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Real-world study on the efficacy and safety of upgrading from bortezomib to carfilzomib for the treatment of NDMM based on early therapeutic assessment

Real-world study on the efficacy and safety of upgrading from bortezomib to carfilzomib for the treatment of NDMM based on early therapeutic assessment

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101593
Enrollment
Unknown
Registered
2025-04-27
Start date
2024-09-11
Completion date
Unknown
Last updated
2025-05-05

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

Conditions

Multiple myeloma

Interventions

treatment group:Carfilzomib-based regimens, including KRd/KPd/DKd/DKRd/DKPd.

Sponsors

Chinese People's Liberation Army Northern Theater Command General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients fully understand this study, voluntarily participate and sign the informed consent form (ICF); 2. Age>=18 years; 3. Newly diagnosed multiple myeloma confirmed by clinical diagnosis; 4. Patients who plan to undergo autologous hematopoietic stem cell transplantation or do not plan to undergo autologous hematopoietic stem cell transplantation; 5. Bortezomib is included in the induction regimen; 6. The efficacy of bortezomib-containing induction therapy for 1 course =CR.

Exclusion criteria

Exclusion criteria: 1. Carfilzomib is not used in induction or consolidation; 2. The efficacy of 1 course of bortezomib-containing induction therapy >=PR; 3. The efficacy of bortezomib-containing induction therapy for 2 courses >=VGPR; 4. MRD detection was not performed at >=CR; 5. Bone marrow dry pumping; 6. Suffering from a serious infection; 7. In the judgment of the investigator, the patient is not suitable to participate in this study; 8. Inability to sign informed consent.

Design outcomes

Primary

MeasureTime frame
MRD negative;Overall response rate;Partial response;Very good partial response;Complete response;Strictly complete response;

Secondary

MeasureTime frame
Sustained minimal residual disease negative;Progression free survival;Adverse event;

Countries

China

Contacts

Public ContactLiu Jinghua

Chinese People's Liberation Army Northern Theater Command General Hospital

mtljh7646@163.com+86 189 0988 5271

Outcome results

None listed

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