Comparison of Immunofixation, Serum Free Light Chain, and Immunophenotyping for Response Evaluation and Prognostication in Multiple Myeloma

Author:

Paiva Bruno1,Martinez-Lopez Joaquin1,Vidriales Maria-Belen1,Mateos Maria-Victoria1,Montalban Maria-Angeles1,Fernandez-Redondo Elena1,Alonso Lourdes1,Oriol Albert1,Teruel Ana-Isabel1,de Paz Raquel1,Laraña José-Garcia1,Bengoechea Enrique1,Martin Alejandro1,Mediavilla Joaquin Diaz1,Palomera Luis1,de Arriba Felipe1,Bladé Joan1,Orfao Alberto1,Lahuerta Juan-Jose1,San Miguel Jesus F.1

Affiliation:

1. From the Hospital Universitario de Salamanca; Servicio General de Citometría, Universidad de Salamanca; Centro de Investigación del Cáncer, Salamanca; Hospital 12 de Octubre; Hospital Universitario La Paz; Hospital Ramon y Cajal; Hospital Clinico San Carlos, Madrid; Hospital Universitari Germans Trias i Pujol, Badalona; Hospital Clinico de Valencia, Valencia; Hospital de Donostia, San Sebastian Hospital Virgen de la Concha, Zamora; Hospital Lozano Blesa, Zaragoza; Hospital Morales Meseguer, Murcia; and...

Abstract

To investigate the impact of immunophenotypic response (IR) versus complete response (CR) and CR plus normal serum free light chain (sFLC) ratio (stringent CR) in elderly patients with multiple myeloma (MM) treated with novel agents. Patients and Methods From a total of 260 elderly patients newly diagnosed with MM included in the GEM05>65y trial, 102 patients achieving at least a partial response with ≥ 70% reduction in M-component after the six planned induction cycles were simultaneously analyzed by immunofixation, sFLC, and multiparameter flow cytometry (MFC) immunophenotyping; this population is the focus of this study. Results Forty-three percent of patients achieved CR, 30% achieved stringent CR, and 30% achieved IR. Patients in stringent CR showed no significant survival advantage compared with those in CR, whereas patients in IR showed significantly increased progression-free survival (PFS) and time to progression (TTP) compared with those in stringent CR or CR; this was confirmed by multivariate analysis (hazard ratio, 4.1; P = .01 for PFS). Discrepancies between the three techniques were relatively common. Notably, in all seven patients achieving IR but remaining immunofixation positive, the M-component disappeared in follow-up analysis. In contrast, MFC-positive patients who were immunofixation negative (n = 20) showed a tendency toward early reappearance of the M-component (median, 3 months). Similarly, in five of 11 stringent CR but MFC-positive patients, symptomatic disease progression was recorded at a median of 13 months after induction. Conclusion Achieving an IR translates into superior PFS and TTP compared with conventional CR or stringent CR. These techniques provide complementary information and thus, an effort should be made to refine response criteria in MM.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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