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      Serum free light chain level at diagnosis in myeloma cast nephropathy—a multicentre study

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          Abstract

          Myeloma cast nephropathy (MCN) is a common cause of severe renal impairment in multiple myeloma (MM). The level of free light chain (FLC) that causes MCN varies substantially and there is uncertainty about the threshold level that should be used to inform clinical practice. In a multicentre cohort study of 103 patients with a diagnosis of MM and biopsy-confirmed MCN made between 2002–2014, we report prospectively measured levels of serum FLC at diagnosis obtained using a single nephelometric assay (Freelite®) and we explore the relationship between serum FLC level at diagnosis with renal outcome and patient survival. Using a landmark approach, overall survival (OS) was compared between patients who achieved independence from dialysis compared to those who remained dialysis dependent at 3-month, 6-month, 9-month, and 12-month time points. The median serum FLC level at diagnosis was 7531 mg/L (range 107–114600). Serum creatinine was 535 μmol/L (range 168–2993) and eGFR 7 ml/min/1.73 m 2 (range 1–34). Six patients (5.8%) had an FLC level <1500 mg/L, which is the International Myeloma Working Group threshold for MCN and two patients were below the International Kidney and Monoclonal Gammopathy working group threshold of 500 mg/L; one was hypercalcaemic, and one had high-normal serum calcium level and had received a non-steroidal anti-inflammatory agent. Sixty-nine (67%) patients required haemodialysis treatment of whom 36 (52.1%) recovered independent renal function. Sixty-six (64%) patients died with a median OS of 2.5 years (95% CI 1.8–3.3). A landmark analysis revealed that independence from dialysis was associated with improved survival at 3-months ( P = 0.003), 6-months ( P = 0.035) and 9-months ( P = 0.014); there was no survival benefit observed beyond 12 months ( P = 0.146). Serum FLC level at diagnosis was neither associated with renal function recovery nor with OS. This is the largest reported cohort of patients with biopsy-confirmed MCN and prospectively measured serum FLC levels. These results indicate that a serum monoclonal FLC > 500 mg/L should be considered the threshold level associated with the development of MCN.

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          Highly sensitive, automated immunoassay for immunoglobulin free light chains in serum and urine.

          Bence Jones proteins or monoclonal immunoglobulin kappa and lambda free light chains (FLCs) are important markers for identifying and monitoring many patients with B-cell tumors. Automated immunoassays that measure FLCs in urine and serum have considerable clinical potential. Sheep antibodies, specific for FLCs, were prepared by immunization with pure kappa and lambda molecules and then adsorbed extensively against whole immunoglobulins. The antibodies were conjugated onto latex particles and used to assay kappa and lambda FLCs on the Beckman IMMAGE protein analyzer. The unconjugated antibodies showed minimal cross-reactivity with intact immunoglobulins or other proteins. With latex-conjugated antibodies, kappa and lambda FLCs could be measured in normal sera and most normal urine samples. Patients with multiple myeloma had increased concentrations of the relevant serum FLC, whereas both FLCs were increased in the sera of patients with systemic lupus erythematosus. We developed sensitive, automated immunoassays for kappa and lambda FLC measurements in serum and urine that should facilitate the assessment of patients with light chain abnormalities.
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            Early reduction of serum-free light chains associates with renal recovery in myeloma kidney.

            Myeloma kidney is the major cause of severe irreversible renal failure in patients with multiple myeloma. This tubulointerstitial injury is a direct consequence of high concentrations of circulating monoclonal free light chains (FLCs) produced by a clonal expansion of plasma cells. Early reduction of serum FLCs associates with renal recovery, but the target threshold of reduction to facilitate renal recovery is unknown. To determine the relationship between the achieved FLC reduction and renal recovery, we identified 39 patients with biopsy-proven myeloma kidney, the majority of whom had severe renal failure at presentation (median estimated GFR 9 ml/min per 1.73 m²). In a multivariable analysis incorporating demographic, hematologic, and renal variables, only the achieved FLC reduction significantly predicted renal recovery (P = 0.003). The relationship between renal recovery and FLC reduction was linear with no absolute threshold for FLC reduction. A 60% reduction in FLCs by day 21 associated with recovery of renal function for 80% of the population. Patient survival strongly associated with renal recovery: the median survival was 42.7 months (range 0 to 80) among those who recovered function compared with 7.8 months (range 0 to 54) among those who did not (P < 0.02). Cox-regression analysis demonstrated that the first presentation of myeloma, the kappa isotype of FLC, and renal recovery were independent predictors of survival. In conclusion, recovery of renal function in myeloma kidney depends on early reduction of serum FLCs, and this recovery associates with a significant survival advantage.
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              Treatment of acute renal failure secondary to multiple myeloma with chemotherapy and extended high cut-off hemodialysis.

