SWOG clinical trial number
S0833
Modified Total Therapy 3 (TT3) for Newly Diagnosed Patients with Multiple Myeloma (MM): A Phase II SWOG Trial for Patients Aged </= 65 Years
Closed
Phase
Accrual
0%
Abbreviated Title
TT3: Ph II New MM for Pts </= 65
Activated
03/15/2011
Closed
05/01/2012
Participants
Research committees
Myeloma
Treatment
Cisplatin
Cyclophosphamide
Dexamethasone
Adriamycin®
Etoposide
Melphalan
Thalidomide
CC-5013 (Lenalidomide)
Bortezomib
Eligibility Criteria Expand/Collapse
Newly diagnosed acitve MM; measurable disease (non-secretory pts elig if >/= 20% plasmacytosis or >3 focal plasmacytomas on skeletal survey/MRI); no more than 1 cycle of prior chemo for this disease; no prior melphalan; no radiation to > half pelvis; prior chemo/radiotherapy must have been completed >/= 4 wks prior to reg; 18-65 years; ejection fraction > 40% by MUGA or 2d ECHO; Zubrod PS 0-2 (or 3-4 based solely on bone pain); platelets >/= 150x10^9/L; ANC >/= 1.5x10^9/L unless myeloma related; total bilirubin </= 1.5xULN; no plans to receive dialysis; no Grade >/= 2 peripheral neuropathy; no known bortezomib, boron or mannitol sensitivity; no uncontrolled diabetes; pts must be offered participation in GEP; pts consenting to GEP must be offered participation in banking; must have serum bilirubin, creatinine, protein electrophoresis, and quantitative immunoglobulins, 24 hr urine for total protein and electrophoresis, serum free light chaines, serum and urine IFE and beta-2-microglobulin tests; pts must be aware of teratogenic potential of thalidomide and agree to comply with contraception guielines and STEPS program, no prior malignancy except adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer or other cancer for which pt has not received treatment for 1 yr prior to reg (other cancers acceptable if life expectancy is > 5 yrs); pts must give informed consent
Other Clinical Trials
SWOG Clinical Trial Number
S2213
A Phase III, Randomized Study of Daratumumab, Cyclophosphamide, Bortezomib and Dexamethasone (Dara-VCD) Induction Followed by Autologous Stem Cell Transplant or Dara-VCD Consolidation and Daratumumab Maintenance in Patients with Newly Diagnosed AL Amyloidosis
Research Committee(s)
Myeloma
Activated
12/01/2023
Accrual
1%
Open
Phase
SWOG Clinical Trial Number
S2209
A Phase III Randomized Trial for Newly Diagnosed Multiple Myeloma Patients Considered Frail or Ineligible for Stem Cell Transplant Comparing Frontline Regimen Bortezomib-Lenalidomide-Dexamethasone-Lite (VRd-Lite) with Daratumumab-Lenalidomide-Dexamethasone (DRd) Followed by Len+/-Dara (R+/-D) Maintenance
Research Committee(s)
Myeloma
Activated
05/30/2023
Accrual
10%
Open
Phase
SWOG Clinical Trial Number
S2005
A PHASE II RANDOMIZED STUDY COMPARING IBRUTINIB AND RITUXIMAB VS. VENETOCLAX AND RITUXIMAB IN PREVIOUSLY UNTREATED WALDENSTROM'S MACROGLOBULINEMIA (WM) /LYMPHOPLASMACYTIC LYMPHOMA (LPL)
Research Committee(s)
Myeloma
Activated
06/24/2021
Accrual
10%
Open
Phase