Kidney Diseases Associated With Monoclonal Immunoglobulin M–Secreting B-Cell Lymphoproliferative Disorders: A Case Series of 35 Patients

Background Kidney diseases associated with immunoglobulin M (IgM) monoclonal gammopathy are poorly described, with few data for patient outcomes and renal response. Study Design Case series. Setting & Participants 35 patients from 8 French departments of nephrology were retrospectively studied....

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Veröffentlicht in:American journal of kidney diseases 2015-11, Vol.66 (5), p.756-767
Hauptverfasser: Chauvet, Sophie, MD, Bridoux, Frank, MD, PhD, Ecotière, Laure, MD, Javaugue, Vincent, MD, Sirac, Christophe, PhD, Arnulf, Bertrand, MD, PhD, Thierry, Antoine, MD, PhD, Quellard, Nathalie, Milin, Serge, MD, Bender, Sébastien, Goujon, Jean-Michel, MD, PhD, Jaccard, Arnaud, MD, PhD, Fermand, Jean-Paul, MD, Touchard, Guy, MD
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Sprache:eng
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Zusammenfassung:Background Kidney diseases associated with immunoglobulin M (IgM) monoclonal gammopathy are poorly described, with few data for patient outcomes and renal response. Study Design Case series. Setting & Participants 35 patients from 8 French departments of nephrology were retrospectively studied. Inclusion criteria were: (1) detectable serum monoclonal IgM, (2) estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73 m2 and/or proteinuria with protein excretion > 0.5 g/d and/or microscopic hematuria, and (3) kidney biopsy showing monoclonal immunoglobulin deposits and/or lymphomatous B-cell renal infiltration. All patients received chemotherapy, including rituximab-based regimens in 8 cases. Predictors Patients were classified into 3 groups according to renal pathology: glomerular AL amyloidosis (group 1; n = 11), nonamyloid glomerulopathies (group 2; n = 15, including 9 patients with membranoproliferative glomerulonephritis), and tubulointerstitial nephropathies (group 3; n = 9, including cast nephropathy in 5, light-chain Fanconi syndrome in 3, and isolated tumor infiltration in 1). Outcomes Posttreatment hematologic response (≥50% reduction in serum monoclonal IgM and/or free light chain level) and renal response (≥50% reduction in 24-hour proteinuria or eGFR ≥ 30 mL/min/1.73 m2 in patients with glomerular and tubulointerstitial disorders, respectively). Results Nephrotic syndrome was observed in 11 and 6 patients in groups 1 and 2, respectively. Patients in group 3 presented with acute kidney injury (n = 7) and/or proximal tubular dysfunction (n = 3). Waldenström macroglobulinemia was present in 26 patients (8, 12, and 6 in groups 1, 2, and 3, respectively). Significant lymphomatous interstitial infiltration was observed in 18 patients (4, 9, and 5 patients, respectively). Only 9 of 29 evaluable patients had systemic signs of symptomatic hematologic disease (2, 5, and 2, respectively). In groups 1, 2, and 3, respectively, hematologic response was achieved after first-line treatment in 3 of 9, 9 of 10, and 5 of 6 evaluable patients, while renal response occurred in 5 of 10, 9 of 15, and 5 of 8 evaluable patients. Limitations Retrospective study; insufficient population to establish the impact of chemotherapy. Conclusions IgM monoclonal gammopathy is associated with a wide spectrum of renal manifestations, with an under-recognized frequency of tubulointerstitial disorders.
ISSN:0272-6386
1523-6838
DOI:10.1053/j.ajkd.2015.03.035