Auto Transplant High Dose Melphalan vs High Dose Melphalan+Bortezomib in Pts With Multiple Myeloma Age 65 Years or Older
In this study the investigators are comparing this standard regimen to the newly established regimen of melphalan and bortezomib.
Inclusion Criteria
- Confirmed diagnosis of multiple myeloma less than 12 months since initiation of systemic therapy
- Age ≥60 years at time of transplantation
- KPS 70-100%
- Recovery from complications of prior therapy
Exclusion Criteria
- Diagnosis other than multiple myeloma
- Chemotherapy or radiotherapy within 8 days of initiating treatment in this study
- Prior dose-intense therapy within 56 days of initiating treatment in this study
- Uncontrolled bacterial, viral, fungal or parasitic infections
- Uncontrolled CNS metastases
- Known amyloid deposition in heart
- Organ dysfunction
- LVEF <40% or cardiac failure not responsive to therapy
- FVC, FEV1 or DLCO < 40% of predicted and/or receiving supplementary continuous oxygen
- Evidence of hepatic synthetic dysfunction or total bilirubin > 2x or AST > 3x ULN
- Measured creatinine < 20ml/min
- Sensory peripheral neuropathy grade 4 within 14 days of enrollment
- Karnofsky score < 70%
- Life expectancy limited by other co-morbid illnesses
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT01453088.
In this study the investigators are comparing this standard regimen to the newly
established regimen of melphalan and bortezomib.
Conditioning Regimens:
Treatment arm A Melphalan is administered at a dose of 200mg/m2 by rapid intravenous
infusion via a central or peripheral vein over 30 minutes to one hour.
Melphalan will be given as a single dose (not split over 2 or more days) and given on
day-1.
Dosing will be based on body surface area calculated using actual body weight
Stem cell infusion:
Stem cell infusion will occur on day 0 and will be at least 20 hours after the infusion
of melphalan. The infusion of peripheral blood stem cells will be done in accordance with
the Blood and Marrow Transplant program standard operating procedures.
Filgrastim will be administered at a dose of 5 mcg/kg (rounded to vial size) every other
day starting on day+3 then daily starting on day 9 until engraftment (at least).
Treatment arm B
Bortezomib:
Bortezomib is administered by rapid I.V. push (over 3-5 seconds) via a central or
peripheral vein into a flowing saline line. Bortezomib will be administered any time on
day -4 and at least 20 hrs after the start of the melphalan infusion on day -1.
Dosing will be based on actual body weight. Dexamethasone is administered at a dose of 20
mg IV prior to each bortezomib infusion.
Melphalan:
Melphalan is administered at a dose of 200mg/m2 by rapid intravenous infusion via a
central or peripheral vein over 30 minutes to one hour.
Melphalan will be given as a single dose (not split over 2 or more days) and given of
day-2.
Dosing will be based body surface area calculated using actual body weight
Stem cell infusion:
Stem cell infusion will occur on day 0 and will be at least 18 hours after the infusion
of the bortezomib. The infusion of peripheral blood stem cells will be done in accordance
with the Blood and Marrow Transplant program standard operating procedures.
Filgrastim will be administered at a dose of 5 mcg/kg (rounded to vial size) every other
day starting on day+3 then daily starting on day 9 until engraftment (at least).
Post-transplant Supportive Care will be administered in accordance to the Blood and
Marrow Transplant program standard operating procedures.
Trial PhasePhase II
Trial Typetreatment
Lead OrganizationHackensack University Medical Center
- Primary IDPRO# 1307
- Secondary IDsNCI-2019-01041
- ClinicalTrials.gov IDNCT01453088