All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Kinetically Guided Neoadjuvant Chemoradiotherapy Based on 5-Fluorouracil in Patients with Locally Advanced Rectal Cancer

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11150%2F15%3A10315478" target="_blank" >RIV/00216208:11150/15:10315478 - isvavai.cz</a>

  • Alternative codes found

    RIV/00179906:_____/15:10315478

  • Result on the web

    <a href="http://dx.doi.org/10.1007/s40262-014-0216-4" target="_blank" >http://dx.doi.org/10.1007/s40262-014-0216-4</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s40262-014-0216-4" target="_blank" >10.1007/s40262-014-0216-4</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Kinetically Guided Neoadjuvant Chemoradiotherapy Based on 5-Fluorouracil in Patients with Locally Advanced Rectal Cancer

  • Original language description

    This study estimated patients' early response following neoadjuvant chemoradiotherapy (CHRT) of locally advanced rectal cancer based on 5-fluorouracil (5-FU). The target was to achieve pathological complete response and toxicities of grade LESS-THAN OR EQUAL TO2, using individual dosing predicted according to the steady-state plasma concentration (Css) and pharmacokinetic parameters of 5-FU: the area under the time-concentration curve at steady state (AUC) and clearance (CL). This open-label prospectivestudy enrolled 33 adult patients treated with 5-FU administered as a continuous intravenous infusion over 4-5 weeks, as follows: in Group 1a (N = 6), the patients received a standard dose of 300 mg/m2/24 h. In Group 1b (N = 7), the patients were treatedwith an escalated dose of 400-1,000 mg/m2/24 h. In Group 2 (N = 20), the patients were given dosing kinetically guided in order to reach the target range of 5-FU Css 50-100 ?g/L. Tolerability was tested according to Common Terminology Cr

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/NS9693" target="_blank" >NS9693: Individual 5-fluorouracil dose individualization in patients with colorectal cancer</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2015

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Clinical Pharmacokinetics

  • ISSN

    0312-5963

  • e-ISSN

  • Volume of the periodical

    54

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    NZ - NEW ZEALAND

  • Number of pages

    13

  • Pages from-to

    503-515

  • UT code for WoS article

    000355338600004

  • EID of the result in the Scopus database

    2-s2.0-84939965747