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. 2008 Aug 14;113(25):6330–6337. doi: 10.1182/blood-2008-04-151860

Table 2.

Univariate analysis of outcome by therapy and CD20 status in de novo precursor B cell ALL: pre-rituximab era

Parameter CD20 negative (N = 133) P* CD20 positive (N = 120) P* P**
No. (%) CR
    All 111 (84) 107 (89) NS
    VAD/CVAD 38 of 56 (68) < .001 45 of 54 (83) .06 .06
    Hyper-CVAD 73 of 77 (95) 62 of 66 (94) NS
No. (%) relapse
    All 47 of 111 (42) 70 of 107 (65)
    VAD/CVAD 20 of 38 (53) .01 32 of 45 (71) .02 .08
    Hyper-CVAD 27 of 73 (37) .01 38 of 62 (61) .005
Percent 3-year remission duration
    All 55 20 < .001
    VAD/CVAD 42 0.04 18 NS NS
    Hyper-CVAD 58 22 < .001
Percent 3-year overall survival
    All 40 27 .03
    VAD/CVAD 28 < .001 26 NS NS
    Hyper-CVAD 60 27 .003

CR, complete remission; VAD, vincristine, Adriamycin, dexamethasone; CVAD, cyclophosphamide, VAD; hyper-CVAD, hyper-fractionated cyclophosphamide, vincristine, Adriamycin, dexamethasone.

*

P values represent significance levels of comparison of VAD/CVAD vs hyper-CVAD with CD20 subsets.

**

P values in final column represent significance levels of comparison of CD20 negative versus CD positive with each subset.