Optimizing treatments for recurrent or metastatic head and neck squamous cell carcinoma

被引:47
作者
Specenier, Pol [1 ,2 ]
Vermorken, Jan B. [1 ,2 ]
机构
[1] Antwerp Univ Hosp, Dept Oncol, Wilrijkstr 10, B-2650 Edegem, Belgium
[2] Univ Antwerp, Fac Med & Hlth Sci, Antwerp, Belgium
关键词
Head and neck cancer; immunotherapy; systemic treatment; recurrent; metastatic; chemotherapy; targeted therapy; PHASE-II TRIAL; CHEMOTHERAPY PLUS CETUXIMAB; PLATINUM-BASED CHEMOTHERAPY; COOPERATIVE-ONCOLOGY-GROUP; PHOSPHATIDYLINOSITOL 3-KINASE INHIBITOR; PREVIOUSLY TREATED RECURRENT; NON-NASOPHARYNGEAL HEAD; ANTI-EGFR ANTIBODY; QUALITY-OF-LIFE; EVERY; WEEKS;
D O I
10.1080/14737140.2018.1493925
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: The majority of patients with locally advanced head and neck squamous cell carcinoma (HNSCC) will recur. The treatment of patients with recurrent/metastatic (R/M HNSCC) is rapidly evolving.Areas covered: This article will comprehensively review the current systemic treatment of R/M HNSCC.Expert commentary: For the time being, the EXTREME regimen (cetuximab in combination with platinum and 5-fluorouracil) still remains standard of care in previously untreated R/M HNSCC patients who are candidates for combination chemotherapy. Single agents with well documented activity in HNSCC include methotrexate, cisplatin, 5-FU, docetaxel, and paclitaxel. The anti-PD-1 monoclonal antibody nivolumab can be considered the current standard of care in patients with R/M HNSCC progressing after platinum-based therapy based on the results of CheckMate 141 showing a survival benefit over standard of care drugs, such as single agent weekly cetuximab, methotrexate, or docetaxel.Multiple randomized phase III trials comparing anti-PD(L)-antibodies either as single agent or in combination with chemotherapy or an anti-CTLA-4 with the EXTREME as fist line treatment are ongoing or planned. The outcome of these trials might change the current treatment paradigm in previously untreated R/M HNSCC. Immunotherapeutic agents under active investigation include Toll-like receptor 8 agonists and inhibitors of IDO1.
引用
收藏
页码:901 / 915
页数:15
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