Bortezomib and Rituximab for Patients With Waldenstrom's Macroglobulinemia

Bortezomib is designed to block a protein that plays a role in cell function and growth,
which may cause cancer cells to die.

Rituximab is designed to attach to cancer cells, which may cause them to die.

Cyclophosphamide, vincristine, doxorubicin, and cladribine are designed to interfere with the
multiplication of cancer cells, which may slow or stop their growth and spread throughout the
body. This may cause the cancer cells to die.

Dexamethasone is designed to decrease inflammation. It is also used to treat certain forms of
cancer.

Before you can start treatment on this study, you will have "screening tests." These tests
will help the doctor decide if you are eligible to take part in this study. The tests may be
performed within 28 days of starting the study drug. You will have a physical exam, including
measurement of vital signs (blood pressure, heart rate, temperature, and breathing rate),
height, and weight. Your medical history will be recorded. You will be asked to fill out a
questionnaire regarding any neuropathy (nerve problems) you may have. The questionnaire will
take about 1 minute to complete. You will have an electrocardiogram (ECG -- a test that
measures the electrical activity of the heart). You will also have blood (about 4-5
teaspoons) drawn one time and urine collected (over 24 hours) to check the status of your WM.
This blood is also used to screen for hepatitis. You will have an x-ray of your chest. You
will have computed tomography (CT) scans of your abdomen and pelvis to see which part of your
body is involved with WM. If your chest x-ray is positive, you will also have a CT scan of
your chest. Women who are able to have children must have a negative blood (about 2
teaspoons) or urine pregnancy test before starting the study. You will also have a bone
marrow aspiration and biopsy. To collect a bone marrow aspirate/biopsy, an area of the hip
bone will be made numb with an anesthetic, and a small amount of bone marrow and bone will be
withdrawn through a large needle.

If you are found to be eligible to participate in this study, you will begin taking the study
drugs. You will be given two 35-day cycles of bortezomib and rituximab. Bortezomib will be
given through a needle in a vein over 3-5 seconds on Days 1, 8, 15, and 22. Rituximab will
also be given through a vein on Days 8 and 22. The first rituximab infusion (by vein) usually
takes 6-8 hours. Later infusions are generally shorter, taking about 4 hours to complete.
While you are receiving bortezomib/rituximab (for 2-3 months), valacyclovir (an anti-viral
drug) is taken by mouth, once a day.

During the study, before each dose of bortezomib, you will have blood (about 2 teaspoons each
time) drawn for routine tests. Your vital signs will be measured. You will be asked about any
side effects you may have experienced. You will also be asked to answer the questionnaire
about any neuropathy you may have.

Stem cells are the cells from which all blood cells develop. If you respond to the first 2
cycles of bortezomib/rituximab, you will then have some of your stems cells collected. You
will have to sign a separate consent form that describes this procedure and its risks. After
the stem cell collection, 1 cycle of cladribine, cyclophosphamide, and rituximab will be
given. Cladribine will be given through a vein once a day over 2 hours on Days 1-5.
Cyclophosphamide is taken by mouth, twice a day on Days 1-5, and rituximab is given through a
vein once a week for 4 weeks.

If you do not respond to the first cycle of bortezomib/rituximab, you will be taken off the
study.

If you respond to the first but do not respond to the second cycle of bortezomib/rituximab,
you will receive a third cycle. The bortezomib/rituximab will be given in the same manner as
your first 2 cycles.

If you respond to the third cycle of bortezomib/rituximab, you will have some of your stems
cells collected. After the stem cell collection, 1 cycle of cladribine, cyclophosphamide, and
rituximab will be given. Cladribine will be given through a vein once a day over 2 hours on
Days 1-5. Cyclophosphamide is taken by mouth, twice a day on Days 1-5, and rituximab is given
through a vein once a week for 4 weeks.

