Table 3 Impact of cytogenetics on time and site of relapse, and overall survival post relapse among non-infant B-ALL patients.
Cytogeneticsa | No. of patients | No. of relapses (%) | 5-yr from diagnosis EFS ± SE | Median time-to-relapse (months) | iBM relapse N (%) | Any BM relapse N (%) | iCNS relapse N (%) | Any CNS relapse N (%) | 5-yr post relapse OS ± SE |
---|---|---|---|---|---|---|---|---|---|
Trisomy 4 + 10 | 2677 | 178 (6.6%) | 92.6 ± 0.5% | 43.3 | 108 (60.7%) | 134 (75.3%) | 31 (17.4%) | 52 (29.2%) | 70.2 ± 3.6% |
ETV6::RUNX1 | 2555 | 213 (8.3%) | 91.7 ± 0.6% | 43.0 | 111 (52.1%) | 151 (70.9%) | 48 (22.5%) | 77 (36.2%) | 74.4 ± 3.1% |
KMT2A-R | 195 | 39 (20.0%) | 70.2 ± 3.4% | 18.0 | 23 (59.0%) | 26 (66.7%) | 6 (15.4%) | 7 (17.9%) | 31.9 ± 7.7% |
TCF3::PBX1 | 414 | 57 (13.8%) | 83.1 ± 1.9% | 15.8 | 28 (49.1%) | 31 (54.4%) | 22 (38.6%) | 25 (43.9%) | 36.8 ± 6.6% |
iAMP21 | 163 | 50 (30.7%) | 68.5 ± 3.7% | 43.6 | 31 (62.0%) | 41 (82.0%) | 8 (16.0%) | 18 (36.0%) | 48.2 ± 7.7% |
BCR::ABL1 | 258 | 65 (25.2%) | 52.4 ± 3.7% | 35.3 | 52 (80.0%) | 55 (84.6%) | 8 (12.3%) | 10 (15.4%) | 47.2 ± 6.6% |
Hypodiploid | 178 | 36 (20.2%) | 56.6 ± 4.1% | 12.5 | 33 (91.7%) | 34 (94.4%) | 1 (2.8%) | 2 (5.6%) | 14.2 ± 6.1% |
B-ALL, other | 3654 | 669 (18.3%) | 77.3 ± 0.7% | 32.5 | 377 (56.4%) | 472 (70.6%) | 161 (24.1%) | 246 (36.8%) | 48.2 ± 2.0% |