Methotrexate (MTX) infusions of 500-1,000 mg/m2 over 24 hours may improve survival and prevent relapse in children with acute lymphoblastic leukemia (ALL). Childrens Cancer Group (CCG) Study 139 compared weekly oral methotrexate 20 mg/m2/ week (oral MTX) to MTX 500 mg/m2 infused over 24 hours (IV MT
Oral mucositis and salivary methotrexate concentration in intermediate-dose methotrexate therapy for children with acute lymphoblastic leukemia
β Scribed by Ishii, Eiichi ;Yamada, Shin-Ichi ;Higuchi, Shun ;Honjo, Tetsu ;Igarashi, Hisaji ;Kanemitsu, Satomi ;Kai, Takashi ;Ueda, Kohji
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 335 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0098-1532
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β¦ Synopsis
The relationship between salivary methotrexate (MTX) concentration and severity of oral mucositis after administration of MTX was investigated in six children with acute lymphoblastic leukemia. They received two administrations of MTX at 500 mgm' with one third given bolusly and the remainder by 24-hour continuous infusion. N o significant difference among patients or administration session was observed in serum MTX concentration. Detectable concentrations of salivary MTX (> 0.01 pM) were observed during nine of the ten infusions. A concentration of 0.1 pM or more, apparently lasting at least 12 hours, was observed during one infusion and followed by severe mucositis.
During two of the ten infusions for different patients, concentrations of 0.04 to 0.07 pM and 0.02 to 0.04 pM, apparently lasting at least 12 and 18 hours, respectively, were observed, followed by moderate mucositis. During the other seven infusions, either much shorter or no increase in salivary MTX concentration was observed, with only mild or no subsequent mucositis. Analysis by Kendall's rank method showed a statistical correlation between concentration at 6 hours of infusion and severity of oral mucositis. The findings suggest that the early secretion of MTX into saliva has a significant role in the development of oral mucositis in leukemic children.
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High-dose methotrexate (HDMTX, 1,000 mg/m2) and cranial irradiation/sequential chemotherapy (RTSC) were compared for ability to extend complete remission durations in children with acute lymphoblastic leukemia (ALL). Three hundred thirty patients were enrolled in the study, according to our criteria
We studied the disposition phannacokinetics of methotrexate (MTX) given orally to 16 children with acute lyrnphoblastic leukemia (ALL) and its relation to the pharrnacokinetics of 6-mercaptopurine (6MP) in the same children. There was an eightfold variability in area-under-concentration tirnecurve (
## Abstract Concentrations of __7__βhydroxyβmethotrexate (__7__βOHβMTX) were determined in serum samples obtained after 266 infusions of methotrexate administered to 58 children with acute lymphoblastic leukemia. The dose of methotrexate (MTX) was in the range of 0.5β33.6 g/m^2^. Pharmacokinetic pa