» Articles » PMID: 23211046

Ratio of Involved/uninvolved Immunoglobulin Quantification by Hevylite™ Assay: Clinical and Prognostic Impact in Multiple Myeloma

Abstract

Unlabelled:

Background: HevyLite™ is a new, recently developed method that facilitates separate quantification of the kappa- and lambda-bounded amounts of a given immunoglobulin (Ig). Using this method, we measured intact immunoglobulin (heavy/light chain; HLC) IgG-kappa, IgG-lambda, IgA-kappa, IgA-lambda individually, as well as their deriving ratios (HLCR) in a series of IgG or IgA multiple myeloma (MM) patients, to investigate and assess the contribution of these tests to disease evaluation.

Patients And Methods: HevyLite™ assays were used in sera from 130 healthy individuals (HI) and 103 MM patients, at time of diagnosis. In patients, the level of paraprotein was IgG in 78 (52 IgG-kappa, 26 IgG-lambda) and IgΑ in 25 (13 IgΑ-kappa, 12 IgΑ-lambda). Durie-Salmon and International Staging System stages were evenly distributed. Symptomatic patients (n = 77) received treatment while asymptomatic ones (n = 26) were followed. Patients' median follow-up was at 32.6 months. HLCR was calculated with the involved Ig (either G or A) as numerator.

Results: In HI, median IgG-kappa was 6.85, IgG-lambda 3.81, IgA-kappa 1.19 and IgA-lambda 0.98 g/L. The corresponding median involving HLC values in MM patients were 25.8, 23.45, 28.9 and 36.4 g/L. HLC-IgG related to anemia, high serum free light chain ratio and extensive bone marrow infiltration, while high HLCR correlated with the same plus increased β2-microglobulin. In addition, increased HLCR and the presence of immunoparesis correlated with time to treatment. Patients with high HLCR had a significantly shorter survival (p = 0.022); HLCR retained its prognostic value in multivariate analysis.

Conclusions: HLC and HLCR quantify the precise amount of the involved immunoglobulin more accurately than other methods; moreover, they carry prognostic information regarding survival in MM patients.

Citing Articles

Laboratory and Clinical Settings of Heavy/Light Chain (HLC) Assays in the Management of Monoclonal Gammopathies and Multiple Myeloma.

Napodano C, Ioannilli L, Basile V, Gulli F, Carnazzo V, Pignalosa S J Pers Med. 2023; 13(5).

PMID: 37240913 PMC: 10220754. DOI: 10.3390/jpm13050743.


The Current Role of the Heavy/Light Chain Assay in the Diagnosis, Prognosis and Monitoring of Multiple Myeloma: An Evidence-Based Approach.

Rios-Tamayo R, Puig N, Algarin M, Garcia de Veas Silva J, Barbosa N, Encinas C Diagnostics (Basel). 2021; 11(11).

PMID: 34829367 PMC: 8620453. DOI: 10.3390/diagnostics11112020.


Multiplexed imaging of immune cells in staged multiple sclerosis lesions by mass cytometry.

Ramaglia V, Sheikh-Mohamed S, Legg K, Park C, Rojas O, Zandee S Elife. 2019; 8.

PMID: 31368890 PMC: 6707785. DOI: 10.7554/eLife.48051.


Heavy+light chain monitoring correlates with clinical outcome in multiple myeloma patients.

Michallet M, Chapuis-Cellier C, Dejoie T, Lombard C, Caillon H, Sobh M Leukemia. 2017; 32(2):376-382.

PMID: 28663581 PMC: 5808078. DOI: 10.1038/leu.2017.209.


Involved/uninvolved heavy/light chain index can predict progression in transplanted multiple myeloma patients.

Espino M, Arteche-Lopez A, Medina S, Munoz-Calleja C, Blanchard M, Alegre A Bone Marrow Transplant. 2017; 52(8):1206-1207.

PMID: 28581457 PMC: 5543252. DOI: 10.1038/bmt.2017.97.


References
1.
Simonsson B, Kallander C, Brenning G, Killander A, Gronowitz J, Bergstrom R . Biochemical markers in multiple myeloma: a multivariate analysis. Br J Haematol. 1988; 69(1):47-53. DOI: 10.1111/j.1365-2141.1988.tb07601.x. View

2.
Greipp P, San Miguel J, Durie B, Crowley J, Barlogie B, Blade J . International staging system for multiple myeloma. J Clin Oncol. 2005; 23(15):3412-20. DOI: 10.1200/JCO.2005.04.242. View

3.
Kyrtsonis M, Maltezas D, Tzenou T, Koulieris E, Bradwell A . Staging systems and prognostic factors as a guide to therapeutic decisions in multiple myeloma. Semin Hematol. 2009; 46(2):110-7. DOI: 10.1053/j.seminhematol.2009.02.004. View

4.
Kim J, Hayton W, Robinson J, Anderson C . Kinetics of FcRn-mediated recycling of IgG and albumin in human: pathophysiology and therapeutic implications using a simplified mechanism-based model. Clin Immunol. 2006; 122(2):146-55. PMC: 2791364. DOI: 10.1016/j.clim.2006.09.001. View

5.
Perosa F, Minoia C, Favoino E, Prete M, Dammacco F . Staging multiple myeloma patients with active disease using serum levels of beta2m-free HLA class I heavy chain together with IgM or platelet count. Blood Cells Mol Dis. 2008; 42(1):71-6. DOI: 10.1016/j.bcmd.2008.09.003. View