Study to Evaluate the Combination of Bendamustine, Bortezomib and Dexamethasone (BBD) in the First-Line Treatment of Patients With Multiple Myeloma Who Are Not Candidates for High Dose Chemotherapy

Phase 2

Completed

• Conditions: Multiple Myeloma
• Interventions: Drug: Bendamustine; Drug: Bortezomib; Drug: Dexamethasone

• Registration Number: NCT01056276
• Lead Sponsor: SCRI Development Innovations, LLC

Brief Summary

In this study, investigators will evaluate the activity of bendamustine, bortezomib and dexamethasone (BBD). This regimen combines 3 agents with high activity in multiple myeloma, with different mechanisms of action and non-overlapping toxicities.

Detailed Description

The purpose of this study is to assess the efficacy, tolerability, and toxicity of bendamustine, bortezomib, and dexamethasone (BBD) as first-line treatment of multiple myeloma (MM) patients who are transplant ineligible or who are not candidates for high dose chemotherapy. Eligible patients will receive protocol treatment for up to 34 weeks plus the screening period (up to 2 weeks). Response assessments will occur every 4 weeks and confirmed using the International Myeloma Working Group Uniform Response Criteria. Patients having an objective response or stable disease will continue to maintenance therapy until disease progression or intolerable toxicity.

Study Timeline

• Study First Submitted: 2010-01-22
• Study First Submitted QC: 2010-01-25
• Study First Posted: 2010-01-26
• Study Start: 2010-05
• Primary Completion: 2015-08
• Study Completion: 2017-02
• Results First Submitted: 2017-02-08
• Results First Submitted QC: 2017-02-08
• Status Verified: 2017-03
• Results First Posted: 2017-03-28
• Last Update Submitted: 2017-03-30
• Last Update Posted: 2017-05-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 59

Inclusion Criteria

1. Patients must meet the Durie and Salmon criteria for initial diagnosis of multiple myeloma.

2. Previously histologically confirmed, multiple myeloma with indication for therapy including one of the following:

   • Hemoglobin <10 g/dl or 2 g/dl below normal
   • Serum calcium >11.5 mg/dl
   • Creatinine >2 mg/dl
   • Lytic bone lesions or severe osteopenia
   • Extramedullary plasmacytomas

3. Patients should not be considered candidates for high dose therapy/autologous stem cell transplantation due to coexistent medical conditions, advanced age, poor performance status, refusal of high dose chemotherapy, or other reasons as judged by the patient and/or physician.

4. ECOG Performance Status 0-2.

5. WBC ≥3000/mL; ANC ≥1000/mL; platelets ≥50,000/mL (patients with platelets ≥30,000/mL are eligible if thrombocytopenia is felt to be due to extensive bone marrow involvement with myeloma).

6. Patients with adequate organ function as measured by:

   Renal: Serum creatinine <2.0 mg/dL or a calculated or measured creatinine clearance of >30 mL/minute.

   Hepatic: Total bilirubin < 1.5 x ULN and ALT and AST <2.5 x the ULN (<5 x ULN for patients with liver involvement).

7. Patients must have measurable or evaluable disease. In patients with disease limited to bone and bone marrow, serial paraprotein measurements are acceptable for evaluable disease.

8. Patients must be accessible for treatment and follow-up procedures.

9. Male or female patients 18 years of age or older.

10. Patients must provide written informed consent prior to receiving protocol therapy.

11. Women of childbearing potential must agree to use a medically acceptable method of birth control(e.g., a hormonal contraceptive, intra-uterine device, diaphragm with spermicide, condom with spermicide, or abstinence) for the duration of the study and for 12 months after their last dose of rituximab. Men must use an acceptable form/method of contraception for the duration of treatment and for 3 months after the end of treatment.

12. Patients must be able to understand the nature of this study and give written informed consent.

Exclusion Criteria

1. Previous therapy for multiple myeloma with the exception of an initial 4-day course of pulsed dexamethasone.

2. Patients with ≥NCI CTCAE v4.0 grade 2 peripheral neuropathy ≤14 days prior to study enrollment.

3. Treatment with investigational agent(s) ≤14 days prior to study enrollment.

4. Active infection or infection requiring intravenous antibiotic treatment at the time of accrual.

5. Known to be HIV positive (HIV test is not required for participation in the trial).

6. Patients with class III/IV cardiac problems as defined by the New York Heart Association (NYHA)criteria:

   • History of uncontrolled or symptomatic angina
   • History of arrhythmias requiring medications, or clinically significant, with the exception of asymptomatic atrial fibrillation requiring anticoagulation
   • Myocardial infarction < 6 months from study entry
   • Uncontrolled or symptomatic congestive heart failure
   • Ejection fraction below the institutional normal limit
   • Any other cardiac condition that, in the opinion of the treatment physician, would make this protocol unreasonably hazardous for the patient
   • Uncontrolled hypertension (systolic blood pressure [BP] >180 or diastolic BP >100mm Hg)or uncontrolled cardiac arrhythmias.
   • Prior to study entry, any ECG abnormality at Screening must be documented by the investigator as not medically relevant.

7. Other serious medical conditions or psychiatric illness that would potentially interfere with patient participation in this trial.

8. A second malignancy, other than basal cell carcinoma of the skin or in situ carcinoma of the cervix,unless the tumor was treated with curative intent at least 2 years previously or low-risk prostate cancer after curative therapy.

9. Known hypersensitivity to bortezomib, boron, or mannitol.

10. Female patient is pregnant or lactating. Confirmation that female patients of childbearing potential are not pregnant must be established by a negative serum pregnancy test ≤7 days prior to start of treatment.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Treatment	Bendamustine	Bendamustine, Bortezomib,and Dexamethasone for 8 cycles or 2 cycles beyond a confirmed complete response, assessed by IMWG criteria. Patients with stable disease and no intolerable toxicity may continue maintenance therapy with Bortezomib and Dexamethasone until disease progression or intolerable toxicity.
Treatment	Dexamethasone	Bendamustine, Bortezomib,and Dexamethasone for 8 cycles or 2 cycles beyond a confirmed complete response, assessed by IMWG criteria. Patients with stable disease and no intolerable toxicity may continue maintenance therapy with Bortezomib and Dexamethasone until disease progression or intolerable toxicity.
Treatment	Bortezomib	Bendamustine, Bortezomib,and Dexamethasone for 8 cycles or 2 cycles beyond a confirmed complete response, assessed by IMWG criteria. Patients with stable disease and no intolerable toxicity may continue maintenance therapy with Bortezomib and Dexamethasone until disease progression or intolerable toxicity.

Primary Outcome Measures

Name	Time	Method
Complete Response Rate	every 8 weeks for approximately 48 months	Defined as the percent of patients having a complete response (CR) to treatment, assessed using the International Myeloma Working Group (IMWG) Uniform Response Criteria. CR=disappearance of soft tissue plasmacytomas and 5% or less plasma cells in bone marrow.
Number of Patients Who Experienced Serious and Non-serious Adverse Events	approximately 36 weeks	All serious adverse events (SAEs) and non-serious adverse events (AEs) were assessed using National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v4.0, and were collected from start of study treatment until 30 days after last dose of study medication. Refer to the Adverse Event module for specific terms.

Secondary Outcome Measures

Name	Time	Method
Progression Free Survival	every 8 weeks for up to 48 months	Defined as the interval of time (in months) that patient are alive from date of first protocol treatment to date of documented tumor progression or date of death from any cause. Progressive disease, assessed according to International Myeloma Working Group Uniform Response Criteria, is defined as at least a 25% increase from the nadir in any one of the following criteria: serum M-protein, urine M-protein, or bone marrow plasma cell percentage of 10% or greater.
Overall Survival	every 4 weeks until progressive disease then every 12 weeks, projected 48 months	Defined as the interval of time, in months, from first study treatment until the earlier of the date of death or date last known alive.
Overall Response Rate	every 4 weeks for approximately 2 years	The number of patients with observed complete or partial response (CR or PR) assessed by International Myeloma Working Group (IMWG) Uniform Response Criteria. PR=50% or greater reduction from baseline in serum M-protein and 90% or greater reduction from baseline in 24-hour urinary M-protein.

Trial Locations

Locations (13)

Hematology Oncology Clinic, LLP; 🇺🇸 Baton Rouge, Louisiana, United States

Los Robles Hospital and Medical Center; 🇺🇸 Thousand Oaks, California, United States

Florida Cancer Specialists; 🇺🇸 Ft. Myers, Florida, United States

Grand Rapids Clinical Oncology Program; 🇺🇸 Grand Rapids, Michigan, United States

South Carolina Oncology Associates; 🇺🇸 Columbia, South Carolina, United States

Chattanooga Oncology Hematology Associates; 🇺🇸 Chattanooga, Tennessee, United States

Leading Edge Research, PA; 🇺🇸 Arlington, Texas, United States

The Center for Cancer and Blood Disorders; 🇺🇸 Fort Worth, Texas, United States

Peninsula Cancer Institute; 🇺🇸 Newport News, Virginia, United States

Oncology Hematology Care Inc.; 🇺🇸 Cincinnati, Ohio, United States

Tennessee Oncology; 🇺🇸 Nashville, Tennessee, United States

Center for Cancer and Blood Disorders; 🇺🇸 Bethesda, Maryland, United States

National Capital Clinical Research Consortium; 🇺🇸 Bethesda, Maryland, United States