Prognostic Impact of the Hevylite Assay in Patients With IgG or IgA Multiple Myeloma Treated Within the GMMG ‐ MM5 Trial
Open Access
- 11 November 2025
- journal article
- Published by Wiley in European Journal of Haematology
- Vol. 116 (3) , 226-234
Abstract
Response assessment during treatment of multiple myeloma (MM) typically relies on immunofixation and serum electrophoresis. However, low levels of IgG and especially IgA paraprotein are difficult to quantify reliably. The Hevylite Assay quantifies the kappa and lambda fractions of IgG and IgA separately and is useful to determine response to therapy. Using serum samples of 360 evaluable patients from the prospective GMMG‐MM5 trial (EudraCT‐No. 2010–019173‐16) we assessed the normalization of the kappa/lambda ratio with the Hevylite Assay (HLCr) at baseline, after induction, mobilization, autologous blood stem cell transplantation, consolidation and every three months during maintenance or follow‐up within two years after the end of consolidation. We observed a steady increase in the proportion of patients with normalized HLCr over the course of therapyAchieving HLCr normalization any time until the end of consolidation was associated with a trend towards a prolonged progression‐free survival (PFS; hazard ratio (HR) = 0.75, 95% confidence interval (95% CI) = 0.56–1.01, p = 0.06) but not overall survival (OS; HR = 0.94, 95% CI = 0.69–1.26, p = 0.66) in multivariable time‐dependent Cox regression analyses. Using a landmark analysis from the end of consolidation there was again a marginally statistically significant effect of HLCr normalization by the end of consolidation on PFS using a multivariable Cox model on the subset of the two study arms with continuous lenalidomide maintenance (HR 0.61, 95% CI 0.37–1.02, p = 0.06). No such effect was observed in study arms in which maintenance was only applied to patients not in CR at the end of consolidation. In conclusion, our analysis of the Hevylite Assay in patients with IgG or IgA myeloma from the GMMG‐MM5 study did not find evidence to support the general use of HLCr normalization as a response parameter for predicting PFS or OS. However, the differential effects of HLCr normalization depending on the way in which treatment was adapted to response may be of interest for future study designs on response‐adapted therapy. Trial Registration: ISRCTN05622749.Keywords
Funding Information
- Celgene
- Chugai Pharmaceutical
- Johnson and Johnson
This publication has 24 references indexed in Scilit:
- Cell-free DNA for the detection of emerging treatment failure in relapsed/ refractory multiple myelomaLeukemia, 2022
- Response-adapted lenalidomide maintenance in newly diagnosed myeloma: results from the phase III GMMG-MM5 trialLeukemia, 2020
- Heavy/light chain assay in the monitoring of multiple myelomaPathology, 2019
- Heavy/light chain assay as a biomarker for diagnosis and follow-up of multiple myelomaClinica Chimica Acta, 2018
- Heavy+light chain monitoring correlates with clinical outcome in multiple myeloma patientsLeukemia, 2017
- International Myeloma Working Group consensus criteria for response and minimal residual disease assessment in multiple myelomaThe Lancet Oncology, 2016
- IgA kappa/IgA lambda heavy/light chain assessment in the management of patients with IgA myelomaCancer, 2014
- Assessment of the diagnostic performances of IgA heavy and light chain pairs in patients with IgA monoclonal gammopathyClinical Biochemistry, 2012
- Immunoglobulin heavy/light chain ratios improve paraprotein detection and monitoring, identify residual disease and correlate with survival in multiple myeloma patientsLeukemia, 2012
- Prognostic value of the serum free light chain ratio in newly diagnosed myeloma: proposed incorporation into the international staging systemLeukemia, 2008