Τόμος 20 (2006) – Τεύχος 2 – Άρθρο 105 – Επιθεώρηση Κλινικής Φαρμακολογίας και Φαρμακοκινητικής-Διεθνής Έκδοση – Volume 20 (2006) – Issue 2 – Article 105 – Epitheorese Klinikes Farmakologias και Farmakokinetikes-International Edition

Title High dose methotrexate therapy of childhood acute lymphoblastic leukaemia:  incidence of nephrotoxicity and glomerular dysfunction
Authors Aggeliki Theodoridou, Fani Athanassiadou-Piperopoulou, Theodotis  Papageorgiou, Magdalini Gatzola-Karaveli and Areti Makedou-Hitoglou

2nd Pediatric Clinic of Aristotle University of Thessaloniki, Department of Pediatric Hematology and Oncology, AHEPA Hospital

Citation Theodoridou, A., Athanassiadou-Piperopoulou, F., Papageorgiou, Th., Gatzola-Karaveli, M., Makedou-Hitoglou, A.: High dose methotrexate therapy of childhood acute lymphoblastic leukaemia:  incidence of nephrotoxicity and glomerular dysfunction, Epitheorese Klin. Farmakol. Farmakokinet. 20(2): 332-334 (2006)
Publication Date Accepted for publication: 19-20 May 2006
Full Text Language English
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Keywords Methotrexate, high dose methotrexate, acute lymphoblastic leukemia, nephrotoxicity, glomerular function.
Other Terms review article
Summary High-dose methotrexate (HDMTX) is used in the treatment of children with acute lymphoblastic leukemia (ALL) during the consolidation phase. Renal dysfunction is considered among the side effects following MTX therapy. The aim of the study was to evaluate the incidence of nephrotoxicity due to HDMTX in children with ALL and to clarify whether glomerular dysfunction is involved. In the sixteen patients included in the study, no serious renal dysfunction occurred. The increase in serum creatinine (sCr) 1 and 2 days after the start of HDMTX infusion was mild and transient and sCr returned to base-line values 7 days after administration of the drug. The mean value of GFR at the end of HDMTX administration decreased significantly compared to the prior to the infusion value (118.15±32.59 vs. 142.93±23.7, p<0.01), but still remained within normal range. No relation was observed between sMTX concentrations and GFR. A de- creased GFR was not associated with an increase in sMTX levels at 24, 42 and 48 hours after HDMTX infusion. Severe renal dysfunction after HDMTX infusion in children with ALL is a very rare complication. HDMTX therapeutic procedures may have a high level of patient safety when exact consideration is given to support therapy.
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