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A joint study of the occurrence, development and prognosis of plasma cell disorders based on multi-omics analysis

A joint study of the occurrence, development and prognosis of plasma cell disorders based on multi-omics analysis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400083869
Enrollment
Unknown
Registered
2024-05-06
Start date
2024-05-13
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

plasma cell disorders

Interventions

newly diagnosed plasma cell disorder group:treatment regimen based on bortezomib
relapsed and/or refractory plasma cell disorder group:treatment regimen based on bortezomib
control group (early stages of plasma cell disorders):treatment regimen based on bortezomib

Sponsors

Department of Hematology, Myeloma & Lymphoma Center, Changzheng Hospital, Naval Medical University, Shanghai, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 95 Years

Inclusion criteria

Inclusion criteria: Patients must meet the following inclusion criteria to be eligible for this clinical study: 1. Know and voluntarily sign the Informed Consent Form (ICF). 2. Age= 18 years old. 3. Diagnosed plasma cell disorders (meeting diagnostic criteria for different plasma cell disorders): A. Diagnostic criteria for multiple myeloma, smoldering multiple myeloma, monoclonal gammopathy of undetermined significance, and solitary plasmacytoma, refer to 2014 Lancet Oncol (Rajkumar et al., 2014); B. Diagnostic criteria for amyloidosis, refer to 2022 Am J Hematol (Gertz, 2022); C. Diagnostic criteria for macroglobulinemia, refer to 2023 Am J Hematol (Gertz, 2023); D. Diagnostic criteria for POEMS syndrome, refer to 2021 Am J Hematol (Dispenzieri, 2021); E. Other plasma cell disorders. 4. Life expectancy is more than 3 months.

Exclusion criteria

Exclusion criteria: Patients who meet any of the following exclusion criteria are not enrolled: 1. Pregnancy or lactation. 2. History of alcoholism, drug addiction and mental illness. 3. Other circumstances deemed by the investigator to be unsuitable for this study.

Design outcomes

Primary

MeasureTime frame
Multi-omics data;

Secondary

MeasureTime frame
Analysis of clinical characteristics;

Countries

China

Contacts

Public ContactJuan Du

Department of Hematology, Myeloma & Lymphoma Center, Changzheng Hospital, Naval Medical University, Shanghai, China

juan_du@live.com+86 158 0070 6091

Outcome results

None listed

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