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. 2020 Feb 20;1(1):68–81. doi: 10.1158/0008-5472.BCD-19-0068

Table 2.

Frequency of del(13q) by FISH analysis in molecular subtypes of MGUS and multiple myeloma

Total % Total % excluding insuff PC % ≥1 FISH abnl Del13/13q Present % del13 Fisher test
Genetic classification MGUS MM MGUS MM MGUS MM MGUS MM MGUS MM MGUS MM P
Insufficient PC 107 190 28% 10%
No FISH abnormality 72 118 19% 6% 26% 7%
CCND: t(11;14) or t(6;14) 64 341 17% 18% 23% 20% 32% 21% 13 125 20% 37% 0.014
MMSET: t(4;14) 8 155 2% 8% 3% 9% 4% 10% 6 127 75% 82% 0.640
MAF: t(14;16) or t(14;20) 16 75 4% 4% 6% 4% 8% 5% 6 57 38% 76% 0.005
HRD11+ 43 444 11% 23% 16% 26% 21% 28% 7 86 16% 19% 0.839
HRD11 13 217 3% 11% 5% 13% 6% 14% 9 107 69% 49% 0.253
nHRD2 59 359 15% 19% 21% 21% 29% 23% 36 219 61% 61% 1.000
Total 382 1899 382 1899 275 1709 203 1591 77 721 38% 45% 0.051

Note: Patients assigned to mutually exclusive groups, starting from the top, after excluding those with insufficient PCs or with no FISH abnormalities. Seventeen patients had a report of hyperdiploidy alone without mention of specific chromosomes and were excluded from the analysis. HRD11+: 11+ and at one of 3+,7+,9+,15+. nHRD2, the remaining patients (no recurrent translocation or hyperdiploidy).

Abbreviation: MM, multiple myeloma.