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. 2021 Apr 15;11:631594. doi: 10.3389/fonc.2021.631594

Table 1.

Clinical characteristics of six infants with KMT2A-rearranged acute lymphoblastic leukemia and corresponding cell lines.

Patient ID Sex Age (days) at diagnosis WBC at presentation (×109/L) CNS status at diagnosis Upfront therapy Relapse Time (months) from diagnosis to relapse Relapse therapy Outcome Corresponding cell line*
P272 Female 336 317.0 CNS1 CCG 1883 BM 3 CCG 1008 Died of Disease;
OS 5 months
PER-494
PER-485 (Relapse)
P287 Female 9 111.8 CNS2 CCG 1883 BM 3 CCG 0922 Died of Disease;
OS 4 months
PER-490
P337 Female 82 564.0 CNS2 CCG 1901 → HSCT BM 16 CCG 1882 → HSCT2 Alive without disease;
26 years of age at last follow-up
PER-784
PER-826
P399 Female 66 670.0 CNS1 CCG 1953 No _ _ Alive without disease; 24 years of age at last follow-up PER-785
P810 Female 52 102.0 CNS2 COG P9407 → HSCT No _ _ Died from hepatic sinusoidal obstruction syndrome post HSCT; OS 4 months PER-703
P899 Male 365 156.6 CNS1 COG AALL0631 No _ _ Alive without disease;
6 years of age at last follow-up
PER-910

*All cell lines were derived at diagnosis except for PER-485 which was derived at first relapse.

BM, Bone Marrow; CCG, Children’s Cancer Group; COG, Children’s Oncology Group; CNS, Central Nervous System; OS, Overall Survival; WBC, White Blood Cell.