Literature DB >> 3719900

Renal function in the elimination of oral melphalan in patients with multiple myeloma.

C G Adair, J M Bridges, Z R Desai.   

Abstract

Pharmacokinetic studies in 11 patients with multiple myeloma were undertaken on the first and last days of one course of chemotherapy. The drug was administered PO in single doses of 6-14 mg daily. Melphalan concentrations were determined by high-performance liquid chromatography. The interpatient variability of pharmacokinetic parameters noted by other authors was observed. Regression analysis showed a significant positive correlation between the elimination rate constant for melphalan and renal function (P = 0.003). The form of the line which describes the overall elimination rate constant for melphalan is given by the equation: Kel = 5.67 X 10(-3) + [4.90 X 10(-5) X GFR]. There was also a significant negative correlation between renal function and the area under the plasma melphalan concentration/time curve (P = 0.006). In vitro stability studies of melphalan in plasma at 37 degrees C and pharmacokinetic data suggest that hydrolysis and renal clearance are the major mechanisms of melphalan elimination. This work shows quantitatively the relationship between renal function and drug elimination and how the data may be used in predicting melphalan half-life from creatinine clearance.

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Year:  1986        PMID: 3719900     DOI: 10.1007/bf00306752

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  13 in total

1.  Prediction of creatinine clearance from serum creatinine.

Authors:  D W Cockcroft; M H Gault
Journal:  Nephron       Date:  1976       Impact factor: 2.847

2.  Prognostic factors and survival in multiple myeloma. Analysis of 91 cases treated by melphalan and prednisone.

Authors:  M Gobbi; M Cavo; G Savelli; M Baccarani; S Tura
Journal:  Haematologica       Date:  1980-08       Impact factor: 9.941

Review 3.  L-phenylalanine mustard (L-PAM): the first 25 years.

Authors:  R L Furner; R K Brown
Journal:  Cancer Treat Rep       Date:  1980 Apr-May

Review 4.  Multiple myeloma.

Authors:  M M Oken
Journal:  Med Clin North Am       Date:  1984-05       Impact factor: 5.456

5.  Comparison of the fed and fasting states on the absorption of melphalan in multiple myeloma.

Authors:  A G Bosanquet; E D Gilby
Journal:  Cancer Chemother Pharmacol       Date:  1984       Impact factor: 3.333

6.  Comparative pharmacokinetics of chlorambucil and melphalan in man.

Authors:  D S Alberts; S Y Chang; H S Chen; B J Larcom; T L Evans
Journal:  Recent Results Cancer Res       Date:  1980

7.  Pharmacokinetics of oral and intravenous melphalan during routine treatment of multiple myeloma.

Authors:  A G Bosanquet; E D Gilby
Journal:  Eur J Cancer Clin Oncol       Date:  1982-04

8.  In vitro degradation of L-phenylalanine mustard (L-PAM).

Authors:  T L Evans; S Y Chang; D S Alberts; I G Sipes; K Brendel
Journal:  Cancer Chemother Pharmacol       Date:  1982       Impact factor: 3.333

9.  Plasma melphalan and prednisolone concentrations during oral therapy for multiple myeloma.

Authors:  I A Taha; R A Ahmad; H Gray; C I Roberts; H J Rogers
Journal:  Cancer Chemother Pharmacol       Date:  1982       Impact factor: 3.333

10.  Effect of renal dysfunction in dogs on the disposition and marrow toxicity of melphalan.

Authors:  D S Alberts; H G Chen; D Benz; N L Mason
Journal:  Br J Cancer       Date:  1981-03       Impact factor: 7.640

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  6 in total

Review 1.  Drug dosage in patients during continuous renal replacement therapy. Pharmacokinetic and therapeutic considerations.

Authors:  P Reetze-Bonorden; J Böhler; E Keller
Journal:  Clin Pharmacokinet       Date:  1993-05       Impact factor: 6.447

Review 2.  Problems in the use of anticancer drugs in the elderly.

Authors:  J E Phister; S G Jue; B J Cusack
Journal:  Drugs       Date:  1989-04       Impact factor: 9.546

3.  Phase II trial and pharmacokinetic assessment of intravenous melphalan in patients with advanced prostate cancer.

Authors:  D C Smith; D I Jodrell; M J Egorin; R M Ambinder; E G Zuhowski; W Kreis; P G Ellis; D L Trump
Journal:  Cancer Chemother Pharmacol       Date:  1993       Impact factor: 3.333

4.  Variability of tumor response to chemotherapy. I. Contribution of host heterogeneity.

Authors:  L Simpson-Herren; P E Noker; S D Wagoner
Journal:  Cancer Chemother Pharmacol       Date:  1987       Impact factor: 3.333

5.  Intratumoral measurement and plasma pharmacokinetics of intravenously administered melphalan. Report of a patient with plasmacytoma.

Authors:  S Friberg; H Ehrsson; S Eksborg; C Carenfeldt
Journal:  Cancer Chemother Pharmacol       Date:  1987       Impact factor: 3.333

6.  Lack of effect of cisplatin on i.v. L-PAM plasma pharmacokinetics in ovarian cancer patients.

Authors:  M Zucchetti; M D'Incalci; Y Willems; F Cavalli; C Sessa
Journal:  Cancer Chemother Pharmacol       Date:  1988       Impact factor: 3.333

  6 in total

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