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Real-world study of pomalidomide-containing regimens in the treatment of relapsed/refractory multiple myeloma

Real-world study of pomalidomide-containing regimens in the treatment of relapsed/refractory multiple myeloma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100054106
Enrollment
Unknown
Registered
2021-12-09
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-11-07

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

Conditions

Multiple myeloma

Interventions

Pomalidomide combined with low-dose dexamethasone group :None
Pomalidomide combined with cyclophosphamide and dexamethasone group :None

Sponsors

Henan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. >= 18 years old, male or female, diagnosed with relapsed or refractory multiple myeloma according to the IMWG diagnostic criteria; 2. When the patient starts using pomalidomide, the hematology routine meets the following requirements: ANC>=500/µL, PLT>=50000/µL; the researchers believe that patients who can benefit from the pomalidomide-containing regimen.

Exclusion criteria

Exclusion criteria: 1. Patients who have had allergic reactions to immunomodulators similar to pomalidomide, dexamethasone or the components contained in the drug; 2. Patients with active new thrombosis or unwilling to undergo antithrombotic therapy; 3. Patients with peripheral neuropathy >= grade 3; 4. Severe mental illness; patients who are judged unsuitable for enrollment after the investigator's evaluation.

Design outcomes

Primary

MeasureTime frame
overall response rate;

Secondary

MeasureTime frame
overall survival;progression free survival;

Countries

China

Contacts

Public ContactFang Baijun

Henan Cancer Hospital

fdation@126.com+86 13027705507

Outcome results

None listed

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