Azacitidine and CAPOX in Metastatic Colorectal Cancer

The Study Drugs:

Azacitidine is designed to block certain proteins in cancer cells whose job is to stop the
function of the tumor-fighting proteins. By blocking the "bad" proteins, the tumor-fighting
genes may be able to work better.

Capecitabine is designed to interfere with the growth of cancer cells.

Oxaliplatin is designed to keep new cancer cells from growing.

Study Groups:

If you are found to be eligible to take part in this study, you will be assigned to a study
group based on when you joined this study. Up to 4 groups of up to 3-6 participants will be
enrolled in the Phase I portion of the study, and up to 30 participants will be enrolled in
Phase II.

If you are enrolled in the Phase I portion, the dose of azacitidine and oxaliplatin you
receive will depend on when you joined this study. All participants will receive the same
dose of capecitabine. The first group of participants will receive a low dose level of the
combination. Each new group will receive a higher dose of the combination than the group
before it, if no intolerable side effects were seen. This will continue until the highest
tolerable dose of the combination of azacitidine, oxaliplatin, and capecitabine is found.

If you are enrolled in the Phase II portion, you will receive the combination of
azacitidine, oxaliplatin, and capecitabine at the highest dose that was tolerated in the
Phase I portion.

Central Venous Catheter (CVC):

Before you can begin to receive oxaliplatin on this study, you will have a CVC placed if you
do not have one already. A CVC is a sterile, flexible tube that will be placed into a large
vein while you are under local anesthesia. Your doctor will explain this procedure to you in
more detail, and you will be required to sign a separate consent form for this procedure.

Study Drug Administration:

A cycle of treatment is defined as 21 days.

Azacitidine will be injected under your skin on Days 1-5 of each cycle.

You will receive oxaliplatin by vein over 2 hours on Day 2 of each cycle.

You will take capecitabine by mouth 2 times each day on Days 1-14 of each cycle.
Capecitabine tablets should be taken 12 hours apart, within 30 minutes after eating a meal.

Study Visits:

Up to 3 days before or on Day 1 of each cycle, the following tests and procedures will be
performed:

- You will have a physical exam, including measurement of your weight and vital signs.

- You will have a neurosensory assessment.

- Your performance status will be recorded.

- You will be asked about any symptoms and/or side effects you may be experiencing and
any drugs you may be taking.

- Blood (about 2 tablespoons) will be drawn for routine tests.

On Day 5 of Cycle 1 and Days 1 and 5 of Cycle 2, before you receive any of the study drugs,
blood (about 2 teaspoons each time) will be drawn to test for CIMP, a chemical "marker" in
the blood that may be related to how the drug may affect the cancer.

After every 3 cycles (Cycles 4, 7, 10 and so on), you will have a CT or MRI scan of the
chest, abdomen, and/or pelvis to check the status of the disease.

Length of Study:

You may continue to take the study drugs for as long as you are benefitting. You will be
taken off the study drugs if the disease gets worse, you experience any intolerable side
effects, or if the study doctor thinks it is in your best interest to stop taking the study
drugs.

If you chose to stop your participation in this study at any time, you should tell the study
doctor or study staff right away. They will make sure that proper procedures are followed
and a final visit is made for your safety.

End-of-Treatment Visit:

Within 10 days after your study treatment ends for any reason, you will return to the clinic
and the following tests and procedures will be performed:

- You will have a physical exam, including measurement of your weight and vital signs.

- You will have a neurosensory assessment.

- Your performance status will be recorded.

- You will have a CT scan or MRI scan of the chest, abdomen, and/or pelvis to check the
status of the disease.

- You will be asked about any symptoms and/or side effects you may be experiencing and
any drugs you may be taking.

- Blood (about 2 tablespoons) will be drawn for routine tests.

Follow-Up:

The study doctor and study staff will follow your health status for the first 30 days after
you stop taking the study drugs to check if you are experiencing any treatment-related side
effects. The follow-up will be done during your regularly scheduled routine clinic visits
and/or by phone call, which should last about 5 minutes.

