Literature DB >> 577182

P-aminosalicylate metabolism in cancer patients sensitive and resistant to chemotherapy.

J G Lavigne, A Barry, C d'Auteuil, J M Delage.   

Abstract

A reduced response of a tumour to chemotherapy may be due to the host's drug metabolism. To test this hypothesis, we measured the metabolism of a model drug, para-aminosalicylate (PAS). Volunteers and cancer patients ingested a single oral dose (2 g) of PAS and we measured the plasma disappearance curve of the drug and its metabolite. In 7 patients suffering from lymphosarcoma, acute or chronic leukaemia and resistant to cancer chemotherapy, we observed low plasma PAS concentrations, an increase in PAS acetylation and an increased number (and a higher frequency) of abnormal liver-function tests. In 14 patients with malignant blood disease, yet responding well to chemotherapy, the metabolism of PAS is similar to that of healthy controls of the same age and sex. The plasma half-life of PAS is similar in sensitive and resistant patients, but slightly longer than in volunteers. Finally, in urine collected 120 min after drug administration, we observed the same results as in plasma. In conclusion, cancer patients resistant to chemotherapy do not metabolize the model drug PAS as volunteers or sensitive patients do, and this might be relevant to the terminal stage of the disease.

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Year:  1977        PMID: 577182      PMCID: PMC2025501          DOI: 10.1038/bjc.1977.91

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


  28 in total

Review 1.  Binding of drugs to serum albumin (first of two parts).

Authors:  J Koch-Weser; E M Sellers
Journal:  N Engl J Med       Date:  1976-02-05       Impact factor: 91.245

2.  Pharmacokinetics in the aged: a review.

Authors:  E J Triggs; R L Nation
Journal:  J Pharmacokinet Biopharm       Date:  1975-12

Review 3.  RENAL COMPLICATIONS OF NEOPLASTIC DISEASE.

Authors:  E FREI; C J BENTZEL; R RIESELBACH; J B BLOCK
Journal:  J Chronic Dis       Date:  1963-07

4.  Importance of pharmacokinetic studies on cyclophosphamide (NSC-26271) in understanding its cytotoxic effect.

Authors:  M G Donelli; I Bartosek; A Guaitani; A Martini; T Colombo; M A Pacciarini; R Modica
Journal:  Cancer Treat Rep       Date:  1976-04

5.  [Antineoplastic drugs: resistance and metabolism].

Authors:  J G Lavigne
Journal:  Union Med Can       Date:  1976-02

Review 6.  Drug disposition and liver disease.

Authors:  G R Wilkinson; S Schenker
Journal:  Drug Metab Rev       Date:  1975       Impact factor: 4.518

7.  Drug metabolism in tumor-bearing rats. I. Activities of NADPH-linked electron transport and drug-metabolizing enzyme systems in liver microsomes of tumor-bearing rats.

Authors:  R Kato; A Takanaka; A Takahashi; K Onoda
Journal:  Jpn J Pharmacol       Date:  1968-06

8.  Some metabolic functions of liver in patients with advanced non-hepatic cancer.

Authors:  T K Basu; R W Raven; D C Williams
Journal:  Oncology       Date:  1974       Impact factor: 2.935

Review 9.  Factors affecting gastrointestinal absorption of drugs.

Authors:  R R Levine
Journal:  Am J Dig Dis       Date:  1970-02

10.  Liver enzymes and pathology in Hodgkin's disease.

Authors:  R E Belliveau; P H Wiernik; A B Abt
Journal:  Cancer       Date:  1974-08       Impact factor: 6.860

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  2 in total

Review 1.  Survey of the human acetylator polymorphism in spontaneous disorders.

Authors:  D A Evans
Journal:  J Med Genet       Date:  1984-08       Impact factor: 6.318

Review 2.  Clinical pharmacokinetics of the antituberculosis drugs.

Authors:  M R Holdiness
Journal:  Clin Pharmacokinet       Date:  1984 Nov-Dec       Impact factor: 6.447

  2 in total

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