Literature DB >> 18370456

[Not Available].

A M Murad1, C A Andrade, C Delfino, S Arikian, J J Doyle, C M Dezii, A Sadana, N Sinha.   

Abstract

The treatment of colorectal cancer continues to pose major challenges for oncologists throughout the world. Uracil and tegafur (UFT), as an oral agent, represents a new patient-focused approach to managing a malignancy with few treatment alternatives other than an intravenous fluorouracil (5-FU)-based regimen. The ability of UFT to achieve equivalent clinical outcomes compared with continuous 5-FU infusion, along with its oral formulation and mild toxicity profile, provide a compelling backdrop for fiscal analysis. An economic assessment of therapy attributes and effects would, therefore, be prudent and necessary when deliberating the adoption of this chemotherapy regimen. We developed a pharmacoeconomic model in Brazil and Argentina identifying clinical practices associated with chemotherapy administration and adverse event management practices from a panel of physicians assembled in each country. Practice patterns and clinical events were then evaluated for resource utilisation trends. The perspective of this pharmacoeconomic analysis was that of the healthcare payor. Country-specific charge data were applied to the identified resources to arrive at an average cost per patient receiving a 6-cycle course of 5-FU with either levamisole and/or leucovorin as a modulator vs a modelled oral UFT/leucovorin regimen. As a comparator, the oral UFT/leucovorin regimen was modelled based on the expert panel's input. Adverse events and incidence data were derived from clinical trial data for both agents. Both agents were analysed in the treatment of metastatic disease and as adjuvant therapy. The principal findings of a cost-minimisation analysis in Brazil revealed approximately equivalent treatment costs for both regimens in the adjuvant setting. When analysing the metastatic treatment arm, costs diverged by $R335/per patient ($R = Reals - the currency of Brazil) in favour of a UFT regimen. The profile in Argentina yielded more dramatic differences, with a UFT regimen costing $P782/per patient ($P = Pesos - the currency of Argentina) less than a 5-FU regimen in the adjuvant setting. In the treatment of metastatic disease, a UFT regimen provided $P1188/per patient in savings over a 5-FU regimen. These differences are predominantly driven by the mild toxicity profile of UFT and its corresponding less severe adverse event management practice patterns. In addition, the oral formulation of UFT versus intravenous 5-FU provides for ease of administration, lowering the total cost of care as well as likely impacting on the patient's quality of life. The pharmacoeconomic results suggest that a UFT regimen is a useful and economical alternative to the standard 5-FU regimen in the treatment of colorectal cancer in Brazil and Argentina.

Entities:  

Year:  1997        PMID: 18370456     DOI: 10.2165/00044011-199713020-00005

Source DB:  PubMed          Journal:  Clin Drug Investig        ISSN: 1173-2563            Impact factor:   2.859


  10 in total

1.  [Analogs of pyrimidine nucleosides. I. N1-(alpha-furanidyl) derivatives of natural pyrimidine bases and their antimetabolities].

Authors:  S A Giller; R A Zhuk; M Iu Lidak
Journal:  Dokl Akad Nauk SSSR       Date:  1967-09-11

2.  Phase II trial of uracil and tegafur plus oral leucovorin: an effective oral regimen in the treatment of metastatic colorectal carcinoma.

Authors:  R Pazdur; Y Lassere; V Rhodes; J A Ajani; S M Sugarman; Y Z Patt; D V Jones; A B Markowitz; J L Abbruzzese; B Bready
Journal:  J Clin Oncol       Date:  1994-11       Impact factor: 44.544

3.  Report on nationwide pooled data and cohort investigation in UFT phase II study.

Authors:  K Ota; T Taguchi; K Kimura
Journal:  Cancer Chemother Pharmacol       Date:  1988       Impact factor: 3.333

4.  Folinic acid does improve 5-fluorouracil activity in vivo. Results of a phase III study comparing 5-fluorouracil to 5-fluorouracil and folinic acid in advanced colon cancer patients.

Authors:  E Bobbio-Pallavicini; C Porta; M Moroni; A Spaghi; I Casagranda; G Nastasi
Journal:  J Chemother       Date:  1993-02       Impact factor: 1.714

5.  Effect of coadministration of uracil or cytosine on the anti-tumor activity of clinical doses of 1-(2-tetrahydrofuryl)-5-fluorouracil and level of 5-fluorouracil in rodents.

Authors:  S Fujii; S Kitano; K Ikenaka; T Shirasaka
Journal:  Gan       Date:  1979-04

6.  Prolonged continuous infusion of fluorouracil with weekly bolus leucovorin: a phase II study in patients with disseminated colorectal cancer.

Authors:  C G Leichman; L Leichman; C P Spears; P J Rosen; S Jeffers; S Groshen
Journal:  J Natl Cancer Inst       Date:  1993-01-06       Impact factor: 13.506

7.  A randomized, double-blind trial of fluorouracil plus placebo versus fluorouracil plus oral leucovorin in patients with metastatic colorectal cancer.

Authors:  L R Laufman; R M Bukowski; M A Collier; B A Sullivan; R A McKinnis; N J Clendennin; A Guaspari; W D Brenckman
Journal:  J Clin Oncol       Date:  1993-10       Impact factor: 44.544

8.  Tegafur-uracil (UFT) plus folinic acid in advanced rectal cancer.

Authors:  F Sanchiz; A Milla
Journal:  Jpn J Clin Oncol       Date:  1994-12       Impact factor: 3.019

9.  Phase I trial of a 5-day infusion of L-leucovorin plus daily bolus 5-fluorouracil in patients with advanced gastrointestinal malignancies.

Authors:  F H Valone; D R Gandara; J A Luce; S Wall; E A Perez; N Braham; M George; L Letvak
Journal:  Cancer Chemother Pharmacol       Date:  1993       Impact factor: 3.333

10.  Fluorouracil plus folinic acid in metastatic adenocarcinoma of unknown primary site suggestive of a gastrointestinal primary.

Authors:  F Nolè; M Colleoni; R Buzzoni; E Bajetta
Journal:  Tumori       Date:  1993-04-30
  10 in total

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