When a Monoclonal Gammopathy Is Not Multiple Myeloma

Author:

Derman Benjamin1,Castillo Jorge J.2,Sarosiek Shayna2,Beksac Meral3

Affiliation:

1. University of Chicago, Chicago, IL

2. Bing Center for Waldenström Macroglobulinemia, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA

3. Department of Hematology, Cebeci Hospital, Ankara University Dikimevi, Ankara, Turkey

Abstract

Our knowledge of monoclonal gammopathies is continuously evolving. Once accepted as a possible precursor condition to multiple myeloma, monoclonal gammopathies as an entity are now associated with many renal, neurologic, and dermatologic disorders of clinical significance. This change has created a challenge for patients and clinicians, as a monoclonal gammopathy may be a harbinger not of multiple myeloma but of other lymphoproliferative disorders such as light-chain amyloidosis and Waldenström macroglobulinemia. Early recognition of monoclonal gammopathies along with a careful workup are essential in determining the next steps in the care of a given patient. Recognition has become all the more important as we understand how to triage the 4% to 9% of patients with monoclonal gammopathies depending on age, with the goal of limiting overdiagnosis and misdiagnosis. In this review, we focus on treatment strategies for patients with monoclonal gammopathies that are not multiple myeloma, including smoldering multiple myeloma, light-chain amyloidosis, and Waldenström macroglobulinemia.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

General Medicine

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