Bortezomib Based Consolidation in Multiple Myeloma Patients Completing Stem Cell Transplant

NCT ID: NCT01706666

Last Updated: 2018-09-17

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 3 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-12-07
• Study Completion Date: 2016-05-17

Brief Summary

This randomized phase II trial studies how well giving bortezomib with or without combination chemotherapy works as consolidation therapy in patients with newly diagnosed multiple myeloma who have completed stem cell transplant. Bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as cyclophosphamide, dexamethasone, and lenalidomide, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. It is not yet known whether giving bortezomib is more effective with or without combination chemotherapy in the post transplant setting.

Detailed Description

PRIMARY OBJECTIVES:

I. To compare the stringent complete response (sCR) rate after 12 cycles among arms.

SECONDARY OBJECTIVES:

I. To compare progression-free and overall survival among arms. II. To describe the adverse event profile of each arm.

TERTIARY OBJECTIVES:

I. To compare sCR after 6 cycles and 24 cycles and quality of life among arms.

OUTLINE: Patients are randomized to 1 of 3 treatment arms.

ARM A: Patients receive bortezomib subcutaneously (SC) on days 1 and 15 of courses 1-12 and day 1 of courses 13-24.

ARM B: Patients receive bortezomib SC as in Arm A, cyclophosphamide orally (PO) on days 1 and 15 of courses 1-12 and day 1 of courses 13-24, and dexamethasone PO on days 1 and 15 of courses 1-12 and day 1 of courses 13-24.

ARM C: Patients receive bortezomib SC as in Arm A and lenalidomide PO once daily (QD) on days 1-28.

In all arms, treatment continues every 28 days for up to 24 courses in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up every 6 months for 3 years.

Conditions

Stage I Multiple Myeloma; Stage II Multiple Myeloma; Stage III Multiple Myeloma

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm A (bortezomib)

Patients receive bortezomib SC on days 1 and 15 of courses 1-12 and day 1 of courses 13-24.

Group Type: EXPERIMENTAL

bortezomib

Intervention Type: DRUG

Given SC

laboratory biomarker analysis

Intervention Type: OTHER

Correlative studies

quality-of-life assessment

Intervention Type: PROCEDURE

Ancillary studies

Arm B (bortezomib, cyclophosphamide, dexamethasone)

Patients receive bortezomib SC as in Arm A, cyclophosphamide PO on days 1 and 15 of courses 1-12 and day 1 of courses 13-24, and dexamethasone PO on days 1 and 15 of courses 1-12 and day 1 of courses 13-24.

Group Type: EXPERIMENTAL

bortezomib

Intervention Type: DRUG

Given SC

cyclophosphamide

Intervention Type: DRUG

Given PO

laboratory biomarker analysis

Intervention Type: OTHER

Correlative studies

dexamethasone

Intervention Type: DRUG

Given PO

quality-of-life assessment

Intervention Type: PROCEDURE

Ancillary studies

Arm C (bortezomib, lenalidomide)

Patients receive bortezomib SC as in Arm A and lenalidomide PO QD on days 1-28.

Group Type: EXPERIMENTAL

bortezomib

Intervention Type: DRUG

Given SC

lenalidomide

Intervention Type: DRUG

Given PO

laboratory biomarker analysis

Intervention Type: OTHER

Correlative studies

quality-of-life assessment

Intervention Type: PROCEDURE

Ancillary studies

Interventions

bortezomib

Given SC

Intervention Type: DRUG

cyclophosphamide

Given PO

Intervention Type: DRUG

lenalidomide

Given PO

Intervention Type: DRUG

laboratory biomarker analysis

Correlative studies

Intervention Type: OTHER

dexamethasone

Given PO

Intervention Type: DRUG

quality-of-life assessment

Ancillary studies

Intervention Type: PROCEDURE

Other Intervention Names

LDP 341; MLN341; VELCADE; CPM; CTX; Cytoxan; Endoxan; Endoxana; CC-5013; IMiD-1; Revlimid; Aeroseb-Dex; Decaderm; Decadron; DM; DXM; quality of life assessment

