TAA Specific Cytotoxic T Lymphocytes in Patients With Pancreatic Cancer

The patient will give blood to make TAA-Specific cytotoxic T cells in a lab. These cells well
be grown and frozen. If the TAA-Specific cytotoxic T cells can be made, the time from
collection of the blood to manufacture of T cells for administration to the patient is about
1 to 2 months.

The cells will be infused by intravenous infusion (IV) into the patient over 1-10 minutes.
The patient may be pre-treated with acetaminophen (Tylenol) and diphenhydramine (Benadryl).
Acetaminophen (Tylenol) and diphenhydramine (Benadryl) are given to prevent a possible
allergic reaction to the TAA-CTL administration.

Patients will be given up to six doses of TAA-CTLs at monthly intervals. The treatments will
be given by the Center for Cell and Gene Therapy at Houston Methodist Hospital (HMH).

MEDICAL TESTS BEFORE TREATMENT:

- Physical exam.

- Blood tests to measure blood cells, kidney and liver function.

- Measurements of the patient's tumor by routine imaging studies and/or blood tests. The
study will use the imaging study that was used before to follow the patient's tumor: CT,
MRI, or PET.

- Blood test to check for pregnancy for female patients who can have children

MEDICAL TESTS DURING TREATMENT:

Standard medical tests will be conducted on the day of the second and subsequent infusions:

- Physical exams prior to each T cell infusion

- Blood tests to measure blood cells, kidney and liver function.

MEDICAL TESTS AFTER TREATMENT:

- Measurements the patient's tumor by routine imaging studies and/or blood tests done as per
standard of care.

To learn more about the way the TAA-CTLs are working in patient's body, an extra 20-40 mL
(4-8 teaspoons) of blood will be taken before the infusion, at Weeks 1 and 2 after each
infusion and at weeks 4, 6 and 8 and months 3, 6, 9 and 12 after the last infusion. The blood
may be drawn from a central line at the time of the patient's regular blood tests.
Investigators will use this blood to see how long the TAA-CTLs last, and to look at the
immune system response to the patient's cancer.

Study Duration: Patients will be active participants in this study for approximately one year
after their last dose. Investigators will contact patients once a year for up to 4 additional
years (total of 5 years follow-up) in order to evaluate disease response long-term.

Inclusion Criteria:

PROCUREMENT:

1. Any patient with biopsy proven pancreatic adenocarcinoma.

2. Patients with life expectancy greater than or equal to 6 months.

3. Age greater than or equal to 18 years

4. Hgb greater than or equal to 7.0 g/dl (transfusions allowed)

TREATMENT:

1. Any patient with biopsy-proven pancreatic adenocarcinoma:

Group A: Patients with locally advanced or metastatic adenocarcinoma who are
responding (defined as stable disease or tumor volume reduction) following 3 cycles of
first line chemotherapy

Group B: Patients with locally advanced or metastatic adenocarcinoma who have failed
first line chemotherapy or are intolerant, ineligible or unwilling to receive standard
of care chemotherapy

Group C: Patients with resectable pancreatic cancer who have completed planned
neo-adjuvant chemotherapy, radiotherapy or combination

2. Patients must have measurable or evaluable disease per RECIST 1.1 criteria.

3. Patients with life expectancy greater than or equal to 12 weeks

4. Age greater than or equal to 18

5. Pulse oximetry of greater than 95 percent on room air in patients who previously
received radiation therapy

6. Patients with an ECOG score of ≤ 2 or Karnofsky score of 50 or greater

7. Patients with bilirubin less than or equal to 2x upper limit of normal, AST less than
or equal to 3x upper limit of normal, Hgb greater than or equal to 7.0 g/dl
(transfusion allowed).

8. Patients with a creatinine less than or equal to 2x upper limit of normal for age

9. Patients should have been off other investigational therapy for one month prior to
receiving treatment on this study.

10. For Groups B or C patients must be off conventional therapy for at least 1 week prior
to receiving treatment on this study.

11. Informed Consent explained to, understood by and signed by patient. Patient given copy
of informed consent.

12. Due to unknown effects of this therapy on a fetus, pregnant women are excluded from
this research. The male partner should use a condom. Females of child-bearing
potential must be willing to utilize one of the more effective birth control methods
during the study unless female has had a hysterectomy or tubal ligation.

Exclusion Criteria:

PROCUREMENT:

1. Patients with severe intercurrent infection.

2. Patients with active HIV infection (can be pending at this time)

TREATMENT:

1. Patients with severe intercurrent infection.

2. Patients receiving systemic corticosteroids (Patients off steroids for at least 48
hours are eligible)

3. Pregnant

4. HIV positive