Parallel Phase I/II Trial of Decitabine and Peg-Interferon in Melanoma: Phase I Portion

The Study Drugs:

Decitabine is designed to damage the DNA of cells, which may cause cancer cells to die.

Peginterferon alfa-2b is designed to strengthen the immune system, which may decrease tumor
growth.

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 6 groups of 3-6 participants will be
enrolled in the Phase I portion of the study, and up to 44 participants will be enrolled in
Phase II.

If you are enrolled in the Phase I portion, the dose of decitabine and peginterferon alfa-2b
you receive will depend on when you joined this study. The first group of participants will
receive the lowest dose level of the study drug combination. Each new group will receive a
higher dose level than the group before it, if no intolerable side effects were seen. This
will continue until the highest tolerable dose of the study drug combination is found.

If you are enrolled in the Phase II portion, the dose of decitabine and peginterferon alfa-2b
you receive will depend on when you joined this study, as well as the research data from the
Phase I portion. You will be randomly assigned (as in the roll of dice) to receive one of the
dose levels (which may be from 1 to 6 dose levels, depending on the available data from the
Phase I portion) that have been found in the Phase I portion to have the least side effects
and to be possibly the most effective. This means you will have an equal chance of being
assigned to any of the dose levels that are being used at that time. As the study goes on, if
the research data suggests that one dose level may be better tolerated than the others, new
participants enrolling into the Phase II portion would be more likely to be assigned to that
possibly better dose level.

No matter which phase you are enrolled in, your dose of the study drugs may be lowered if you
do not tolerate the study drug combination well.

Study Drug Administration:

A "cycle" on this study is 28 days. Decitabine will be given by vein, over 1 hour, on Days
1-5 of each cycle. Peginterferon alfa-2b will be given by injection under the skin, once a
week (on Days 1, 8, 15, and 21). You will be giving peginterferon alfa-2b to yourself under
nursing supervision on the days you are receiving decitabine.

On Day 6 of each cycle, you will either receive Neulasta (pegfilgrastim) or Neupogen
(filgrastim). Pegfilgrastim or filgrastim will be injected under your skin. If you receive
pegfilgrastim, it will be injected only on Day 6 of each cycle. If you receive filgrastim, it
will be injected 1 time a day for as many days as the doctor decides is needed to raise your
white blood cell count.

Study Visits:

On Day 1 of each cycle, the following procedures will be performed:

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

- You will be asked about any medications or treatments you may be currently receiving and
any side effects you may have experienced.

- You will have a performance status evaluation.

- Blood (about 1 teaspoon) will be drawn for routine tests.

These same tests listed above will be repeated at additional visits with the research nurse
during Week 3 of Cycles 1 and 2. If you do not experience severe side effects during Cycles 1
and 2, these extra Week 3 visits with the research nurse will no longer be necessary in later
cycles. They may, however, be started again if needed.

At the end of of Cycle 3, and every odd cycle after that (Cycles 5, 7, 9, and so on), you
will have a scan performed (such as CT or MRI) to check the status of the disease.

Length of Study Participation:

You may remain on study for as long as you are benefitting. If the disease gets worse or
intolerable side effects occur, you will be taken off study early.

End-of-Study Visit:

Once you go off study for any reason, you will have an end-of-study visit with the same
procedures performed as the Day 1 study visits. You may also have a scan performed (such as
CT or MRI) to check the status of the disease if you have not had one performed in the last 4
weeks.

Long-Term Follow-Up:

Every 3 months for about 2 years, researchers will call you to see how you are doing.

This is an investigational study. Decitabine is FDA approved and commercially available for
the treatment of myelodysplastic syndrome (MDS). Peginterferon alfa-2b is FDA approved and
commercially available for the treatment of hepatitis C. Their use together in this study in
the treatment of melanoma is considered experimental. At this time, the combination is being
used in research only.

Up to 80 patients will take part in this study. All will be enrolled at M. D. Anderson.

Inclusion Criteria:

1. Patients must have pathologically confirmed malignant melanoma that is unresectable
stage III or stage IV.

2. Patients must have measurable disease as defined by RECIST criteria.

3. No more than two prior chemotherapy for unresectable stage III or IV melanoma.

4. Patients must be >/= 28 days beyond the last administration of anticancer therapy, and
must have recovered from the toxicities of prior therapy. If the patient was recently
treated with a nitrosurea, they must be >/= 42 days beyond the last administration.

5. Patients must have no other active malignancies. Patients with prior history of any in
situ cancer, lobular carcinoma of the breast in situ, cervical cancer in situ,
atypical melanocytic hyperplasia or Clark I melanoma in situ or basal or squamous cell
skin cancer are eligible. Patients with other malignancies are eligible, if their
disease has been inactive for 2 years prior to the time of study entry.

6. Patients must be >/= 18 years of age.

7. Patients must give written informed consent prior to initiation of therapy in keeping
with the policies of the institution. Patients with a history of major psychiatric
illness must be judged able to fully understand the investigational nature of this
study and the risks associated with the therapy.

8. Women of childbearing potential (WOCBP) must not be pregnant (negative urine human
chorionic gonadotropin (HCG) within 2 weeks of treatment) or lactating. A WOCBP is
defined as a woman who has not undergone a hysterectomy or who has had menses at any
time in the preceding 24 consecutive months.

9. Women of childbearing potential and sexually active males must be counseled to use an
accepted and effective method of contraception (including abstinence) while on
treatment and for a period of 3 months after completing or discontinuing treatment.

10. Patients must have Eastern Cooperative Oncology Group (ECOG) performance status 0 or
1.

11. Patients must have adequate organ and marrow function, measured within 14 days of
study entry, as defined below: All Patients: - Absolute neutrophil count >/=1,500/uL -
Platelets >/=100,000/uL - Creatinine (serum) mg/dL - AST(SGOT)/ALT(SGPT)
12. Patients with any number of prior targeted or cytokine therapies, but no more than two
chemotherapy containing regimens.

Exclusion Criteria:

1. Patients with active autoimmune disorders or who are receiving immunosuppressive
therapy (including steroids or methotrexate) for any indication are excluded. An
exception may be made, by the PI, to include patients with adrenal insufficiency
requiring physiologic steroid hormone replacement only.

2. Patients who have previously received adjuvant high dose interferon.

3. Patients may not receive any other investigational agents within four weeks of study
entry. Patients may not receive any other investigational agents while on study.

4. Patients who have had major surgery within 2 weeks prior to entering the study, or
have otherwise not adequately recovered from prior surgery.

5. Patients who have had palliative radiation therapy within 2 weeks prior to entering
the study.

6. Patients with brain metastases.

7. Patients with a history of active ischemic heart disease or cerebro-vascular disease,
congestive heart failure (NYHA class >2) or anginal syndrome requiring ongoing medical
treatment.

8. Patients with myocardial ischemia (MI), stroke, or transient ischemic attack (TIA)
within the last 6 months.

9. Patients with a diagnosis or evidence of organic brain syndrome or significant
impairment of basal cognitive function or any psychiatric disorder that might preclude
participation in the protocol.

10. Patients with a history of central nervous system (CNS) demyelinating, inflammatory
disease or hereditary or acquired peripheral neuropathy.

11. Patients with known history of HIV and hepatitis infection or any other significant
medical or surgical condition or psychiatric disorder that may interfere with the
completion of this trial or with the evaluation of safety and efficacy of the study
combination.

12. Patients with thyroid dysfunction not responsive to therapy.