Table 1

Baseline patient characteristics and clinical responses (n = 15)

PatientAge, yStage/subtypePrior therapy no./typeClinical responseTTR, wkDOR, wkTTP, wk
Single immunization procedure        
    1 60 IIB 3/TS, RT, UVB SD n/a n/a 19.4 
    2 61 IIB 6/NM, UVB, PUVA + bex, bex, anti-CD4 PR 7.9 12.4 20.3 
    3 34 IIB 6/TS, TSEBT, NM, bex, bex + IFN, b-gel SD n/a n/a n/a (EOS week 10.6) 
    4 61 IB 9/TS, UVB, PUVA, bex, NM, anti-CD4, RT, b-gel, forodesine SD n/a n/a n/a (EOS week 28.9) 
    5 65 IIB 5/TS, TSEBT, NM, bex, b-gel PR 7.3 7.0 n/a (EOS week 14.3) 
    6 60 IIB/LCT 7/TS, TSEBT, NM, PUVA, b-gel, anti-CD4, RT PD n/a n/a 11.4 
    7 38 IB 2/NM + TS, UVB SD n/a n/a n/a (EOS week 17.0) 
Dual immunization procedure        
    8 69 IIB/LCT 8/TSEBT, IFN, TS, bex, chlorambucil, MTX, RT, gem, comb chemo PD n/a n/a 4.0 
    9 71 IB 3/TS, UVB, NM PR 12.0 6.1 n/a (EOS week 18.1) 
    10 47 IIB/FMF 5/TS, RT, bex, MTX, IFN PD n/a n/a 2.4 
    11 57 IB/FMF 3/UVB, TS, bex PR 11.1 6.0 n/a (EOS week 17.1) 
    12 38 IIB/GMF 3/RT, UVB, TS PR 7.1 37.0 n/a (EOS week 44.1) 
    13 55 IIB 2/TS, UVB SD n/a n/a n/a (EOS week 2; grade 3 injection-site reaction) 
    14 46 IB 2/TS, NM SD n/a n/a 15.1 
    15 18 IIB 5/NM, TS, bex, UVB, RT SD n/a n/a n/a (EOS week 15.0) 
PatientAge, yStage/subtypePrior therapy no./typeClinical responseTTR, wkDOR, wkTTP, wk
Single immunization procedure        
    1 60 IIB 3/TS, RT, UVB SD n/a n/a 19.4 
    2 61 IIB 6/NM, UVB, PUVA + bex, bex, anti-CD4 PR 7.9 12.4 20.3 
    3 34 IIB 6/TS, TSEBT, NM, bex, bex + IFN, b-gel SD n/a n/a n/a (EOS week 10.6) 
    4 61 IB 9/TS, UVB, PUVA, bex, NM, anti-CD4, RT, b-gel, forodesine SD n/a n/a n/a (EOS week 28.9) 
    5 65 IIB 5/TS, TSEBT, NM, bex, b-gel PR 7.3 7.0 n/a (EOS week 14.3) 
    6 60 IIB/LCT 7/TS, TSEBT, NM, PUVA, b-gel, anti-CD4, RT PD n/a n/a 11.4 
    7 38 IB 2/NM + TS, UVB SD n/a n/a n/a (EOS week 17.0) 
Dual immunization procedure        
    8 69 IIB/LCT 8/TSEBT, IFN, TS, bex, chlorambucil, MTX, RT, gem, comb chemo PD n/a n/a 4.0 
    9 71 IB 3/TS, UVB, NM PR 12.0 6.1 n/a (EOS week 18.1) 
    10 47 IIB/FMF 5/TS, RT, bex, MTX, IFN PD n/a n/a 2.4 
    11 57 IB/FMF 3/UVB, TS, bex PR 11.1 6.0 n/a (EOS week 17.1) 
    12 38 IIB/GMF 3/RT, UVB, TS PR 7.1 37.0 n/a (EOS week 44.1) 
    13 55 IIB 2/TS, UVB SD n/a n/a n/a (EOS week 2; grade 3 injection-site reaction) 
    14 46 IB 2/TS, NM SD n/a n/a 15.1 
    15 18 IIB 5/NM, TS, bex, UVB, RT SD n/a n/a n/a (EOS week 15.0) 

FMF indicates folliculotropic MF; LCT, large cell transformation; GMF, granulomatous MF; TS, topical steroid; UVB, ultraviolet light B therapy; NM, topical nitrogen mustard/mechlorethamine; PUVA, ultraviolet light A with oral psoralen; bex, oral bexarotene; anti-CD4, fully human anti-CD4 monoclonal antibody; TSEBT, total skin electron beam therapy; b-gel, topical bexarotene gel; forodesine, purine nucleoside phosphorylase inhibitor; MTX, methotrexate; gem, gemcitabine; TTP time to progression; n/a, not applicable; EOS, end of study–withdrawal of consent to initiate MF therapy due to worsening symptoms without documented progressive disease; RT, radiation therapy; comb chemo, combination chemotherapy; and n/a, not applicable.

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