Monoclonal gammopathies consist of. Monoclonal GammopathyeAssociated Proliferative Glomerulonephritis REVIEW

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REVIEW Monoclonal GammopathyeAssociated Proliferative Glomerulonephritis Sanjeev Sethi, MD, PhD, and S. Vincent Rajkumar, MD Abstract Monoclonal gammopathy is characterized by circulating monoclonal immunoglobulin owing to clonal proliferation of immunoglobulin-producing B lymphocytes or plasma cells. Clonal proliferation of B lymphocytes is seen in B-cell lymphoma/leukemia, and clonal plasma cell proliferation is seen in multiple myeloma and monoclonal gammopathy of undetermined significance. The monoclonal immunoglobulin in the setting of a B-cell or plasma cell disorder can cause a proliferative glomerulonephritis via 2 mechanisms: (1) glomerular deposition of the monoclonal immunoglobulin with activation of the classical pathway of complement (direct mechanism), resulting in an immunoglobulin-positive C3-positive glomerulonephritis, and (2) glomerular deposition of complement factors of the alternative and terminal pathway via inhibition of alternative pathwayeregulating proteins by the monoclonal immunoglobulin (indirect mechanism), resulting in immunoglobulin-negative C3-positive glomerulonephritis (C3 glomerulopathy). Evaluation should include serum and urine electrophoresis and immunofixation as well as serum-free light-chain assay. If a monoclonal immunoglobulin is detected on these tests, bone marrow biopsy or imaging is needed to exclude more advanced plasma cell dyscrasia. Evaluation of alternative pathway of complement should be done in patients with Ig-negative C3-positive glomerulonephritis. If monoclonal gammopathy is due to an underlying malignant disease such as myeloma, lymphoma, or chronic lymphocytic leukemia, then specific treatment should be aimed at treating the malignant disease, with the goal of eradicating the clonal cells producing the immunoglobulin. In contrast, if monoclonal gammopathy is due to a monoclonal gammopathy of undetermined significance, treatment options include bortezomib, cyclophosphamide, and dexamethasone for a non- IgM monoclonal immunoglobulin and rituximab alone or in combination with cyclophosphamide and dexamethasone for an IgM monoclonal immunoglobulin. ª 2013 Mayo Foundation for Medical Education and Research n Mayo Clin Proc. 2013;88(11):1284-1293 From the Division of Anatomic Pathology, Department of Laboratory Medicine and Pathology (S.S.), and Division of Hematology, Department of Internal Medicine (S.V.R.), Mayo Clinic, Rochester, MN. Monoclonal gammopathies consist of a heterogeneous group of disorders characterized by clonal proliferation of immunoglobulin-producing B lymphocytes or plasma cells. 1,2 In most patients, the proliferating cells continue to secrete immunoglobulin, which can be detected in the blood or the urine as a monoclonal immunoglobulin (M protein). There is frequent secretion of the light chain component of the immunoglobulin molecule (k or l light chains) in addition to intact immunoglobulin, suggesting dysregulation of the normal antibody synthetic pathways. 3 In some instances, the neoplastic cells lose the ability to synthesize the normal heavy chain component of the immunoglobulin molecule and instead secrete only k or l light chains. 4 The clinical spectrum of monoclonal gammopathies is wide and includes classic malignant diseases such as multiple myeloma and Waldenström macroglobulinemia; clonal, but nonmalignant, paraprotein-related disorders such as light chain amyloidosis; and the incidentally detected premalignant plasma cell dyscrasia termed monoclonal gammopathy of undetermined significance (MGUS). 1,5 Monoclonal gammopathy of undetermined significance is present in approximately 3% of the general population aged 50 years and older. 6,7 It is associated with a risk of progression to multiple myeloma or related plasma cell malignancy, as well as to paraprotein-related disorders such as light chain amyloidosis. 1 Although, by definition, MGUS is a premalignant process, the secreted M protein is often a functioning antibody and can thus be associated with various clinical diseases depending on the antigen being targeted or the intrinsic property of the antibody. 8 Because MGUS is present in 3% of the population, numerous disease associations have been reported in the literature, but most are coincidental and not causally related to the 1284 Mayo Clin Proc. n November 2013;88(11):1284-1293 n http://dx.doi.org/10.1016/j.mayocp.2013.08.002 n ª 2013 Mayo Foundation for Medical Education and Research

