Carfilzomib, Bendamustine Hydrochloride, and Dexamethasone in Treating Patients With Relapsed or Refractory Multiple Myeloma

PRIMARY OBJECTIVES:

I. To determine the maximum tolerated dose (MTD) of carfilzomib in combination with
bendamustine (bendamustine hydrochloride) and dexamethasone, up to a maximum bendamustine
dose of 90 mg/m^2.

SECONDARY OBJECTIVES:

I. To evaluate the safety of carfilzomib in combination with bendamustine and dexamethasone,
at the MTD.

II. To evaluate the response rate and duration of response of carfilzomib in combination with
bendamustine and dexamethasone, in patients with relapsed and or refractory multiple myeloma.

OUTLINE: This is a dose-escalation study of carfilzomib and bendamustine hydrochloride.

Patients receive dexamethasone orally (PO) or intravenously (IV) over 20 minutes on days 1,
2, 8, 9, 15, 16, 22, and 23 of courses 1-3; on days 1, 2, 15, and 16 of courses 4-12; and on
days 1 and 2 of all subsequent courses. Patients also receive bendamustine hydrochloride IV
over 10 minutes on days 1 and 2 of courses 1-3 and on day 1 of all subsequent courses and
carfilzomib IV over 30 minutes on days 1, 2, 8, 9, 15, and 16 of courses 1-12 and on days 1,
2, 15, and 16 of all subsequent courses. Courses repeat every 28 days in the absence of
disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up for 30 days, every 3 months for
1 year, and then every 6 months thereafter.

Inclusion Criteria:

- Relapsed and or refractory multiple myeloma after at least one prior line of therapy;
there is no upper limit of prior lines of therapy; patients who are ineligible for
stem cell transplantation are allowed; patients should have received at least one
prior novel agent (immunomodulatory agents or proteasome inhibitors); patients
eligible for bone marrow transplant must have undergone bone marrow transplant (BMT)
prior to enrollment

- Measurable disease, as defined by one or all of the following (assessed within 30 days
prior to initiation of therapy): a) serum M-protein >= 0.5 g/d; b) urine Bence-Jones
protein >= 200 mg/24 hours; c) patients with light chain only myeloma are eligible;
the involved free light chain level 100 mg/L with abnormal serum free light chain
ratio

- Documented relapse or progressive disease on or after any regimen (subjects refractory
to the most recent regimen are eligible)

- Primary refractory patients (never responded to any therapy) are eligible

- Eastern Cooperative Oncology Group performance status 0 - 2

- Serum alanine aminotransferase (ALT) < 3.5 times the upper limit of normal within 30
days prior to cycle 1 day 1

- Serum direct bilirubin < 2 mg/dL (34 Omol/L) within 30 days prior to cycle 1 day 1

- Absolute neutrophil count (ANC) >= 1.0 x 10^9/L within 30 days prior to cycle 1 day 1,
without granulocyte-colony stimulating factor (G-CSF)

- Hemoglobin > 9 g/dL (80 g/L) within 30 days prior to cycle 1 day 1 (subjects may be
receiving red blood cell transfusions in accordance with institutional guidelines)

- Platelet count > 100 x 10^9/L (30 x 10^9/L if myeloma involvement in the bone marrow
aspirate is > 50%) within 30 days prior to cycle 1 day 1; subjects may receive
platelet transfusions within institutional guidelines

- Creatinine clearance > 50 mL/minute within 30 days prior to cycle 1 day 1, either
measured or calculated using a standard formula

- Patient should have a normalized or normal uric acid level prior to study entry

- Written informed consent in accordance with federal, local, and institutional
guidelines

- Females of childbearing potential must have a negative pregnancy test and agree to
ongoing pregnancy testing and to practice contraception; (birth control methods should
be determined in consultation with the investigator)

- Male subjects must agree to practice contraception

Exclusion Criteria:

- Intolerance to previous bendamustine, carfilzomib or dexamethasone or mannitol;
subjects who are allergic to bortezomib are not excluded

- Chemotherapy (approved or investigational) within 3 weeks prior to the first day of
treatment or antibody therapy within 6 weeks prior to the first day of treatment

- Radiotherapy to >= 3 sites at the same time within 1 week prior to the first day of
treatment

- Immunomodulatory therapy such as immunomodulatory drugs (Imids) or stem cell
transplant within 28 days prior to the first day of treatment

- Pregnant or lactating females

- Major surgery within 21 days prior to the first day of treatment

- Acute active infection requiring treatment (IV antibiotics, antivirals, or
antifungals) within 14 days prior to the first day of treatment

- Known human immunodeficiency virus infection

- Known active hepatitis B or C infection

- Unstable angina or myocardial infarction within 4 months prior to the first day of
treatment, the New York Heart Association (NYHA) class III or IV heart failure,
uncontrolled angina, history of severe coronary artery disease, severe uncontrolled
ventricular arrhythmias, sick sinus syndrome, or electrocardiographic evidence of
acute ischemia or grade 3 conduction system abnormalities unless subject has a
pacemaker

- Uncontrolled hypertension or uncontrolled diabetes within 14 days prior to the first
day of treatment

- Non-hematologic malignancy within the past 3 years with the exception of a) adequately
treated basal cell carcinoma, squamous cell skin cancer, or thyroid cancer; b)
carcinoma in situ of the cervix or breast; c) prostate cancer of Gleason grade 6 or
less with stable prostate-specific antigen levels; or d) cancer considered cured by
surgical resection or unlikely to impact survival during the duration of the study,
such as localized transitional cell carcinoma of the bladder or benign tumors of the
adrenal or pancreas

- Significant neuropathy (grades 3 - 4, or grade 2 with pain) within 14 days prior to
the first day of treatment

- Known history of allergy to Captisol (a cyclodextrin derivative used to solubilize
carfilzomib)

- Contraindication to any of the required concomitant drugs or supportive treatments or
intolerance to hydration due to preexisting pulmonary or cardiac impairment

- Subjects with known or likely systemic amyloidosis

- Ongoing graft-vs-host disease

- Subjects with pleural effusions requiring thoracentesis or ascites requiring
paracentesis within 14 days prior to the first day of treatment

- Any other clinically significant medical disease or condition that, in the
investigator's opinion, may interfere with protocol adherence or a subject's ability
to give informed consent