Literature DB >> 6402917

A comparative study of oral tegafur and intravenous 5-fluorouracil in patients with metastatic colorectal cancer.

A Y Bedikian, J Stroehlein, J Korinek, D Karlin, G P Bodey.   

Abstract

A randomized study was conducted in patients who had measurable metastatic colorectal cancer to compare the relative efficacy and toxicities of oral tegafur (1 gm/m2/days 1-21) with those of 5-fluorouracil (5-Fu, 500 mg/m2/days 1-4, then 250 mg/m2 on days 6, 8, 10, 12). The treatment courses were repeated every 4 weeks. Patients not responding to 5-Fu treatment were switched to tegafur. Randomization was stratified for presence or absence of liver metastasis and performance status. Partial responses were observed with 5-Fu, 6/32 (19%), tegafur, 7/35 (20%), and in patients who had been switched to tegafur after failing on 5-Fu, 1/20 (5%) with patients evaluable for response. Neutropenia was more common with 5-Fu (32% vs. 1% of treatment courses). Nausea occurred in about half the treatment courses; vomiting occurred in only 22%. Mucositis and diarrhea were more common with 5-Fu and severe in patients with liver function impairment. Neurologic toxicities due to tegafur were mild and occurred in less than 10% of the treatment courses. Oral tegafur and I.V. 5-Fu were equally effective against colorectal cancer, but tegafur was associated with minimal myelosuppression, which makes it suitable for use in combination with myelosuppressive antitumor agents.

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Year:  1983        PMID: 6402917     DOI: 10.1097/00000421-198304000-00007

Source DB:  PubMed          Journal:  Am J Clin Oncol        ISSN: 0277-3732            Impact factor:   2.339


  6 in total

1.  Tegafur and 5-fluorouracil pelvic tissue concentrations in rectal cancer patients receiving preoperative chemoradiation.

Authors:  F A Calvo; A Aldaz; L Zufía; D de la Mata; J Serrano; R García; J A Arranz; A Alvarado; J Giráldez
Journal:  Clin Transl Oncol       Date:  2006-07       Impact factor: 3.405

2.  Open-label trial on efficacy and security of treatment with gemcitabine and oral modulation with tegafur and levofolinic acid (GEMTG) in patients with advanced pancreatic cancer.

Authors:  Carles Pericay Pijaume; Pilar Escudero Emperador; Román Bastús Piulats; Juan Manuel Campos Cervera; Gaspar Esquerdo Galiana; Manuel Gallén Castillo; Jordi Alfaro Gamero; Emma Dotor Navarro; Aleydis Pisa Gatell; Inmaculada Guasch Jordán; Eugeni Saigí Grau
Journal:  Clin Transl Oncol       Date:  2011-01       Impact factor: 3.405

Review 3.  Cellular pharmacology of fluorinated pyrimidines in vivo in man.

Authors:  J S Kovach; R W Beart
Journal:  Invest New Drugs       Date:  1989-04       Impact factor: 3.850

Review 4.  Oral versus intravenous fluoropyrimidines for colorectal cancer.

Authors:  Fiona Chionh; David Lau; Yvonne Yeung; Timothy Price; Niall Tebbutt
Journal:  Cochrane Database Syst Rev       Date:  2017-07-28

5.  Quantitative analysis of hydrogen and chalcogen bonds in two pyrimidine-5-carbonitrile derivatives, potential DHFR inhibitors: an integrated crystallographic and theoretical study.

Authors:  Lamya H Al-Wahaibi; Kushumita Chakraborty; Nora H Al-Shaalan; Mohamed Yehya Annavi Syed Majeed; Olivier Blacque; Aamal A Al-Mutairi; Ali A El-Emam; M Judith Percino; Subbiah Thamotharan
Journal:  RSC Adv       Date:  2020-10-06       Impact factor: 4.036

6.  Structural Insights of Three 2,4-Disubstituted Dihydropyrimidine-5-carbonitriles as Potential Dihydrofolate Reductase Inhibitors.

Authors:  Lamya H Al-Wahaibi; Althaf Shaik; Mohammed A Elmorsy; Mohammed S M Abdelbaky; Santiago Garcia-Granda; Subbiah Thamotharan; Vijay Thiruvenkatam; Ali A El-Emam
Journal:  Molecules       Date:  2021-05-29       Impact factor: 4.411

  6 in total

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