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Retrospective chart review study to evaluate mobilization effectiveness of G CSF+plerixafor or G-CSF+/-chemotherapy for the first mobilization attempt in patients with multiple myeloma

Retrospective chart review study to evaluate mobilization effectiveness of G CSF+plerixafor or G-CSF+/-chemotherapy for the first mobilization attempt in patients with multiple myeloma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0008532
Enrollment
500
Registered
2023-06-16
Start date
2023-04-20
Completion date
Unknown
Last updated
2023-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Sanofi-Aventis Korea
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. = 19 years of age 2. Consecutive patients who attempt the first mobilization for ASCT between Oct 2019 and Feb 2023 3. Multiple Myeloma patients undergoing first mobilization for ASCT with G-CSF+/-chemotherapy or G-CSF + preemptive plerixafor according to cohort definition as below: a) Cohort A (G+P group): Patients who receive G-CSF and plerixafor in the first mobilization attempt b) Cohort B (G+/-chemotherapy group): - Cohort B-1 (G alone group): Patients who receive G-CSF alone in the first mobilization attempt - Cohort B-2 (G+chemotherapy group): Patients who receive G-CSF and chemotherapeutic-mobilizing agent in the first mobilization attempt Note: The chemotherapeutic-mobilizing agents include cyclophosphamide, etoposide, vinorelbine, gemcitabine, cytarabine or its combination.

Exclusion criteria

Exclusion criteria: 1. Autologous stem cell transplant eligible patients other than MM patients (ie, non Hodgkin’s lymphoma [NHL]) 2. Patients who receive G-CSF, chemotherapy and plerixafor triple combination for mobilization 3. Re-mobilizing patients with prior mobilization failure

Design outcomes

Primary

MeasureTime frame
Total PB CD34+ cells collected after first mobilization attempt

Secondary

MeasureTime frame
Percentage of patients achieving =2×106 (minimum target) and =4×106 (optimal target);Mobilization failure rate% (fail to harvest minimum target);Total PB CD34+ cells collected on the first apheresis day;Successful mobilization (=2×106/kg) rate% on the first apheresis day;Days of mobilization and collection;Days of hospital stay ;Number of red blood cell (RBC) transfusions ;Number of platelet transfusions

Countries

Korea, Republic of

Contacts

Public ContactKihyun Kim

Samsung Medical Center

kihyunk@skku.edu+82-2-9933-3456

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026