Evaluation of Total Hepatocellular Cancer Lifespan, Including Both Clinically Evident and Preclinical Development, Using Combined Network Phenotyping Strategy and Fisher Information Analysis
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F15%3A10319693" target="_blank" >RIV/00216208:11320/15:10319693 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1053/j.seminoncol.2014.12.025" target="_blank" >http://dx.doi.org/10.1053/j.seminoncol.2014.12.025</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1053/j.seminoncol.2014.12.025" target="_blank" >10.1053/j.seminoncol.2014.12.025</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Evaluation of Total Hepatocellular Cancer Lifespan, Including Both Clinically Evident and Preclinical Development, Using Combined Network Phenotyping Strategy and Fisher Information Analysis
Popis výsledku v původním jazyce
We previously showed that for hepatocellular cancer (HCC) prognostication, disease parameters need to be considered within a total personal clinical context. This requires preserving the coherence of data values, observed simultaneously for each patientduring baseline diagnostic evaluation. Application of the Network Phenotyping Strategy (NPS) provided quantitative descriptors of these patient coherences. Combination of these descriptors with Fisher information about the patient tumor mass and the histogram of the tumor masses in the whole cohort permitted estimation of the time from disease onset until clinical diagnosis (t(baseline)). We found faster growth of smaller tumors having total masses <70 (80% of cohort) which involved about three times more interacting cellular processes than were observed for slower growing larger tumors (20% of cohort) with total masses >70. Combining the clinical survival and tbasth normalized all HCC patients to a common 1,045 days of mean total disea
Název v anglickém jazyce
Evaluation of Total Hepatocellular Cancer Lifespan, Including Both Clinically Evident and Preclinical Development, Using Combined Network Phenotyping Strategy and Fisher Information Analysis
Popis výsledku anglicky
We previously showed that for hepatocellular cancer (HCC) prognostication, disease parameters need to be considered within a total personal clinical context. This requires preserving the coherence of data values, observed simultaneously for each patientduring baseline diagnostic evaluation. Application of the Network Phenotyping Strategy (NPS) provided quantitative descriptors of these patient coherences. Combination of these descriptors with Fisher information about the patient tumor mass and the histogram of the tumor masses in the whole cohort permitted estimation of the time from disease onset until clinical diagnosis (t(baseline)). We found faster growth of smaller tumors having total masses <70 (80% of cohort) which involved about three times more interacting cellular processes than were observed for slower growing larger tumors (20% of cohort) with total masses >70. Combining the clinical survival and tbasth normalized all HCC patients to a common 1,045 days of mean total disea
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
BB - Aplikovaná statistika, operační výzkum
OECD FORD obor
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Návaznosti výsledku
Projekt
<a href="/cs/project/LL1201" target="_blank" >LL1201: Komplexní Struktury: Regularita v Kombinatorice a Diskrétní Matematice</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2015
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Seminars in Oncology
ISSN
0093-7754
e-ISSN
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Svazek periodika
42
Číslo periodika v rámci svazku
2
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
8
Strana od-do
339-346
Kód UT WoS článku
000352757700014
EID výsledku v databázi Scopus
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