scholarly journals Folinic Acid Rescue Increases Ability to Deliver Full Course of Methotrexate GVHD Prophylaxis for Pediatric HSCT Recipients

2011 ◽  
Vol 17 (2) ◽  
pp. S262
Author(s):  
M. Hudspeth ◽  
T. Heath ◽  
C. Chiuzan ◽  
E. Garrett-Mayer ◽  
E. Nista ◽  
...  
Author(s):  
Riitta Niinimäki ◽  
Henri Aarnivala ◽  
Joanna Banerjee ◽  
Tytti Pokka ◽  
Kaisa Vepsäläinen ◽  
...  

Abstract Purpose Low doses of folinic acid (FA) rescue after high-dose methotrexate (HD-MTX) have been associated with increased toxicity, whereas high doses may be related to a decreased antileukemic effect. The optimal dosage and duration of FA rescue remain controversial. This study was designed to investigate, whether a shorter duration of FA rescue in the setting of rapid HD-MTX clearance is associated with increased toxicity. Methods We reviewed the files of 44 children receiving a total of 350 HD-MTX courses during treatment for acute lymphoblastic leukemia according to the NOPHO ALL-2000 protocol. Following a 5 g/m2 HD-MTX infusion, pharmacokinetically guided FA rescue commenced at hour 42. As per local guidelines, the patients received only one or two 15 mg/m2 doses of FA in the case of rapid MTX clearance (serum MTX ≤ 0.2 μmol/L at hour 42 or hour 48, respectively). Data on MTX clearance, FA dosing, inpatient time, and toxicities were collected. Results Rapid MTX clearance was observed in 181 courses (51.7%). There was no difference in the steady-state MTX concentration, nephrotoxicity, hepatotoxicity, neutropenic fever, or neurotoxicity between courses followed by rapid MTX clearance and those without. One or two doses of FA after rapid MTX clearance resulted in a 7.8-h shorter inpatient time than if a minimum of three doses of FA would have been given. Conclusion A pharmacokinetically guided FA rescue of one or two 15 mg/m2 doses of FA following HD-MTX courses with rapid MTX clearance results in a shorter hospitalization without an increase in toxic effects.


1989 ◽  
Vol 59 (4) ◽  
pp. 627-630 ◽  
Author(s):  
A Thyss ◽  
G Milano ◽  
MC Etienne ◽  
P Paquis ◽  
JL Roche ◽  
...  

Author(s):  
Juliana Gomes Poli ◽  
Gabriela Paiva ◽  
Fernanda Freitas ◽  
Paulo Mora ◽  
Luis Guillermo Coca Velarde ◽  
...  

1978 ◽  
Vol 16 (6) ◽  
pp. 24-24

Folic acid injection (15 mg/ml) can still be obtained, but only direct from the manufacturers, The Boots Company Limited.


2020 ◽  
Vol 4 (16) ◽  
pp. 3822-3828
Author(s):  
Moshe Yeshurun ◽  
Uri Rozovski ◽  
Oren Pasvolsky ◽  
Ofir Wolach ◽  
Ron Ram ◽  
...  

Abstract The use of methotrexate (MTX) for graft-versus-host disease (GVHD) prophylaxis is associated with increased rates of organ-specific toxicities. Despite limited data, the European Society for Blood and Marrow Transplantation-European LeukemiaNet working group recommend the use of folinic acid (FA) rescue to reduce MTX toxicity after allogeneic hematopoietic cell transplantation (allo-HCT). In a multicenter, double-blind, randomized, controlled trial, we explored whether FA rescue reduces MTX-induced toxicity. We enrolled patients undergoing allo-HCT with myeloablative conditioning with peripheral blood stem cell grafts, with GVHD prophylaxis consisting of cyclosporine and MTX. Patients were randomized to receive FA or placebo starting 24 hours after each MTX dose and continuing over 24 hours in 3 to 4 divided doses. The primary end point was the rate of grades 3 and 4 oral mucositis. After enrollment of 52 patients (FA, n = 28; placebo, n = 24), preplanned interim analysis revealed similar rates of grade 3 and 4 (46.6% vs 45.8%; P = .97) and grades 1 to 4 (83.3% vs 77.8%; P = .65) oral mucositis. With a median follow-up of 17 (range, 4.5-50) months, there was no difference in the rates of acute and chronic GVHD, disease relapse, nonrelapse mortality, and overall survival. These interim results did not support continuation of the study. We conclude that FA rescue after MTX GVHD prophylaxis does not decrease regimen-related toxicity or affect transplantation outcomes. This study was registered at clinicaltrials.gov as #NCT02506231.


2007 ◽  
Vol 88 (7) ◽  
pp. 780-782 ◽  
Author(s):  
L Riva ◽  
V Conter ◽  
C Rizzari ◽  
M Jankovic ◽  
A Sala ◽  
...  

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