Clinical Trials Directory

Trials / Terminated

TerminatedNCT01548573

Tandem Auto Transplantation in Myeloma Patients With <12 Months of Prior Treatment

Tandem Autotransplantation for Multiple Myeloma in Participants With Less Than 12 Months of Preceding Therapy, Incorporating Velcade (Bortezomib) With the Transplant Chemotherapy and During Maintenance

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
19 (actual)
Sponsor
University of Iowa · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

This study is designed to decrease toxicity associated with prior tandem transplant protocols by reducing the intensity of induction, consolidation and maintenance therapy, while increasing event-free survival by adding bortezomib (Velcade®), thalidomide, gemcitabine and carmustine to the transplant regimens to down-regulate the rescue of myeloma cells by the micro-environment and to prevent DNA repair post high-dose alkylating agent therapy. By reducing drug resistance, it is hoped that 3-year event-free survival will be increased significantly when compared to Total Therapy II. Additionally, participants will have the option of providing biospecimens for a sub-study evaluating gene expression profiling at specific timepoints to better understand drug-resistance in myeloma, and to determine whether there are genes or gene products in the resistant population that can be targeted by novel therapies.

Detailed description

This study is targeted towards patients who have been diagnosed with Multiple Myeloma, POEMS(Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes), or myeloma plus amyloidosis and have had no more than 12 months of prior treatment. Furthermore, participants cannot have had a prior autologous or allogeneic transplant. The study schema consists of one round of induction chemotherapy, two transplants, one round of consolidation chemotherapy, and two years of maintenance treatment. This study design differs from its historical predecessors in the following manner: * In contrast to Total Therapy II and III, which only allow enrollment of patients with one cycle or one month of treatment prior to enrollment, the proposed study allows enrollment of participants with up to 12 months of prior treatment. * Induction therapy has been reduced to a single cycle. * Bortezomib and thalidomide have been added to the transplant regimen. * Carmustine is added to the second transplant. * Gemcitabine is added to the second transplant regimen. * Consolidation treatment has been reduced to a single cycle. * The first year of maintenance consists of 12 28-day cycles of bortezomib,dexamethasone, and either thalidomide, lenalidomide, or cyclophoshamide. The second year of maintenance therapy consists of lenalidomide and dexamethasone. * The novel agents thalidomide and bortezomib are not introduced upfront, but only with transplantation, consolidation, and maintenance.

Conditions

Interventions

TypeNameDescription
DRUGDexamethasoneGiven PO
PROCEDURETandem autologous stem cell transplant
DRUGCisplatinGiven IV
DRUGDoxorubicinGiven IV
DRUGCyclophosphamideGiven IV or PO
DRUGEtoposideGiven IV
DRUGBortezomibGiven IV
DRUGThalidomideGiven PO
DRUGMelphalanGiven IV

Timeline

Start date
2012-05-01
Primary completion
2013-07-01
Completion
2014-08-01
First posted
2012-03-08
Last updated
2017-06-14
Results posted
2017-06-14

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT01548573. Inclusion in this directory is not an endorsement.