G-CSF, Multiple Myeloma, Febrile Episode, Filgrastim, Leograstim Clinical Trial
Official title:
Study on the Incidence of Febrile Episodes During Stem Cells Collection After Chemotherapy in Patients With Multiple Myeloma
To evaluate the difference in the incidence of febrile episodes in patients undergoing stem
cells mobilization with chemotherapy and filgrastim versus chemotherapy and lenograstim.
A febrile episode will be considered as: body temperature > 38°C for two measurements in the
24 hours with an interval of 6 hours at least between the two measurements.
Status | Active, not recruiting |
Enrollment | 180 |
Est. completion date | |
Est. primary completion date | April 2007 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: 1. Age > 18 and < 70 years 2. Diagnosis of multiple myeloma 3. ECOG < 2 to be evaluated at baseline, after the induction chemotherapy 4. Indication to the mobilization with high dose cyclophosphamide chemotherapy 5. Normal blood counts: neutrophils > 1500/µl; platelets > 100.000/µl; hemoglobin > 10 g/dl. 6. Liver and renal function: SGOT/AST, SGPT/ALT; bilirubin < 1.5 times the upper limit of the normal ranges; creatinine < 2 times the upper limit of the normal ranges. 7. Interval from previous induction chemotherapy to high dose chemotherapy between 30 and 60 days 8. ECG e/o Echocardiogram within age related normal range 9. Negative HCV and HbsAg 10. Must be willing and able to fill in the patient's diary 11. Written informed consent Exclusion Criteria: 1. Documented and/or suspected infections 2. Uncontrolled concurrent illness 3. Documented cardiac dysfunction |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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University of Pisa |
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* Note: There are 18 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | febrile episode | 30 days | Yes | |
Secondary | Documented infectious episodes Collection efficiency (CD34+ cells/kilo) Mobilization days Safety | 30 days | Yes |