AL amyloidosis
   

Freelite® serum free light chains can be identified in 98% of AL amyloidosis patients.

AL amyloidosis is a protein conformation disorder characterised by the accumulation of monoclonal free light chain fragments as amyloid deposits. For patients with either primary systemic Amyloidosis or light chain deposition disease, sensitivity of immunofixation electrophoresis (IFE) is low. These patients often do not have an M-protein peak and consequently it has been difficult to monitor their haematological response. Freelite® can aid diagnosis and follow up in these patients.1

Kaplan-Meier estimate of survival in 137 patients with AL amyloidosis showing a reduction of Freelite free light chain concentrations
Kaplan-Meier estimate of survival in 137 patients with AL amyloidosis showing a reduction of Freelite® free light chain concentrations by greater than 50% following chemotherapy was associated with increased survival 2 

Recommendations of the UK Myeloma Forum Guidelines1 based on Freelite® include:

  • "Serum free light chain assay is required for investigation in suspected AL amyloid patients"
  • "Treatment strategies in individual patients are presently best guided by their early effect on quantifiable measurements of circulating free immunoglobulin light chains"
  • Reduction of amyloidogenic serum free light chain concentration can suppress accumulation of AL amyloid deposits
  • Use of Freelite® serum FLC (free light chain) "measurement enables response to chemotherapy to be evaluated effectively and rapidly, for example, on a monthly basis during cyclical treatments"

A consensus opinion from the 10th International Symposium on Amyloid and Amyloidosis3 based on Freelite® states:

  • "All patients should have an immunonephelometric immunoglobulin serum-free light chain assay"
  • "The use of the serum free light chain assay has been important for quantification of hematologic responses and has been proposed as a useful tool to define hematologic response"

In a 2006 publication4 the authors concluded that the absolute levels of Freelite® immunoglobulin free light chain appeared more relevant than the FLC ratio. Also that the achievement of a low absolute level of the involved immunoglobulin FLC was the best predictor of haematologic response, organ response and overall survival after peripheral blood stem cell transplantation.

Summary

  • Serum free light chains have a circulation life of several hours compared to several weeks for intact immunoglobulin, and so can be a much earlier indicator of response to therapy5
  • Freelite® serum free light chains provide a more sensitive marker than electrophoresis and immunofixation in serum. This enables detection of most amyloidosis from a serum sample
 
View Belinda Ng’s webinar, Amyloidosis: The Secrets Behind These Elusive Diseases’

 

Freelite® is a valuable tool at all stages of patient management. It is useful when screening  to support an initial diagnosis. It adds valuable prognosis information and can be used throughout treatment management as a reliable monitoring  tool.

  1. United Kingdom Myeloma Forum on behalf of the British Committee for Standards in Haematology (BCSH). Guidelines on the diagnosis and management of AL amyloidosis. BJH 2004; 125:681-700 Request your copy - code MKG227
  2. Lachmann HJ, et al. Outcome in systemic AL amyloidosis in relation to changes in concentration of circulating free immunoglobulin light chains following chemotherapy. BJH 2003; 122:78-84 Request your copy - code MKG200
  3. Gertz MA, et al. Definition of Organ Involvement and Treatment Response in Immunoglobulin Light Chain Amyloidosis (AL): A Consensus Opinion From the 10th International Symposium on Amyloid and Amyloidosis. Am J Hematol 2005; 79:319-328 Request your copy - code MKG293
  4. Dispenzieri, et al. Absolute values of Free Light chains are prognostic in patients with primary amyloidosis undergoing peripheral blood stem cell transplant. Blood 2006; 107:3378-3383 Request your copy - code MKG311
  5. Brockhurst I, et al. Diagnosis and monitoring a case of light-chain deposition disease in the kidney using a new sensitive immunoassay. Nephrol Dial Transplant 2005; 20:1251-1253