MONOCLONAL GAMMOPATHY AND PROLIFERATIVE GLOMERULONEPHRITIS M protein. 8 A true association is considered only when the prevalence of an M protein in a given disease approaches levels far higher than what would be expected by the known prevalence of MGUS. 8 In addition, there should be clear pathologic and laboratory evidence to support a causal relationship. On the basis of these criteria, it is well accepted that the M protein in MGUS can lead to disorders such as peripheral neuropathy, monoclonal immunoglobulin deposition diseases, cold agglutinin disease, and cryoglobulinemia. More recently, we have found that a substantial proportion of cases of idiopathic proliferative glomerulonephritis are related to MGUS or associated monoclonal gammopathies. 9-13 Proliferative glomerulonephritis results when immune complexes and/or complement factors are deposited in the glomerulus. 14 The deposition of immune complexes and/or complement factors results in an inflammatory response with an influx of leukocytes and ensuing glomerular injury. Immune complexes are deposited in the glomeruli in the setting of infections, autoimmune diseases, and monoclonal gammopathy. 14 In contrast, complement factors, in the absence of significant immune deposits, are deposited in conditions associated with dysregulation of the alternative pathway of complement components. The term C3 glomerulopathy is used to define conditions associated with abnormalities of the alternative pathway and includes C3 glomerulonephritis (C3GN) and dense deposit disease (DDD). 15-18 Monoclonal gammopathies can lead to proliferative glomerulonephritis via 2 mechanisms: direct and indirect (Figure 1). The direct mechanism involves deposition of monoclonal immunoglobulin (also referred to as monotypic immunoglobulin) in the mesangium and along capillary walls, resulting in an immune complexemediated proliferative glomerulonephritis. 10,12 Monoclonal immunoglobulins activate the classical and terminal pathways of complement, resulting in the glomerular deposition of complement factors of the classical and terminal complement pathways along with monoclonal immunoglobulins. The indirect mechanism involves the activation of the alternative pathway of complement by the monoclonal immunoglobulin, resulting in the deposition of complement factors of the alternative and classical pathways in the absence ARTICLE HIGHLIGHTS n Monoclonal gammopathy can be associated with a proliferative glomerulonephritis. n A proliferative glomerulonephritis may result from the direct glomerular deposition of monoclonal immunoglobulins (direct mechanism). Monoclonal immunoglobulins also activate the classical and terminal pathways of complement. Thus, on kidney biopsy, both the monotypic immunoglobulin and the complement factor C3 are present. n A proliferative glomerulonephritis may result when monoclonal immunoglobulins cause activation of the alternative pathway via functional inhibition of complement-regulating proteins (indirect mechanism), resulting in the deposition of complement factors of the alternative and terminal pathways. Thus, on kidney biopsy, only the complement factor C3 is present. n The evaluation of monoclonal gammopathy should include serum and urine electrophoresis and immunofixation as well as serum-free light chain assay, followed by bone marrow and imaging studies to identify the underlying disorder. n Treatment should be aimed at eradicating the population of clonal cells responsible for the offending immunoglobulin. of significant immunoglobulin deposition (C3 glomerulopathy). 9,19 In addition, monoclonal gammopathy may be associated with a proliferative glomerulonephritis with specific pathologic findings such as fibrillary glomerulonephritis, immunotactoid glomerulopathy, and monoclonal immunoglobulin deposition diseases. These specific pathologic entities are not considered here. The term monoclonal gammopathy of renal significance has recently been proposed to include various renal disorders associated with MGUS. 11 This new term is a generic term that is useful in highlighting the potential relationship of MGUS with kidney disease in clinical settings. However, once a pathologic diagnosis is made, we recommend that the specific disorder should be stated, such as monoclonal gammopathye associated proliferative glomerulonephritis and monoclonal gammopathyeassociated fibrillary glomerulonephritis. PubMed was searched for the terms monoclonal gammopathy, proliferative glomerulonephritis, membranoproliferative glomerulonephritis, C3 glomerulopathy, alternative pathway of complement, and glomerulonephritis. Mayo Clin Proc. n November 2013;88(11):1284-1293 n http://dx.doi.org/10.1016/j.mayocp.2013.08.002 1285

