Table 1.
Molecular cytogenetic classification and risk stratification of multiple myeloma (MM).
Cytogenetic abnormality | Gene/chromosome (s) affected | Risk stratificationa |
---|---|---|
Primary cytogenetic abnormality | ||
Trisomic MM | Trisomies of one or more odd-numbered chromosomes | Standard risk |
t (11;14) MM | CCND1 | Standard risk |
t (4;14) MM | FGFR3 and MMSET | High risk |
MAF MM | High risk | |
t(14;16) | C-MAF | |
t(14;20) | MAF-B | |
Other | Standard risk | |
Secondary cytogenetic abnormality | ||
Gain (1q) | 1q | High risk |
Del (17p) | p53 | High risk |
p53 mutation | p53 | High risk |
Other | Variable |
aPresence of any two high-risk cytogenetic abnormalities is considered double-hit MM. Presence of any three or more high-risk cytogenetic abnormalities is considered triple-hit MM.