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The Risk Stratification in Patients With Multiple Myeloma Based on Fluorescence Flow Cytometry Quantitative Determination of the Circulating Plasma Cells in the Peripheral Blood

The Risk Stratification in Patients With Multiple Myeloma Based on Fluorescence Flow Cytometry Quantitative Determination of the Circulating Plasma Cells in the Peripheral Blood

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04242121
Enrollment
24
Registered
2020-01-27
Start date
2020-01-15
Completion date
2024-05-06
Last updated
2024-05-08

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

Conditions

Myeloma Multiple

Brief summary

The main aim of this study is to evaluate the effectiveness of the clinical application of the XN-1000/20 hematology analyzer for risk stratification in patients with multiple myeloma based on the number of detected plasma cells in peripheral blood at the different stages of treatment. This clinical study is observational and does not involve drugs. 100 subjects with newly diagnosed multiple myeloma will be enrolled in this study and followed for 3 years.

Detailed description

The presence of circulating plasma cells in patients with multiple myeloma is considered as a marker for highly proliferative disease and associated with a worse prognosis. Plasma cell counting is conventionally done by means of peripheral blood film morphology using light microscopy. However, this manual method is laborious as well as imprecise due to the low number of cells counted, and inter-observer variability. Flow cytometry with monoclonal antibodies is unsuitable as a screening test. The procedure is not automated, and it is expensive and time consuming. Therefore, new rapid, effective and inexepensive methods are needed for risk-stratification in patients with multiple myeloma. Automated antibody-synthesizing or secreting cells counting from routine haematology systems (XN-1000/20) without sample preparation and in less than 1 minute will further reduce the workload in haematology laboratories and it can be used for counting circulating plasma cells in peripheral blood in patients with multiple myeloma.

Interventions

DIAGNOSTIC_TESTfluorescence flow cytometry

Countification of plasma cells by fluorescence flow cytometry (hematology analyzer XN-1000/20)

Sponsors

Ivan S Moiseev
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis: Newly diagnosed symptomatic multiple myeloma * Signed informed consent * No second tumors

Exclusion criteria

* Monoclonal gammopathies of undefined significance * Smoldering Multiple Myeloma * Plasma cell leukemia

Design outcomes

Primary

MeasureTime frameDescription
Time-to-progression according to circulating plasma cells[Time Frame: 3 years]Measured by cumulative incidence estimates

Secondary

MeasureTime frameDescription
Progression-free survival[Time Frame: 3 years]Measured by Kaplan-Meier estimates
Overall survival[Time Frame: 3 years]Measured by Kaplan-Meier estimates

Countries

Russia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026