A Phase II Study of Ziv-aflibercept in Combination With Capecitabine/Oxaliplatin (XELOX) Chemotherapy in the Front-Line Treatment of Patients With Metastatic Colorectal Cancer

Inclusion Criteria:

- The study will be limited to subjects with newly diagnosed mCRC without any prior
systemic chemotherapy for metastatic disease.

- The diagnosis of metastatic colorectal cancer will be based on histologic or
cytologic confirmation.

- Subjects must have the ability to swallow oral medication.

- Subjects must have measurable disease, defined as at least one lesion that can be
accurately measured in at least one dimension (longest diameter to be recorded for
non-nodal lesions and short axis for nodal lesions) as ≥ 20 mm with conventional
techniques or as ≥ 10 mm with spiral CT scan, MRI, or calipers by clinical exam.

- Any prior chemotherapy for mCRC is not allowed. Adjuvant chemotherapy with
oxaliplatin-containing regimen CRC within the last 12 months is not allowed. Adjuvant
chemotherapy with Fluorouracil (5-FU) or capecitabine alone within the last 6 months
is allowed.

- Age ≥ 18 years.

- Both men and women of all races and ethnic groups are eligible for this trial.

- Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1 (Karnofsky ≥ 60%).

- Life expectancy of greater than 12 months.

- Patients must have normal organ and marrow function as defined below:

- Absolute Neutrophil Count ≥ 1,500/mm3

- Platelets ≥ 100,000/mm3

- Total Bilirubin 2 × institutional upper limit of normal (ULN)

- Aspartate aminotransferase (AST) and Alanine transaminase (ALT) 2.5 ×
institutional upper limit of normal (AST and ALT ≤ 5.0 x ULN is acceptable if
liver has tumor involvement).

- Creatinine Clearance (CrCl) 30 mL/min.

- The effects of the combination of ziv-aflibercept, oxaliplatin and capecitabine on
the developing human fetus are unknown. For this reason, women of child-bearing
potential and men must agree to use adequate contraception (hormonal or barrier
method of birth control; abstinence) prior to study entry and for the duration of
study participation, and 6 months after last administration of ziv-aflibercept.
Should a woman become pregnant or suspect she is pregnant while she or her partner is
participating in this study, she should inform her treating physician immediately.
Men treated or enrolled on this protocol must also agree to use adequate
contraception prior to the study, for the duration of study participation, and 4
months after completion of therapeutic agents administration and 6 months after last
administration of ziv-aflibercept.

- Ability to understand and to sign a written informed consent document.

Exclusion Criteria:

- Unwilling or unable to follow protocol requirements or to give informed consent.

- Any prior chemotherapy for mCRC.

- Adjuvant chemotherapy with oxaliplatin-containing regimen CRC within the last 12
months.

- Adjuvant chemotherapy with 5-FU or capecitabine alone within the last 6 months is
allowed.

- CrCl < 30 mL/min

- Any peripheral neuropathy of grade ≥ 2

- Patients with known dihydropyrimidine dehydrogenase (DPD) deficiency

- Patients with urine protein creatinine ration > 1 or urine protein > 500 mg/24 hours.

- Patients who have had radiotherapy within 4 weeks to entering the study or those who
have not recovered from adverse events due to radiotherapy administered more than 4
weeks earlier.

- Patients with uncontrolled or symptomatic brain metastases should be excluded from
this clinical trial because of their poor prognosis and because they often develop
progressive neurologic dysfunction that would confound the evaluation of neurologic
and other adverse events.

- Presence of metastatic disease that, in the opinion of the investigator, would
require palliative treatment within 4 weeks of enrollment.

- Uncontrolled intercurrent illness including, but not limited to, ongoing or active
infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac
arrhythmia, or psychiatric illness/social situations that would limit compliance with
study requirements.

- Pregnant women are excluded from this study because ziv-aflibercept, capecitabine,
and oxaliplatin are agents with the potential for teratogenic or abortifacient
effects. Because there is an unknown but potential risk for adverse events in nursing
infants secondary to treatment of the mother with ziv-aflibercept, capecitabine, and
oxaliplatin, breastfeeding should be discontinued if the mother is treated with
ziv-aflibercept, capecitabine, and oxaliplatin.

- HIV-positive patients on combination antiretroviral therapy are ineligible because of
the potential for pharmacokinetic interactions with ziv-aflibercept, capecitabine,
and oxaliplatin. In addition, these patients are at increased risk of lethal
infections when treated with marrow-suppressive therapy. Appropriate studies will be
undertaken in patients receiving combination antiretroviral therapy when indicated.

- Malabsorption syndrome, ulcerative colitis, inflammatory bowel disease, resection of
the stomach or small bowel, or other disease or condition significantly affecting
gastrointestinal function.

- Serious or non-healing wound, skin ulcer, or bone fracture.

- History of bleeding diathesis or coagulopathy or active anticoagulation with
Coumadin.

- Any documented stroke or Transient Ischemic Attack (TIA) within 6 months prior to
study entry

- Any grade 3/4 hemorrhage within 3 months prior to study entry

- Any pulmonary embolism (PE) within 3 months prior to study entry

- Any deep vein thrombosis (DVT) within 3 months prior to study entry

- Uncontrolled hypertension defined as > 140/90 mmHg or isolated systolic hypertension
> 160 mmHg on 2 separate days in past 3 months prior to study inclusion.

- Any of the following cardiac conditions:

- Documented congestive heart failure

- Myocardial infarction within 6 months prior to study entry

- Unstable angina within 6 months prior to study entry

- Symptomatic arrhythmia