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      Paraprotein-Related Kidney Disease: Evaluation and Treatment of Myeloma Cast Nephropathy

      , , , 1
      Clinical Journal of the American Society of Nephrology
      American Society of Nephrology (ASN)

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          Abstract

          <p class="first" id="d2069036e153">Nearly 50% of patients with multiple myeloma develop renal disease, most commonly from AKI caused by cast nephropathy. Development of AKI is associated with poor 1-year survival and reduces the therapeutic options available to patients. There is a great need for more effective therapies. Cast nephropathy is caused by the interaction and aggregation of filtered free light chains and Tamm–Horsfall protein causing intratubular obstruction and damage. The key to treating cast nephropathy is rapid lowering of free light chains, because this correlates with renal recovery. Newer chemotherapy agents rapidly lower free light chains and have been referred to as renoprotective. There is additional great interest in using extracorporeal therapies to remove serum free light chains. Small trials initially showed benefit of therapeutic plasma exchange to improve renal outcomes in cast nephropathy, but a large randomized trial of therapeutic plasma exchange failed to show benefit. A newer technique is extended high–cutoff hemodialysis. This modality uses a high molecular weight cutoff filter to remove free light chains. To date, trials of high–cutoff hemodialysis use in patients with cast nephropathy have been encouraging. However, there are no randomized trials showing the benefit of high-cutoff hemodialysis when used in addition to newer chemotherapeutic regimens. Until these studies are available, high-cutoff hemodialysis cannot be recommended as standard of care. </p>

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          Most cited references43

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          Cancer statistics, 2000

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            Proteasome inhibitors in multiple myeloma: 10 years later.

            Proteasome inhibition has emerged as an important therapeutic strategy in multiple myeloma (MM). Since the publication of the first phase 1 trials of bortezomib 10 years ago, this first-in-class proteasome inhibitor (PI) has contributed substantially to the observed improvement in survival in MM patients over the past decade. Although first approved as a single agent in the relapsed setting, bortezomib is now predominantly used in combination regimens. Furthermore, the standard twice-weekly schedule may be replaced by weekly infusion, especially when bortezomib is used as part of combination regimens in frontline therapy. Indeed, bortezomib is an established component of induction therapy for patients eligible or ineligible for autologous stem cell transplantation. Bortezomib has also been incorporated into conditioning regimens before autologous stem cell transplantation, as well as into post-ASCT consolidation therapy, and in the maintenance setting. In addition, a new route of bortezomib administration, subcutaneous infusion, has recently been approved. Recently, several new agents have been introduced into the clinic, including carfilzomib, marizomib, and MLN9708, and trials investigating these "second-generation" PIs in patients with relapsed/refractory MMs have demonstrated positive results. This review provides an overview of the role of PIs in the treatment of MM, focusing on developments over the past decade.
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              International Myeloma Working Group Recommendations for the Diagnosis and Management of Myeloma-Related Renal Impairment

              The aim of the International Myeloma Working Group was to develop practical recommendations for the diagnosis and management of multiple myeloma-related renal impairment (RI).
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                Author and article information

                Journal
                Clinical Journal of the American Society of Nephrology
                Clinical Journal of the American Society of Nephrology
                American Society of Nephrology (ASN)
                1555-9041
                1555-905X
                December 07 2016
                August 15 2016
                : 11
                : 12
                : 2273-2279
                Affiliations
                [1 ]for the American Society of Nephrology Onco-Nephrology Forum
                Article
                10.2215/CJN.01640216
                5142056
                27526708
                6f3d8d96-8764-4946-973a-5b17c8f74988
                © 2016
                History

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