Literature DB >> 2439582

Induction of remission in hepatocellular carcinoma with a new thymidylate synthase inhibitor, CB3717. A phase II study.

M F Bassendine, N J Curtin, H Loose, A L Harris, O F James.   

Abstract

In a Phase II clinical trial, 14 consecutive, unselected patients with primary hepatocellular carcinoma were treated with a new inhibitor of thymidylate synthase, CB3717. On the basis of previously reported criteria, 6 patients were considered to have a good prognosis (Grade A) and 8 a poor prognosis (Grade B). Three Grade B patients died after only one treatment. Six patients responded (4 Grade A and 2 Grade B) with a decrease in tumour size and greater than 50% fall in serum alphafetoprotein levels; 3 of these had a greater than 1 log fall in alphafetoprotein. A further patient (Grade B) showed static disease during treatment. Thus, of 11 patients receiving two or more treatments 7 showed clinical benefit, with a median survival from start of CB3717 therapy of 46 weeks (2 still alive at 33 and 67 weeks). Our results suggest that CB3717 will be a useful new therapeutic agent in hepatocellular carcinoma. Further controlled trials are indicated to confirm these preliminary findings, using the drug both as a single agent and in combination with inhibitors of thymidine uptake by cells, which may further increase efficacy.

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Year:  1987        PMID: 2439582     DOI: 10.1016/s0168-8278(87)80545-7

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  7 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

2.  Biochemical effects of folate-based inhibitors of thymidylate synthase in MGH-U1 cells.

Authors:  B Mitrovski; J Pressacco; S Mandelbaum; C Erlichman
Journal:  Cancer Chemother Pharmacol       Date:  1994       Impact factor: 3.333

Review 3.  New targets for pyrimidine antimetabolites in the treatment of solid tumours. 1: Thymidylate synthase.

Authors:  C L van der Wilt; G J Peters
Journal:  Pharm World Sci       Date:  1994-04-15

4.  Biological activity of a novel rationally designed lipophilic thymidylate synthase inhibitor.

Authors:  B M O'Connor; S Webber; R C Jackson; J Galivan; M S Rhee
Journal:  Cancer Chemother Pharmacol       Date:  1994       Impact factor: 3.333

5.  The efficacy of 5-fluorouracil in human colorectal cancer is not enhanced by thymidylate synthetase inhibition with CB3717 (N10-propargyl-5,8 dideazafolic acid).

Authors:  B M Cantwell; A L Harris
Journal:  Br J Cancer       Date:  1988-08       Impact factor: 7.640

6.  A phase I study of the lipophilic thymidylate synthase inhibitor Thymitaq (nolatrexed dihydrochloride) given by 10-day oral administration.

Authors:  D I Jodrell; A Bowman; R Rye; B Byrne; A Boddy; I Rafi; G A Taylor; A Johnston; N J Clendeninn
Journal:  Br J Cancer       Date:  1999-02       Impact factor: 7.640

7.  The renal effects of N10-propargyl-5,8-dideazafolic acid (CB3717) and a non-nephrotoxic analogue ICI D1694, in mice.

Authors:  D I Jodrell; D R Newell; S E Morgan; S Clinton; J P Bensted; L R Hughes; A H Calvert
Journal:  Br J Cancer       Date:  1991-11       Impact factor: 7.640

  7 in total

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