SZTURZ, Petr a S. FAIVRE. 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. Oral Oncology. Amsterdam: Elsevier Science BV, 2016, roč. 62, "neuvedeno", s. "e3"-"e4", 2 s. ISSN 1368-8375. Dostupné z: https://dx.doi.org/10.1016/j.oraloncology.2016.08.007.
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Základní údaje
Originální název 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.
Autoři SZTURZ, Petr (203 Česká republika, garant, domácí) a S. FAIVRE (250 Francie).
Vydání Oral Oncology, Amsterdam, Elsevier Science BV, 2016, 1368-8375.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30200 3.2 Clinical medicine
Stát vydavatele Nizozemské království
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 4.794
Kód RIV RIV/00216224:14110/16:00092818
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1016/j.oraloncology.2016.08.007
UT WoS 000392635300002
Klíčová slova anglicky squamous-cell carcinoma; recurrent; methotrexate; trial
Štítky EL OK
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Ing. Mgr. Věra Pospíšilíková, učo 9005. Změněno: 1. 3. 2017 09:23.
Anotace
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.
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