review article | Q7318358 |
scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1005989173 |
P356 | DOI | 10.2165/00003495-199958003-00011 |
P698 | PubMed publication ID | 10711845 |
P2093 | author name string | Pazdur R | |
Hoff PM | |||
Lassere Y | |||
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Pharmacokinetics of Leucovorin Metabolites in Human Plasma as a Function of Dose Administrated Orally and Intravenously | Q41135720 | ||
Preoperative combined oral UFT plus leucovorin and radiation therapy for rectal cancer | Q42666008 | ||
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Impact of protracted venous infusion fluorouracil with or without interferon alfa-2b on tumor response, survival, and quality of life in advanced colorectal cancer. | Q53639104 | ||
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Thymidylate synthase inhibition by an oral regimen consisting of tegafur-uracil (UFT) and low-dose leucovorin for patients with gastric cancer | Q71422133 | ||
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Mechanism-based improvement in the therapeutic selectivity of 5-FU prodrug alone and under conditions of metabolic modulation | Q71934546 | ||
Clinical application of biochemical modulation in cancer chemotherapy: biochemical modulation for 5-FU | Q71934549 | ||
Biochemical factors affecting the tightness of 5-fluorodeoxyuridylate binding to human thymidylate synthetase | Q72004501 | ||
A fixed-ratio combination of uracil and Ftorafur (UFT) with low dose leucovorin. An active oral regimen for advanced colorectal cancer | Q72425285 | ||
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Fluorouracil plus levamisole as effective adjuvant therapy after resection of stage III colon carcinoma: a final report | Q72525174 | ||
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Phase I trial of uracil-tegafur (UFT) plus oral leucovorin: 14-day schedule | Q73504125 | ||
P921 | main subject | colorectal cancer | Q188874 |
fluorouracil | Q238512 | ||
colorectal carcinoma | Q25493920 | ||
P304 | page(s) | 77-83 | |
P577 | publication date | 1999-01-01 | |
P1433 | published in | Drugs | Q3040094 |
P1476 | title | Tegafur/uracil + calcium folinate in colorectal cancer: double modulation of fluorouracil | |
P478 | volume | 58 Suppl 3 |
Q33370792 | A phase I dose-finding clinical pharmacokinetic study of an oral formulation of irinotecan (CPT-11) administered for 5 days every 3 weeks in patients with advanced solid tumours |
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