Anthracycline/dexamethasone-based induction chemotherapy
Drug4 cycles of anthracycline/dexamethasone-based chemotherapy
Other names: ID, VAD, CAD
NCT Number: NCT02288741
Patients 60 to 70 years of age with newly diagnosed multiple myeloma were prospectively randomized between 4 cycles of anthracycline/dexamethasone-based induction chemotherapy (A1) or only 2 x 4 days of dexamethasone (A2). A reference arm included patients who could not be randomized (B). Tandem melphalan 140 mg/m² (MEL140) with autologous transplantation was scheduled for all patients.
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Notify Me60 year–70 year
All sexes
Interventional
Phase 3
In arm A1, patients received 4 cycles of conventional induction therapy with anthracycline/dexamethasone-based regimens. Specified in the protocol were vincristine/doxorubicin/dexamethasone (VAD), idarubicin/dexamethasone (ID) and cyclophosphamide/doxorubicin/dexamethasone (CAD). In arm A2, patients were planned to receive only dexamethasone 40 mg orally on days 1-4 and 8-11 for symptom control before stem cell mobilization. For the patients in arm B, a maximum of 6 cycles of induction chemotherapy was allowed. Following this, the treatment was identical for all patients. For stem cell mobilization, an age-adjusted IEV-regimen with granulocyte-colony stimulating factor (G-CSF) was recommended. The target dose for stem cell collection was 6 x 10E+6 CD34 (cluster of differentiation 34)-positive cells/kg (2 transplants and one back-up). The standard dose for each transplantation was 2 x 10E+6 CD34-positive cells/kg. High-dose melphalan at a total dose of 140 mg/m² (MEL140) was given in two doses of 70 mg/m² on days -3 and -2. Stem cell transplantation (SCT) was performed on day 0. A second MEL140 course was planned two months after the first. Regular bisphosphonate treatment was recommended.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
4 cycles of anthracycline/dexamethasone-based chemotherapy
Other names: ID, VAD, CAD
2 x 4 days of dexamethasone (day 1-4 and day 8-11: 40mg)
Other names: dexamethasone
Ifosfamide (day 1-3: 1.900mg/m² iv), epirubicin (day 1: 75 mg/m² iv), etoposide (day 1-3: 120 mg/m² iv) and G-CSF (day 5 until end of apheresis: 5µg/kg sc)
Other names: IEV + G-CSF
stem cell apheresis in peripheral blood, sought amount of CD34-cells: 6 * 10E6/kg
Other names: SC-apheresis
Two cycles of high-dose melphalan (day -3 and day -2: 70mg/m²)
Other names: Tandem melphalan
Two infusions of collected stem cells (day 0: 2*10E6 CD34-cell/kg per transplantation)
Other names: PBSCT
Time frame: From randomization to 10 years follow up
Calculated according to the method of Kaplan and Meier
Time frame: From randomization to 10 years follow up
Calculated according to the method of Kaplan and Meier
Time frame: After last therapy to at least 6 weeks thereafter
Evaluation of the overall response rate. Overall repose is defined as complete response + partial response. The definition of remission followed the criteria of Bladé.
Time frame: After last therapy to at least 6 weeks thereafter
Evaluation of the best response. Response is evaluated after induction therapy, tumor-reduction chemotherapy and stem cell mobilization and each high-dose chemotherapy. The definition of remission followed the criteria of Bladé.
Time frame: From randomization until 2 years after last therapy
Examination of the maximum grade of toxicity according to NCI Common Terminology Criteria for Adverse Events (CTCAE)
Time frame: From randomization to 10 years follow up
Examination of cytogenetic abnormalities wich are of major importance to define longer or shorter survival. Univariate analysis according to the method of Kaplan and Meier. Multivariate analysis according to the method of Cox´s proportional hazards regression analysis.
WiSP Wissenschaftlicher Service Pharma GmbH
Other
Phase III-study for Evaluation of Induction Therapy Before Stem Cell Mobilization and Tandem High-dose Melphalan in Multiple Myeloma Patients 60 to 70 Years of Age
Acronym: DSMM-II
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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