Literature DB >> 3829494

Effect of razoxane on metastases from colorectal cancer.

K Hellmann, J Gilbert, M Evans, P Cassell, R Taylor.   

Abstract

At a median follow-up of 5 years, adjuvant razoxane (125 mg b.d.) given 5 days/week indefinitely following resection of colorectal cancer provided no benefit in terms of survival or recurrence for Dukes' A or B patients when compared to untreated controls. However in Dukes' C patients this treatment reduced the recurrence rate (P = 0.05) and possibly increased survival time (P = 0.08). Analysis now of the development of metastases in this trial which entered 272 patients over 7 years shows that in the Dukes' C group the incidence of liver metastases in the razoxane-treated patients is only about half that of the untreated patients (18 per cent versus 34 per cent) and that the time to first appearance of the liver metastases is twice as long in the razoxane-treated group as it is in the untreated group (80 weeks versus 40 weeks). It is concluded that the benefit of adjuvant razoxane observed in the Dukes' C patients is due to the antimetastatic activity of the drug in reducing and slowing down the development of hepatic secondaries.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3829494

Source DB:  PubMed          Journal:  Clin Exp Metastasis        ISSN: 0262-0898            Impact factor:   5.150


  4 in total

1.  Phase II study of ICRF-159 (NSC-129943) in advanced colorectal carcinoma.

Authors:  T A Marciniak; C G Moertel; A J Schutt; R G Hahn; R J Reitemeier
Journal:  Cancer Chemother Rep       Date:  1975 Jul-Aug

2.  Adjuvant chemotherapy of large bowel cancer.

Authors:  J M Gilbert
Journal:  Cancer Treat Rev       Date:  1982-09       Impact factor: 12.111

3.  Randomized trial of oral adjuvant razoxane (ICRF 159) in resectable colorectal cancer: five-year follow-up.

Authors:  J M Gilbert; K Hellmann; M Evans; P G Cassell; R H Taylor; B Stoodley; H Ellis; C Wastell
Journal:  Br J Surg       Date:  1986-06       Impact factor: 6.939

4.  Metastases and the normalization of tumour blood vessels by ICRF 159: a new type of drug action.

Authors:  A W Le Serve; K Hellmann
Journal:  Br Med J       Date:  1972-03-04
  4 in total
  1 in total

1.  Antitumor activity of MST-16, a novel derivative of bis(2,6-dioxopiperazine), in murine tumor models.

Authors:  T Narita; S Yaguchi; T Komatsu; M Takase; A Hoshino; M Inaba; S Tsukagoshi
Journal:  Cancer Chemother Pharmacol       Date:  1990       Impact factor: 3.333

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.