Survival of patients with head and neck cancer treated with definitive radiotherapy and concurrent cisplatin or concurrent cetuximab: A Surveillance, Epidemiology, and End Results-Medicare analysis

被引:27
|
作者
Xiang, Michael [1 ]
Holsinger, F. Christopher [2 ]
Colevas, A. Dimitrios [3 ]
Chen, Michelle M. [2 ]
Quynh-Thu Le [1 ]
Beadle, Beth M. [1 ]
机构
[1] Stanford Univ, Dept Radiat Oncol, 875 Blake Wilbur Dr,Room CC-G226, Stanford, CA 94304 USA
[2] Stanford Univ, Dept Otolaryngol, Div Head & Neck Surg, Stanford, CA 94304 USA
[3] Stanford Univ, Div Oncol, Dept Med, Stanford, CA 94304 USA
关键词
cetuximab; chemoradiotherapy; cisplatin; head and neck neoplasms; Medicare; propensity score; squamous cell carcinoma; SQUAMOUS-CELL CARCINOMA; LOCALLY ADVANCED HEAD; RADIATION-THERAPY; HUMAN-PAPILLOMAVIRUS; CONCOMITANT CHEMOTHERAPY; TRIAL; CHEMORADIOTHERAPY; ASSOCIATION; TOXICITY; OUTCOMES;
D O I
10.1002/cncr.31708
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Cisplatin and cetuximab are both systemic therapies commonly used in combination with radiation (RT) for the definitive treatment of head and neck cancers, but their comparative efficacy is unclear. Methods Patients with locoregionally advanced (American Joint Committee on Cancer stage III-IVB) squamous cell carcinomas of the oropharynx, larynx, or hypopharynx were identified in the Surveillance, Epidemiology, and End Results -Medicare database. Patients received either cisplatin or cetuximab concurrent with RT, as determined by Medicare claims. The primary study outcome was head and neck cancer-specific mortality (CSM) analyzed with competing risks. Filtering, propensity score matching, and multivariable Fine-Gray regression were used to adjust for differences between the cisplatin and cetuximab cohorts, including age, comorbidity, and cycles of systemic therapy received. Results The total cohort consisted of 1395 patients, of whom 786 (56%) received cisplatin and 609 (44%) received cetuximab; the median follow-up was 3.5 years in the patients who remained alive. In the cetuximab cohort, CSM was significantly higher than in the cisplatin cohort (39% vs 25% at 3 years; P < .0001). In the matched cohorts (n = 414), the adjusted hazard ratio of CSM for cetuximab was 1.65 (95% confidence interval, 1.30-2.09; P < .0001) relative to cisplatin, corresponding to an absolute difference of approximately 10% in both CSM and overall survival at 3 years. Cetuximab was associated with less dysphagia, more dermatitis, and a similar incidence of mucositis. Conclusions In this sizeable, national patient population, treatment with cetuximab was associated with significantly higher CSM than cisplatin. These results suggest that cisplatin may be the preferred chemotherapeutic agent in this setting. (C) 2018 American Cancer Society.
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收藏
页码:4486 / 4494
页数:9
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