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. 2010 Apr 12;116(5):679–686. doi: 10.1182/blood-2010-02-268862

Table 5.

Percentages of patients achieving a best response of VGPR or better to lenalidomide-bortezomib-dexamethasone and estimated 18-month PFS rates after lenalidomide-bortezomib-dexamethasone with/without ASCT, according to disease stage, baseline β2-microglobulin, baseline albumin, and presence of baseline cytogenetic abnormalities

Characteristic/value n Response of VGPR or better, n (%) Estimated 18-month PFS, % (95% CI)
Baseline characteristic
    ISS disease stage
        I 29 21 (72) 89 (70-96)
        II/III 37 23 (62) 65 (47-78)
    Durie-Salmon disease stage
        I 22 12 (55) 82 (59-93)
        II/III 44 32 (73) 72 (56-83)
    β2-microglobulin, mg/L
        < 3.5 44 32 (73) 77 (61-87)
        ≥ 3.5 22 12 (55) 73 (49-87)
    Albumin, g/dL
        < 3.5 24 17 (71) 63 (40-78)
        ≥ 3.5 42 27 (64) 83 (67-91)
Cytogenetics present
    Abnormal metaphase cytogenetics
        Yes 6 5 (83) 83 (27-97)
        No 60 39 (65) 75 (62-84)
    Del 13/13q by FISH
        Yes 24 18 (75) 79 (57-91)
        No 27 16 (59) 65 (43-80)
    Del 17p by FISH
        Yes 5 3 (60) 100
        No 45 30 (67) 68 (52-80)
    t(4;14) by FISH
        Yes 2 2 (100) 100
        No 39 24 (62) 63 (46-77)
    t(11;14) by FISH
        Yes 11 7 (64) 73 (37-90)
        No 40 28 (70) 72 (55-83)
    Del 17p and/or t(4;14) by FISH
        Yes 6 4 (67) 100
        No 44 29 (66) 68 (51-79)

FISH indicates fluorescence in situ hybridization; ISS, International Staging System; PFS, progression-free survival after lenalidomide-bortezomib-dexamethasone with/without transplantation; and VGPR, very good partial response.

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