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. 2015 Oct 23;5(10):e363. doi: 10.1038/bcj.2015.91

Table 4. Baseline characteristics and response according by treatment group.

  Primary Rd until progression (n=9) Primary Rd stopped before progression (n=11) Primary Rd stopped with progression and restarted (n=5) Rd induction followed by SCT (n=8)
Age, years, median (range) 65 (36–70) 60 (40–78) 55 (32–75) 62 (36–73)
Prior plasma cell disorder, N 6 (3 MGUS/SMM; 3 plasmacytoma) 3 (3 MGUS/SMM) 3 (2 MGUS/SMM; 1 plasmacytoma) 3 (1 MGUS/SMM; 2 plasmacytoma)
MDE at presentation Bone, 8 Anemia, 1 Bone, 10 Anemia, 1 Bone, 3 Anemia, 1 Hypercalcemia, 1 Bone, 7 Anemia, 1
Molecular classification, N Trisomies, 5 t(11;14) 1t(11;14) plus trisomy, 1Isolated del 13, 1Normal/insufficient, 1 Trisomies, 6t(11;14), 1 Not done, 4 Trisomies, 3 Normal/insufficient, 1 Not done, 1 Trisomies, 4 Isolated del 13, 2 Normal/insufficient, 2
Best response to therapy CR, 7 VGPR, 2 CR, 9 VGPR, 1 PR, 1 CR, 2 VGPR, 2 PR, 1 CR, 7 PR, 1

Abbreviations: CR, complete response; MDE, myeloma defining event; MGUS, monoclonal gammopathy of undetermined significance; Rd, lenalidomide–dexamethasone; SCT, stem cell transplantation; SMM, smoldering multiple myeloma.