MAYO CLINIC PROCEEDINGS FIGURE 1. Schematic model for monoclonal gammopathyeassociated proliferative glomerulopathy. Left, Direct mechanism: binding of monoclonal immunoglobulin to complement factors of the classical pathway results in the activation of the classical pathway (red oval structures) and the terminal pathway (purple oval structures) of complement components. Mesangial and subendothelial deposition of the monoclonal immunoglobulin and factors of the classical and terminal pathways then results in mesangial and capillary wall injury. Right, Indirect mechanism: monoclonal immunoglobulins cause the activation of the alternative pathway by acting as autoantibodies to complement-regulating proteins (red/green squares or blue/red circles) or C3 convertase (C3 nephritic factor; yellow oval structures), which is followed by the activation of the terminal pathway of complement components. The mesangial and subendothelial deposition of the complement factors of the alternative and terminal pathways then results in mesangial and capillary wall injury with the development of C3 glomerulopathy. Note the lack of immunoglobulin deposition along capillary walls. The injury phase in both direct (left) and indirect (right) mechanisms is followed by leukocyte influx, leading to a proliferative phase with damage to the capillary walls from the release of cytokines and proteases (P) and ensuing hematuria and proteinuria. The endothelial cells exhibit loss of fenestrations; the glomerular basement is disrupted; and podocytes exhibit the effacement of foot processes. Reparative changes follow with new basement membrane formation and entrapment of immune complexes with or without complement factors (left) or complement factors only (right), cellular elements, and matrix material, resulting in double contours along the capillary walls. 1286 Mayo Clin Proc. n November 2013;88(11):1284-1293 n http://dx.doi.org/10.1016/j.mayocp.2013.08.002

MONOCLONAL GAMMOPATHY AND PROLIFERATIVE GLOMERULONEPHRITIS DIRECT MECHANISM In the direct mechanism, proliferative glomerulonephritis results from the deposition of the monoclonal immunoglobulin and complement factors of the classical and terminal pathways in the glomeruli. Pathologic Findings On kidney biopsy, the most common pattern of injury is a membranoproliferative glomerulonephritis. Less commonly, other patterns of proliferative glomerulonephritis can be seen, such as mesangial proliferative glomerulonephritis, diffuse proliferative glomerulonephritis, crescentic and necrotizing glomerulonephritis, and sclerosing glomerulonephritis. 10,12 The most important element for the diagnosis is immunofluorescence microscopy, which characteristically reveals monoclonal immunoglobulin deposits in the mesangium and along capillary walls. The deposits are composed of a heavy chain component, typically IgG, and a light chain component, either k or l light chain. However, it is important to note that any class of monoclonal immunoglobulin can cause a proliferative glomerulonephritis. 13 Less commonly, only heavy or light chains may be present. Electron microscopy reveals mesangial and subendothelial electron dense deposits and rarely subepithelial and intramembranous deposits. Glomerular capillary wall remodeling with double contour formation is often present. In rare instances, the deposits may be difficult to locate on electron microscopy, even though immunofluorescence studies report monoclonal immunoglobulin deposition. Representative kidney biopsy findings of proliferative glomerulonephritis due to monoclonal immunoglobulin deposition are illustrated in Figure 2. Clinical Studies In a recent study, a serum M protein was detected in 28 of the 61 patients (46%) with proliferative glomerulonephritis after exclusion of systemic lupus erythematosus and viral hepatitis B and C. 12 In 20 of the 28 patients (71%), monoclonal immunoglobulin deposits of the FIGURE 2. Representative kidney biopsy findings in a patient with membranoproliferative glomerulonephritis and monoclonal immunoglobulin deposits. The patient is a 73-year-old man with nephrotic syndrome, hypertension, and worsening kidney function. Kidney biopsy reveals a (A) membranoproliferative pattern of injury on light microscopy (periodic acid Schiff stain, original magnification 40); granular mesangial and capillary wall staining for (B) IgG, (C) C3, (D) k light chains, and (E) negative l light chains staining on immunofluorescence microscopy (B-E, original magnification 40); and (F) subendothelial deposits (arrows) on electron microscopy (original magnification 23,000). On further evaluation, serum immunofixation studies did not reveal monoclonal bands. However, k free light chains were elevated at 5.15 mg/dl, with l free light chain of 2.45 mg/dl and ratio of 2.1. Mayo Clin Proc. n November 2013;88(11):1284-1293 n http://dx.doi.org/10.1016/j.mayocp.2013.08.002 1287

