Multiple Myeloma Clinical Trials

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Individualized Dynamic Frailty-tailored Therapy (DynaFiT) in Elderly Patients With Newly Diagnosed Multiple Myeloma: a Prospective and Multi-center Study

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

Frailty is dynamic and confers poor outcomes in elderly patients with newly diagnosed multiple myeloma (NDMM), mainly because of the high prevalence of treatment discontinuation due to intolerability. We designed a multi-center prospective study (DynaFiT) based on our real-life practice to evaluate the feasibility and benefits of a dynamic frailty-tailored therapy in elderly patients with different fitness/frailty statuses. Since Dara-based treatment have recently become the new standard regimens, in this amendment of the study, daratumumab added to VRd is recommended as induction therapy regimen.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 65
Healthy Volunteers: f
View:

• Adult males and females aged ≥65 years who were either transplant-ineligible or had no intent for immediate transplant;

• Subject must have documented multiple myeloma as defined by the criteria below:

∙ Monoclonal plasma cells in the bone marrow 10% or presence of a biopsy-proven plasmacytoma;

∙ Measurable disease as defined by any of the following:

• Serum monoclonal paraprotein (M-protein) level ≥1.0 g/dL or urine M-protein level ≥200 mg/24 hours; or

• IgA multiple myeloma: serum M-protein level ≥0.5 g/dL or urine M-protein level ≥200 mg/24 hours; or

• Light chain multiple myeloma: Serum immunoglobulin free light chain ≥10 mg/dL and abnormal serum immunoglobulin kappa lambda free light chain ratio.

‣ Has not had prior systemic therapy for multiple myeloma;

⁃ The functional reserve of the organs can withstand systemic therapy;

⁃ Each subject (or their legally acceptable representative) must sign an informed consent form (ICF) indicating that he or she understands the purpose of and procedures required for the study and are willing to participate in the study. Subject must be willing and able to adhere to the prohibitions and restrictions specified in this protocol, as referenced in the ICF.

Locations
Other Locations
China
The First Hospital of Jilin University
RECRUITING
Changchun
Time Frame
Start Date: 2021-09-08
Estimated Completion Date: 2029-09-08
Participants
Target number of participants: 131
Related Therapeutic Areas
Sponsors
Collaborators: The First Affiliated Hospital of Air Force Medicial University, Sun Yat-Sen University Cancer Center, Ruijin Hospital, Second Hospital of Shanxi Medical University
Leads: FengYan Jin

This content was sourced from clinicaltrials.gov