If you do not respond to the third cycle of bortezomib/rituximab, you will be given a
chemotherapy regimen containing the drugs rituximab, cyclophosphamide, vincristine, and
doxorubicin, together with dexamethasone. This combination is known as modified R-Hyper-CVAD.
Rituximab will be given through a vein over about 4 hours on Day 1 only. Cyclophosphamide
will be given through a vein every 12 hours on Days 1-4. Doxorubicin and vincristine will be
given through a vein continuously over 24 hours on Days 1-4. Dexamethasone is taken by mouth
daily on Days 1-4, 9-12, and 17-20.

If a partial response is seen with modified R-Hyper-CVAD, you will have some of your stem
cells collected. You will receive 1 cycle of cladribine, cyclophosphamide, and rituximab.
Cladribine will be given through a vein once a day over 2 hours on Days 1-5. Cyclophosphamide
is taken by mouth, twice a day on Days 1-5, and rituximab is given through a vein once a week
for 4 weeks.

About 1 week before the start of each cycle of chemotherapy, you will have blood (about 4-5
teaspoons) drawn for routine tests and to see how your WM is responding. You may also need to
collect your urine over 24 hours, depending on if the first test was initially positive or
not. You will also have a complete physical exam, including measurement of vital signs,
height, and weight.

If your CT scans were positive initially, you will need to have them repeated after 2 cycles
of bortezomib/rituximab and then every 6 months. Once you have a partial response confirmed
by CT scans, you will not need to repeat the CT scans anymore.

If your disease does not respond to modified R-Hyper-CVAD, you will be taken off the study.

Responding participants will be followed at least every 6 months for the first 36 months
(from the end of therapy). After that, you will be followed at least once a year unless the
disease gets worse and needs to be re-treated. For the follow-up evaluations, you will have a
physical exam, including measurement of vital signs. Blood (about 4 tablespoons) will be
drawn for routine tests. Blood (about 4-5 teaspoons) and urine (over 24 hours) will be
collected to check the status of your WM. If the x-rays and/or CT scans done at the beginning
of the study were positive, you will have repeat x-rays and/or CT scans.

For patients who have not had a partial response, follow-up evaluations will be at least
every 3 months. You will have a physical exam, including measurement of vital signs. Blood
(about 4 tablespoons) will be drawn for routine tests. Blood (about 4-5 tablespoons) and
urine (over 24 hours) will be collected to check the status of your WM.

You will be taken off the study if you do not have a partial or complete response following 3
cycles of bortezomib/rituximab and 2 cycles of modified R-Hyper-CVAD. You will be taken off
the study if the disease gets worse after all planned therapy that the study doctor feels
requires repetition. You will be taken off the study if intolerable side effects occur. You
will be taken off the study if treatment with bortezomib is delayed for more than 2 weeks.
You will be taken off the study if you develop certain other illnesses, or if there are
certain changes in your health that the study doctor decides may make further treatment with
the study drugs to be unacceptable.

Once you are taken off the study, you will have an end-of-study visit. At this visit, a
physical exam, including measurement of vital signs, height, and weight will be performed.
You will be asked about any side effects that you may have experienced. You will be asked to
answer the questionnaire regarding any neuropathy you may have. Blood (about 4-6 teaspoons)
will be drawn for routine tests and to check the status of your WM. You will need to collect
your urine over 24 hours to see how your WM is responding. If your initial CT scans showed
lesions that appear to be caused by WM, you will have a CT scan repeated at this time.

If you have had a partial or complete response at the end of all planned therapy, you will
need to return to the clinic for follow-up visits at least once every 6 months for the first
36 months (from the end of therapy). After that, you will have follow-up visits at least once
a year, unless the disease gets worse and re-treatment is necessary. At the follow-up visits,
you will have a physical exam, including measurement of vital signs, height, and weight. You
will be asked about any side effects that you may have experienced. Blood (about 4-6
teaspoons) will be drawn for routine tests and to check the status of your WM. Depending on
the results of your original urine tests, you may need to collect your urine over 24 hours to
see how your WM is responding. If your initial CT scans showed lesions that appear to be
caused by WM, you will have CT scans and an x-ray of your chest repeated at this time.