MAYO CLINIC PROCEEDINGS same isotype as the serum M protein could be detected in the glomeruli on immunofluorescence microscopy. The isotype of monoclonal immunoglobulin included IgG, IgM, and, in one case, IgA. Patients most often presented with hypertension, proteinuria, and kidney failure. C3 and C4 levels were both low in approximately 40% of the patients, indicating activation of the classical pathway of complement components. Monoclonal gammopathy of undetermined significance was the most common (57%) underlying monoclonal gammopathy in these patients; other causes include chronic lymphocytic leukemia (CLL), lymphoplasmacytic lymphoma/waldenström macroglobulinemia, low-grade B-cell lymphoma, and multiple myeloma. 20 Nasr et al 10 retrospectively examined 37 patients with proliferative glomerulonephritis with monoclonal immunoglobulin deposits. In this study, a corresponding serum M protein was documented in only 11 patients (30%), which suggests that proliferative glomerulonephritis can be caused by small amounts of monoclonal immunoglobulin that are well below the level of detection in the systemic circulation through serum immunofixation. In fact, 1 of the 11 patients (9%) had no serum M protein in the initial evaluation; the systemic monoclonal gammopathy became detectable only 3 years later on follow-up testing. It is possible that additional evaluation by using more sensitive methods such as the serumfree light chain assay or multiparametric flow cytometry of the bone marrow could have detected a systemic monoclonal gammopathy in more patients. All the patients in this series had a monoclonal immunoglobulin deposit of the IgG isotype: IgG1 (28.1%), IgG2 (6.3%), and IgG3 (65.6%). IgG3 monotypic deposits were more likely to be associated with the absence of the M protein on serum immunofixation. On follow-up, available in 32 of the 37 patients (86%), 37.5% recovered kidney function, 37.5% developed persistent renal dysfunction, and 22% progressed to end-stage kidney disease. The causal nature of the relationship between monoclonal immunoglobulin and proliferative glomerulonephritis is illustrated by a study of 4 patients with monotypic IgG3 on kidney biopsy who underwent renal transplant. Despite negative results of serum studies for M protein at the time of transplant, all 4 patients had early recurrence of proliferative glomerulonephritis with monotypic immunoglobulin deposits in the graft. 21 The recurrence in these patients also supports the hypothesis that some patients may have circulating monoclonal immunoglobulin below the threshold of detection by current techniques. INDIRECT MECHANISM In the indirect mechanism, monoclonal immunoglobulin causes dysregulation of the alternative pathway, and thus, there is deposition of complement factors of the alternative and terminal pathways in the glomeruli, with the development of C3 glomerulopathy. Pathologic Findings As in the direct mechanism, the most common pattern of injury in both DDD and C3GN is a membranoproliferative glomerulonephritis. Less common patterns of injury include mesangial proliferative glomerulonephritis, diffuse proliferative glomerulonephritis, crescentic and necrotizing glomerulonephritis, and sclerosing glomerulonephritis. 15,16,22 The most important diagnostic finding is the presence of bright mesangial and capillary wall staining for C3 and the absence of any significant immunoglobulin deposits on immunofluorescence microscopy (Figure 3). The difference between DDD and C3GN is in the electron microscopy findings: DDD is characterized by dense intramembranous deposits, whereas C3GN exhibits mesangial, intramembranous, subendothelial, and occasionally subepithelial deposits. 16,17 Although DDD and C3GN may occur in the de novo setting, secondary causes or insults that result in the unmasking of an abnormality of the alternative pathway are more likely to cause C3 glomerulopathy. The dysregulation of the alternative pathway of complement can result from either autoantibodies to or sequence variations in complement-regulating proteins, such as complement factor H. 23,24 Infections are another important secondary cause of C3 glomerulopathy, as they may unmask an underlying abnormality in the alternative pathway of complement components. 25 Monoclonal immunoglobulins inhibit regulation of the alternative pathway of complement by interfering with the function of complement-regulating proteins, which 1288 Mayo Clin Proc. n November 2013;88(11):1284-1293 n http://dx.doi.org/10.1016/j.mayocp.2013.08.002

