Table 3.
Outcome for Adults With De Novo Philadelphia Chromosome–Negative Precursor B-Lineage Acute Lymphoblastic Leukemia by Pretreatment Characteristics (n = 282)
| Characteristic | No. | % | % CR | P (χ2) | % CRD |
P | % OS |
P (χ2) | ||
|---|---|---|---|---|---|---|---|---|---|---|
| 3 Year | 5 Year | 3 Year | 5 Year | |||||||
| Age, years | ||||||||||
| Overall | 282 | 95 | — | 60 | 50 | — | 58 | 50 | — | |
| ≤ 30 | 96 | 34 | 99 | .02 | 63 | 50 | NS | 70 | 64 | < .001 |
| 31-59 | 128 | 45 | 98 | 66 | 55 | 60 | 50 | |||
| ≥ 60 | 58 | 21 | 88 | 53 | 47 | 29 | 21 | |||
| Sex | ||||||||||
| Male | 282 | 57 | 96 | NS | 57 | 60 | .1 | 57 | 48 | NS |
| Female | 120 | 43 | 96 | 69 | 45 | 57 | 50 | |||
| Performance status | ||||||||||
| 0-1 | 219 | 78 | 96 | NS | 65 | 55 | .04 | 60 | 50 | NS |
| 2-3 | 63 | 22 | 97 | 50 | 40 | 50 | 44 | |||
| Leukocyte count, ×109/L | ||||||||||
| < 5 | 142 | 50 | 96 | NS | 65 | 54 | < .001 | 60 | 49 | < .01 |
| 5-29.9 | 91 | 32 | 98 | 65 | 54 | 64 | 54 | |||
| ≥ 30 | 49 | 17 | 94 | 47 | 44 | 42 | 35 | |||
| Hemoglobin, g/dL | ||||||||||
| < 10 | 219 | 78 | 97 | NS | 60 | 62 | NS | 55 | 45 | NS |
| ≥ 10 | 63 | 22 | 94 | 67 | 48 | 59 | 55 | |||
| Platelet count, ×109/L | ||||||||||
| < 100 | 214 | 76 | 95 | NS | 60 | 48 | .03 | 53 | 43 | < .01 |
| ≥ 100 | 68 | 24 | 98 | 68 | 61 | 69 | 67 | |||
| Serum creatinine, mg/dL | ||||||||||
| < 1.3 | 252 | 89 | 97 | < .01 | 64 | 54 | .06 | 60 | 56 | < .01 |
| ≥ 1.3 | 30 | 11 | 87 | 51 | 35 | 43 | 25 | |||
| Serum bilirubin, mg/dL | ||||||||||
| < 1.3 | 254 | 91 | 96 | NS | 64 | 50 | NS | 59 | 50 | NS |
| ≥ 1.3 | 27 | 10 | 93 | 45 | 45 | 46 | 41 | |||
| Serum albumin, g/dL | ||||||||||
| < 3 | 232 | 83 | 94 | NS | 42 | 39 | .01 | 45 | 40 | .04 |
| ≥ 3 | 49 | 17 | 97 | 65 | 53 | 60 | 50 | |||
| β–2 microglobulin, mg/dL (n = 232) | ||||||||||
| < 3 | 128 | 55 | 98 | NS | 70 | 55 | NS | 65 | 55 | .05 |
| ≥ 3 | 104 | 45 | 95 | 53 | 55 | 52 | 46 | |||
| Lactate dehydrogenase, U/L | ||||||||||
| < 1,400 | 161 | 57 | 95 | NS | 60 | 48 | NS | 57 | 50 | NS |
| ≥ 1,400 | 121 | 43 | 98 | 60 | 52 | 57 | 48 | |||
| Systemic risk classification | ||||||||||
| Low | 81 | 29 | 99 | NS | 64 | 52 | NS | 72 | 65 | < .001 |
| High | 200 | 71 | 95 | 63 | 50 | 51 | 43 | |||
| Karyotype (n = 275) | ||||||||||
| Diploid | 113 | 40 | 96 | NS | 68 | 55 | NS | 60 | 50 | .06 |
| Hyperdiploid | 29 | 10 | 97 | 75 | 75 | 65 | 65 | |||
| Hypodiploid | 14 | 5 | 100 | 48 | 39 | 55 | 42 | |||
| t(1;19) | 8 | 3 | 100 | 85 | 68 | 62 | 62 | |||
| del 9p | 13 | 5 | 92 | 67 | 45 | 69 | 61 | |||
| t(4;11), t(11;19), 11q | 18 | 6 | 94 | 14 | 14 | 20 | 10 | |||
| Other | 44 | 16 | 93 | 64 | 56 | 59 | 48 | |||
| Insufficient metaphases | 36 | 13 | 94 | 49 | 39 | 50 | 42 | |||
| CD20 expression | ||||||||||
| Positive | 150 | 53 | 94 | NS | 53 | 48 | .002* | 60 | 52 | NS |
| Without rituximab | 55 | 93 | 40 | 40 | 45 | 39 | ||||
| With rituximab | 95 | 96 | 67 | 53 | 61 | 49 | ||||
| Negative | 132 | 47 | 96 | 69 | 52 | 54 | 46 | |||
| Myeloid marker expression (n = 269) | ||||||||||
| Positive | 125 | 46 | 94 | NS | 64 | 50 | NS | 55 | 45 | NS |
| Negative | 144 | 54 | 97 | 53 | 50 | 57 | 52 | |||
| Regimen | ||||||||||
| Hyper-CVAD | 109 | 39 | 96 | NS | 53 | 46 | < .01 | 55 | 49 | NS |
| Modified hyper-CVAD 1 | 47 | 17 | 99 | 54 | 44 | 55 | 44 | |||
| Modified hyper-CVAD 2 | 126 | 45 | 94 | 78 | 56 | 60 | 50 | |||
Abbreviations: CRD, complete remission duration; OS, overall survival; CR, complete remission; NS, not significant; Systemic risk classification: High risk, WBC > 5 × 109/L, > 1 course to CR, Philadelphia chromosome or CNS disease; Low risk, none of these features; Hyper-CVAD, fractionated cyclophosphamide, vincristine, doxorubicin, dexamethasone; Modified hyper-CVAD 1, anthracycline intensification with or without rituximab; Modified hyper-CVAD 2, no anthracycline intensification with or without rituximab.
P value represents comparison with or without rituximab within the CD20-positive group. No differences in rates of CR, CRD, or OS by French-American-British subtype; presence or absence of peripheral blasts; CNS disease at presentation; CNS risk classification; or presence or absence of lymphadenopathy, splenomegaly, and/or hepatomegaly.