Safety Study of Autologous Dendritic Cells Injected Into the Prostate After Cryoablation for Advanced Prostate Cancer

Prostate Cancer Clinical Trial

— CRITICAL  

Official title:

A Phase I/IIa Trial of Combined Cryotherapy and Intra-tumoral Immunotherapy With Autologous Immature Dendritic Cells (VDC2008) in Chemo-naïve Men With Prostatic Adenocarcinoma and Limited Metastases to Lymph Nodes and/or Bone

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00753220
• Other study ID #: CRITICAL001
• Status: Terminated
• Phase: Phase 1/Phase 2
• First received: September 12, 2008
• Last updated: November 3, 2014
• Start date: August 2009
• Est. completion date: December 2011

Study information

• Verified date: November 2014
• Source: Bostwick Laboratories
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine if the intra-tumoral injection of a subject's own dendritic cells after cryotherapy of the prostate is a safe and effective treatment for advanced prostate cancer.

In theory, the injected dendritic cells will internalize antigens from the tumor cells which have been damaged by cryotherapy and activate the subject's immune system against that specific tumor.

Subjects will also receive a low dose chemotherapy designed to lower the number of T-regulatory cells which have been shown to lower or stop some immune system responses.

Hypothesis 1: Dendritic cell injection into cryotreated prostate cancer is non-toxic;

Hypothesis 2: Dendritic cell injection into cryotreated prostate cancer is medically beneficial to the subject.

Description:

The study treatment dendritic cells (VDC2008) will be injected into the prostate following prostatic cryoablation. It is speculated that antigen from the cryoablated cancer will be available in the vicinity of the cryoablation field immediately following the procedure. Autologous, immature dendritic cells are capable of internalizing antigen, migrating to the lymphatic system, and presenting antigenic epitopes to T lymphocytes. In this way, dendritic cells are capable of initiating a cell-mediated systemic immune response.

In concept, the cancer itself should provide a specific and potentially broad spectrum of cancer-related antigens. Regulatory T lymphocytes, which have been implicated in dampening or halting cell-mediated, antigen-specific immune responses, will be selectively depleted using a regimen of low-dose cyclophosphamide. Low-dose cyclophosphamide has been empirically shown to selectively deplete the number of circulating regulatory T cells.

Using this combination of therapies, it is thought that a clinically significant anti-cancer immune response might be elicited.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 7
• Est. completion date: December 2011
• Est. primary completion date: May 2011
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria

• Men = 18 years of age and any race.

• Signed Informed Consent document obtained prior to the initiation of screening procedures.

• Histologically documented primary adenocarcinoma of the prostate. A specimen of the primary tumor must be submitted to the Central Pathology Laboratory for confirmation of prostatic adenocarcinoma and determination of Gleason Sum grading.

• Prior history of:

1. Androgen Deprivation Therapy; or

2. Organ-preserving therapy (i.e., non-prostatectomy) for primary prostate cancer (e.g., radiation therapy).

• In case of recurrence, subject must have evidence of prostate cancer by a positive biopsy revealing adenocarcinoma within the past 6 months of screening and confirmed by the Central Pathology Laboratory.

• TxNxM1a and/or TxNxM1b disease limited to three total metastatic sites as evidenced by lymph node metastases and /or bone metastases at time of screening.

1. TxNxM1a : Lymph node metastases histologically proven and confirmed by Central Pathology Laboratory;

2. TxNxM1a: Lymph node metastases not histologically proven, given that the following are satisfied in the temporal order listed:

1. Computed tomography (CT) or Magnetic Resonance Imaging (MRI) for positive lymph nodes negative at original diagnosis of prostate cancer;

2. Definitive local treatment undertaken;

3. Evidence of local treatment failure on the basis of rising serum PSA;

4. Prostatic biopsy positive for carcinoma;

5. Subsequent CT or MRI reveals lymph node(s) of 2 cm diameter or greater

3. TxNxM1b: Bone metastases demonstrated by radionuclide bone scan, CT, or MRI.

• Androgen-independent prostate cancer as defined by:

1. Three consecutive rises of at least 10% each in serum PSA, in which all serum PSA measurements are separated by at least one week and results are obtained within 60 days of study screening; OR

2. Three rises that involve an increase of 50% over the nadir serum PSA, in which all serum PSA measurements are separated by at least one week and results are obtained within 60 days of study screening;

3. A castrate level of testosterone (<50 ng/dl) obtained within 60 days of study screening.

• Life expectancy of greater than or equal to 12 months.

• Adequate hematological function as defined by:

1. Total WBC > 4,500/mm3

2. Total lymphocyte count > 500/mm3

3. Hemoglobin > 12.0 g/dl

4. Neutrophils > 1,500/mm3

5. Platelets > 150,000/mm3

• Adequate renal function with creatinine < 2.0 mg/dl.