              Extended hemodialysis using a high cut-off dialyzer (HCO-HD) removes large quantities of free light chains in patients with multiple myeloma. However, the clinical utility of this method is uncertain. This study assessed the combination of chemotherapy and HCO-HD on serum free light chain concentrations and renal recovery in patients with myeloma kidney (cast nephropathy) and dialysis-dependent acute renal failure. An open-label study of the relationship between free light chain levels and clinical outcomes in 19 patients treated with standard chemotherapy regimens and HCO-HD. There were sustained early reductions in serum free light chain concentrations (median 85% [range 50 to 97]) in 13 patients. These 13 patients became dialysis independent at a median of 27 d (range 13 to 120). Six patients had chemotherapy interrupted because of early infections and did not achieve sustained early free light chain reductions; one of these patients recovered renal function (at 105 d) the remaining 5 patients did not recover renal function. Patients who recovered renal function had a significantly improved survival (P < 0.012). In dialysis-dependent acute renal failure secondary to myeloma kidney, patients who received uninterrupted chemotherapy and extended HCO-HD had sustained reductions in serum free light chain concentrations and recovered independent renal function.
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                Author and article information

                Contributors
                paul.cockwell@uhb.nhs.uk
                Journal
                Blood Cancer J
                Blood Cancer J
                Blood Cancer Journal
                Nature Publishing Group UK (London )
                2044-5385
                3 March 2020
                3 March 2020
                March 2020
                : 10
                : 3
                : 28
                Affiliations
                [1 ]ISNI 0000 0004 0376 6589, GRID grid.412563.7, Department of Renal Medicine, , University Hospitals Birmingham NHS Foundation Trust, ; Birmingham, UK
                [2 ]ISNI 0000 0004 1936 7486, GRID grid.6572.6, Institute of Inflammation and Ageing, , University of Birmingham, ; Birmingham, UK
                [3 ]Mayo Clinic, Rochester NY, USA
                [4 ]ISNI 0000000106344187, GRID grid.265892.2, Department of Pathology, , University of Alabama at Birmingham, ; Birmingham AL, USA
                [5 ]ISNI 0000 0004 0376 6589, GRID grid.412563.7, Department of Haematology, , University Hospitals Birmingham NHS Foundation Trust, ; Birmingham, UK
                [6 ]ISNI 0000000106344187, GRID grid.265892.2, Department of Medicine, , University of Alabama at Birmingham, ; Birmingham, AL USA
                [7 ]ISNI 0000 0004 0419 1326, GRID grid.280808.a, Birmingham Veterans Affairs Medical Center, ; Birmingham, AL USA
                Author information
                http://orcid.org/0000-0002-5651-1411
                Article
                295
                10.1038/s41408-020-0295-4
                7054310
                32127527
                a668ba29-6925-4a63-8550-ccf81830b90e
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 27 March 2019
                : 29 July 2019
                : 23 August 2019
                Funding
                Funded by: Dr. Brown was supported by grants from the National Cancer Institute (R01 CA186646).
                Funded by: Dr. Sanders was supported by a Merit Award (1 I01 CX001326) from the United States (U.S.) Department of Veterans Affairs Clinical Sciences R&D (CSRD) Service, a National Institutes of Health George M. O'Brien Kidney and Urological Research Centres Program (P30 DK079337), and an Anderson Innovation Award
                Funded by: P.C. is a medical advisor to the The Binding Site
                Categories
                Article
                Custom metadata
                © The Author(s) 2020

                Oncology & Radiotherapy
                medical research,translational research
                Oncology & Radiotherapy
                medical research, translational research

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