PROSTVAC (PSA-TRICOM) in Preventing Disease Progression in Patients With Localized Prostate Cancer Undergoing Active Surveillance

PRIMARY OBJECTIVES:

I. To determine the effect of rilimogene-galvacirepvec (PROSTVAC) on the change (from pre to
post-intervention) in CD8+ positive cells in the stroma adjacent to tumor and within the
malignant portion of the prostate biopsies.

II. To determine the effect of PROSTVAC on the change in CD4+ positive cells in the stroma
adjacent to tumor and within the malignant portion of the prostate biopsies.

SECONDARY OBJECTIVES:

I. To assess the effect of PROSTVAC on PD-L1 positive cells in the stroma adjacent to tumor
and within the malignant portion of the prostate biopsies.

II. To assess the correlation between the change in CD8+ and the change in PSA. III. To
assess the effect of PROSTVAC on CD8+, CD4+, and PD-L1 positive cells in the benign portion
of the prostate biopsies.

IV. To assess the effect of PROSTVAC on the change in PSA. V. To assess the effect of
PROSTVAC on tumor grade (Gleason score). VI. To assess the effect of PROSTVAC on tumor extent
(percent of positive random biopsy cores).

VII. To compare the proportion of men on the two study arms with no cancer on
post-intervention biopsy.

VIII. To assess the effect of PROSTVAC on the size of the dominant lesion on magnetic
resonance imaging (MRI) (largest histopathologically confirmed lesion) in the subgroup of
patients with MRIs pre and postintervention.

IX. To assess the effect of PROSTVAC on circulating 15-Mer PSA-specific, MUC-1 and
Brachyury-specific T cells.

X. To assess the effect of PROSTVAC on soluble antibodies to tumor-associated antigens.

XI. To assess the immunologic effects of PROSTVAC in prostate tissue using multiplex
immunofluorescence.

XII. To assess the safety and feasibility of PROSTVAC in the active surveillance population.

XIII. To assess the effect of PROSTVAC on lower urinary tract symptoms (LUTS) in the active
surveillance population.

OUTLINE: Patients are randomized to 1 of 2 treatment arms.

ARM I: Patients receive rilimogene-galvacirepvec subcutaneously (SC) at baseline and on days
14, 28, 56, 84, 112, and 140.

ARM II: Patients receive placebo SC at baseline and on days 14, 28, 56, 84, 112, and 140.

After completion of study treatment, patients are followed up for 30 days and then at 6
months.

Inclusion Criteria:

- Biopsy-proven (consisting of >= 10 tissue cores) adenocarcinoma of the prostate with
cancer present in at least one biopsy core, either random or targeted, in the most
recent biopsy

- All prior biopsies must meet the following: =< 50% of the total number of random
biopsy cores positive for cancer

- Gleason score =< (3+4)

- Clinical stage =< T2a by digital rectal exam (DRE)

- Biopsies performed at outside institutions should have Gleason score confirmed at the
study site by a genitourinary (GU) pathologist to ensure eligibility

- Pre-intervention biopsy tissue (most proximal to enrollment) with sufficient tumor
tissue to cut 5-10 unstained slides confirmed to be available upon request

- Screening serum PSA < 20 ng/mL; for men treated with 5-alpha-reductase inhibitors
(e.g., finasteride, dutasteride), PSA needs to be < 10 ng/mL

- Neutrophil count >= 1,200/mm^3 (>= 1.2 k/uL)

- Stable platelet count >= 75,000/mm^3 (>= 75 k/uL)

- Bilirubin =< 1.5 mg/dL (or =< 3.0 mg/dL for patients with Gilbert's syndrome)

- Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) =< 2.5 x upper
limit of normal (ULN)

- Serum creatinine =< 1.5 x ULN

- Karnofsky >= 70%

- Must agree to use medically acceptable barrier and/or chemical method of contraception
while on study and for at least one month following the last vaccine injection; should
a participant's partner become pregnant or suspect she is pregnant while the
participant is participating in this study, the study physician should be informed
immediately; in the event a participant's partner becomes pregnant, the study sponsor
may request additional information regarding the course of the pregnancy and if the
pregnancy is carried to term, the birth of the child (i.e., the outcome of the
pregnancy)

- Ability to understand and the willingness to sign a written informed consent document

- No planned prostate biopsies during the intervention until after the post-intervention
biopsy

- Men on stable doses of 5-alpha reductase inhibitors are eligible as long as there is
no planned dose change while on study

Exclusion Criteria:

- Have had prior treatment for prostate cancer by surgery, irradiation, local ablative
(i.e., cryosurgery or high-intensity focused ultrasound), or androgen-deprivation
therapy

- Patients who have prostate cancer with distant metastases

- Have undergone treatment of hormone therapy, immunotherapy, chemotherapy and/or
radiation for any malignancies within the past 2 years

- Uncontrolled intermittent illnesses or medical conditions which, in the opinion of the
treating physician, would make this protocol unreasonably hazardous for the patient;
such illnesses/conditions may include, but are not limited to, ongoing or active
infection, symptomatic congestive heart failure, unstable angina pectoris, symptomatic
or unstable cardiac arrhythmia, or psychiatric illness/social situations that would
limit compliance with study requirements

- Positive for human immunodeficiency virus (HIV) or active infections for hepatitis B,
and/or hepatitis C, based on medical history

- Prior solid organ or bone marrow transplant

- Immunodeficiency or splenectomy

- Chronic immunosuppressive therapy within 30 days of screening

- Inflammatory eye disease requiring steroid treatment within 28 days of screening

- Chronic administration (defined as daily or every other day for continued use > 14
days) of systemic corticosteroids within 28 days of the first planned dose of
PROSTVAC-V/F; use of inhaled steroids, nasal sprays, and topical creams for small body
areas is allowed

- History of or active autoimmune disease including but not limited to autoimmune
neutropenia, thrombocytopenia, or hemolytic anemia, systemic lupus erythematosus,
Sjogren's syndrome, scleroderma, myasthenia gravis, Goodpasture's syndrome; persons
with vitiligo are not excluded; Persons with well-controlled autoimmune
endocrinopathies, e.g., diabetes mellitus, Graves' disease, Hashimoto's thyroiditis,
Addison's disease are not excluded; persons with well-controlled rheumatoid arthritis,
psoriatic arthritis and polymyalgia rheumatica are not excluded

- Known allergy to eggs, egg products

- Prior or concurrent eczema or other eczemoid skin disorders or active skin condition
(acute, chronic, or exfoliative) that disrupts the epidermis; persons with psoriasis
are not excluded except in cases of:

- any active lesion

- any active lesion in the previous 6 months that required treatment, either
systemic or topical

- any prior episode, at any time, extensive enough or severe enough as to require
systemic treatment

- Previous adverse reactions to smallpox vaccination

- Unable to avoid close contact or household contact with the following high-risk
individuals for three weeks after the day 1 vaccination or until the vaccination site
heals completely: (a) children =< 3 years of age, (b) pregnant or nursing women, (c)
individuals with prior or concurrent extensive eczema or other eczemoid skin
disorders, (d) individuals with other acute, chronic, or exfoliative skin condition,
or (e) immunocompromised or immunosuppressed persons (by disease or therapy)

- Participants may not be receiving any other investigational agents

- History of allergic reactions attributed to compounds of similar chemical or biologic
composition of PROSTVAC