The purpose of this study is to evaluate the real-world characteristics and outcomes of participants with smoldering multiple myeloma (SMM) overall and by high-risk and non-high-risk SMM according to (AQUILA study criteria \[NCT03301220\], Mayo 20-2-20 and international myeloma working group (IMWG) 2020 risk classification models), and to evaluate the risk of progressing of SMM to multiple myeloma (MM) and outcomes in participants after progressing to MM.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Participant Characteristics and Treatment Patterns: Number of Participants With Type of Treatment
Timeframe: Data collection up to 1 year and 2 months
Participant Characteristics and Treatment Patterns: Duration of Treatment
Timeframe: Data collection up to 1 year and 2 months
Participant Characteristics and Treatment Patterns: Time to Best Response
Timeframe: Data collection up to 1 year and 2 months
Participant Characteristics and Treatment Patterns: Overall Survival in Participants With SMM Overall and for High-risk and Non-high-risk Participants
Timeframe: Data collection up to 1 year and 2 months
Observation Patterns for High-risk and Non-high-risk SMM Participants and Overall
Timeframe: Data collection up to 1 year and 2 months
Time to Progression to Multiple Myeloma (MM) in Participants With High-risk SMM
Timeframe: Data collection up to 1 year and 2 months
Progression-free Survival
Timeframe: Data collection up to 1 year and 2 months
Rates of Progression From SMM to MM for High and Non-high-risk Participants
Timeframe: Data collection up to 1 year and 2 months
Risk Factors of Progression From SMM to MM
Timeframe: Data collection up to 1 year and 2 months
Number of Participants With Myeloma-related Organ Damage Who Progress From SMM to MM
Timeframe: Data collection up to 1 year and 2 months