Letter to the editor referring to the publication entitled "The role of antagonists of the PD-1: PD-L1/PD-L2 axis in head and neck cancer treatment" by Pai et al
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F16%3A00066737" target="_blank" >RIV/65269705:_____/16:00066737 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216224:14110/16:00092818
Výsledek na webu
<a href="http://www.oraloncology.com/article/S1368-8375(16)30135-X/abstract" target="_blank" >http://www.oraloncology.com/article/S1368-8375(16)30135-X/abstract</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.oraloncology.2016.08.007" target="_blank" >10.1016/j.oraloncology.2016.08.007</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Letter to the editor referring to the publication entitled "The role of antagonists of the PD-1: PD-L1/PD-L2 axis in head and neck cancer treatment" by Pai et al
Popis výsledku v původním jazyce
As addressed by Pai with co-workers in their comprehensive review, novel immunotherapeutic strategies using immune checkpoint inhibitors represent a promising area of research in squamous cell carcinoma of the head and neck (SCCHN) [1]. Results from a phase III trial and preliminary data from three early clinical studies demonstrated the efficacy of monoclonal antibodies against programmed death-1 (PD-1) receptor (nivolumab, pembrolizumab) and its ligand PD-L1 (durvalumab) as second-line treatments in the recurrent and/or metastatic (R/M) setting. With relatively low incidence of serious adverse events, these agents elicited durable responses even in patients with refractory disease. Moreover, nivolumab, as the first drug ever, significantly improved overall survival (OS) by 2.4 months compared with investigator's choice (single-agent chemotherapy or cetuximab) [1-4]. From a broader perspective, these pioneering studies have important implications for future trial design with one of the challenges being the selection of appropriate clinical endpoints associated with benefits of immune checkpoint inhibitors.
Název v anglickém jazyce
Letter to the editor referring to the publication entitled "The role of antagonists of the PD-1: PD-L1/PD-L2 axis in head and neck cancer treatment" by Pai et al
Popis výsledku anglicky
As addressed by Pai with co-workers in their comprehensive review, novel immunotherapeutic strategies using immune checkpoint inhibitors represent a promising area of research in squamous cell carcinoma of the head and neck (SCCHN) [1]. Results from a phase III trial and preliminary data from three early clinical studies demonstrated the efficacy of monoclonal antibodies against programmed death-1 (PD-1) receptor (nivolumab, pembrolizumab) and its ligand PD-L1 (durvalumab) as second-line treatments in the recurrent and/or metastatic (R/M) setting. With relatively low incidence of serious adverse events, these agents elicited durable responses even in patients with refractory disease. Moreover, nivolumab, as the first drug ever, significantly improved overall survival (OS) by 2.4 months compared with investigator's choice (single-agent chemotherapy or cetuximab) [1-4]. From a broader perspective, these pioneering studies have important implications for future trial design with one of the challenges being the selection of appropriate clinical endpoints associated with benefits of immune checkpoint inhibitors.
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
—
Návaznosti
N - Vyzkumna aktivita podporovana z neverejnych zdroju
Ostatní
Rok uplatnění
2016
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Oral oncology
ISSN
1368-8375
e-ISSN
—
Svazek periodika
62
Číslo periodika v rámci svazku
NOV
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
2
Strana od-do
"E3"-"E4"
Kód UT WoS článku
000392635300002
EID výsledku v databázi Scopus
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