TY - JOUR
T1 - Individualized toxicity-titrated 6-mercaptopurine increments during high-dose methotrexate consolidation treatment of lower risk childhood acute lymphoblastic leukemia
T2 - A Nordic Society of Paediatric Haematology and Oncology (NOPHO) pilot study
AU - Frandsen, Thomas Leth
AU - Abrahamsson, Jonas
AU - Lausen, Birgitte Frederiksen
AU - Vettenranta, Kim
AU - Heyman, Mats
AU - Behrentz, Michael
AU - Castor, Anders
AU - Wehner, Peder Skov
AU - Frost, Britt-marie
AU - Andersen, Elisabeth Anne Wreford
AU - Schmiegelow, Kjeld
PY - 2011/10
Y1 - 2011/10
N2 - This study explored the feasibility and toxicity of individualized toxicity-titrated 6-mercaptopurine (6MP) dose increments during post-remission treatment with High-dose methotrexate (HDM) (5000 mg/m2, ×3) in 38 patients with Childhood (ALL). Patients were increased in steps of 25 mg 6MP/m2 per day if they did not develop myelotoxicity within 2 weeks after HDM. 6MP could be increased in 31 patients (81%). Toxicity was acceptable and did not differ significantly between groups. Patients receiving 75 mg/m2 per day had significantly shorter duration of treatment interruptions of 6MP than the remaining patients (P = 0·03). This study shows individualized toxicity-titrated 6MP dosing during consolidation is feasible without increased risk of toxicity.
AB - This study explored the feasibility and toxicity of individualized toxicity-titrated 6-mercaptopurine (6MP) dose increments during post-remission treatment with High-dose methotrexate (HDM) (5000 mg/m2, ×3) in 38 patients with Childhood (ALL). Patients were increased in steps of 25 mg 6MP/m2 per day if they did not develop myelotoxicity within 2 weeks after HDM. 6MP could be increased in 31 patients (81%). Toxicity was acceptable and did not differ significantly between groups. Patients receiving 75 mg/m2 per day had significantly shorter duration of treatment interruptions of 6MP than the remaining patients (P = 0·03). This study shows individualized toxicity-titrated 6MP dosing during consolidation is feasible without increased risk of toxicity.
U2 - 10.1111/j.1365-2141.2011.08835.x
DO - 10.1111/j.1365-2141.2011.08835.x
M3 - Journal article
C2 - 21848519
SN - 0007-1048
VL - 155
SP - 244
EP - 247
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 2
ER -