Multiple Myeloma Clinical Trial
Official title:
High-dose Etoposide +G-CSF Versus High-dose Cyclophosphamide +G-CSF in Peripheral Blood Stem Cell Mobilization in Patients With Multiple Myeloma:a Multicenter,Randomized,Prospective Study
This study was a multi-center, randomized, prospective study. The purpose is to clarify that high-dose VP-16+G-CSF has better mobilization efficiency and less toxic and side effects compared with high-dose CTX+G-CSF, and minimize mobilization failure, so as to provide convenient and high-quality mobilization programs for clinical practice and enable more patients to enter the transplantation stage smoothly.
Status | Recruiting |
Enrollment | 164 |
Est. completion date | October 1, 2025 |
Est. primary completion date | October 1, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: - Confirmed MM patients: patients who were initially diagnosed and treated, who were suitable for autologous transplantation and planned to be treated with ASCT; - Age limitation: 18-70 years old patients; ? Physical status: ECOG physical status score was 0 or 1; ? The adverse reactions caused by chemotherapy had recovered: peripheral blood leukocytes =3.0×109/L, hemoglobin =80g/L, platelet =80×109/L; Liver function glutamic-pyruvic transaminase and glutamic-oxalacetic transaminase = 2 times the upper limit of normal value, total bilirubin = 1.5 times the upper limit of normal value, serum creatinine = 1.5 times the upper limit of normal value, chest CT normal, ecg normal; (5) Patients participate voluntarily and informed consent is signed by patients themselves (or their legal representatives); Take effective contraceptive measures during the childbearing age. Exclusion Criteria: ? According to the clinical judgment of the researcher: According to NCI CTCAE (4th edition May 28, 2009), patients with =3 grade cardiopulmonary insufficiency and severe kidney disease, currently diagnosed as coronary heart disease, myocardial infarction, arrhythmia, glutamic-oxalacetic transaminase, glutamic-pyruvic transaminase = 2 times the upper limit of normal value, Total bilirubin = 1.5 times the upper limit of normal; - With active infection, including fever of unknown cause (axillary temperature > 37.5?); ? Patients with severe history of mental system. |
Country | Name | City | State |
---|---|---|---|
China | Hospital 307 | Beijing | Beijing |
Lead Sponsor | Collaborator |
---|---|
Affiliated Hospital to Academy of Military Medical Sciences |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Main purpose | Compared with the literature data, The primary efficacy endpoint was the difference in the proportion of patients who reached the target CD34+ cells =5×106/kg and CD34+ cells =5×106/kg within 3 days of monotherapy between the study group and the control group. | Enrollment is expected to last for one year, followed up for two years. |
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