Antigen-presenting cells 8015 (Provenge) in patients with androgen-dependent, biochemically relapsed prostate cancer

Garth Beinart1, Brian I Rini, Vivian Weinberg

  • 1Department of Hematology/Oncology, M. D. Anderson Cancer Center, USA.

Clinical Prostate Cancer
|July 5, 2005
PubMed
Abstract

Insights

Antigen-presenting cells 8015 (APC8015) immunotherapy showed potential in modulating prostate-specific antigen doubling time in patients with androgen-dependent prostate cancer. Further immune system manipulation may be needed for significant antitumor effects.

Area of Science:

  • Immunotherapy
  • Oncology
  • Prostate Cancer Research

Background:

  • Antigen-presenting cells 8015 (APC8015) is an immunotherapy targeting prostatic acid phosphatase, overexpressed in prostate cancer.
  • Previous trials indicated APC8015 elicits immune and clinical responses in androgen-independent prostate cancer.
  • This study evaluated APC8015's effect on prostate-specific antigen (PSA) in androgen-dependent prostate cancer (ADPC) with biochemical progression.

Purpose of the Study:

  • To assess the PSA-modulating effects of APC8015 in patients with ADPC and biochemical progression.
  • To evaluate the safety and tolerability of APC8015 in this patient population.

Main Methods:

  • Phase II trial involving patients with nonmetastatic recurrent ADPC and rising PSA levels.
  • Patients received three infusions of APC8015 at weeks 0, 2, and 4.
  • PSA levels were monitored monthly to determine disease progression, defined by PSA doubling or metastasis.

Main Results:

  • Thirteen out of 18 patients experienced an increase in PSA doubling time (PSADT).
  • The median increase in PSADT was 62% (4.9 to 7.9 months; P=0.09).
  • APC8015 did not achieve a >=50% decrease in PSA from baseline in any patient.

Conclusions:

  • APC8015 was well-tolerated as a single agent in patients with ADPC and biochemical progression.
  • The immunotherapy demonstrated a potential to modulate PSADT in a subset of patients.
  • Significant antitumor effects may necessitate further immune system modulation strategies.

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