Literature DB >> 18282

Weekly methotrexate-calcium leucovorin rescue: effect of alkalinization on nephrotoxicity; pharmacokinetics in the CNS; and use in CNS non-Hodgkin's lymphoma.

S W Pitman, E Frei.   

Abstract

Urinary alkalinization with oral sodium bicarbonate has decreased the incidence of acute nephrotoxicity and subsequent myelotoxicity in 18 adults receiving high-dose methotrexate with calcium leucovorin rescue (MTX-LCV) weekly in doses of 1-7.5 g/m2. Close monitoring of 24-hour serum creatinine and MTX levels can predict patients at risk for serious toxicity. By a prompt (24-36 hours) increase in the LCV dose rate, hematologic and biochemical evidence of myelosuppression has been prevented. Kinetic parameters in serum and lumbar cerebrospinal fluid (CSF) were studied in two patients following iv injection of 3 and 7.5 g/m2 respectively. Lumbar CSF MTX concentrations greater than 1 muM are achieved. The half-life of MTX in the CSF (11.95 hours) is twice as long as the serum half-life. In the presence of carcinomatous meningitis, further delay in the clearance of MTX from the CSF was seen. With weekly MTX-LCV, there have been four objective responses in six patients with non-Hodgkin's lymphoma in CNS relapse, including complete regression in two. It is suggested that therapeutic concentrations can be achieved in the central nervous system following MTX-LCV.

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Year:  1977        PMID: 18282

Source DB:  PubMed          Journal:  Cancer Treat Rep        ISSN: 0361-5960


  31 in total

1.  Acetazolamide for alkalinisation of urine in patients receiving high-dose methotrexate.

Authors:  J Shamash; H Earl; R Souhami
Journal:  Cancer Chemother Pharmacol       Date:  1991       Impact factor: 3.333

2.  Population pharmacokinetics of high-dose methotrexate in children with acute lymphoblastic leukaemia.

Authors:  Dolores Aumente; Dolores Santos Buelga; John C Lukas; Pedro Gomez; Antonio Torres; Maria José García
Journal:  Clin Pharmacokinet       Date:  2006       Impact factor: 6.447

3.  [High-dose methotrexate therapy in osteogenic sarcoma: plasma pharmakokinetics to predict toxicity (author's transl)].

Authors:  G E Janka; H Wiesner; F Bidlingmaier; R J Haas
Journal:  Klin Wochenschr       Date:  1979-04-17

4.  Effective therapy for Burkitt's lymphoma: high-dose cyclophosphamide + high-dose methotrexate with coordinated intrathecal therapy.

Authors:  I Ramirez; M P Sullivan; Y Wang; R G Martin; J J Butler
Journal:  Cancer Chemother Pharmacol       Date:  1979       Impact factor: 3.333

5.  Urinary pH and urine flow independent renal clearance of methotrexate in dogs.

Authors:  C Y Lui; M G Lee; W L Chiou
Journal:  J Pharmacokinet Biopharm       Date:  1985-04

6.  Renal and hepatic toxicity after high-dose 7-hydroxymethotrexate in the rat.

Authors:  E Smeland; R M Bremnes; A Andersen; R Jaeger; T J Eide; N E Huseby; J Aarbakke
Journal:  Cancer Chemother Pharmacol       Date:  1994       Impact factor: 3.333

7.  CCND1 G870A polymorphism is associated with toxicity of methotrexate in childhood acute lymphoblastic leukemia.

Authors:  Yao Xue; Liucheng Rong; Na Tong; Meilin Wang; Zhengdong Zhang; Yongjun Fang
Journal:  Int J Clin Exp Pathol       Date:  2015-09-01

Review 8.  The practical use of methotrexate in psoriasis.

Authors:  J P Tung; H I Maibach
Journal:  Drugs       Date:  1990-11       Impact factor: 9.546

9.  Clinical pharmacokinetics of 6-hour infusion of high-dose methotrexate. Preliminary trial of monitoring high infusion doses.

Authors:  M Luyckx; J L Cazin; C Brunet; P Gosselin; M C Demaille
Journal:  Eur J Clin Pharmacol       Date:  1985       Impact factor: 2.953

10.  Theoretically required urinary flow during high-dose methotrexate infusion.

Authors:  K Sasaki; J Tanaka; T Fujimoto
Journal:  Cancer Chemother Pharmacol       Date:  1984       Impact factor: 3.333

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