Eligibility Criteria

Inclusion Criteria

• Creatinine =< 2 mg/dL
• Absolute neutrophil count (ANC) >= 1000/mm^3
• Platelet count >= 75000/mm^3
• Hemoglobin >= 8.0 g/dL
• Total bilirubin =< 1.5 x upper limit of normal (ULN)
• Treated myeloma: Prior induction therapy (any) and followed by autologous stem cell transplantation
• Measurable disease at initial diagnosis, pre-stem cell transplant (SCT) or post-SCT of multiple myeloma as defined by at least ONE of the following:

• Serum monoclonal protein >= 0.5 g/dL
• > 200 mg of monoclonal protein in the urine on 24 hour electrophoresis
• Serum immunoglobulin free light chain >= 5 mg/dL AND abnormal serum immunoglobulin kappa to lambda free light chain ratio
• Monoclonal bone marrow plasmacytosis >= 30% (evaluable disease)
• Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1 or 2
• < 120 days post SCT with no evidence of relapse or progression prior to registration
• Provide voluntary informed written consent before performance of any study-related procedure not part of normal medical care, with the understanding that consent may be withdrawn by the subject at any time without prejudice to future medical care
• Negative serum pregnancy test done =< 7 days prior to registration, for women of childbearing potential only
• Willing to return to enrolling institution for follow-up during the active monitoring phase of the study
• Ability to complete questionnaire(s) by themselves or with assistance
• Female patients who:

• Are postmenopausal for at least 1 year before the screening visit, OR
• Are surgically sterile, OR
• If they are of childbearing potential, agree to practice 2 effective methods of contraception, at the same time, from the time of signing the informed consent through 30 days after the last dose of study treatment, OR agree to completely abstain from heterosexual intercourse
• Male patients, even if surgically sterilized (ie, status postvasectomy), who:

• Agree to practice effective barrier contraception during the entire study treatment period and through 30 days after the last dose of study treatment, OR
• Agree to completely abstain from heterosexual intercourse

Exclusion Criteria

• Other active malignancy =< 3 years prior to registration; EXCEPTIONS: Non-melanotic skin cancer or carcinoma-in-situ of the cervix; NOTE: If there is a history of prior malignancy, they must not be receiving other specific treatment for their cancer
• 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
• Known to be human immunodeficiency virus (HIV), hepatitis C virus (HCV) or hepatitis B virus positive (HBV+)
• Hypersensitivity to study drugs, boron or mannitol
• Patient refractory to bortezomib (defined as patients who progressed while on bortezomib or within 60 days of receiving bortezomib)
• Any serious medical or psychiatric condition that would prevent the subject from complying with the protocol treatment and procedures
• Grade >= 2 peripheral neuropathy
• 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 electrocardiogram (ECG) abnormality at screening must be documented by the investigator as not medically relevant
• Participation in clinical trials with other investigational agents not included in this trial, within 14 days of the start of this trial and throughout the duration of this trial
• Radiation therapy within 3 weeks before randomization; enrollment of subjects who require concurrent radiotherapy (which must be localized in its field size) should be deferred until the radiotherapy is completed and 3 weeks have elapsed since the last date of therapy
• Female patients who are lactating or pregnant

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Mayo Clinic

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Craig B. Reeder, M.D.

Role: PRINCIPAL_INVESTIGATOR

Mayo Clinic

Locations

Mayo Clinic in Arizona

Scottsdale, Arizona, United States

Johns Hopkins University

Baltimore, Maryland, United States

Washington University School of Medicine

St Louis, Missouri, United States

Baylor Medical Center

Garland, Texas, United States

Countries

United States

Other Identifiers

NCI-2012-01579

Identifier Type: REGISTRY

Identifier Source: secondary_id

MC1186

Identifier Type: -

Identifier Source: org_study_id