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. Author manuscript; available in PMC: 2015 Nov 1.
Published in final edited form as: Cancer Chemother Pharmacol. 2014 Oct 28;75(1):59–66. doi: 10.1007/s00280-014-2613-7

Table 1. Patient characteristics and event rate in relation to thiopurine methyltransferase activity.

High activity Intermediate activity P
Patient distribution
 No. of patients 362 49
 Male/female 192/170 28/21 0.59
 Standard risk/Intermediate risk 200/162 24/25 0.41
 Pharmacologyb/control groupc 176/186 27/22 0.39
Median (50 % range)
 Age at diagnosis, years 4.0 (2.9-6.0) 4.5 (3.2-6.4) 0.11
 WBC at diagnosis, × 109/L 6.0 (3.0-13.0) 5.0 (2.0-11.5) 0.46
Survival outcomes
 Dead in CR1 2 0
 SMN 2 2
 Relapse 54 4
 pEFS at 15 years (± SE) 83.8 (2.0) 87.4 (4.8) 0.47
a

Patients were classified as TPMT high activity if TPMT was >14 IU/ml and TPMT intermediate activity if TPMT was <14 IU/ml. Patients with TPMT deficiency (n=2) were excluded from the study.

b

Pharmacology group had dose adjustments by red blood cell levels of MTX and 6MP metabolites in addition to dose adjustments by toxicity.

c

Control group, see text and Schmiegelow et al., 2003.

Dead in CR1, dead in first complete remission; SMN, second malignant neoplasm; pEFS, probability of event-free survival; SE, standard error.