Abstract

In the first part of this study the availability of folinic acid (FA) and its main active circulating metabolite, 5-methyltetrahydrofolate (5-MTHF), were studied in plasma and cerebrospinal fluid (CSF) from normal subjects after i.v. administration of 100 and 250 mg of FA. 5-MTHF rapidly appeared in plasma, the maximum value being reached at the first observation time point (1 h). FA was eliminated in plasma more slowly than 5-MTHF. Between the two doses, there was no evidence of modification in pharmacokinetic parameters (terminal half-life, clearance) for either FA or 5-MTHF in plasma and CSF; 5-MTHF was the only product detectable in CSF. Considering FA plus 5-MTHF together, the AUC (area under the curve) ratios between CSF and plasma were close to 1%. 5-MTHF was cleared very slowly from CSF (t 1/2 = 85 h). This finding suggested possible accumulation of 5-MTHF in CSF during repeated administration of FA combined with medium or high dose MTX. In the second part of the study, dealing with a group of eight children treated by such protocols, an increase in CSF 5-MTHF was detected from cycle to cycle in five (r = 0.91, P less than 0.01) with a maximum at 5 x 10(-8) M. This progressive accumulation of 5-MTHF in CSF may have a negative effect on the local action of MTX and should be taken into account for therapeutic strategies designed for the management of meningeal leukaemia.

Highlights

  • Ratios between cerebrospinal fluid (CSF) and plasma were close to 1%. 5-MTHF was cleared very slowly from CSF (t1/2 = 85 h)

  • In the second part of the study, dealing with a group of eight children treated by such protocols, an increase in CSF 5-MTHF was detected from cycle to cycle in five (r=0.91, P

  • This progressive accumulation of 5-MTHF in CSF may have a negative effect on the local action of MTX and should be taken into account for therapeutic strategies designed for the management of meningeal leukaemia

Read more

Summary

Methods

Each patient received a specific dose of FA; samples (concomitant blood and CSF) were obtained at fixed times after FA injection: 1, 2, 6, 12 and 24 h. The other group (G2) was the patients group It consisted of eight patients (six males and two females) with acute lymphocytic leukaemia, mean age 5 years (2-9), without signs of meningeal disease. They were treated by MTX (2.5 gm-2) and FA rescue according to the EORTC Children's Leukaemia Cooperative group protocol which follows the general guidelines of the BFM protocol (Riehm et al, 1980). CSF samples were obtained 8 h after the beginning of the 24-h administration of MTX and just before injection of the intrathecal MTX dose.

Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call