Literature DB >> 3157512

A radioimmunoassay for GnRH agonist analogue in serum of patients with prostate cancer treated with D-Ser (tBu)6 AZA Gly10 GnRH.

R N Clayton, L C Bailey, J Cottam, D Arkell, T J Perren, G R Blackledge.   

Abstract

A radioimmunoassay is described for D-Ser (tBu)6 AZA Gly10 GnRH (ICI 118630) in serum of prostate cancer patients treated chronically with this peptide to produce a medical castration. With 125I-118630 as the label, and an anti-GnRH serum, the specificity of the assay is directed to the N-terminal end of the peptide, and putative degradation products have less than 6% cross-reactivity. The assay appears specific for intact 118630 which, after subcutaneous administration of 250 micrograms, has a half-time of disappearance from the serum of 4.9 +/- 0.4 h and a volume of distribution of 13.7 +/- 0.8 litres. Continuous subcutaneous infusion of 120 micrograms 118630/d gave stable serum concentrations of between 2-3 ng/ml for up to 63 d which were very similar to values predicted from pharmacokinetic analysis of the analogue clearance rate. This contrasts with the "peak and trough' pattern of serum 118630 levels measured in two subjects after 118630 administration from a subcutaneous implant containing 3.6 mg of peptide in a biodegradable formulation. Serum 118630 levels peaked at between 6-8 ng/ml 15 d after the implant and fell to less than 1 ng/ml at 29 d, immediately before the next implant. Serum 118630 levels following a second 3.6 mg implant were almost identical with respect to absolute concentration and time to peak value as after the first implant. This assay will be of value not only for evaluation of the pharmacokinetics of GnRH analogue release from new long-acting formulations, but also for correlation of serum peptide concentrations with pituitary gonadotroph desensitization.

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Year:  1985        PMID: 3157512     DOI: 10.1111/j.1365-2265.1985.tb00144.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.478


  9 in total

Review 1.  Clinical pharmacokinetics of endocrine agents used in advanced breast cancer.

Authors:  P E Lønning; E A Lien; S Lundgren; S Kvinnsland
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Review 2.  Gonadotropin releasing hormone (GnRH) analogs for the treatment of breast and prostatic carcinoma.

Authors:  R J Santen; A Manni; H Harvey
Journal:  Breast Cancer Res Treat       Date:  1986       Impact factor: 4.872

Review 3.  Clinical pharmacokinetics of goserelin.

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Review 4.  Goserelin. A review of its pharmacodynamic and pharmacokinetic properties, and clinical use in sex hormone-related conditions.

Authors:  P Chrisp; K L Goa
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Review 5.  Goserelin. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in benign gynaecological disorders.

Authors:  C M Perry; R N Brogden
Journal:  Drugs       Date:  1996-02       Impact factor: 9.546

Review 6.  Goserelin. A review of its pharmacodynamic and pharmacokinetic properties and therapeutic efficacy in prostate cancer.

Authors:  R N Brogden; D Faulds
Journal:  Drugs Aging       Date:  1995-04       Impact factor: 3.923

Review 7.  A risk benefit assessment of drugs used in the treatment of endometriosis.

Authors:  R W Shaw
Journal:  Drug Saf       Date:  1994-08       Impact factor: 5.606

8.  Pharmacokinetic and endocrinological parameters of a slow-release depot preparation of the GnRH analogue ICI 118630 (zoladex) compared with a subcutaneous bolus and continuous subcutaneous infusion of the same drug in patients with prostatic cancer.

Authors:  T J Perren; R N Clayton; G Blackledge; L C Bailey; G Holder; S S Lynch; D G Arkell; J Cottam; D Farrar; C H Young
Journal:  Cancer Chemother Pharmacol       Date:  1986       Impact factor: 3.333

9.  Zoladex: endocrine and therapeutic effects in post-menopausal breast cancer.

Authors:  A L Harris; J Carmichael; B M Cantwell; M Dowsett
Journal:  Br J Cancer       Date:  1989-01       Impact factor: 7.640

  9 in total

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