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AJNR - American Journal of Neuroradiology

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American Journal of Neuroradiology 22:781-785 (4 2001)
© 2001 American Society of Neuroradiology

ARTICLE

CT-guided Biopsy of Focal Lesions in Patients with Multiple Myeloma May Reveal New and More Aggressive Cytogenetic Abnormalities

Ramesh Avva^a, Rudy L. Vanhemert^a, Bart Barlogie^a, Nikhil Munshi^a and Edgardo J. Angtuaco^,a

^a From the Department of Radiology, Division of Neuroradiology (R.A., R.L.V., E.J.A.), and the Myeloma and Transplantation Research Center, Arkansas Cancer Research Center (B.B., N.M.), University of Arkansas for the Medical Sciences, Little Rock.

BACKGROUND AND PURPOSE: Cytogenetic abnormalities, especially chromosome 13 deletion, are high-risk factors for multiple myeloma. Attaining the highest detection rates of cytogenetic abnormalities is important to provide accurate prognostic information to the referring oncologist. The purpose of this study was to use CT-guided percutaneous fine-needle aspiration bone biopsy (CT-guided FNA) of MR-detected focal lesions in patients with multiple myeloma to increase identification of abnormal cytogenetics.

METHODS: Patients enrolled in two clinical trials for myeloma therapy underwent MR imaging of the entire spine and pelvis. CT-guided FNA biopsy samples obtained from MR-detected focal lesions in these patients were sent for cytogenetic analysis. FNA results were then compared with random bone marrow sampling of the iliac crest done at or near the same time as the FNA to provide the data revealed in this study.

RESULTS: Forty-one patients (47 lesions) in one of the trials and 37 patients (38 lesions) in the other trial had biopsies performed. CT-guided FNA revealed cytogenetic abnormalities in 21% of the total patient population and new information in nearly 10% of the patients in one trial and in 20% of those in the other trial.

CONCLUSION: CT-guided biopsy of MR-detected focal lesions is a safe technique that can provide important cytogenetic information in a significant number of patients with multiple myeloma not identified during random marrow sampling.

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