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. Author manuscript; available in PMC: 2014 Mar 24.
Published in final edited form as: Int J Hematol. 2013 Feb 28;97(3):313–323. doi: 10.1007/s12185-013-1291-2

Table 1.

Survival of high-risk genetic subgroups on randomized controlled clinical trials of thalidomide and bortezomib in untreated MM

Genetics N1/N2 Endpoint Arm 1 Arm 2 Arm 1 (%) Arm 2 (%) Comment
t(4;14) 26/24 3-year OS V-AD/ASCT/Thal Bz-AD/ASCT/Bz 44 66 HOVON/GMMG [77]
98/106 4-year OS VA-D Bz-D 32 63 IFM-2005 [68]
21/23 2-year OS Thal Placebo 67 87 TT2 [72]
21/29 2-year OS Thal-TT2 Bz-TT3 67 97 TT2 v. TT3 [71]
del17p 21/16 3-year OS V-AD/ASCT/Thal Bz-AD/ASCT/Bz 17 69 HOVON/GMMG [77]
119/54 4-year OS VA-D Bz-D 36 50 IFM-2005 [68]
Non-hyperdiploid 92 3-year OS Thal-D-Bz Mel-P-Bz 53 72 PETHEMA [76]
Unfav. FISH 152/141 3-year OS Thal-D-Cyclo VA-D-Cyclo 58 56 MRC-IX intensive [86]
96/90 3-year OS Thal-D-Cyclo Placebo-P-Mel 34 26 MRC-IX non-intens [75]
99/98 3-year OS Thal maint Placebo maint 45 69 MRC-IX maint [73]

The drugs randomized in Arm 1 vs Arm 2 are highlighted in bold, as are the survival outcomes that are significantly superior

V vincristine, A adriamycin, D dexamethasone, ASCT autologous stem cell transplant, Thal thalidomide, Bz bortezomib, TT2 total therapy 2, TT3 total therapy 3, Mel low dose oral melphalan, P prednisone, Cyclo cyclophosphamide, / implies sequential therapies