← Back to Clinical Trials
Recruiting NCT06463717

Primary Multiple Myeloma Who Achieved MRD Negativity After Induction Therapy, ASCT or Not

Trial Parameters

Condition Multiple Myeloma
Sponsor First Affiliated Hospital of Zhejiang University
Study Type OBSERVATIONAL
Phase N/A
Enrollment 210
Sex ALL
Min Age 18 Years
Max Age 70 Years
Start Date 2023-12-01
Completion 2028-11
Interventions
Transplant, AutologousChemotherapy drug

Brief Summary

The goal of this observational study is to compare the efficacy and safety of autologous hematopoietic stem-cell transplantation (ASCT) versus non ASCT regimens in primary multiple myeloma patients achieved MRD negativity after induction. The main question it aims to answer is: In primary multiple myeloma patients who achieved MRD negativity after induction, non ASCT regimens are not inferior to ASCT or not? Participants will receive ASCT or non ASCT regimen according to their own choice. Researchers will compare ASCT and non ASCT group see if any significant difference in efficacy and safety.

Eligibility Criteria

Inclusion Criteria: 1. Newly diagnosed multiple myeloma according to the criteria of International Working Group of Myeloma 2. Age ranges from 18-70 years old 3. Achieved MRD negativity and at least very good partial response in clinical response after 4-6 courses of induction therapy. MRD is measured by MRD by multicolor flow with a sensitivity of 10-5. 4. At enrollment, score of Eastern Cooperative Oncology Group (ECOG) should be 0-2. 5. Organ function requirement: Blood bilirubin ≤ 2mg/dL (35 μ mol/L), Alanine aminotransferase/Aspartate aminotransferase below 2 times the upper limit of normal value, Creatinine clearance rate (Ccr) ≥ 30ml/min and Cardiac ejection fraction ≥50%. 6. Expected survival more than 3 months. Exclusion Criteria: 1. Two or more high-risk cytogenetic abnormalities, including del (17p), t (4; 14), t (14; 16), del (1p), amp (1q). Fluorescence in situ hybridization was used to analyze CD138 positive sorted cells, with cut off value of 15% for translocation, 10% f

Related Trials