MONOCLONAL GAMMOPATHY AND PROLIFERATIVE GLOMERULONEPHRITIS FIGURE 3. Representative kidney biopsy findings in a patient with C3GN and monoclonal gammopathy. The patient is a 53-year-old woman with nephrotic syndrome and hypertension. Serum immunofixation studies revealed IgG k. Bone marrow studies revealed slightly increased numbers of plasma cells (5%) with k light chain restriction. Laboratory studies were negative for cryoglobulins. Kidney biopsy revealed a (A) membranoproliferative pattern of injury on light microscopy (periodic acid Schiff stain, original magnification 40), (B) bright C3 staining (original magnification 40) and negative immunoglobulin staining on immunofluorescence microscopy, and (C) subendothelial deposits (arrow) on electron microscopy (original magnification 5800). Further evaluation revealed abnormalities in the alternative pathway of complement components. leads to overactivation of the alternative pathway, resulting in DDD or C3GN. Clinical Studies In a recent series of 14 patients with DDD aged 49 years and older, 10 (71%) had a concomitant diagnosis of MGUS. 19 The mean age was 61.2 years. Six of the 10 patients (60%) had progression to end-stage kidney disease, and 1 (10%) received a kidney transplant with early recurrence of DDD. In an index case, low levels of factor H autoantibodies, a permissive genetic background (H402 allele of the complement factor H), and the activation of the alternative pathway of complement were detected. The study raises the possibility that in some patients the monoclonal immunoglobulin may act as factor H antibody, resulting in the activation of the alternative pathway of complement and the resultant DDD. Others have also reported an association between a proportion of patients with DDD and monoclonal gammopathy. 26 Dense deposit disease tends to have a worse prognosis in adults than in children. 26 Bridoux et al 27 reported 6 cases of monoclonal gammopathyeassociated C3GN. Anticomplement factor H activity was positive in one patient. Five patients had progression to end-stage kidney disease over a median period of 47 months, despite chemotherapy in 4 patients. In a study of 32 cases of C3GN at Mayo Clinic between January 1, 2009, and December 31, 2012, 10 (31%) had evidence of a monoclonal immunoglobulin in the serum. 9 Bone marrow biopsy, done in 9 patients, revealed MGUS in 5 patients, CLL in 1 patient, and no abnormal clones in the remaining 3 patients. Importantly, 2 patients who received therapy targeting the monoclonal proliferative process had a marked decrease in hematuria and proteinuria and stabilization of renal function. The mechanism by which monoclonal immunoglobulin activates the alternative pathway is not entirely known. In an elaborate study by Meri et al, 28 monoclonal l light chains from a patient with DDD were found to result in the activation of the alternative pathway by directly interacting with factor H. Later, Jokiranta et al 29 reported that monoclonal l light chains bind to the third short consensus repeat domain, resulting in the inhibition of factor H function. Antibodies to the C3 convertase (C3 nephritic factor) are commonly detected in C3GN and DDD. 16,24 The C3 nephritic factor stabilizes the C3 convertase, increasing its half-life, and it prevents its breakdown by complement-regulating proteins, leading to overactivation of the alternative pathway of complement. We found abnormalities of the alternative pathway of complement components in 7 of the 9 patients (78%) with monoclonal gammopathyeassociated C3GN. 9 Two patients also had the C3 nephritic factor, suggesting that the monoclonal immunoglobulin may act as a C3 nephritic factor. Sequence variations in complement-regulating proteins have not been found in monoclonal gammopathye associated C3GN. 9,27 Mayo Clin Proc. n November 2013;88(11):1284-1293 n http://dx.doi.org/10.1016/j.mayocp.2013.08.002 1289

MAYO CLINIC PROCEEDINGS RECURRENT GRAFT INJURY Membranoproliferative glomerulonephritis of any etiology tends to recur in the graft, and recent studies have reported a recurrence rate of 40% to 60%. 