TY - JOUR
T1 - Effect of azole antifungal therapy on vincristine toxicity in childhood acute lymphoblastic leukaemia
AU - van Schie, Rosalin M.
AU - Brüggemann, Roger J.M.
AU - Hoogerbrugge, Peter M.
AU - te Loo, D. M.W.M.
N1 - Funding Information:
This work was supported by the Department of Pediatric Hemato-Oncology, Radboud University Nijmegen-Medical Centre, Nijmegen, the Netherlands.
PY - 2011/8
Y1 - 2011/8
N2 - Background: Vincristine is one of the cornerstones of the treatment of children with acute lymphoblastic leukaemia (ALL). Constipation, and peripheral and central neurotoxicities are the most common side effects. A comparative study exploring vincristine toxicity in individual patients receiving vincristine with and without azoles, however, is lacking. Methods: In total, 20 paediatric patients with de novo ALL were included. In each patient, vincristine toxicity in the period with and without azole co-medication was retrospectively graded according to the US National Cancer Institute toxicity scale. Statistical analysis was performed using the Wilcoxon signed rank test and McNemar's test. Results: Patients receiving vincristine in combination with azole treatment experienced significantly more constipation and peripheral neurotoxicity (P=0.001 and P<0.001, respectively). Vincristine-induced CNS toxicity was only seen in patients (30%) receiving vincristine in combination with azole treatment. Conclusions: Vincristine toxicity is significantly enhanced when combined with azole treatment and can even be life threatening. Therefore, we advise avoidance of the combination of azole and vincristine treatments in patients with ALL.
AB - Background: Vincristine is one of the cornerstones of the treatment of children with acute lymphoblastic leukaemia (ALL). Constipation, and peripheral and central neurotoxicities are the most common side effects. A comparative study exploring vincristine toxicity in individual patients receiving vincristine with and without azoles, however, is lacking. Methods: In total, 20 paediatric patients with de novo ALL were included. In each patient, vincristine toxicity in the period with and without azole co-medication was retrospectively graded according to the US National Cancer Institute toxicity scale. Statistical analysis was performed using the Wilcoxon signed rank test and McNemar's test. Results: Patients receiving vincristine in combination with azole treatment experienced significantly more constipation and peripheral neurotoxicity (P=0.001 and P<0.001, respectively). Vincristine-induced CNS toxicity was only seen in patients (30%) receiving vincristine in combination with azole treatment. Conclusions: Vincristine toxicity is significantly enhanced when combined with azole treatment and can even be life threatening. Therefore, we advise avoidance of the combination of azole and vincristine treatments in patients with ALL.
KW - Anticancer agents
KW - Children
KW - Clinical pharmacology
UR - http://www.scopus.com/inward/record.url?scp=79960452198&partnerID=8YFLogxK
U2 - 10.1093/jac/dkr223
DO - 10.1093/jac/dkr223
M3 - Article
C2 - 21652620
AN - SCOPUS:79960452198
SN - 0305-7453
VL - 66
SP - 1853
EP - 1856
JO - Journal of Antimicrobial Chemotherapy
JF - Journal of Antimicrobial Chemotherapy
IS - 8
M1 - dkr223
ER -