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Prepublished online as a Blood First Edition Paper on March 20, 2003; DOI 10.1182/blood-2002-12-3674.
Submitted December 4, 2002
Hematology Service, Division of Hematologic Oncology, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY, USA * Corresponding author; email: comenzor{at}mskcc.org.
Optimal methods of stem cell mobilization in multiple myeloma are undefined, and contaminating clonotypic cells could contribute to disease recurrence. A phase 2 trial of intravenous melphalan (60mg/m2) and G-CSF (10ug/kg/d) for mobilization was performed. To enhance reliability, contamination was assessed with two sensitive methods, immunoglobulin light- and heavy-chain variable region patient-specific limiting-dilution PCR. We evaluated 29 stem cell components (SCC) from fifteen patients; for 9 SCC, only VL PCR was used because of light chain disease or technical problems with VH primers. For 20 SCC, VL and VH PCR results were highly correlated (r2 = 0.93, p << 0.01) with 35% (7/20) having identical estimates. VH PCR gave significantly higher estimates for 8, and VL PCR for 5, SCC, supporting the utility of employing two methods. Estimated clonotypic contamination per SCC was 0.0009% (0-0.1) or 0.5 x 104 clonotypic cells per kg (0-41.2), and contamination correlated with CD34+ cells collected (r2 = 0.42, p << 0.01). Melphalan-mobilized SCC contain minimal clonotypic contamination.
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