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Panobinostat maintenance in patients with multiple myeloma that have achieved less than complete remission following autologous stem cell transplantation.

Phase 2
Completed
Conditions
Multiple myeloma less than complete remission following Autologous Stem Cell Transplant
Blood - Haematological diseases
Cancer - Myeloma
Registration Number
ACTRN12613000219785
Lead Sponsor
The Alfred Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
25
Inclusion Criteria

Inclusion criteria at registration - pre-ASCT
1. Age > 18 years
2. Diagnosis of multiple myeloma
3. Must have been previously exposed to thalidomide, and/or lenalidomide and/or bortezomib containing induction regimen pre-ASCT (no more than 12 months total prior standard-dose chemotherapy)
4. No previous high-dose chemotherapy or ASCT
5. Eastern Cooperative Oncology Group (ECOG) performance status 0 - 2
6. > 2 X 10^6 CD34+ stem cells available for infusion
7. Normal liver and kidney function (within 2 x the institutional upper limit of normal)
8. Written informed consent
Inclusion criteria to commence panobinostat post-ASCT
10. Have reached Day 42 post-ASCT with evidence of haematology recovery (neutrophils > 1.5 x 10^9/L, platelets unsupported > 50 x 10^9/L
11. Have failed to achieve CR and without progressive disease at 6 to 8 weeks post-ASCT
12. Eastern Cooperative Oncology Group (ECOG) performance status 0 - 2
13. Normal liver and kidney function (within 2 x the institutional upper limit of normal); serum potassium, magnesium, phosphate, sodium, total corrected calcium within normal limits

Exclusion Criteria

1. Patients with monoclonal gammopathy of uncertain significance (MGUS)
2. Patient has been treated with allogeneic transplant
3. Patient has received any anti-MM therapy after ASCT including but not limited to:
- chemotherapy prior to start of study
- biologic immunotherapy including monoclonal antibodies or experimental therapy prior to start of study
- radiation therapy
4. Patients with progressive MM post-ASCT
5. Patient has received prior treatment with DAC in ihibitors including panobinostat
6. Patient has received an investigational agent of any kind within 28 days of ASCT
7. Patient is taking any anti-cancer therapy concomitantly
8. Patient needs valproic acid within 5 days prior to first administration of panobinostat
9. Patients with evidence of another malignancy not in remission, or history of such a malignancy within the last 3 years (except for treated basal or squamous cell carcinoma,
or in situ cancer of the cervix)
10. Patient has undergone major surgery < 2 weeks prior to starting study drug or whohave not recovered from side effects of such therapy to < grade 1 CTCAE 4.0 or baseline
11. Patient has impaired cardiac function, including any one of the following:
- Left Ventricular Ejection Fraction < the lower limit of institutional norm
- Complete left bundle branch block, bifascicular block
- Obligate use of a permanent cardiac pacemaker
- Congenital long QT syndrome
- History or presence of ventricular tachy-arrhythmias
- Resting bradycardia defined as < 50 bpm
- QTcF > 480 msec on screening ECG
- Any clinically significant ST segment and/or T-wave abnormalities
- Presence of unstable atrial fibrillation (ventricular response rate > 100 bpm). Patients with stable atrial fibrillation are allowed in the study provided they do not meet the other cardiac exclusion criteria
- Myocardial infarction or unstable angina pectoris < 6 months prior to starting the study drug
- Congestive cardiac failure (New York Heart Association class III-IV)
- Other clinically significant heart disease and vascular disease (eg. uncontrolled hypertension)
12. Patient is taking medications with relative risk of prolonging the QT interval or inducing torsade de pointes, if such treatment cannot be discontinued or switched to a different medication prior to starting study drug
13. Patient has impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of panobinostat, such as:
- ulcerative disease
- uncontrolled nausea
- vomiting
- diarrhoea CTCAE 4.0 Grade > 2 (despite antidiarrheal medications)
- malabsorption syndrome
- obstruction
- stomach and/or small bowel resection
14. Patient has any other concurrent severe and/or uncontrolled medical conditions that could cause unacceptable safety risks or compromise compliance with the protocol such as:
- uncontrolled diabetes
- active or uncontrolled infection
- chronic obstructive or chronic restrictive pulmonary disease including dyspnea at rest from any cause
- uncontrolled thyroid dysfunction
- recent, acute or active bleeding
15. Patient has a known history of human immunodeficiency virus (HIV) seropositivity or history of active/treated hepatitis B or C (a test for screening is not required)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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