NCT05986682 · OUTCOME
Treatment Characteristics: Dosing Patterns - Delays in Treatment With BLENREP Therapy
Real-World Analysis of Belantamab Mafodotin Care Patterns in Patients With Relapsed and/or Refractory Multiple Myeloma · Source last updated 2025-02-03
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- COUNT_OF_PARTICIPANTS
- Unit
- Participants
- Interval / dispersion
- Not reported
- Time frame
- Between baseline and earliest of end of BLENREP treatment, death, lost to contact or end of study timeframe, up to 40 months.
What was measured
Number of participants for whom BLENREP dosing was delayed during treatment as categorized by reason.
Groups in this outcome
Multiple Myeloma/Blenrep Participants
Participants with relapsed and/or refractory multiple myeloma who were treated with Belantamab Mafodotin - blmf (BLENREP) in the DCI Oncology outpatient clinics between August 5, 2020 and November 7, 2023.
Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.
Analysis denominator · Participants
| Group | Source count |
|---|
| Multiple Myeloma/Blenrep Participants | 30 |
|---|
Reported measurements
Delay for any reason
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Multiple Myeloma/Blenrep Participants | 27 | Not reported | Not reported | Not reported | Not reported |
|---|
Delay for Corneal AE
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Multiple Myeloma/Blenrep Participants | 27 | Not reported | Not reported | Not reported | Not reported |
|---|
Delay for Other Ocular Toxicity
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Multiple Myeloma/Blenrep Participants | 2 | Not reported | Not reported | Not reported | Not reported |
|---|
Delay for Hematologic Toxicity
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Multiple Myeloma/Blenrep Participants | 3 | Not reported | Not reported | Not reported | Not reported |
|---|
Delay for Physician/Patient Choice
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Multiple Myeloma/Blenrep Participants | 2 | Not reported | Not reported | Not reported | Not reported |
|---|
Delay for any other reason
Values in Participants · Interval/dispersion: Not reported| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Multiple Myeloma/Blenrep Participants | 10 | Not reported | Not reported | Not reported | Not reported |
|---|
Complete source fields
- classes
- title
- Delay for any reason
- title
- Delay for Corneal AE
- title
- Delay for Other Ocular Toxicity
- title
- Delay for Hematologic Toxicity
- title
- Delay for Physician/Patient Choice
- title
- Delay for any other reason
- description
- Number of participants for whom BLENREP dosing was delayed during treatment as categorized by reason.
- groups
- description
- Participants with relapsed and/or refractory multiple myeloma who were treated with Belantamab Mafodotin - blmf (BLENREP) in the DCI Oncology outpatient clinics between August 5, 2020 and November 7, 2023.
- id
- OG000
- title
- Multiple Myeloma/Blenrep Participants
- param Type
- COUNT_OF_PARTICIPANTS
- reporting Status
- POSTED
- time Frame
- Between baseline and earliest of end of BLENREP treatment, death, lost to contact or end of study timeframe, up to 40 months.
- title
- Treatment Characteristics: Dosing Patterns - Delays in Treatment With BLENREP Therapy
- type
- PRIMARY
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice