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Prospective Research Assessment in Multiple Myeloma: An Observational Evaluation (PREAMBLE)

Recruiting
Conditions
Multiple Myeloma
Registration Number
NCT01838512
Lead Sponsor
Bristol-Myers Squibb
Brief Summary

The purpose of this study is to assess the clinical effectiveness of all approved multiple myeloma (MM) therapies in the newly-diagnosed (NDMM) and the relapsed/refractory MM (RRMM) settings in real-world clinical practice.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
2555
Inclusion Criteria

For RRMM participants who have received at least one prior line of therapy (LoT) for MM:

  • Have documented progression from a prior LoT
  • Participants who have initiated treatment with one of the following therapies within 90 days before consent for this study OR in the case where treatment has not yet been initiated, documentation that the treatment strategy was determined before consent for this study must be provided, and treatment must be initiated within 30 days after consent:
  • IMiDs
  • PIs
  • Combination of IMiD + PI
  • Newer agents with novel MOAs alone or in combination (eg, mAbs, HDACIs, Akt inhibitors, SINE, or CAR T-cell therapies)

For NDMM participants receiving frontline therapy:

  • Eligible to receive frontline therapy for MM (no prior MM treatment)
  • Participants who have initiated treatment for MM with one of the following therapies within 90 days before consent for this study OR in the case where treatment has not yet been initiated, documentation that the treatment strategy was determined before consent for this study must be provided, and treatment must be initiated within 30 days after consent:
  • IMiDs
  • PIs
  • Combination of IMiD + PI
  • Newer agents with novel MOAs alone or in combination (eg, mAbs, HDACIs, Akt inhibitors, SINE, or CAR T-cell therapies)
Exclusion Criteria
  • Participants who are currently participating in a clinical trial for MM
  • Participants who are currently receiving treatment for primary cancer other than MM
  • Participants who are not willing or able to provide informed consent
  • Participants who are incarcerated
  • Participants under compulsory detention for treatment of a physical (eg, infectious) or psychiatric illness

Other protocol-defined inclusion/exclusion criteria apply

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Overall Survival (OS) for participants with newly-diagnosed multiple myeloma (NDMM)Up to 8 years
Progression-Free Survival (PFS) for participants with NDMMUp to 8 years
Overall Survival (OS) for participants with relapsed/refractory multiple myeloma (RRMM)Up to 5 years
Progression-Free Survival (PFS) for participants with RRMMUp to 5 years
Secondary Outcome Measures
NameTimeMethod
Healthcare resource utilization (HCRU) for participants with NDMMFrom the day of enrollment until death, withdrawal of consent, enrollment into a clinical trial for MM, loss to follow-up, or end of study, whichever comes first; assessed up to 96 months
Incidence of Adverse Events (AEs) for participants with RRMMUp to 5 years
Incidence of Adverse Events (AEs) for participants with NDMMUp to 8 years
Treatment patterns of approved MM therapies as measured by the Response Rate for participants with RRMMFrom study index date until the enrollment date, assessed up to 5 years
Treatment patterns of approved MM therapies as measured by the Response Rate for participants with NDMMFrom study index date until the enrollment date, assessed up to 8 years
Healthcare resource utilization (HCRU) for participants with RRMMFrom the day of enrollment until death, withdrawal of consent, enrollment into a clinical trial for MM, loss to follow-up, or end of study, whichever comes first; assessed up to 60 months
Patient reported outcomes as measured by EQ-5D summary index for participants with NDMMFrom start of initial therapy to questionnaire completion, assessed up to 8 years
Patient reported outcomes as measured by EQ-5D summary index for participants with RRMMFrom start of initial therapy to questionnaire completion, assessed up to 5 years
Patient reported outcomes as measured by EORTC-QLQ-MY20 for participants with NDMMFrom start of initial therapy to questionnaire completion, assessed up to 8 years
Patient reported outcomes as measured by EORTC-QLQ-C30 for participants with RRMMFrom start of initial therapy to questionnaire completion, assessed up to 5 years
Patient reported outcomes as measured by EORTC-QLQ-C30 for participants with NDMMFrom start of initial therapy to questionnaire completion, assessed up to 8 years
Patient reported outcomes as measured by EORTC-QLQ-MY20 for participants with RRMMFrom start of initial therapy to questionnaire completion, assessed up to 5 years

Trial Locations

Locations (118)

Local Institution - 0011

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Indianapolis, Indiana, United States

Local Institution - 0028

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Sherman, Texas, United States

Local Institution - 0106

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Cannes Cedex, France

Local Institution - 0051

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Santa Rosa, California, United States

Local Institution - 0045

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Burbank, California, United States

Local Institution - 0046

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Savannah, Georgia, United States

Local Institution - 0041

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Springfield, Illinois, United States

Local Institution - 0064

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London, Kentucky, United States

Local Institution - 0012

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Urbana, Illinois, United States

Local Institution - 0013

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Muscle Shoals, Alabama, United States

Local Institution - 0017

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Jacksonville, Florida, United States

Florida Cancer Specialists & Research Institute

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Brooksville, Florida, United States

Local Institution - 0019

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Cleveland, Ohio, United States

Local Institute

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Swansea, United Kingdom

Local Institution - 0015

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Saint Louis, Missouri, United States

Local Institution - 0043

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Pottstown, Pennsylvania, United States

Local Institution - 0026

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Spokane, Washington, United States

Local Institution - 0044

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Fort Lauderdale, Florida, United States

Local Institution - 0025

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Dallas, Texas, United States

Local Institution - 0115

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Pesaro, Italy

Local Institution - 0099

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Chalon sur Saone, France

Local Institution - 0065

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Toronto, Ontario, Canada

Local Institution - 0101

🇫🇷

Perigueux, France

Local Institution - 0086

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Rostock, Germany

Local Institution - 0058

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Anderson, Indiana, United States

Local Institution - 0032

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Garland, Texas, United States

Local Institution - 0020

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Springfield, Missouri, United States

Local Institution - 0067

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Magdeburg, Germany

Local Institution - 0082

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Dresden, Germany

Local Institution - 0102

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Nantes, France

Local Institution - 0071

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Heidelberg, Germany

Local Institution - 0076

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Ludwigsburg, Germany

Local Institution - 0073

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Muenchen, Germany

Local Institution - 0075

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Reutlingen, Germany

Local Institution - 0033

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Cary, North Carolina, United States

Local Institution - 0037

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Missoula, Missouri, United States

Local Institution - 0089

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Goslar, Germany

Local Institution - 0078

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Traunstein, Germany

Local Institution - 0030

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Woodbury, Minnesota, United States

Local Institution - 0014

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Dallas, Texas, United States

Local Institution - 0124

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Messina, Italy

Local Institution - 0122

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San Giovanni Rotondo (FG), Italy

Local Institution - 0105

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Meaux, France

Local Institution - 0097

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Manchester, United Kingdom

Local Institution - 0109

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Roma, Italy

Local Institution - 0049

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Stony Brook, New York, United States

Local Institution - 0039

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Seattle, Washington, United States

Local Institution - 0100

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La Roche-sur-yon Cedex 9, France

Generic Country - Canada

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No City Provided, New Jersey, United States

Local Institution - 0103

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Rennes, France

Local Institution - 0068

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Berlin, Germany

Tulsa Cancer Institute PLLC

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Tulsa, Oklahoma, United States

Local Institution - 0077

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Frankfurt-oder, Germany

Local Institution - 0070

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Hamm, Germany

Local Institution - 0088

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Kiel, Germany

Local Institution - 0079

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Mutlangen, Germany

Local Institution - 0111

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Firenze, Italy

Local Institution - 0085

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Wiesbaden, Germany

Local Institution - 0113

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Lecce, Italy

Local Institution - 0120

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Messina, Italy

Local Institution - 0121

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Pescara, Italy

Local Institution - 0069

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Dresden, Germany

Local Institution - 0117

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Vicenza, Italy

Local Institution - 0087

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Köln, Germany

Local Institution - 0080

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Oldenburg, Germany

Local Institution - 0074

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Rostock, Germany

Local Institution - 0096

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Stafford, United Kingdom

Local Institution - 0108

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Ancona, Italy

Local Institution - 0119

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Cagliari, Italy

Local Institution - 0116

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Milano, Italy

Local Institution - 0110

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Roma, Italy

Local Institution - 0114

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Napoli, Italy

Local Institution - 0091

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Liverpool, United Kingdom

Local Institution - 0107

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Terni, Italy

Local Institution - 0092

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Leeds, United Kingdom

Local Institution - 0027

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San Antonio, Texas, United States

Local Institution - 0059

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Jackson, Mississippi, United States

Cancer Center of Acadiana at Lafayette General Health

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Lafayette, Louisiana, United States

Local Institution - 0057

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Washington, District of Columbia, United States

Local Institution - 0009

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Shreveport, Louisiana, United States

Local Institution - 0060

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Lincoln, Nebraska, United States

Local Institution - 008

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Does Not Exist, New Jersey, United States

Generic Country - France

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No City Provided, New Jersey, United States

Local Institution - 0038

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Knoxville, Tennessee, United States

Generic Country - Italy

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No City Provided, New Jersey, United States

Generic Country - UK

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No City Provided, New Jersey, United States

Generic Country - USA

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No City Provided, New Jersey, United States

Local Institution - 0035

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Memphis, Tennessee, United States

Generic Country - Germany

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No City Provided, New Jersey, United States

Local Institution - 0118

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Roma, Italy

Local Institution - 0112

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Torino, Italy

Local Institution

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Liverpool, United Kingdom

Local Institution - 0021

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Birmingham, Alabama, United States

Local Institution - 0024

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Omaha, Nebraska, United States

Local Institution - 0023

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Anaheim, California, United States

Local Institution - 0048

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Downey, California, United States

Local Institution - 0052

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Fountain Valley, California, United States

Local Institution - 0047

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Valdosta, Georgia, United States

Local Institution - 0018

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Sioux City, Iowa, United States

Local Institution - 0010

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Gastonia, North Carolina, United States

Local Institution - 0022

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Canton, Ohio, United States

Local Institution - 0063

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Bryan, Texas, United States

Local Institution - 0029

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Amarillo, Texas, United States

Local Institution - 0066

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Toronto, Ontario, Canada

Local Institution - 0072

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Aschaffenburg, Germany

Local Institution - 0104

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Limoges, France

Local Institution - 0081

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Bielefeld, Germany

Local Institution - 0084

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Gelsenkirchen, Germany

Local Institution - 0098

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Harrow, Greater London, United Kingdom

Local Institution - 0095

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Nottingham, United Kingdom

Local Institution - 0093

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Swansea, United Kingdom

Local Institution - 0094

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Truro, United Kingdom

Local Institution - 0061

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Des Moines, Iowa, United States

Local Institution - 0062

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Lexington, Kentucky, United States

Local Institution - 0042

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Louisville, Kentucky, United States

Local Institution - 0050

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Kansas City, Missouri, United States

Local Institution - 0016

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Charleston, South Carolina, United States

Local Institution - 0031

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Yakima, Washington, United States

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