A Prospective Cohort Study of Patients With Plasma Cell Disorders (PCDs) in PKUFH

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

The primary aim is to establish a prospective cohort of patients with plasma cell disorders (PCDs). All of the hospitalized PCD patients who are willing to sign the informed consent form (ICF) will be included in this study. Clinical characteristics, treatment options and responses will be collected. Peripheral blood, bone marrow aspirate and urine samples before and after the treatment will banked for future research. Our team will focus on the clinical and pathological features of PCDs, the correlation between the minimal residual disease (MRD) status and prognosis, and the role of Tumor Microenvironment (TME) in the pathogenesis and progress of PCDs.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: t
View:

• Patients included are those with confirmed diagnosis of PCDs and hospitalized into Peking University First Hospital (PKUFH)

• Patients of plasma cell disorders (PCDs) are recruited. PCDs include monoclonal gammopathy of uncertain significance; smoldering myeloma; multiple myeloma; plasma cell leukemia; amyloidosis; light chain deposition disease; heavy chain deposition disease; Castleman's disease (CD); Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal gammopathy and Skin changes syndrome; cryoglobulinemia; Monoclonal Gammopathy of Renal Significance (MGRS); Monoclonal gammopathy of neurological significance (MGNS).

• Patients are included into this cohort after signing the ICFs.

Locations
Other Locations
China
Peking University First Hospital
RECRUITING
Beijing
Contact Information
Primary
Bo Tang, PhD
tangbo8809@163.com
008613521776195
Backup
Yujun Dong, M.D.
dongy@hsc.pku.edu.cn
008618210264969
Time Frame
Start Date: 2021-07-01
Estimated Completion Date: 2030-12-31
Participants
Target number of participants: 2000
Sponsors
Leads: Peking University First Hospital

This content was sourced from clinicaltrials.gov