Role of urine immunofixation in the complete response assessment of MM patients other than light-chain-only disease

Author:

Lahuerta Juan-José1,Jiménez-Ubieto Ana1,Paiva Bruno2,Martínez-López Joaquín1ORCID,González-Medina José1,López-Anglada Lucía1ORCID,Cedena María-Teresa1ORCID,Puig Noemi3,Oriol Albert4ORCID,Blanchard María-Jesús5,Ríos Rafael6ORCID,Martin Jesús7,Martínez Rafael8,Sureda Anna9,Hernández Miguel Teodoro10,de la Rubia Javier11,Krsnik Isabel12ORCID,Cabañas Valentín13ORCID,Palomera Luis14,Bargay Joan15,Mateos María-Victoria3,Rosiñol Laura16,San Miguel Jesús F.2ORCID,Blade Joan16

Affiliation:

1. Hospital Universitario 12 de Octubre, Centro de Investigación Biomédica en Red Cáncer (CIBERONC), Madrid, Spain;

2. Clínica Universidad de Navarra, Centro de Investigación Médica Aplicada, Instituto de Investigación Sanitaria de Navarra, CIBERONC, Pamplona, Spain;

3. Hospital Universitario de Salamanca-IBSAL, Instituto de Biología Molecular y Celular del Cáncer–Centro Superior de Investigaciones Científicas, Salamanca, Spain;

4. Hospital Germans i Trials, Barcelona, Spain;

5. Hematology Department, Hospital Ramón y Cajal, Madrid, Spain;

6. Hospital Universitario Virgen de las Nieves de Granada, Granada, Spain;

7. Hospital Universitario Virgen del Rocío, Seville, Spain;

8. Hospital Clínico San Carlos, Madrid, Spain;

9. Institut Catalá d’Oncologia-l’Hospitalet, Barcelona, Spain;

10. Hospital Universitario de Canarias, Santa Cruz de Tenerife, Spain;

11. Hospital Dr Peset, Valencia, Spain;

12. Hospital Puerta de Hierro, Madrid, Spain;

13. Hospital Virgen de la Arrixaca, El Palmar, Spain;

14. Hospital Clínico Universitario Lozano Blesa, IIs Aragón, Zaragoza, Spain;

15. Hospital Son Llatzer, Palma, Spain; and

16. Hospital Clinic, Institut d’Investigacions Biomèdiques August Pi I Sunyer, Barcelona, Spain

Abstract

Abstract Response criteria for multiple myeloma (MM) require monoclonal protein (M-protein)–negative status on both serum immunofixation electrophoresis (sIFE) and urine (uIFE) immunofixation electrophoresis for classification of complete response (CR). However, uIFE is not always performed for sIFE-negative patients. We analyzed M-protein evaluations from 384 MM patients (excluding those with light-chain-only disease) treated in the GEM2012MENOS65 (NCT01916252) trial to determine the uIFE-positive rate in patients who became sIFE-negative posttreatment and evaluate rates of minimal residual disease (MRD)–negative status and progression-free survival (PFS) among patients achieving CR, CR but without uIFE available (uncertain CR; uCR), or very good partial response (VGPR). Among 107 patients with M-protein exclusively in serum at diagnosis who became sIFE-negative posttreatment and who had uIFE available, the uIFE-positive rate was 0%. Among 161 patients with M-protein in both serum and urine at diagnosis who became sIFE-negative posttreatment, 3 (1.8%) were uIFE positive. Among patients achieving CR vs uCR, there were no significant differences in postconsolidation MRD-negative (<10−6; 76% vs 75%; P = .9) and 2-year PFS (85% vs 88%; P = .4) rates; rates were significantly lower among patients achieving VGPR. Our results suggest that uIFE is not necessary for defining CR in MM patients other than those with light-chain-only disease.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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