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. 2019 May 27;85(7):1585–1597. doi: 10.1111/bcp.13943

Table 1.

Patient characteristics (139 paediatric patients with acute lymphoblastic leukaemia)

Sex, n (%)
Male 64 (46)
Female 75 (54)
Age, median (IQR), years 5.1 (3.7–10.6)
Follow‐up period, median (IQR), years 5.9 (3.6–7.9)
Body weight, median (IQR), kg 19.4 (15.2–37.5)
Body surface area, median (IQR), m2 0.79 (0.66–1.19)
Diagnosis
B‐lymphoblastic leukaemia, n (%) 131 (94)
T‐lymphoblastic leukaemia, n (%) 8 (6)
Risk group
Standard risk, n (%) 86 (62)
High risk, n (%) 53 (38)
Number of thiopurine metabolite measurements per patient, median (range) 7 (1–14)
6‐MP daily dose, median (IQR), mg m−2 per day 30.1 (22.2–38.9)
6‐TGN level, median (IQR), pmol per 8 × 108 RBCs 388.5 (301.1–555.2)
6‐MeMPN level, median (IQR), pmol per 8 × 108 RBCs 5089.0 (2064.2–9363.7)
6‐MeMPN/6‐TGN ratio, median (IQR) 13.9 (5.2–23.5)
6‐TGN/6‐MP dose ratio, median (IQR) 12.8 (9.3–18.1)
TPMT genotype, n (%)
*1/*1 133 (96)
*1/*3C 2 (1)
*1/*6 2 (1)
*1/*32 1 (1)
*1/? (c.532T>C) (novel allele) 1 (1)
Toxicity, n (%)a
Leukopenia (WBC < 1.5 x 109 L−1) 38 (27)
Neutropenia (ANC < 0.5 x 109 L−1) 40 (29)
Hepatotoxicity 64 (46)
Treatment interruption, n (%) 114 (82)

Abbreviations: ANC, absolute neutrophil count; IQR, interquartile range; WBC, white blood cell.

a

Any toxicity experienced during the follow‐up period.