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SERUM FREE LIGHT CHAIN RATIO IS AN INDEPENDENT RISK FACTOR FOR PROGRESSION IN MONOCLONAL GAMMOPATHY OF UNDETERMINED SIGNIFICANCE
Author(s): ,
Rahali Cherif
Affiliations:
Hematology,Central Hospital Mohammed Seghir Nekkache, Algiers, Algeria,Algiers,Algeria
Belakehal Salah Eddine
Affiliations:
Hematology,Central Hospital Mohammed Seghir Nekkache, Algiers, Algeria,Algiers,Algeria
(Abstract release date: 05/18/17) EHA Library. Rahali C. 05/18/17; 182656; PB1942
Cherif Rahali
Cherif Rahali
Contributions
Abstract

Abstract: PB1942

Type: Publication Only

Background
Monoclonal gammopathy of undetermined significance (MGUS) is a premalignant plasma cell proliferative disorder found in approximately 3% of the general population 50 years of age and older. MGUS is associated with progression to multiple myeloma or related malignancy at a rate of 1% per year. Thus the risk of malignancy for a 50-year-old patient with a 25-year life span is 25%.

Aims
We hypothesized that the presence of monoclonal free kappa or lambda immunoglobulin light chains in monoclonal gammopathy of undetermined significance (MGUS), as detected by the serum free light chain (FLC) assay increases the risk of progression to malignancy.

Methods
90 Patients seen at the Hematology consultation from 2010 to 2015 with MGUS have a serum Mprotein less than 30 g/L, bone marrow plasma cells less than 10%, and no anemia, hypercalcemia, lytic bone lesions, or renal failure that would be indicative of a malignant plasma cell disorder.

The prognostic effect of abnormal kappa-to-lambda FLC ratio on progression of MGUS was studied. We also examined whether the risk of progression varied depending on the extent to which the FLC ratio was abnormal (the normal reference range of ĸ/ʎ ratio 0.26 to 1.65).

Results
The median age at diagnosis of MGUS was 59 years (35-92years). 62 Womans and 28 Mans Sex ratio=2.2. Serum electrophoresis and immunoelectrophoresis or immunofixation was done in 85 patients. Of these, The median serum M protein size at diagnosis was 12 g/L (1.7-28.5g/L)

IgG monoclonal : 68 patients (75%), and non IgG monoclonal : 22 patients (25%). A monoclonal light chain was detected in 62 patients, as detected by the serum free light chain (FLC) assay increases the risk of progression to malignancy. An abnormal FLC ratio (kappa-lambda ratio < 0.26 or > 1.65) was detected in 27 (30%) patients. At a median follow-up of 5 years, malignant progression had occurred in 6 patients (6,6%) with an abnormal serum FLC ratio.

Conclusion
A novel, highly sensitive serum free light chain (FLC) assay is now available for clinical practice.The risk of progression in patients with an abnormal FLC ratio was significantly higher compared with patients with a normal ratio, and was independent of the size and type of the serum monoclonal (M) protein. Patients with an abnormal serum FLC ratio, non–immunoglobulin G (non-IgG) MGUS, and a high serum M protein level (> 15 g/L) had a major risk of progression.

Session topic: 13. Myeloma and other monoclonal gammopathies - Biology

Keyword(s): Free light chain, MGUS

Abstract: PB1942

Type: Publication Only

Background
Monoclonal gammopathy of undetermined significance (MGUS) is a premalignant plasma cell proliferative disorder found in approximately 3% of the general population 50 years of age and older. MGUS is associated with progression to multiple myeloma or related malignancy at a rate of 1% per year. Thus the risk of malignancy for a 50-year-old patient with a 25-year life span is 25%.

Aims
We hypothesized that the presence of monoclonal free kappa or lambda immunoglobulin light chains in monoclonal gammopathy of undetermined significance (MGUS), as detected by the serum free light chain (FLC) assay increases the risk of progression to malignancy.

Methods
90 Patients seen at the Hematology consultation from 2010 to 2015 with MGUS have a serum Mprotein less than 30 g/L, bone marrow plasma cells less than 10%, and no anemia, hypercalcemia, lytic bone lesions, or renal failure that would be indicative of a malignant plasma cell disorder.

The prognostic effect of abnormal kappa-to-lambda FLC ratio on progression of MGUS was studied. We also examined whether the risk of progression varied depending on the extent to which the FLC ratio was abnormal (the normal reference range of ĸ/ʎ ratio 0.26 to 1.65).

Results
The median age at diagnosis of MGUS was 59 years (35-92years). 62 Womans and 28 Mans Sex ratio=2.2. Serum electrophoresis and immunoelectrophoresis or immunofixation was done in 85 patients. Of these, The median serum M protein size at diagnosis was 12 g/L (1.7-28.5g/L)

IgG monoclonal : 68 patients (75%), and non IgG monoclonal : 22 patients (25%). A monoclonal light chain was detected in 62 patients, as detected by the serum free light chain (FLC) assay increases the risk of progression to malignancy. An abnormal FLC ratio (kappa-lambda ratio < 0.26 or > 1.65) was detected in 27 (30%) patients. At a median follow-up of 5 years, malignant progression had occurred in 6 patients (6,6%) with an abnormal serum FLC ratio.

Conclusion
A novel, highly sensitive serum free light chain (FLC) assay is now available for clinical practice.The risk of progression in patients with an abnormal FLC ratio was significantly higher compared with patients with a normal ratio, and was independent of the size and type of the serum monoclonal (M) protein. Patients with an abnormal serum FLC ratio, non–immunoglobulin G (non-IgG) MGUS, and a high serum M protein level (> 15 g/L) had a major risk of progression.

Session topic: 13. Myeloma and other monoclonal gammopathies - Biology

Keyword(s): Free light chain, MGUS

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