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Phase 2 Completed N=24 Randomized Single-blind Treatment

Safety and Effectiveness of a Vaccine for Prostate Cancer That Uses Each Patients' Own Immune Cells.

Source: ClinicalTrials.gov NCT00289341 ↗
Enrolled (actual)
24
Serious AEs
3.3%
Results posted
Jan 2013
Primary outcomePrimary: Adverse Event — 22; 2; 4; 0 Adverse Events — p=0.001

Summary

The purpose of this study is to assess the safety and activity of a type of vaccine as immune therapy for prostate cancer. This vaccine will be made for each participant's own immune cells (called dendritic cells) obtained by blood donation. Dendritic cells are immune cells, whose role is to identify foreign antigens (bacteria, viruses, or tumor cells, for example) in the body and to activate other cells of the immune system to mount an attack on that foreign antigen. Each participant will be randomized into either Arm 1 (experimental treatment only) or Arm 2 (placebo first, then the experimental treatment). Participants will be given the vaccine and three boosters as an injection. After the placebo phase, each participant in Arm 2 will crossover to the treatment phase so that all participants will eventually receive the experimental treatment.

Outcome Measures

OutcomeResultp-value
PRIMARY
Adverse Event
22; 2; 4; 0; 0; 1 0.001 sig
PRIMARY
Immunogenicity of the DC/LNCaP Vaccine. Pre- vs Post-vaccination Bulk T Cell Proliferation (3H Thymidine Incorporation) by Type of Antigen. The "Number" Indicated is the Median Difference of Post-Pre, of Each Antigen Group.
4375.64; 16873.92; 20334.1581; 23950.125; 10299.3967
SECONDARY
Change in PSA Slope, Pre- vs Post-vaccination.
-0.093 0.016 sig

Eligibility Criteria

Inclusion Criteria

Disease Characteristics

  • Histologically confirmed prostate carcinoma
  • Progressive, disease required, i.e.: elevated PSA documented to be rising on 3 occasions, either despite castrate testosterone levels (below 50 ng/dl), or after definitive local therapy (prostatectomy or radiation).

Prior/Concurrent Therapy

-Biologic therapy:

  • Recovered from toxicity of any prior therapy

-Chemotherapy:

  • At least 4 weeks since chemotherapy -Endocrine evaluation/therapy
  • 3 rising PSA values at least 2 weeks apart
  • At least 2 weeks since concurrent corticosteroids (other than for replacement therapy for adrenal insufficiency)
  • Medical hormonal therapy to maintain castrate testosterone levels permitted

-Radiotherapy:

  • At least 4 weeks since radiotherapy

-Surgery:

  • Prior surgery allowed

Patient Characteristics

  • Age: 18 and over, able to give written informed consent. Individuals unable to provide informed consent must have consent provided by the legal guardian, or person designated by the subject to give consent on his behalf.
  • Performance status: Karnofsky 70-100%
  • Life expectancy: At least 1 year
  • Hematopoietic: obtained twice, once within 45 days prior to study entry, and again within 72 hours of study entry.
  • WBC greater than 3,800
  • Absolute neutrophils greater than 1,500
  • Absolute lymphocytes greater than 500
  • Platelets greater than 120,000
  • Hb at least 10 g/dl
  • Hepatic:

--Bilirubin less than 2.0 mg/dl OR

--SGOT less than 2 x ULN

  • Renal:
  • Creatinine no greater than 2.0 mg/dl OR
  • Creatinine clearance at least 40 ml/min
  • Rheumatologic:

--ANA no greater than upper limit of normal, or ANA abnormal in absence of clinical signs of autoimmunity.

  • Rheumatoid factor (RF) no greater than upper limit of normal, or RF abnormal in absence of clinical signs of autoimmunity.
  • Anti-ds DNA no greater than upper limit of normal, or anti ds DNA abnormal in absence of clinical signs of autoimmunity.
  • Immunologic:
  • Influenza serology (assessment made at time of screening).
  • Assessment of DTH response to a standard anergy panel (to include candida, trichophyton and tetanus) or to a Multitest CMI (a disposable kit for DTH testing with standardized preloaded antigens).
  • Endocrine:

--TSH, T3, and T4 no greater than upper limit of normal

  • Radiographic:
  • Baseline bone scan
  • Baseline CT or MRI of abdomen and pelvis

Exclusion Criteria

Disease Characteristics -No active CNS metastases

Prior/Concurrent Therapy

  • Biologic therapy:
  • No prior autologous or allogeneic tumor vaccines
  • No concurrent other immunotherapy
  • Chemotherapy

--Not previously treated with more than 2 chemotherapy regimens

  • No concurrent chemotherapy
  • Radiotherapy --No concurrent radiotherapy

Patient Characteristics -Cardiovascular: No NYHA class III/IV status No active angina, clinically significant cardiac arrythmia, recent (6 months) myocardial infarction

  • Pulmonary:

--No severe debilitating pulmonary disease

  • Other:
  • No active infection requiring antibiotics
  • No active pain requiring chronic opioid analgesics.
  • Not HIV, hepatitis B or hepatitis C virus positive; anti-HIV, HbsAg and Hep C antibody negative
  • No history of hypersensitivity to vaccine components
  • No serious uncontrolled medical illness
  • No currently active second malignancy other than non-melanoma skin cancer (note: a patient is NOT considered to have currently active malignancy if they have completed therapy and are now considered by their physician to be at less than 30% risk for relapse)
  • No history of total lymph node irradiation
  • No history of vasculitis, including but not limited to systemic necrotizing vasculitides (polyarteritis nodosa group), hypersensitivity vasculitis, Wegener's granulomatosis.
  • No history of autoimmune disease.
  • No use of hydroxyurea within 45 days of study entry
  • No receipt of immune modulators or suppressors within 30 days prior to study entry, including but not limited to interferons and thalidomide. No active
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00289341). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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