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Immunological monitoring in transplant-ineligible myeloma patients treated with lenalidomide

Immunological monitoring in transplant-ineligible myeloma patients treated with lenalidomide - Immunological analysis of lenalidomide therapy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000034399
Enrollment
40
Registered
2018-11-01
Start date
2018-11-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Multiple myeloma

Interventions

None listed

Sponsors

Kyoto University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. A 20 to 80 year-old patient who was diagnosed with multiple myeloma according to the diagnostic criteria of the Hematologic Malignancy Practice Guideline published by the Japanese Society of Hematology. 2. A patient who was judged as ineligible for both autologous and allogeneic hematopoietic cell transplantation by the attending physician. 3. A patient who has measurable M-protein in serum or urine. 4. A patient who agreed with the registration for RevMate and can keep its administrative procedures. 5. A newly diagnosed myeloma patient who will be treated with lenalidemide and dexamethasone (Ld) as the first-line treatment, or a relapsed or refractory myeloma patient who will be treated with a combination of Ld and elotuzumab (ELd) or daratumumab (DLd). 6. A patient who provided written informed consent for this study.

Exclusion criteria

Exclusion criteria: A patient who is judged to be inappropriate to participate in this study by the attending physician.

Design outcomes

Primary

MeasureTime frame
Best therapeutic effect

Secondary

MeasureTime frame
Immunological parameters, progression-free survival, overall survival, time to next treatment, safety

Countries

Japan

Contacts

Public ContactToshio Kitawaki

Kyoto University Hospital Department of Hematology and Oncology

hemato@kuhp.kyoto-u.ac.jp(075)751-4694

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026