • Five patients presented stable disease

Kondo et al. [48]

MUC1, Mucinl; AA, amino acid; DCs, dendritic cells; IFNγ, Interferon gamma; BCG, Bacillus-Calmette-Guérin; SB-AS2, adjuvant composed of monophosphoryl lipid A and QS-21; CEA, Carcinoembryonic antigen; TRICOM, formulation including the costimulatory molecules B7.1, ICAM-1, and LFA-3; GM-CSF, granulocyte-macrophage colony-stimulating factor; CTLs, cytotoxic T lymphocytes