Anti-CD3 x Anti-Erbitux® Armed Activated T Cells (Phase Ib) for Gastrointestinal (GI Cancer)

The purpose of this study is to determine in a dose-escalation phase Ib trial the safety of 3
infusions of EGFR2Bi armed activated T cells (aATC), after chemotherapy, for patients with
advanced colorectal and pancreatic cancer

Inclusion Criteria:

- Histological or cytological proof of colorectal or pancreatic adenocarcinoma

- Must have metastatic colorectal cancer or pancreatic cancer with stable disease after
first line chemotherapy or patients with colorectal or pancreatic cancer who have
progressed with standard chemotherapy options*

- Standard chemotherapy for metastatic colorectal cancer include 5-FU/capecitabine with
either oxaliplatin or irinotecan based regimen with or without bevacizumab or
cetuximab.

- Standard chemotherapy for metastatic pancreatic cancer include gemzar based regimen or
FOLFIRINOX (5-FU, oxaliplatin, and irinotecan)

- Prior cetuximab, panitumumab, or other monoclonal antibody therapy allowed if given 28
days prior to the 1st infusion of armed T cells

- Absolute Neutrophil Count (ANC) ≥ 1,000/mm3

- Lymphocyte count ≥ 400/mm3

- Platelet Count ≥ 50,000/mm3

- Hemoglobin ≥ 8 g/dL

- Serum Creatinine < 2.0 mg/dl, Creatinine Clearance ≥50 ml/mm (can be calculated)

- Total Bilirubin ≤ 2 mg/dl (biliary stent is allowed)

- SGPT and SGOT < 5.0 times normal

- LVEF ≥ 45% at rest (MUGA or Echo)

- Pulse Oximetry of >88%

- Age ≥ 18 years at the time of consent

- Written informed consent and HIPAA authorization for release of personal health
information

- Females of childbearing potential, and males, must be willing to use an effective
method of contraception

- Females of childbearing potential must have a negative pregnancy test within 7 days of
being registered for protocol therapy

- KPS ≥ 70% or SWOG Performance Status 0 or 1

Exclusion Criteria:

- Any chemotherapy related toxicities from prior treatment.(> grade I per CTCAE v4.0

- Known hypersensitivity to cetuximab or other EGFR antibody

- Treatment with any investigational agent within 14 days prior to being registered for
protocol therapy Protocol version: 07/13/2011 8

- Symptomatic brain metastasis

- Chronic treatment with systemic steroids or another immuno-suppressive agent

- Serious non-healing wound, ulcer, bone fracture, major surgical procedure, open biopsy
or significant traumatic injury within 28 days prior to being registered for protocol
therapy

- Active liver disease such as cirrhosis, chronic active hepatitis or chronic persistent
hepatitis

- HIV infection

- Positive HbsAg

- Positive Hepatitis C

- Active bleeding or a pathological condition that is associated with a high risk of
bleeding

- Uncontrolled systemic disease like active infections

- Nonmalignant medical illnesses that are uncontrolled or a controlled illness that may
be jeopardized by the treatment with protocol therapy

- Females must not be breastfeeding

- Patient may be excluded if, in the opinion of the PI and investigator team, the
patient is not capable of being compliant

Minor changes from these guidelines will be allowed at the discretion of the attending team
under special circumstances. The reasons for exceptions will be documented.