The serum free light chain FLC assay. Tutorial. #MedTwitter #MyelomaVR
Frequently ordered and frequently abnormal. This thread will reduce unnecessary headaches and referrals.
1/ Donโt order it unless you are suspecting myeloma, amyloid or related disorder
Frequently ordered and frequently abnormal. This thread will reduce unnecessary headaches and referrals.
1/ Donโt order it unless you are suspecting myeloma, amyloid or related disorder
2/ The assay itself consists of 2 separate assays: a free kappa assay and a free lambda assay.
The lab also CALCULATES and reports a free kappa/lambda light chain ratio using the absolute levels.
The lab also CALCULATES and reports a free kappa/lambda light chain ratio using the absolute levels.
5) The serum FLC assay is more sensitive than serum immunofixation is detecting free (unbound) circulating monoclonal light chains. But it is NOT more sensitive and in fact cannot pick up intact monoclonal proteins. So for eg., it picks up free kappa but not IgG kappa.
6) We all make a slight excess of free kappa and free lambda light chains. So we all have small measurable levels. And we have a normal range for the kappa/ lambda ratio.
For the Binding Site free light chain assay the normal kappa/lambda ratio is reported as 0.26-1.65
For the Binding Site free light chain assay the normal kappa/lambda ratio is reported as 0.26-1.65
7) The normal FLC levels and FLC ratio and range are not set in stone. They were established using levels in young normal volunteers. But we know now that in renal failure and with increasing age the true normal range is wider.
So donโt lose sleep over slight abnormalities.
So donโt lose sleep over slight abnormalities.
8) When the kappa/lambda FLC ratio is more than the upper limit, especially >4, it means there is likely a monoclonal kappa plasma cell disorder.
When the kappa/lambda ratio is less than the lower limit, especially <0.125, it means a monoclonal lambda plasma cell disorder.
When the kappa/lambda ratio is less than the lower limit, especially <0.125, it means a monoclonal lambda plasma cell disorder.
9) Iโm not good at math. So rather than the kappa/lambda ratio the lab reports, I do involved/uninvolved ratio which provides a nice whole number.
So take the higher level and divide by lower level. This involved/uninvolved ratio is what we use for risk stratification.
So take the higher level and divide by lower level. This involved/uninvolved ratio is what we use for risk stratification.
10) So we can use a involved/uninvolved ratio >4 to say whether there is a monoclonal plasma cell disorder or not.
Or a ratio >20 to say whether smoldering myeloma is high or low risk.
Or a ratio of >100 to say whether someone has myeloma defining event or not.
Or a ratio >20 to say whether smoldering myeloma is high or low risk.
Or a ratio of >100 to say whether someone has myeloma defining event or not.
11) FLC Assay USE #1
To follow patients with myeloma and other plasma cell disorders
We follow the level & ratio to assess response to therapy & to detect progression. We have specific cut offs for how much reduction qualifies for response & how much qualifies for progression
To follow patients with myeloma and other plasma cell disorders
We follow the level & ratio to assess response to therapy & to detect progression. We have specific cut offs for how much reduction qualifies for response & how much qualifies for progression
12) FLC Assay USE #2
To diagnose whether patients have a monoclonal plasma cell disorder or not.
It complements serum protein electrophoresis and immunofixation. For myeloma, without FLC assay, sensitivity is 93%. If you also do the FLC assay your sensitivity increases to 98%
To diagnose whether patients have a monoclonal plasma cell disorder or not.
It complements serum protein electrophoresis and immunofixation. For myeloma, without FLC assay, sensitivity is 93%. If you also do the FLC assay your sensitivity increases to 98%
15) FLC assay USE #5
As a myeloma defining event. To diagnose myeloma.
An involved/uninvolved ratio of >100 coupled with an absolute involved level of >100 mg/L, and urine M protein >200 mg/24 H is a myeloma defining event.
As a myeloma defining event. To diagnose myeloma.
An involved/uninvolved ratio of >100 coupled with an absolute involved level of >100 mg/L, and urine M protein >200 mg/24 H is a myeloma defining event.
16) FLC Assay Use #6
To diagnose light chain MGUS. Here the serum & urine immunofixation do not show any heavy chain expression. ie. there is no IgG or IgA or IgM M protein. The clonal plasma cells are only making light chains.
Unless ratio is >8, risk of progression is low.
To diagnose light chain MGUS. Here the serum & urine immunofixation do not show any heavy chain expression. ie. there is no IgG or IgA or IgM M protein. The clonal plasma cells are only making light chains.
Unless ratio is >8, risk of progression is low.
17) FLC assay Use #7
Prognosis of solitary plasmacytoma after radiation.
If the FLC ratio doesnโt normalize by one year after radiation, the risk of progression or relapse is higher.
Prognosis of solitary plasmacytoma after radiation.
If the FLC ratio doesnโt normalize by one year after radiation, the risk of progression or relapse is higher.
18) FLC assay Caveat #1
Some labs report the absolute level in mg/L. Some in mg/dl
Please check units when following. Otherwise you may think there is a massive change when all thatโs happened is the lab changed.
Some labs report the absolute level in mg/L. Some in mg/dl
Please check units when following. Otherwise you may think there is a massive change when all thatโs happened is the lab changed.
19) FLC assay Caveat #2
The ratio can be affected greatly and swing wildly if the uninvolved normal light chain (lambda in a patient with kappa myeloma for example) is very low. So follow both the actual level and the ratio. Not just the ratio.
The ratio can be affected greatly and swing wildly if the uninvolved normal light chain (lambda in a patient with kappa myeloma for example) is very low. So follow both the actual level and the ratio. Not just the ratio.
20) FLC assay caveat #3
You need a change of >10 mg/dl or 100 mg/L to be sure that itโs a real change and not a lab variation in most settings. Except in amyloid small changes are not very reliable.
You need a change of >10 mg/dl or 100 mg/L to be sure that itโs a real change and not a lab variation in most settings. Except in amyloid small changes are not very reliable.
21) FLC assay caveat #4
Some people donโt excrete the light chain due to dimerization. So a high level may be related to decreased excretion and not increased production. To verify check urine M spike. To consider as myeloma defining event, you need urine M spike >200 mg/24h
Some people donโt excrete the light chain due to dimerization. So a high level may be related to decreased excretion and not increased production. To verify check urine M spike. To consider as myeloma defining event, you need urine M spike >200 mg/24h
22) FLC assay caveat #5
The levels and even the ratio may be perturbed by renal failure. Usually both light chains are higher. nature.com
The levels and even the ratio may be perturbed by renal failure. Usually both light chains are higher. nature.com
23) FLC assay caveat #6
Like the sed rate, FLC levels increase in any inflammatory process. Both kappa and lambda levels go up. Ratio is normal or only mildly perturbed. This is polyclonal process. Not monoclonal gammopathy.
Like the sed rate, FLC levels increase in any inflammatory process. Both kappa and lambda levels go up. Ratio is normal or only mildly perturbed. This is polyclonal process. Not monoclonal gammopathy.
24) Algorithm for using FLC assay in managing MGUS. When to refer. How to follow. When can follow up be deferred. When can Bone marrow biopsy and bone imaging be deferred. #MedTwitter #MGUSVR
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