30 A recent study by Lorenz et al 30 found that the risk of recurrence is particularly high in the presence of circulating monoclonal immunoglobulin. The increased risk of recurrence is not surprising because monoclonal gammopathy has not been the target of treatment in these patients. Recurrence tends to be early and is often clinically much more severe than the native disease. EVALUATION The diagnosis of monoclonal gammopathye associated glomerulonephritis should be suspected in any patient with clinical or histopathologic evidence of proliferative glomerulonephritis in whom there are no other identifiable causes such as infections (especially hepatitis C) or autoimmune disease. Immunofluorescence examination of the kidney biopsy is essential for the evaluation of all cases of proliferative glomerulonephritis (Figure 4). In the direct mechanism, immunofluorescence microscopy will reveal monoclonal immunoglobulin deposits in the mesangium and along capillary walls. The deposits will have evidence of light chain restriction (either k or l light chain staining but not both), indicating the clonal nature of the process. However, in the indirect mechanism in which monoclonal immunoglobulins cause dysregulation of the complement pathway, the actual deposits consist only of complement factors. Thus, the kidney biopsy will reveal bright mesangial and capillary wall staining for C3 with no significant immunoglobulin deposits on immunofluorescence microscopy. In all patients with suspected monoclonal gammopathyeassociated glomerulonephritis, direct or indirect, laboratory tests to determine the presence of a systemic monoclonal gammopathy should be undertaken. Proliferative glomerulonephritis Direct mechanism IF: monotypic immunoglobulin deposits with or without C3 Indirect mechanism IF: C3 deposits, absence of monotypic immunoglobulin deposits DDD or C3GN Positive for circulating M protein Negative for circulating M protein Positive for circulating M protein VCD (non-igm) or RCD (IgM) CP and/or rituximab VCD (non-igm) or RCD (IgM) FIGURE 4. Evaluation and management of monoclonal gammopathyeassociated proliferative glomerulonephritis. On the basis of the immunofluorescence findings (IF), proliferative glomerulonephritis can be broadly divided into monoclonal immunoglobulin-positive with or without C3 and monoclonal immunoglobulin-negative C3-positive proliferative glomerulonephritis. Evaluation of both conditions necessitates a work-up to detect circulating monoclonal immunoglobulin, referred to as M protein. In patients with detectable M protein of the non-igm isotype, bortezomib, cyclophosphamide, and dexamethasone (VCD) is recommended as the initial therapy, whereas in patients with an M protein of the IgM isotype, rituximab, cyclophosphamide, and dexamethasone (RCD) is preferred. In patients without a detectable circulating M protein, standard therapy with cyclophosphamide and prednisone (CP) as used in idiopathic glomerulonephritis should be tried first. DDD ¼ dense deposit disease. 1290 Mayo Clin Proc. n November 2013;88(11):1284-1293 n http://dx.doi.org/10.1016/j.mayocp.2013.08.002

MONOCLONAL GAMMOPATHY AND PROLIFERATIVE GLOMERULONEPHRITIS The most sensitive tests to detect M proteins in the serum and urine consist of the serum and urine electrophoresis and immunofixation and serum-free light chain assay. 31 M proteins appear as a localized band on electrophoresis and immunofixation. Immunofixation also permits the determination of the heavy and light chain type of the M protein, which can then be correlated with the immunofluorescence results for concordance. If a paraprotein is detected on these tests, usual work-up to exclude more advanced plasma cell dyscrasia such as a bone marrow biopsy or imaging may be needed, depending on the size and type of the M protein. 32 By definition, documentation of a circulating M protein is required for the diagnosis of monoclonal gammopathyeassociated DDD or C3GN (indirect mechanism). However, not all patients with monoclonal gammopathye associated proliferative glomerulonephritis mediated by the direct mechanism will have evidence of an M protein in the serum or urine (Figure 4). In some of these patients, the monoclonal process may be limited and the levels of the M protein in circulation are too low to be detected. In such patients, the diagnosis requires documentation of light chain restriction on renal histopathology. In addition to immunofluorescence microscopy, mass spectrometry may be helpful in identifying clonal immunoglobulin deposits in proliferative glomerulonephritis, although additional studies are needed for validation. 33 An evaluation of the alternative pathway of complement is warranted in monoclonal immunoglobulinenegative C3- positive proliferative glomerulonephritis to determine the cause of dysregulation of the alternative pathway. In most patients, the specific plasma cell disorder associated with the proliferative glomerulonephritis is MGUS; in some patients, a more advanced disorder such as multiple myeloma, macroglobulinemia, or CLL is detected. In the latter cases, the renal process serves as the harbinger of the malignant disease. In some patients, proliferative glomerulonephritis precedes the diagnosis of a plasma cell malignant disease by months to years. MANAGEMENT Because monoclonal gammopathyeassociated glomerulonephritis is a newly described entity, there