Source:http://linkedlifedata.com/resource/pubmed/id/17170721
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
2007-1-25
|
pubmed:abstractText |
The objective of the study was to assess acute neurotoxicity associated with triple intrathecal therapy (TIT)+/-high-dose methotrexate (HD MTX) in children with acute lymphoblastic leukemia (ALL). 1395 children were enrolled on FRALLE 93 protocol from 1993 to 1999. Lower-risk group (LR, n=182) were randomized to weekly low-dose MTX at 25 mg/m(2)/week (LD MTX, n=81) or HD MTX at 1.5 g/m(2)/2 weeks x 6 (n=77). Intermediate-risk group (IR, n=672) were randomized to LD MTX (n=290) or HD MTX at 8 g/m(2)/2 weeks x 4 (n=316). Higher-risk group (HR, n=541) prednisone-responder patients received LD MTX and cranial radiotherapy. HR group steroid resistant cases were grafted (autologous or allogenic). TIT (MTX, cytarabine and methylprednisolone) was given every 2 weeks during 16-18 weeks and every 3 months during maintenance therapy in LR and IR patients. 52 patients (3.7%) developed neurotoxicity. Isolated seizures: n=15 (1.1%), peripheral and spinal neuropathy: n=17 (1.2%) and encephalopathy: n=20 (1.4%). Age >10 years was significantly associated with neurotoxicity (P=0.01) and use of HD MTX is associated with encephalopathy (P=0.03). Sequels are reported respectively in 60 and 33% of spinal neuropathy and encephalopathy cases. Current strategies tailoring risk of neurological sequels has to be defined.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0887-6924
|
pubmed:author |
pubmed-author:AuclercM FMF,
pubmed-author:BaruchelAA,
pubmed-author:CouillaultGG,
pubmed-author:DemeocqFF,
pubmed-author:DufourgM NMN,
pubmed-author:GandemerVV,
pubmed-author:Landman-ParkerJJ,
pubmed-author:LeblancTT,
pubmed-author:LevergerGG,
pubmed-author:LevyPP,
pubmed-author:MichelGG,
pubmed-author:PerexMM,
pubmed-author:SchmittCC,
pubmed-author:TaboneM DMD,
pubmed-author:VannierJ PJP
|
pubmed:issnType |
Print
|
pubmed:volume |
21
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
238-47
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:17170721-Adolescent,
pubmed-meshheading:17170721-Age Factors,
pubmed-meshheading:17170721-Antimetabolites, Antineoplastic,
pubmed-meshheading:17170721-Brain Diseases, Metabolic,
pubmed-meshheading:17170721-Child,
pubmed-meshheading:17170721-Child, Preschool,
pubmed-meshheading:17170721-Combined Modality Therapy,
pubmed-meshheading:17170721-Dose-Response Relationship, Drug,
pubmed-meshheading:17170721-Female,
pubmed-meshheading:17170721-Humans,
pubmed-meshheading:17170721-Infant,
pubmed-meshheading:17170721-Male,
pubmed-meshheading:17170721-Methotrexate,
pubmed-meshheading:17170721-Neurotoxins,
pubmed-meshheading:17170721-Precursor Cell Lymphoblastic Leukemia-Lymphoma,
pubmed-meshheading:17170721-Risk Assessment
|
pubmed:year |
2007
|
pubmed:articleTitle |
Age and high-dose methotrexate are associated to clinical acute encephalopathy in FRALLE 93 trial for acute lymphoblastic leukemia in children.
|
pubmed:affiliation |
Service d'Hématologie et d'Oncologie Pédiatrique Hôpital d'Enfant Armand Trousseau, AP-HP, Paris, France.
|
pubmed:publicationType |
Journal Article,
Randomized Controlled Trial
|