Cytogenetic and Fluorescence In Situ Hybridization Studies in Multiple Myeloma
Cytogenetic and Fluorescence In Situ Hybridization Studies in Multiple Myeloma
RATIONALE: Studying the chromosomes in samples of bone marrow and blood in the laboratory from patients with cancer or other blood diseases may help doctors learn more about the disease.
PURPOSE: This laboratory study is analyzing chromosomes in patients with newly diagnosed multiple myeloma or other blood disease.
OBJECTIVES:
OUTLINE: Patients receive treatment as directed by the treatment clinical trial on which they are registered. Patients undergo bone marrow or blood sample collection periodically for conventional cytogenetic analysis and fluorescence in situ hybridization studies (FISH). Samples are analyzed for deleted 13q/monosomy 13 and chromosomal abnormalities.
PROJECTED ACCRUAL: A total of 500 patients will be accrued for this study.
DISEASE CHARACTERISTICS:
Diagnosis of 1 of the following:
Newly diagnosed disease
Must be currently registered, but have not begun therapy, on 1 of the following Southwest Oncology Group (SWOG) treatment clinical trials:
PATIENT CHARACTERISTICS:
PRIOR CONCURRENT THERAPY: