p16, HPV, and Cetuximab: What Is the Evidence?

被引:19
作者
Bonner, James A. [1 ]
Mesia, Ricard [2 ]
Giralt, Jordi [3 ]
Psyrri, Amanda [4 ]
Keilholz, Ulrich [5 ]
Rosenthal, David I. [6 ]
Beier, Frank [7 ]
Schulten, Jeltje [7 ]
Vermorken, Jan B. [8 ]
机构
[1] Univ Alabama Birmingham, Ctr Comprehens Canc, Birmingham, AL USA
[2] Univ Barcelona, IDIBELL, Catalan Inst Oncol Hosp, Med Oncol Dept, Barcelona, Spain
[3] Univ Autonama Barcelona, Hosp Vall Hebron, Dept Med, Barcelona, Spain
[4] Univ Athens, Athens, Greece
[5] Charite Comprehens Canc Ctr, Berlin, Germany
[6] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[7] Merck KGaA, Darmstadt, Germany
[8] Antwerp Univ Hosp, Edegem, Belgium
关键词
Cetuximab; p16; Human papillomavirus; Squamous cell carcinoma of the head and neck; IMCL-9815; EXTREME; SQUAMOUS-CELL CARCINOMA; CHEMOTHERAPY PLUS CETUXIMAB; FACTOR RECEPTOR BLOCKADE; NECK-CANCER PATIENTS; QUALITY-OF-LIFE; HUMAN-PAPILLOMAVIRUS; OROPHARYNGEAL CANCER; REGISTRATION TRIAL; HEAD; RADIOTHERAPY;
D O I
10.1634/theoncologist.2016-0433
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Squamous cell carcinoma of the head and neck (SCCHN) is the sixth most common cancer worldwide. It has recently been appreciated that human papillomavirus (HPV) status (or p16 status, which is a frequently used surrogate for HPV status) is prognostic for oropharyngeal SCCHN. Here, we review and contextualize existing p16 and HPV data, focusing on the cetuximab registration trials in previously untreated, locoregionally advanced, nonmetastatic SCCHN (LA SCCHN) and in recurrent and/or metastatic SCCHN (R/M SCCHN): the IMCL-9815 and EXTREME clinical trials, respectively. Taken together, the available data suggest that, while p16 and HPV are prognostic biomarkers in patients with LA SCCHN and R/M SCCHN, it could not be shown that they are predictive for the outcomes of the described cetuximab-containing trial regimens. Consequently, although HPV status provides prognostic information, it is not shown to predict therapy response, and so is not helpful for assigning first-line therapy in patients with SCCHN. In addition, we discuss assays currently used to assess p16 and HPV status, as well as the differentiation between these two biomarkers. Ultimately, we believe HPV E6/E7 polymerase chain reaction-based mRNA testing may represent the most informative technique for assessing HPV status in patients with SCCHN. While p16 is a valid surrogate for HPV status in oropharyngeal carcinoma (OPC), there is a higher risk of discordance between p16 and HPVstatus in non-OPC SCCHN. Collectively, these discussions hold key implications for the clinical management of SCCHN.
引用
收藏
页码:811 / 822
页数:12
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