MedPath

Long-term KRd in Relapsed and/or Refractory Multiple Myeloma

Conditions
Multiple Myeloma in Relapse
Multiple Myeloma, Refractory
Interventions
Registration Number
NCT05495620
Lead Sponsor
Dong-A University Hospital
Brief Summary

Research question: Is KRd therapy effective and safe in the real-world Asian patients?

Primay objective: To evaluate the effectiveness of KRd in RRMM patients

Secondary objectives:

To evaluate the effectiveness of investigational treatment strategy by

* PFS difference according to the high-risk disease subgroups and previous treatment

* OS

* Overall response rate and clinical benefit rate

* Duration of response To evaluate the safety and tolerability of KRd in RRMM patients

Detailed Description

Key study variables:

Demographic data, ISS, R-ISS, cytogenetic abnormalities on FISH and G-banding, previous treatment regimens, response to previous treatment regimens, existence of extramedullary plasmacytoma, MM-related symptoms, whether or not M protein has increased twice or more in 2-3 months at the time of KRd commencement, response to KRd therapy, duration of KRd treatment, adverse events during KRd therapy, disease progression and progression date, survival, and censored date or day of death

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
300
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Relapsed and/or refractory multiple myelomaCarfilzomibMultiple myeloma in relapsed but not refractory, relapsed and refractory, and primary refractory status
Relapsed and/or refractory multiple myelomaLenalidomideMultiple myeloma in relapsed but not refractory, relapsed and refractory, and primary refractory status
Relapsed and/or refractory multiple myelomaDexamethasoneMultiple myeloma in relapsed but not refractory, relapsed and refractory, and primary refractory status
Primary Outcome Measures
NameTimeMethod
Progression-free survivalup to 54 months

the time from the first date of KRd to the date of disease progression or death or censored date

Secondary Outcome Measures
NameTimeMethod
Overall survivalup to 54 months

the time from the first date of KRd treatment to the time of death or censored date

Overall response rate, clinical benefit rateup to 54 months

the proportion of patients who achieved a PR or better, which response is defined by the IMWG criteria, the proportion of patients who achieved a MR or better

Duration of responseup to 54 months

the time from the first date of response to the time of disease progression or death or censored date

Toxicity profileup to 2 years

toxicities as determined by the incidence of clinical and laboratory findings occurred from the time of the first date of KRd treatment to the date of disease progression or death or censored date

© Copyright 2025. All Rights Reserved by MedPath