Department of Radiation Oncology, Stanford University, Stanford, California, United States.
Department of Otolaryngology, Division of Head and Neck Surgery, Stanford University, Stanford, California, United States.
Cancer. 2018 Dec 1;124(23):4486-4494. doi: 10.1002/cncr.31708. Epub 2018 Oct 17.
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.
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.
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.
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.
顺铂和西妥昔单抗都是常用于联合放疗(RT)治疗头颈部癌症的系统治疗药物,但它们的疗效比较尚不清楚。
从监测、流行病学和最终结果-医疗保险数据库中确定局部晚期(美国癌症联合委员会分期 III-IVB 期)口咽、喉或下咽鳞状细胞癌患者。根据医疗保险索赔确定患者接受顺铂或西妥昔单抗联合 RT 治疗。主要研究结果是头颈部癌症特异性死亡率(CSM),采用竞争风险分析。采用筛选、倾向评分匹配和多变量 Fine-Gray 回归调整顺铂和西妥昔单抗队列之间的差异,包括年龄、合并症和接受的系统治疗周期。
总队列包括 1395 例患者,其中 786 例(56%)接受顺铂治疗,609 例(44%)接受西妥昔单抗治疗;在仍存活的患者中,中位随访时间为 3.5 年。在西妥昔单抗组中,CSM 显著高于顺铂组(3 年时为 39% vs 25%;P<0.0001)。在匹配队列(n=414)中,西妥昔单抗组的 CSM 调整风险比为 1.65(95%置信区间,1.30-2.09;P<0.0001),与顺铂相比,3 年时 CSM 和总生存率的绝对差异约为 10%。西妥昔单抗与较少的吞咽困难、更多的皮炎和相似的粘膜炎发生率相关。
在这个相当大的全国性患者人群中,西妥昔单抗治疗与顺铂相比,CSM 显著更高。这些结果表明,在这种情况下,顺铂可能是首选的化疗药物。