Back to Authors

McElroy, Edwin

Mayo Clinic

Mayo Clinic

Citations 2

Chemotherapy for Advanced Esthesioneuroblastoma: The Mayo Clinic Experience
McElroy, Edwin, Buckner, Jan C. , Lewis, Jean E.

Neurosurgery | July 30, 2004 | Volume: 42 | Issue: 5 | Pages: 1023-1027

10.1097/00006123-199805000-00040 Get It

Circulating peripheral blood plasma cells as a prognostic indicator in patients with primary systemic amyloidosis
Pardanani, Animesh , Schroeder, Georgene, McElroy, Edwin, Fonseca, Rafaël , Dispenzieri, Angela , Lacy, Martha Q. , Lust, John A., Kyle, Robert A. , Greipp, Philip R., Rajkumar, S. Vincent , Witzig, Thomas E. , Gertz, Morie A. , Rajkumar, S Vincent , Dispenzieri, Angela , Fonseca, Rafael

Blood | January 15, 2003 | Volume: 101 | Issue: 3 | Pages: 827-830

10.1182/blood-2002-06-1698 Get It

Abstract This study examined the prognostic value of circulating peripheral blood plasma cells (PBPCs) in patients with primary systemic amyloidosis (AL). A sensitive slide-based immunofluorescence technique was used to assess 147 patients for circulating PBPCs. Circulating monoclonal plasma cells were quantified as a percentage of circulating cytoplasmic immunoglobulin-positive cells (PBPC%). The absolute circulating plasma cell count was also determined. When analyzed retrospectively, 24 (16%) of 147 patients were found to have detectable circulating PBPCs. Overall survival for patients with high PBPC%'s (> 1%) was poorer (median survival, 10 vs 29 months;P = .002). Similarly, overall survival for patients with high PBPC counts (> 0.5 × 106/L) was significantly poorer (median, 13 vs 31 months;P = .003). Increased percentages of bone marrow plasma cells (BMPC%; P = .0004), increased levels of serum β2-microglobulin (P = .04), and dominant cardiac amyloid involvement (P = .03) also predicted poorer survival. The combined consideration of circulating PBPCs and BMPC% identified low-, intermediate-, and high-risk groups with median survivals of 37.5, 15.5, and 10 months, respectively (P = .0003). Multivariate analysis revealed circulating PBPCs and BMPC% to be independent prognostic factors for survival. Patients with PBPC%'s of 2% or higher were significantly more likely to have a coexisting clinical diagnosis of multiple myeloma (50% vs 12%, P = .008). The prognostic value of circulating PBPCs may help select treatment for patients with AL.