TP53-related clonal competition and disrupted molecular processes in CLL
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14740%2F24%3A00137827" target="_blank" >RIV/00216224:14740/24:00137827 - isvavai.cz</a>
Výsledek na webu
<a href="https://ericll2024.org/" target="_blank" >https://ericll2024.org/</a>
DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
TP53-related clonal competition and disrupted molecular processes in CLL
Popis výsledku v původním jazyce
The presence of either TP53 gene loss or mutation defined high-risk CLL especially in the era of chemoimmunotherapy. Its prognostic and predictive impact remains a matter of debate in the setting of BTKi- and BCL2i-based treatment, which does not act directly via the TP53 pathway, but yet seems to associate with worse clinical outcomes. The adverse effect on overall survival, at least upon chemoimmunotherapy, is notable not only in patients with expanded but also in lowburden TP53 mutations, which were identified in 5–35% of CLL patients. In this study, we aimed to scrutinize the principles of clonal competition in CLL and identify factors influencing the development of TP53-mutated subclones in various clinical contexts.
Název v anglickém jazyce
TP53-related clonal competition and disrupted molecular processes in CLL
Popis výsledku anglicky
The presence of either TP53 gene loss or mutation defined high-risk CLL especially in the era of chemoimmunotherapy. Its prognostic and predictive impact remains a matter of debate in the setting of BTKi- and BCL2i-based treatment, which does not act directly via the TP53 pathway, but yet seems to associate with worse clinical outcomes. The adverse effect on overall survival, at least upon chemoimmunotherapy, is notable not only in patients with expanded but also in lowburden TP53 mutations, which were identified in 5–35% of CLL patients. In this study, we aimed to scrutinize the principles of clonal competition in CLL and identify factors influencing the development of TP53-mutated subclones in various clinical contexts.
Klasifikace
Druh
O - Ostatní výsledky
CEP obor
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OECD FORD obor
30204 - Oncology
Návaznosti výsledku
Projekt
Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2024
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů