In-Situ Therapeutic Cancer Vaccine for Metastatic Cancer Combining AlloStim With Tumor Cryoablation

This is a Phase I/II clinical study to investigate the feasibility of creating a personalized
anti-tumor vaccine within the body of patients with advanced cancers. The aim of the study is
to evaluate the safety of administration and anti-tumor effect of a vaccine protocol that has
three separate phases. Cancer patients generally present with an immune response to cancer
biased to a Th2 response, while a Th1 response is considered necessary for mediating
anti-tumor immunity. The first step of the study consists of three (3) weekly intradermal
priming doses of AlloStim. The aim of this step is to create Th1 immunity to the alloantigens
in AlloStim, thus increasing the number of Th1 cells in circulation. The second step of the
protocol involves the cryoablation of a selected tumor lesion followed by an intratumoral
AlloStimTM injection. The aim of this step is to generate tumor-specific CTL killer cells in
the circulation. The final step is an intravenous infusion of AlloStim. The aim of this step
is to activate circulating Th1 cells, killer cells, and natural killer cells The further aim
of this step is to create an inflammatory environment that can break-down the ability of the
tumor to avoid an anti-tumor immune response.

Inclusion Criteria:

- 18 years or older

- Metastatic cancer refractory to at least one course of active chemotherapy or prior
radiation therapy, including metastatic breast cancer, colorectal cancer, non-small
cell lung cancer, ovarian or other gynecological cancer, prostate cancer, pancreatic
or other GI cancer, melanoma, head or neck cancer or lymphoma/plasmacytoma.

- Measurable disease determined upon review of abdominal and/or chest CT scan within 60
days of evaluation for study inclusion with a target tumor lesion for cryoablation
located in liver, kidney, bone, pancreas, lymph node, skin, neck or prostate deemed to
be accessible for percutaneous access.

- Acceptable cryoablation procedure technique risk: the target tumor for ablation must
have adequate distance from adjacent vasculature and other organs to permit safe
application of cryoprobe (generally, more than a 2.5cm clearance of the cryoprobe from
any vital structure such as the bowel, inferior vena cava, or aorta). The safety
assessment of the cryoprobe placement will be made an attending radiologist based on
imaging studies.

- Life expectancy >180 days

- No bevacizumab (Avastin®) within 6 weeks of planned cryoablation procedure

- ECOG status 0-1

- No concurrent medication known to interfere with platelet function or coagulation
(e.g., aspirin, ibuprofen, clopidogrel, or warfarin) unless such medications can be
discontinued for an appropriate time period based on the drug half-life and known
activity (e.g., aspirin for 7 days) prior to cryoablation procedure

- No low molecular weight heparin preparations unless can be discontinued 8 hours prior
to cryoablation

- At least 2 weeks since prior cytotoxic chemotherapy

- Absolute granulocyte count ≥ 1,200/mm3

- Platelet count ≥ 100,000/mm3

- PT/INR ≤ 1.5

- INR correctable to ≤ 1.5 or a PT/PTT correctable to normal limits. Patients
receiving anti-coagulation treatment with an agent such as warfarin or heparin
may be allowed to participate. For patients on warfarin, the INR should be
monitored weekly prior to the cryoablation day 21 to assure INR is stable.
However, heparin or warfarin must be withheld prior to cryoablation such that the
above criteria are met.

- Hemoglobin ≥ 9 g/dL

- Creatinine ≤ 1.5 mg/dL

- Total bilirubin ≤ 1.5 times normal

- Alkaline phosphatase ≤ 2.5 times normal (≤ 5 times normal if liver involvement)

- Aspartate aminotransferase (AST) or (SGOT) ≤ 2.5 times ULN

- Alanine aminotransferase (ALT) or (SGPT) ≤ 2.5 times ULN

- Not pregnant or lactating

- Patients with child bearing potential must agree to use adequate contraception

- No psychiatric or addictive disorders or other condition that, in the opinion of the
investigator, would preclude study participation

- Study specific informed consent

Exclusion Criteria:

- Taking anticoagulant medication for concomitant medical condition (unless can be
safely discontinued for cryoablation procedure)

- Prior allogeneic bone marrow/stem cell or solid organ transplant

- Chronic use (> 2 weeks) of greater than physiologic doses of a corticosteroid agent
(dose equivalent to > 10 mg/day of prednisone) within 30 days of the first day of
study drug treatment

- Topical and inhaled corticosteroids are permitted

- Concomitant autoimmune disease (e.g., rheumatoid arthritis, multiple sclerosis,
autoimmune thyroid disease, uveitis)

- Prior experimental cancer vaccine treatment (e.g., dendritic cell therapy, heat shock
vaccine)

- Immunosuppressive therapy, including: cyclosporine, antithymocyte globulin, or
tacrolimus within 3 months of study entry