Literature DB >> 4038385

Metoclopramide kinetics at high-dose infusion rates for prevention of cisplatin-induced emesis.

R Saller, D Hellenbrecht, L Briemann, A Hellstern, H Hess, P Mitrou, M Hodgson, G Achtert, P Brockmann, H J Hausleiter.   

Abstract

Eleven male subjects aged 24 to 58 yr received cisplatin, 90 to 120 mg/m2 iv, in combination with other cytostatic drugs such as doxorubicin HCl and bleomycin. To prevent emesis, two high-dose metoclopramide regimens were started 2 hr before cytostatic therapy. Regimen A (n = 7) consisted of a loading dose infusion of 1 mg/kg/hr over 2 hr, followed by a maintenance infusion of 0.5 mg/kg/hr over 24 hr (total dose was 14 mg/kg in each cytostatic cycle). Regimen B (n = 6) consisted of half the metoclopramide dose. The following kinetics were derived from the metoclopramide steady-state plasma levels and the t1/2 of the elimination phase 26 to 38 hr after dosing (median value and range are listed): Steady-state plasma concentration in group A and group B was 750 (480 to 1520) and 360 (300 to 480) ng/ml plasma. Drug clearance in group A and group B was 0.67 (0.3 to 1.0) and 0.70 (0.5 to 0.8) l/hr/kg. Volumes of drug distribution in group A and group B were 4.4 (1.9 to 6.5) and 4.3 (3.2 to 5.9) l/kg. Values for the t1/2 in the elimination phase in group A and group B were 4.7 (3.0 to 5.4) and 4.3 (3.7 to 5.1) hr. It appears that metoclopramide kinetics at high doses were dose linear, i.e., without evidence of cumulation. There were few side effects; vomiting was effectively suppressed by both regimens.

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Year:  1985        PMID: 4038385     DOI: 10.1038/clpt.1985.9

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  7 in total

1.  Continuous infusion of high-dose metoclopramide: comparison of pharmacokinetically adjusted and standard doses for the control of cisplatin-induced acute emesis.

Authors:  J M Brechot; J P Dupeyron; C Delattre; C Chastang; J P Laaban; J Rochemaure
Journal:  Eur J Clin Pharmacol       Date:  1991       Impact factor: 2.953

2.  Antiemetic effect and pharmacokinetics of high dose metoclopramide in cancer patients treated with cisplatin-containing chemotherapy regimens.

Authors:  H Havsteen; H Nielsen; M Kjaer
Journal:  Eur J Clin Pharmacol       Date:  1986       Impact factor: 2.953

3.  High-dose metoclopramide by infusion: a double-blind study of plasma concentration-effect relationships in patients receiving cancer chemotherapy.

Authors:  W B Taylor; J M Simpson; D N Bateman
Journal:  Eur J Clin Pharmacol       Date:  1987       Impact factor: 2.953

4.  Minimal biliary excretion and enterohepatic recirculation of metoclopramide in patients with extrahepatic cholestasis.

Authors:  A Hellstern; D Hellenbrecht; R Saller; M Gatzen; G Achtert; P Brockmann; H J Hausleiter
Journal:  Eur J Clin Pharmacol       Date:  1993       Impact factor: 2.953

Review 5.  Pharmacokinetics of high-dose metoclopramide in cancer patients.

Authors:  E M McGovern; J Grevel; S M Bryson
Journal:  Clin Pharmacokinet       Date:  1986 Nov-Dec       Impact factor: 6.447

6.  [Benefit and risk of high-dose metoclopramide in comparison to high-dose haloperidol or triflupromazine in cisplatin-induced vomiting].

Authors:  R Saller; D Hellenbrecht
Journal:  Klin Wochenschr       Date:  1985-05-02

7.  Improved benefit/risk ratio of higher-dose metoclopramide therapy during cisplatin-induced emesis.

Authors:  R Saller; D Hellenbrecht; A Hellstern; H Hess
Journal:  Eur J Clin Pharmacol       Date:  1985       Impact factor: 2.953

  7 in total

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