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Pomalidomide, Bortezomib, and Dexamethasone in Treating Patients With Relapsed or Refractory Multiple Myeloma

Information source: Mayo Clinic
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Refractory Multiple Myeloma

Intervention: pomalidomide (Drug); bortezomib (Drug); dexamethasone (Drug); laboratory biomarker analysis (Other); gene expression analysis (Other)

Phase: Phase 1/Phase 2

Status: Active, not recruiting

Sponsored by: Mayo Clinic

Official(s) and/or principal investigator(s):
Martha Lacy, M.D., Study Chair, Affiliation: Mayo Clinic
Joseph R. Mikhael, M.D., Principal Investigator, Affiliation: Mayo Clinic in Arizona
Vivek Roy, M.D., Principal Investigator, Affiliation: Mayo Clinic in Florida


RATIONALE: Pomalidomide and bortezomib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Bortezomib may also stop the growth of tumor cells by blocking blood flow to the tumor. Drugs used in chemotherapy, such as dexamethasone, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving pomalidomide and bortezomib together with dexamethasone may kill more tumor cells. PURPOSE: This phase I/II trial is studying the side effects and best dose of bortezomib when given together with pomalidomide and dexamethasone and to see how well it works in treating patients with relapsed or refractory multiple myeloma.

Clinical Details

Official title: MC1082: A Phase I/II Trial of Pomalidomide (CC-4047), Bortezomib, and Dexamethasone in Patients With Relapsed or Refractory Multiple Myeloma

Study design: Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Primary outcome:

Maximum tolerated dose (MTD) of bortezomib in combination with pomalidomide and dexamethasone out to 2.5 years.

Hematologic response rate (PR, VGPR, or CR) of pomalidomide, bortezomib and dexamethasone in patients with relapsed or refractory myeloma out to 2.5 years

Secondary outcome:

Time to progression.

Toxicity of pomalidomide, bortezomib and dexamethasone in this patient population.

Detailed description: PRIMARY OBJECTIVES: I. Determine the maximum tolerated dose (MTD) of bortezomib in combination with pomalidomide and dexamethasone. II. To evaluate the hematologic response rate (PR, VGPR, or CR) of pomalidomide, bortezomib and dexamethasone in patients with relapsed or refractory myeloma. SECONDARY OBJECTIVES: I. Time to progression. II. To assess the toxicity of pomalidomide, bortezomib and dexamethasone in this patient population. OUTLINE : This is a phase I, dose-escalation study of bortezomib followed by a phase II study. Patients receive oral pomalidomide on days 1-21; bortezomib IV on days 1, 8,15, 22; and oral dexamethasone on days 1, 8, 15, 22 . Treatment repeats every 28 days for 8 courses. Patients then receive maintenance therapy comprising oral pomalidomide on days 1-21. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up every 6 months.


Minimum age: 18 Years. Maximum age: N/A. Gender(s): Both.


Inclusion Criteria:

- Serum Creatinine =< 3 mg/dL

- Absolute neutrophil count >= 1000/uL

- Platelet count >= 75,000/uL

- Measurable disease of multiple myeloma as defined by at least ONE of the following:

- serum monoclonal protein >= 1. 0 g/dL

- > 200 mg of monoclonal protein in the urine on 24 hour electrophoresis

- serum immunoglobulin free light chain >= 10 mg/dL AND abnormal serum

immunoglobulin kappa to lambda free light chain ratio

- monoclonal bone marrow plasmacytosis >= 30% (evaluable disease)

- measurable plasmacytoma that has not been radiated

- ECOG Performance status (PS) 0, 1, or 2

- Previously treated relapsed or refractory multiple myeloma

- Patients must have received at least one prior therapy but no more than 4 therapies.

- one or more of the prior regimens must have included lenalidomide and it has

been determined the patient is refractory, resistant, or relapsed this therapy

- prior bortezomib not required but if prior exposure, patients should not be

refractory (Refractory means progression on therapy or within 60 days from the last dose of bortezomib.)

- Provide informed written consent

- Females of childbearing potential (FCBP) must have a negative serum or urine

pregnancy test with a sensitivity of at least 50 mIU/mL within 10 - 14 days prior to

and again within 24 hours of starting pomalidomide and must either commit to continued abstinence from heterosexual intercourse or begin TWO acceptable methods of birth control, one highly effective method and one additional effective method AT THE SAME TIME, at least 28 days before she starts taking pomalidomide; FCBP must also agree to ongoing pregnancy testing

- Men must agree to use a latex condom during sexual contact with a FCBP even if they

have had a vasectomy

- All patients must be counseled at a minimum of every 28 days about pregnancy

precautions and risks of fetal exposure

- Willing and able to take aspirin or alternate prophylactic anticoagulation

- All previous cancer therapy, including chemotherapy, high dose corticosteroids,

immune modulatory drugs or proteosome inhibitors must have been discontinued >= 2 weeks prior to study registration

- Any prior treatment with investigational agents must be discontinued >= 28 days prior

to study registration

- Willing to abstain from donating blood during study participation and for 28 days

after discontinuation of study drug

- Men must agree to abstain from donating semen or sperm during study participation and

for 28 days after discontinuation of study drug

- Willingness to return to enrolling institution for follow-up

Exclusion Criteria:

- Concomitant high dose corticosteroids (concurrent use of corticosteroids); EXCEPTION:

Patients may be on chronic steroids (maximum dose 20 mg/day prednisone equivalent) if they are being given for disorders other than myeloma, i. e., adrenal insufficiency, rheumatoid arthritis, etc

- Another malignancy undergoing active treatment with the exception of non melanoma

skin cancer or in situ cervical or breast cancer

- Pregnant women or women of reproductive ability who are unwilling to use effective


- Nursing women

- Men who are unwilling to use a condom (even if they have undergone a prior vasectomy)

while having intercourse with any woman, while taking the drug and for 4 weeks after stopping treatment

- Other co-morbidity which would interfere with patient's ability to participate in

trial, e. g. uncontrolled infection, uncompensated heart or lung disease

- Other concurrent chemotherapy, radiotherapy, or any ancillary therapy considered

investigational: NOTE: Bisphosphonates are considered to be supportive care rather than therapy, and are thus allowed while on protocol treatment

- Active DVT or PE that has not been therapeutically anticoagulated

- Known positive for HIV or active hepatitis infection

- Any condition, including the presence of laboratory abnormalities, which places the

subject at unacceptable risk if he/she were to participate in the study or confounds the ability to interpret data from the study

- Known hypersensitivity to thalidomide or lenalidomide including development of

erythema nodosum if characterized by a desquamating rash

- > grade 2 peripheral neuropathy

- Any prior use of pomalidomide

Locations and Contacts

Mayo Clinic in Arizona, Scottsdale, Arizona, United States

Mayo Clinic in Florida, Jacksonville, Florida, United States

Mayo Clinic, Rochester, Minnesota 55905, United States

Additional Information

Starting date: September 2011
Last updated: March 23, 2015

Page last updated: August 23, 2015

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