Literature DB >> 9460992

Comparison of plasma and tissue levels of ZD1694 (Tomudex), a highly polyglutamatable quinazoline thymidylate synthase inhibitor, in preclinical models.

G W Aherne1, E Ward, N Lawrence, D Dobinson, S J Clarke, H Musgrove, F Sutcliffe, T Stephens, A L Jackman.   

Abstract

ZD1694 (Tomudex, raltitrexed) is a specific quinazoline antifolate thymidylate synthase inhibitor that relies on polyglutamation for high potency. Antibodies to ZD1694 have been used to establish a sensitive radioimmunoassay as an alternative to high-performance liquid chromatography (HPLC). The radioimmunoassay is reproducible, accurate and provides a means of determining low levels of ZD1694 in plasma (< 1 nM). By virtue of the high cross-reactivity of the antibodies with polyglutamated forms of ZD1694, it is also possible to measure the total concentration of drug in tissues. Results obtained in L1210 mouse leukaemia cells and in mouse tissues were similar to those previously determined using radiolabelled drug. Pharmacokinetic studies in mice have confirmed that the compound is rapidly eliminated from the plasma and that there is a prolonged terminal elimination phase. ZD1694 was measured in plasma (0.56 ng ml(-1); 1.2 pmol ml(-1)) up to 7 days after a single i.p. dose of 100 mg kg(-1) ZD1694. Liver, kidney and gut epithelium had a substantially higher level of ZD1694 immunoreactivity than plasma. For example, 24 h after a single i.p. dose at 1, 10 and 100 mg kg(-1), total drug levels in the liver were 480, 325 and 152 times higher than plasma levels respectively. In kidney and gut epithelium, total drug levels at these doses were approximately 55 and 34 times those of plasma. The high tissue to plasma ratios were maintained for at least 7 days after administration. Similarly, high tissue to plasma ratios (> 100) were found in dogs treated with a clinically relevant dose of ZD1694. These were maintained for 4 weeks in liver and kidney tissue (> 100). Total gastrointestinal concentrations of ZD1694 were approximately 10 times higher than plasma 3 days after administration, but levels were near to the limit of detection at 4 weeks. These results are consistent with extensive polyglutamation of ZD1694 within tissues in both mice and dog and provide further support for the infrequent schedule that has been used clinically. Although it has not been possible to measure individual polyglutamated forms of ZD1694, the radioimmunoassay provides a convenient means of assessing total drug levels in tissues and is currently the only method suitable for measuring the extent of drug retention in normal tissue and tumour biopsies obtained from patients treated with ZD1694.

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Year:  1998        PMID: 9460992      PMCID: PMC2151243          DOI: 10.1038/bjc.1998.37

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  26 in total

1.  Quinazoline antifolate thymidylate synthase inhibitors: alkyl, substituted alkyl, and aryl substituents in the C2 position.

Authors:  L R Hughes; A L Jackman; J Oldfield; R C Smith; K D Burrows; P R Marsham; J A Bishop; T R Jones; B M O'Connor; A H Calvert
Journal:  J Med Chem       Date:  1990-11       Impact factor: 7.446

2.  Development of an assay for the estimation of N10-propargyl-5,8-dideazafolic acid polyglutamates in tumor cells.

Authors:  E Sikora; D R Newell; A L Jackman; A J Simmonds; T R Jones; A H Calvert
Journal:  Anal Biochem       Date:  1988-08-01       Impact factor: 3.365

3.  Quinazoline antifolates inhibiting thymidylate synthase: synthesis of gamma-linked peptide and amide analogues of 2-desamino-2-methyl-N10-propargyl- 5,8-dideazafolic acid (ICI 198583).

Authors:  V Bavetsias; A L Jackman; T J Thornton; K Pawelczak; F T Boyle; G M Bisset
Journal:  Adv Exp Med Biol       Date:  1993       Impact factor: 2.622

4.  The measurement of polyglutamate metabolites of the thymidylate synthase inhibitor, ICI D1694, in mouse and human cultured cells.