This is an investigational study. Cyclophosphamide, vincristine, doxorubicin, and rituximab
are commercially available and FDA-approved for treatment of Waldenstrom's macroglobulinemia.
Bortezomib, dexamethasone, cladribine, and the drug combinations used in this study have been
authorized for use in research only. Bortezomib has been FDA approved and it is registered in
Europe for the treatment of multiple myeloma patients who have received at least one prior
therapy. Tests/procedures that are required for this study are considered to be part of your
routine medical care. Up to 38 patients will be enrolled in this study. All will be enrolled
at MD Anderson.

Inclusion Criteria:

1. Patients with symptomatic macroglobulinemic lymphoma who have had no prior treatment,
or whose prior treatment has been limited to steroids and/or alpha-interferon, are
eligible. Macroglobulinemic lymphoma includes patients with either biopsy proven
clonal lymphocytic or lymphoplasmacytic proliferation and monoclonal IgM. Also
included are symptomatic patients with clonal proliferation producing a pathologic
monoclonal IgM that causes cryoglobulinemia, peripheral neuropathy or cold agglutinin
hemolytic anemia.

2. Patients must have acceptable liver function (total bilirubin < 2.5mg/dL) and renal
function (creatinine < 2.0mg/dL). Patients with impaired renal function will only be
included if the renal failure is secondary to macroglobulinemic lymphoma (i.e. Bence
Jones proteinuria, cryoglobulinemia, ureteral obstruction due to mass) that might
reverse with improvement of disease.

3. Female subject is either post-menopausal or surgically sterilized or willing to use an
acceptable method of birth control (i.e., a hormonal contraceptive, intra-uterine
device, diaphragm with spermicide, condom with spermicide, or abstinence) for the
duration of the study.

4. Male subject agrees to use an acceptable method for contraception for the duration of
the study.

5. Patients must voluntarily sign an informed consent form indicating that they are aware
of the investigational nature of the study, with the understanding that consent may be
withdrawn by the subject at any time without prejudice to future care.

6. Patient has a heart rate (HR) of greater than or equal to 50 bpm.

Exclusion Criteria:

1. Patient has a platelet count of <30x10^9/L within 28 days before enrollment unless due
to >/= 75% marrow infiltration by macroglobulinemic lymphoma or splenomegaly.

2. Patient has an absolute neutrophil count of <1.0x10^9/L within 28 days before
enrollment unless due to >/= 75% marrow infiltration by macroglobulinemic lymphoma.

3. Patient has a calculated or measured creatinine >/= to 2.0mg/dL on baseline
evaluation. Patients with impaired renal function will only be included if the renal
failure is secondary to macroglobulinemic lymphoma (i.e. Bence Jones proteinuria,
cryoglobulinemia, ureteral obstruction due to mass).

4. Patient has >/= Grade 2 peripheral neuropathy on baseline evaluation.

5. Myocardial infarction within 6 months prior to enrollment or has New York Heart
Association (NYHA) Class III or IV heart failure, uncontrolled angina, severe
uncontrolled ventricular arrhythmias, or electrocardiographic evidence of acute
ischemia or active conduction system abnormalities. Prior to study entry, any ECG
abnormality at Screening has to be documented by the investigator as not medically
relevant.

6. Patient has hypersensitivity to boron, mannitol, or murine proteins.

7. Female subject is pregnant or breast-feeding. Confirmation that the subject is not
pregnant must be established by a negative serum or urine Beta -human chorionic
gonadotropin (B-hCG) pregnancy test result obtained during screening. Pregnancy
testing is not required for post-menopausal or surgically sterilized women.

8. Patient has received other investigational drugs within 14 days before enrollment

9. Patient has a serious medical or psychiatric illness that is likely to interfere with
participation in this clinical study.

10. Eastern Cooperative Oncology Group (ECOG) performance status of > 2.

11. Patient with a "currently active" second malignancy, other than non-melanoma skin
cancer and carcinoma in situ of the cervix, should not be enrolled. Patients are not
considered to have a "currently active" malignancy if they have completed therapy for
a prior malignancy, are disease free from prior malignancies for > 5 years and are
considered by their physician to be at less than 30 % risk of relapse.

12. Patient with a lifetime cumulative dose of > 450 mg/m^2 of anthracyclines.

13. Patients with an active hepatitis B infection.