Monoclonal gammopathy of undetermined significance medical therapy

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Associate Editor(s)-in-Chief: Omer Kamal, M.D.[2]Shyam Patel [3]

Overview

There is no specific treatment for monoclonal gammopathy of undetermined significance; the mainstay of therapy is active surveillance and supportive care. The goal is to detect other plasma cell dyscrasias at an early time point such that corrective intervention can be undertaken. Trials using lenalidomide and bisphosphonates are been conducted to determine whether they decrease the progression of the disease both for MGUS and multiple myeloma.

Medical Therapy

There is no specific treatment for monoclonal gammopathy of undetermined significance. The mainstay of therapy is active surveillance and supportive care. A typical management regimen includes once yearly blood checks, including assessment of:

Anti-resorptive therapy

Vitamin D and calcium can be given as anti-resorptive therapy.[2]

Peripheral neuropathy

Corticosteroids may be helpful with peripheral neuropathy. Gabapentin can be considered also.

Advances

Trials using lenalidomide and bisphosphonates are begin run to determine whether they decrease the progression of the disease both for MGUS and multiple myeloma.[3][4][5]

References

  1. Bird J, Behrens J, Westin J, Turesson I, Drayson M, Beetham R, D'Sa S, Soutar R, Waage A, Gulbrandsen N, Gregersen H, Low E (October 2009). "UK Myeloma Forum (UKMF) and Nordic Myeloma Study Group (NMSG): guidelines for the investigation of newly detected M-proteins and the management of monoclonal gammopathy of undetermined significance (MGUS)". Br. J. Haematol. 147 (1): 22–42. doi:10.1111/j.1365-2141.2009.07807.x. PMID 19673884.
  2. Berenson JR, Anderson KC, Audell RA, Boccia RV, Coleman M, Dimopoulos MA, Drake MT, Fonseca R, Harousseau JL, Joshua D, Lonial S, Niesvizky R, Palumbo A, Roodman GD, San-Miguel JF, Singhal S, Weber DM, Zangari M, Wirtschafter E, Yellin O, Kyle RA (July 2010). "Monoclonal gammopathy of undetermined significance: a consensus statement". Br. J. Haematol. 150 (1): 28–38. doi:10.1111/j.1365-2141.2010.08207.x. PMID 20507313.
  3. Pozzi S, Raje N (2011). "The role of bisphosphonates in multiple myeloma: mechanisms, side effects, and the future". Oncologist. 16 (5): 651–62. doi:10.1634/theoncologist.2010-0225. PMC 3228190. PMID 21493759.
  4. Mateos MV, Hernández MT, Giraldo P, de la Rubia J, de Arriba F, López Corral L, Rosiñol L, Paiva B, Palomera L, Bargay J, Oriol A, Prosper F, López J, Olavarría E, Quintana N, García JL, Bladé J, Lahuerta JJ, San Miguel JF (August 2013). "Lenalidomide plus dexamethasone for high-risk smoldering multiple myeloma". N. Engl. J. Med. 369 (5): 438–47. doi:10.1056/NEJMoa1300439. PMID 23902483.
  5. Mahindra A, Pozzi S, Raje N (September 2012). "Clinical trials of bisphosphonates in multiple myeloma". Clin Adv Hematol Oncol. 10 (9): 582–7. PMID 23073123.

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