Authors:  W Gibson; G M Bisset; P R Marsham; L R Kelland; I R Judson; A L Jackman
Journal:  Biochem Pharmacol       Date:  1993-02-24       Impact factor: 5.858

5.  Decreased polyglutamylation of methotrexate in acute lymphoblastic leukemia blasts in adults compared to children with this disease.

Authors:  E Göker; J T Lin; T Trippett; Y Elisseyeff; W P Tong; D Niedzwiecki; C Tan; P Steinherz; B I Schweitzer; J R Bertino
Journal:  Leukemia       Date:  1993-07       Impact factor: 11.528

6.  Syntheses and thymidylate synthase inhibitory activity of the poly-gamma-glutamyl conjugates of N-[5-[N-(3,4-dihydro-2-methyl-4-oxoquinazolin-6-ylmethyl)-N-methylamino ]-2-thenoyl]-L-glutamic acid (ICI D1694) and other quinazoline antifolates.

Authors:  G M Bisset; K Pawelczak; A L Jackman; A H Calvert; L R Hughes
Journal:  J Med Chem       Date:  1992-03-06       Impact factor: 7.446

7.  ICI D1694, a quinazoline antifolate thymidylate synthase inhibitor that is a potent inhibitor of L1210 tumor cell growth in vitro and in vivo: a new agent for clinical study.

Authors:  A L Jackman; G A Taylor; W Gibson; R Kimbell; M Brown; A H Calvert; I R Judson; L R Hughes
Journal:  Cancer Res       Date:  1991-10-15       Impact factor: 12.701

8.  The pharmacokinetics of the quinazoline antifolate ICI D 1694 in mice and rats.

Authors:  D I Jodrell; D R Newell; W Gibson; L R Hughes; A H Calvert
Journal:  Cancer Chemother Pharmacol       Date:  1991       Impact factor: 3.333

9.  The biochemical pharmacology of the thymidylate synthase inhibitor, 2-desamino-2-methyl-N10-propargyl-5,8-dideazafolic acid (ICI 198583).

Authors:  A L Jackman; D R Newell; W Gibson; D I Jodrell; G A Taylor; J A Bishop; L R Hughes; A H Calvert
Journal:  Biochem Pharmacol       Date:  1991-10-24       Impact factor: 5.858

10.  A phase II study in advanced breast cancer: ZD1694 ('Tomudex') a novel direct and specific thymidylate synthase inhibitor.

Authors:  I Smith; A Jones; M Spielmann; M Namer; M D Green; J Bonneterre; H E Wander; T Hatschek; N Wilking; J Zalcberg; J Spiers; L Seymour
Journal:  Br J Cancer       Date:  1996-08       Impact factor: 7.640

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  5 in total

Review 1.  Clinical and preclinical pharmacokinetics of raltitrexed.

Authors:  S J Clarke; P J Beale; L P Rivory
Journal:  Clin Pharmacokinet       Date:  2000-12       Impact factor: 6.447

Review 2.  Progress in colorectal cancer chemotherapy: how far have we come, how far to go?

Authors:  M E Royce; P M Hoff; R Pazdur
Journal:  Drugs Aging       Date:  2000-09       Impact factor: 3.923

Review 3.  Novel chemotherapy agents for colorectal cancer: oral fluoropyrimidines, oxaliplatin, and raltitrexed.

Authors:  M E Royce; P M Hoff; R Padzur
Journal:  Curr Oncol Rep       Date:  1999       Impact factor: 5.075

4.  Population pharmacokinetics of raltitrexed in patients with advanced solid tumours.

Authors:  Elaine Y L Blair; Laurent P Rivory; Stephen J Clarke; Andrew J McLachlan
Journal:  Br J Clin Pharmacol       Date:  2004-04       Impact factor: 4.335

5.  Phase I study of irinotecan and raltitrexed in patients with advanced gastrointestinal tract adenocarcinoma.

Authors:  H E Ford; D Cunningham; P J Ross; S Rao; G W Aherne; T S Benepal; T Price; A Massey; L Vernillet; G Gruia
Journal:  Br J Cancer       Date:  2000-07       Impact factor: 7.640

  5 in total

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