If you continue to experience any treatment-related side effects after the 30 days of
follow-up, the study staff will continue to follow up with you during your regularly
scheduled clinic visits until the side effects have gotten better or become stable.

Long-Term Follow-Up:

Every 3 months after the end-of-treatment visit, the study staff will contact you by phone
or email to check on how you are doing. If you are contacted by phone, the call should last
about 5 minutes. Your medical records may also be reviewed.

This is an investigational study. Azacitidine is FDA approved and commercially available for
myelodysplastic syndrome (MDS - a blood disease that often leads to cancer). Its use in
colorectal cancer is investigational.

Oxaliplatin and capecitabine are both FDA approved and commercially available as treatment
for colorectal cancer.

The use of azacitidine, oxaliplatin, and capecitabine in combination is investigational.

Up to 54 patients will take part in this study. All will be enrolled at MD Anderson.

Inclusion Criteria:

1. Phase I: Patient must have histologically or cytologically confirmed colorectal
adenocarcinoma with metastatic disease documented on diagnostic imaging studies.
Disease may be measurable or non-measurable as per RECIST version 1.1.

2. Eastern Cooperative Oncology Group (ECOG) performance status 0-2

3. For patients on full-dose low-molecular weight anticoagulation, no active bleeding or
pathological condition that carries a high risk of bleeding (e.g., tumor involving
major vessels or know varices) is allowed.

4. Serum bilirubin levels laboratory (ULN)

5. Serum aspartate aminotransferase (AST) or serum alanine aminotransferase (ALT) levels

6. Serum creatinine levels
7. Absolute neutrophil count of >/=1,500/mm^3 (ie, >/=1.5 x 10^9/L by International
Units [IU]).

8. Platelet count >/=100,000/mm^3 (IU: ≥100 x 10^9/L).

9. Hemoglobin value of >/=9.0 g/dL.

10. No limit to number of prior therapies.

11. Women of childbearing potential must have a negative serum pregnancy test and must be
advised to avoid becoming pregnant. Men should be advised to not father a child while
receiving treatment. Sexually active women of childbearing potential and men must use
an effective method of birth control during the course of the study, in a manner such
that risk of failure is minimized.

12. Patient must be refractory to treatment with 5-FU (either intravenous 5-FU or as the
oral prodrug, capecitabine) and oxaliplatin, defined as previous clinical or
radiographic progression on or within 3 months of treatment with 5-FU and
oxaliplatin. There is no limit to the number of prior lines of therapy.

13. Phase II: Patient must have histologically or cytologically confirmed colorectal
adenocarcinoma with measurable metastatic disease documented on diagnostic imaging
studies by RECIST version 1.1 criteria

14. Phase II: Patient must be known to have CpG island methylator phenotype.

Exclusion Criteria:

1. Patients with known brain metastases or carcinomatous meningitis

2. Patients unable to swallow oral medications or with gastrointestinal disorders that
might interfere with proper absorption of oral drugs.

3. Known dihydropyrimidine (DPD) deficiency

4. Grade 3 or more peripheral neuropathy

5. Chemotherapy or any other investigational agents within 14 days of first receipt of
study treatment, or major surgery within 28 days of first receipt of study treatment,
or palliative radiation within 7 days of first receipt of study treatment.

6. Concurrent severe and/or uncontrolled medical conditions which could compromise
participation in the study such as unstable angina, myocardial infarction within 6
months, unstable symptomatic arrhythmia, uncontrolled diabetes, serious active or
uncontrolled infection.

7. Known or suspected hypersensitivity to azacitidine or mannitol

8. Pregnant or breast feeding

9. Because of the interaction between coumadin and capecitabine patients taking
therapeutic doses of coumarin-derivative anticoagulants, are not eligible. Low-dose
Coumadin (e.g. 1 mg PO per day) in patients with in-dwelling venous access devices is
allowed but increased frequency of international normalized ratio (INR) monitoring is
recommended.

10. Interstitial pneumonia or extensive and symptomatic interstitial fibrosis of the
lung.