Advances in multiple myeloma therapy during two past decades
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F14%3A10291741" target="_blank" >RIV/00216208:11110/14:10291741 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00064165:_____/14:10291741
Výsledek na webu
<a href="http://dx.doi.org/10.1016/j.csbj.2014.05.005" target="_blank" >http://dx.doi.org/10.1016/j.csbj.2014.05.005</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.csbj.2014.05.005" target="_blank" >10.1016/j.csbj.2014.05.005</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Advances in multiple myeloma therapy during two past decades
Popis výsledku v původním jazyce
Multiple myeloma (MM) is a clonal B-cell malignancy characterized by aberrant expansion of plasma cells within bone marrow and extramedullary sites. It is one of the most common haematological malignancies; it accounts for 1.4% of all tumours and is responsible for 2% of cancer-related mortality. Over the last decades, the paradigm of MM therapy has changed dramatically - from the conventional combination of oral melphatan + prednisone, high-dose chemotherapy with stem cell (ASCT) support for younger patients to the present paradigm with the use of one (or more) of 3 major new targeted agents - the first-in class proteasome inhibitor bortezomib, the immunomodulatory drug thalidomide, and its more potent derivative lenalidomide. Their use as a part of initial therapy is associated with high overall response rates as well as high rates of complete response (CR), both for elderly patients unable to undergo ASCT and for younger patients treated prior to ASCT. Altogether, the advent of nove
Název v anglickém jazyce
Advances in multiple myeloma therapy during two past decades
Popis výsledku anglicky
Multiple myeloma (MM) is a clonal B-cell malignancy characterized by aberrant expansion of plasma cells within bone marrow and extramedullary sites. It is one of the most common haematological malignancies; it accounts for 1.4% of all tumours and is responsible for 2% of cancer-related mortality. Over the last decades, the paradigm of MM therapy has changed dramatically - from the conventional combination of oral melphatan + prednisone, high-dose chemotherapy with stem cell (ASCT) support for younger patients to the present paradigm with the use of one (or more) of 3 major new targeted agents - the first-in class proteasome inhibitor bortezomib, the immunomodulatory drug thalidomide, and its more potent derivative lenalidomide. Their use as a part of initial therapy is associated with high overall response rates as well as high rates of complete response (CR), both for elderly patients unable to undergo ASCT and for younger patients treated prior to ASCT. Altogether, the advent of nove
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
FD - Onkologie a hematologie
OECD FORD obor
—
Návaznosti výsledku
Projekt
<a href="/cs/project/NT12215" target="_blank" >NT12215: Racionalizace léčby mnohočetného myelomu</a><br>
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2014
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Computational and Structural Biotechnology Journal
ISSN
2001-0370
e-ISSN
—
Svazek periodika
10
Číslo periodika v rámci svazku
16
Stát vydavatele periodika
SE - Švédské království
Počet stran výsledku
3
Strana od-do
38-40
Kód UT WoS článku
—
EID výsledku v databázi Scopus
—