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S0309, Repository: Blood/Bone Marrow From Pts. With Myeloma, WM, Amyloidosis, or MGUS.

S0309, Myeloma Specimen Repository Protocol, Ancillary

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00919139
Enrollment
190
Registered
2009-06-12
Start date
2003-11-30
Completion date
2010-11-30
Last updated
2015-04-03

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

Conditions

Amyloidosis, Monoclonal Gammopathy of Undetermined Significance, Multiple Myeloma, Smoldering Myeloma, Waldenstrom's Macroglobulinemia

Keywords

multiple myeloma, Waldenström macroglobulinemia, monoclonal gammopathy of undetermined significance, primary systemic amyloidosis

Brief summary

RATIONALE: Collecting and storing samples of blood and bone marrow from patients with cancer to study in the laboratory may help doctors find better ways to ways to treat the cancer. PURPOSE: The purpose of this study is to collect and store blood and bone marrow samples from patients with multiple myeloma, smoldering myeloma, Waldenstrom's macroglobulinemia, amyloidosis, and monoclonal gammopathy of undetermined significance to be tested in the laboratory.

Detailed description

OBJECTIVES: * Maintain and expand tissue repositories of myeloma specimens from uniformly treated Southwest Oncology Group (SWOG) patients with multiple myeloma, smoldering myeloma, Waldenstrom's macroglobulinemia, amyloidosis, or monoclonal gammopathy of undetermined significance. * Utilize scientific information generated from intergroup and collaborative studies to assist the SWOG Myeloma Committee in the development of new and more effective treatment regimens for these patients. OUTLINE: Patients receive treatment as directed by the treatment protocols on which they are registered. Specimens of blood and/or marrow are submitted to the Myeloma Repository. The status of the patient (e.g., pre-study, post-remission, or relapse) will be recorded prior to specimen collection. PROJECTED ACCRUAL: Not specified

Interventions

OTHERbiologic sample preservation procedure

Blood and 3-4 cc bone marrow aspirate collected at same time (in association with treatment protocols on which patient is registered)

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
SWOG Cancer Research Network
Lead SponsorNETWORK

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Diagnosis of 1 of the following: * Multiple myeloma * Smoldering myeloma * Waldenstrom's macroglobulinemia * Amyloidosis * Monoclonal gammopathy of undetermined significance * Must be currently registered on a Southwest Oncology Group-coordinated treatment study (SWOG or Intergroup) * Must have pretreatment specimens to submit to this study * No cytogenetic samples PATIENT CHARACTERISTICS: * Not specified PRIOR CONCURRENT THERAPY: * Not specified

Design outcomes

Primary

MeasureTime frame
Maintenance and expansion of tissue repositories of myeloma specimens from uniformly treated SWOG patients with multiple myeloma, smoldering myeloma, Waldenstrom's macroglobulinemia, amyloidosis, or monoclonal gammopathy of undetermined significance7 years
Development of new and more effective treatment regimens for these patients using scientific information generated from intergroup and collaborative studies7 years

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026