are no studies to determine the optimal approach to therapy. Recommendations for therapy are therefore primarily based on clinical opinion and experience, as well as data on the feasibility, response rate, and toxicity of various regimens used in the treatment of multiple myeloma and related plasma cell malignant diseases, in which the goal of therapy is essentially the same, that is, eradication of clonal plasma cells (Figure 4). In patients with an underlying malignant disease such as myeloma, lymphoma, or CLL, the treatment of the primary malignant disease is the first step, and it will accomplish the desired goal of eradicating the population of clonal cells that are responsible for the offending immunoglobulin. In patients with proliferative glomerulonephritis with positive immunoglobulin deposits on immunofluorescence microscopy as well as the presence of the corresponding M protein on serum and urine studies, the diagnosis is straightforward and there is a clear rationale to justify chemotherapy, provided the renal process is sufficiently severe. In such patients, any of the regimens used to treat multiple myeloma is reasonable if the M protein is of the non-igm type. On the basis of relative efficacy, tolerance, and cost, we prefer bortezomib, cyclophosphamide, and dexamethasone (VCD). We administer VCD as follows: bortezomib, 1.3 mg/m 2 once a week subcutaneously; cyclophosphamide, 500 mg (total dose) once a week orally; and dexamethasone, 40 mg once a week orally. 34,35 This regimen is followed for 3 weeks on and 1 week off. Patients are monitored every 4 weeks, and treatment is administered for approximately 6 months if there is evidence of renal response and low toxicity. In our opinion, 6 months of VCD is probably no more toxic overall than other regimens used to treat glomerulonephritis, which usually consist of cyclophosphamide and daily corticosteroids. In patients with an IgM type of the M protein, we prefer the use of rituximab (anti-cd20 monoclonal antibody) alone or in combination with cyclophosphamide and dexamethasone because IgM-secreting cells are almost always CD20 positive. In patients with proliferative glomerulonephritis who have positive immunoglobulin deposits on immunofluorescence microscopy but no evidence of an M protein on serum and urine studies, there needs to be more circumspection concerning the use of chemotherapy. Mayo Clin Proc. n November 2013;88(11):1284-1293 n http://dx.doi.org/10.1016/j.mayocp.2013.08.002 1291

MAYO CLINIC PROCEEDINGS A decision to use the approach described earlier is still reasonable if 2 to 3 months of conservative therapy fails to produce a renal response. In addition to specific therapy aimed at eradicating the cause, patients need usual supportive care measures such as adjustment of medications for hypertension, fluid balance, and dialysis, as needed. Renal transplant is typically associated with the recurrence of the same process in the graft unless the monoclonal plasma cell disorder is successfully eradicated before such a procedure. CONCLUSION Monoclonal gammopathyeassociated proliferative glomerulonephritis can occur either from the deposition of the monoclonal immunoglobulin and complement factors of the classical and terminal pathways (direct mechanism) or from the deposition of complement factors of the alternative and terminal pathways as a consequence of the activation of the alternative pathway of complement by the monoclonal immunoglobulin (indirect mechanism). We have proposed an algorithm for the evaluation and treatment of these cases. Clearly, clinical trials are desperately needed for all patients with monoclonal gammopathyeassociated proliferative glomerulonephritis. Abbreviations and Acronyms: C3GN = C3 glomerulonephritis; CLL = chronic lymphocytic leukemia; DDD = dense deposit disease; MGUS = monoclonal gammopathy of undetermined significance; VCD = bortezomib, cyclophosphamide, and dexamethasone Correspondence: Address to Sanjeev Sethi, MD, PhD, Division of Anatomic Pathology, Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First St SW, Rochester, MN 55905 (sethi.sanjeev@mayo.edu). REFERENCES 1. Kyle RA, Therneau TM, Rajkumar SV, et al. A long-term study of prognosis in monoclonal gammopathy of undetermined significance. N Engl J Med. 2002;346(8):564-569. 2. Kyle RA, Rajkumar SV. Criteria for diagnosis, staging, risk stratification and response assessment of multiple myeloma. Leukemia. 2008;23(1):3-9. 3. Rajkumar SV, Kyle RA, Therneau TM, et al. Serum free light chain ratio is an independent risk factor for progression in monoclonal gammopathy of undetermined significance. Blood. 2005;106(3):812-817. 4. 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