• Adequate liver function as defined by:

1. AST and ALT < 2 times the upper limit of normal;

2. Serum bilirubin < 2.0 mg/dl;

3. Alkaline Phosphatase < 2.0 upper limit of normal.

• Assessment of superficial veins as adequate for the performance of leukapheresis.

• No active major medical or psychological problems that could be complicated by study participation.

Exclusion Criteria

• The presence of lung, liver or brain metastases, malignant pleural effusions or malignant ascites.

• Moderate or severe symptomatic metastatic disease. Subjects who meet either of the following criteria must be excluded:

1. A requirement for treatment with opioid analgesics for any reason within 21 days prior to study screening;

2. Average weekly pain score of 4 or more as reported on the 11-point Pain Intensity - Numerical Rating Scale (Appendix III) over the two weeks prior to study enrollment.

• Eastern Cooperative Oncology Group (ECOG) performance status = 2 accessed at study screening visit.

• Chemotherapy treatment at any time prior to study screening.

• Radiation therapy for metastatic disease, including intravenous radioactive strontium therapy.

• Initiation or discontinuation of bisphosphonate therapy within 28 days prior to study screening. Subjects taking bisphosphonate medication must not have their dosing regimen altered until objective disease progression is independently confirmed.

• Treatment with any of the following medications or interventions within 28 days of study screening:

1. Systemic corticosteroids (use of inhaled, intranasal and topical steroids is acceptable);

2. External beam radiation therapy or surgery;

3. PC-SPES (or PC-SPEC) or Saw Palmetto extract;

4. Megestrol acetate (Megace®), diethyl stilbesterol (DES), or cyproterone acetate;

5. Ketoconazole;

6. High dose calcitriol (i.e., > 7.0 µg/week);

7. Any other systemic therapy for prostate cancer.

• Treatment with any investigational vaccine within 2 years of enrollment to this study.

• Treatment with any other investigational product within 28 days of study screening.

• Pathologic long-bone fractures, imminent pathologic long-bone fracture (cortical erosion on radiography > 50%) or spinal cord compression.

• Impending untreated spinal cord compression or urinary outlet obstruction.

• Paget's Disease of bone.

• History of stage III or greater cancer, excluding prostate cancer:

1. Basal or squamous cell skin cancers must have been adequately treated and the subject must be disease-free at the time of study screening visit;

2. Subjects with a history of stage I or II cancer must have been adequately treated and be disease-free for = 3 years at the time of study screening

• Requirement for systemic immunosuppressive therapy for any reason

• Prior or currently active autoimmune disease requiring management with systemic immunosuppression. Such conditions include inflammatory bowel disease, systemic vasculitis, scleroderma, psoriasis, multiple sclerosis, hemolytic anemia, immune-related thrombocytopenia, rheumatoid arthritis, systemic lupus erythematosus, Sjögren's syndrome, sarcoidosis, or other rheumatological disease.

• Any infection requiring parenteral antibiotic therapy or causing fever (body temperature > 100.5°F or 38.1°C) within 1 week prior to study screening.

• Known allergy, intolerance, or medical contraindication to receiving the contrast dye required for the protocol-specified CT imaging

• History of asthma, anaphylaxis, or other known serious adverse reactions to vaccines.

• Any medical intervention or other condition which, in the opinion of the Physician-Investigator could compromise adherence with study requirements or otherwise compromise study subject safety and the study's objectives.

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Prostate Cancer
• Prostatic Neoplasms

Intervention

Biological:
• VDC2008
Intratumoral injection of VDC2008 post-cryotherapy. Dosage will depend on cohort: 2.5 x 10^7, 7.5 x 10^7 or 1.0 x 10^8 cells

Drug:
• Cyclophosphamide
Cyclophosphamide i.v. given at day -3 (dose: 300mg/m2); Low-dose Cyclophosphamide pill given twice daily (dose: 25 mg, p.o., b.i.d. for 7 days on and 7 days off; a total of 6 cycles [1 cycle = 4 weeks] starting Week 2 after cryoablation and going to Week 26)

Locations

Country	Name	City	State
United States	Community Memorial Hospital	Ventura	California

Sponsors (4)

Lead Sponsor	Collaborator
Bostwick Laboratories	Community Memorial HealthCenter, HemaCare Corporation, Prostate Institute of America

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum Tolerated Dose (MTD)	PROTOCOL EXCERPT: The primary objective of the Phase I Portion of this study is the determination of the maximum tolerated dose (MTD) of intratumorally injected study agent VDC2008 administered following cryoablation of the prostate, and pre- and post-treatment with a low-dose cyclophosphamide therapy, as determined by toxicity and adverse event monitoring following treatment of metastatic androgen-independent prostate cancer.; ADDITIONAL INFORMATION: MTD was not reached by any study participant prior to end of the study. Additional participants would have been necessary to determine MTD.	Up to 1 year	Yes