Tandem High Dose Melphalan Versus Triple Intermediate Dose Melphalan and Stem Cell Transplantation in Induction Phase and Prednisolone/IFN Versus IFN in Maintenance Therapy

Multiple Myeloma Clinical Trial

Official title:

Randomised, Non-blind, Parallel Group Study to Compare Tandem High Dose Melphalan (200mg/m²) Versus Triple Intermediate Dose Melphalan (100mg/m²) and Stem Cell Transplantation in Induction Phase and Prednisolone/IFN Versus IFN in Maintenance Therapy in Newly Diagnosed Patients With Multiple Myeloma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00205764
• Other study ID #: 03/99
• Status: Completed
• Phase: Phase 3
• First received: September 12, 2005
• Last updated: November 21, 2013
• Start date: March 1999
• Est. completion date: October 2009

Study information

• Verified date: November 2013
• Source: Austrian Forum Against Cancer
• Contact: n/a
• Is FDA regulated: No
• Health authority: Austria: Federal Ministry for Health and Women
• Study type: Interventional

Clinical Trial Summary

This is an international,multicenter, prospective, open, double randomised and controlled phase III study to compare the therapeutic efficacy of tandem high dose Melphalan versus triple intermediate dose Melpahaln in newly-diagnosed myeloma patients

Description:

Patients will be enrolled into this protocol before start of Induction therapy which consists of 3 cycles or VAD with a 4 week interval followed by 1 cycle of IEV after which stem cell harvesting is performed. After stem cell harvesting is completed Patients will be randomised to one of the high dose therapy arms after response evaluation (Complete remission, Partial remission or stable disease). One group is receiving 2 Cycles of Melphalan 200mg/m² each followed by stem cell transplantation, the other group is receiving 3 Cycles of Melphalan 100mg/m² also followed by stem cell transplantation each time.

After completing high dose therapy patients will be randomised into Maintenance responding with CR, PR or SD. The maintenance therapy will be continued until relapse or progression of disease as defined by the response criteria.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 212
• Est. completion date: October 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 19 Years to 70 Years

Eligibility

Inclusion Criteria:

• Patients with newly diagnosed multiple myeloma of either IgG, IgG, IgD, IgE, IgM (but excluding Waldenstöm´s macroglobulinemia) lambda of kappa light chain, low-secretory, non-secretory disease or plasma cell leukemia

• Performance status of 0, 1, 2, or 3

• Patients not pre-treated with cytostatic drugs

• Patients who clearly require treatment (usually Durie and Salmon stage II or III)

• Patients in stage I who are symptomatic and/or show progression of their disease

• Patients must have an anticipated life expectancy of at least 3 months

• Patients must have adequate organ function

• Patients must have had a minimum recovery period of 2 weeks following any major surgical procedure before entry into this study

• Patients must be between 19 and 70 years of age, also it is understood that most of the patients above 65 will not be eligible because of poor performance status or multimorbidity

• Women of childbearing potential must have a negative pregnancy test and must take adequate precautions to prevent pregnancy during treatment

• Patients must have signed an informed consent

Exclusion Criteria:

• Patients with more than 3 irradiation fields

• Patients presenting initially with one of the following conditions:

• Extramedullary plasmacytoma or solitary plasmacytoma

• Monoclonal gammopathy of undetermined significance

• Smouldering myeloma

• Patients with an irreversible performance status of 4

• Medical of psychiatric conditions that compromise the patient´s ability to give informed consent or complete the study

• Patients with congestive heart failure, NYHA III, IV

• Known HIV positivity

• Known intolerance to any of the study drugs or components

• Acute infection requiring systemic antibiotics at study entry until fully resolved

• Patients with any underlying medical condition which cannot be adequately controlled

• Patients with second primary malignancies (with the exception of cervical carcinoma in situ and non-melanoma skin malignancies) are not eligible unless the patient has been disease-free for at least five years

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Multiple Myeloma
• Neoplasms, Plasma Cell

Intervention

Drug:
• Melphalan

Locations

Country	Name	City	State
Austria	Wilhelminenspital, 1st Medical Department-center for oncology and hematology	Vienna

Sponsors (1)

Lead Sponsor	Collaborator
Austrian Forum Against Cancer

Country where clinical trial is conducted

Austria, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time to treatment failure
Secondary	Response rate
Secondary	Time to response
Secondary	Tolerance of treatment
Secondary	Quality of life
Secondary	Overall survival