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Mexican Concensus of Multiple Myeloma.

Authors :
de la Peña-Celaya JA
Aguilar-Luevano J
Alcivar-Cedeño LM
Álvarez-Vera JL
Anaya-Cuellar I
Añorve-Hernández E
Arana-Luna LL
Arteaga-Ortíz L
Báez-Islas PE
Banda-García LI
Bates-Martín RA
Campa-Monroy DI
Cardiel-Silva M
Castillo-Salas ÁJ
Cota-Rangel X
Díaz-Vargas G
Espitia-Ríos ME
Estrada-Domínguez P
Fermín-Caminero D
García-Camacho A
García-Castillo C
Garzón-Velásquez KB
Gil-Rondero C
Guerra-Alarcón LV
Hernández-Colín AK
Hernández-Ruiz E
Hernández-Alcántara AE
Hernández-Cervantes SA
Herrera-Olivares W
Ignacio-Ibarra G
Inclán-Alarcón SI
Leyto-Cruz F
Macías-Flores JP
Vega AM
Martínez-Ramírez MA
Martínez-Coronel J
Medina-Coral JE
Meza-Dávalos L
Montoya-Jiménez L
Morales-Hernández A
Morales-López E
Morales-Adrián JJ
Azcué MM
Mújica-Martínez A
Murillo-Cruz JL
Nájera-Martínez J
Narváez-Sarmiento IM
Nava-Villegas L
Nava-Alpide MA
Orellana Garibay JJ
Palafox-Zaldívar MT
Palma-Moreno OG
Paredes-Lozano EP
Pedraza-Colín ML
Pérez-Zúñiga JM
Pérez-Lizardi AB
Rojas-Castillejos F
Romero-Martínez E
Romero-Rodelo H
Ruiz-Contreras J
Saavedra-González A
Saucedo-Montes E
Silva-Michel LG
Silva-Vera K
Teomitzi-Sánchez Ó
Tepepa-Flores F
Ventura-Enríquez Y
Villela-Peña A
Vilchis-González SP
Zapata-Canto N
Zárate-Rodríguez PA
Alvarado-Ibarra M
Source :
Gaceta medica de Mexico [Gac Med Mex] 2020; Vol. 156 (Suppl 1), pp. S1-S45.
Publication Year :
2020

Abstract

To identify this increasingly common pathology, known as multiple myeloma (MM), it is necessary to refer to the specific factors that characterize it; to this end, the classic criteria known as CRAB (hyperkalemia, renal failure, anemia, and lytic lesions) are available, in which renal failure is one of the most frequent complications. Recently, three indisputable biomarkers have been described for the diagnostic support for MM, which are: more than 10% of clonal plasma cells in bone marrow or, a biopsy that corroborates the presence of a plasmacytoma, light chain ratio ≥ 100 mg/dL and more than one focal lesion on magnetic resonance imaging. A differential diagnosis for plasma cell leukemia, solitary bone plasmacytoma, and extramedullary plasmacytoma should always be considered. Being this an incurable disease, a lot of research has been done regarding its therapeutic management, whose main objective is the disappearance of plasma cells and the patient clinical improvement. Melphalan was the first drug that showed a benefit in 1958 and afterward, with the addition of a steroid as a second drug, it was possible to improve response rates. Subsequently, different molecules were studied, forming multiple combinations, and achieving better rates of overall survival and progression-free survival. Years later, with the arrival of proteasome inhibitors such as bortezomib, and immunomodulators such as thalidomide and lenalidomide, an important turnaround in the disease has been seen, as deeper responses, more prolonged remissions, and improvement in the quality of life of patients have been achieved. This consensus has the purpose of integrating a group of Mexican specialists and promoting the updating of this pathology.<br /> (Copyright: © 2020 Permanyer.)

Details

Language :
English
ISSN :
0016-3813
Volume :
156
Issue :
Suppl 1
Database :
MEDLINE
Journal :
Gaceta medica de Mexico
Publication Type :
Academic Journal
Accession number :
33103663
Full Text :
https://doi.org/10.24875/GMM.M20000393