Machtay Mitchell, Moughan Jennifer, Trotti Andrew, Garden Adam S, Weber Randal S, Cooper Jay S, Forastiere Arlene, Ang K Kian
Jefferson Medical College and Kimmel Cancer Center of Thomas Jefferson University, Philadelphia, PA, USA.
J Clin Oncol. 2008 Jul 20;26(21):3582-9. doi: 10.1200/JCO.2007.14.8841. Epub 2008 Jun 16.
Concurrent chemoradiotherapy (CCRT) for squamous cell carcinoma of the head and neck (SCCHN) increases both local tumor control and toxicity. This study evaluates clinical factors that are associated with and might predict severe late toxicity after CCRT.
Patients were analyzed from a subset of three previously reported Radiation Therapy Oncology Group (RTOG) trials of CCRT for locally advanced SCCHN (RTOG 91-11, 97-03, and 99-14). Severe late toxicity was defined in this secondary analysis as chronic grade 3 to 4 pharyngeal/laryngeal toxicity (RTOG/European Organisation for the Research and Treatment of Cancer late toxicity scoring system) and/or requirement for a feeding tube >or= 2 years after registration and/or potential treatment-related death (eg, pneumonia) within 3 years. Case-control analysis was performed, with a multivariable logistic regression model that included pretreatment and treatment potential factors.
A total of 230 patients were assessable for this analysis: 99 patients with severe late toxicities and 131 controls; thus, 43% of assessable patients had a severe late toxicity. On multivariable analysis, significant variables correlated with the development of severe late toxicity were older age (odds ratio 1.05 per year; P = .001); advanced T stage (odds ratio, 3.07; P = .0036); larynx/hypopharynx primary site (odds ratio, 4.17; P = .0041); and neck dissection after CRT (odds ratio, 2.39; P = .018).
Severe late toxicity after CCRT is common. Older age, advanced T-stage, and larynx/hypopharynx primary site were strong independent risk factors. Neck dissection after CCRT was associated with an increased risk of these complications.
头颈部鳞状细胞癌(SCCHN)的同步放化疗(CCRT)可提高局部肿瘤控制率,但也会增加毒性。本研究评估与CCRT后严重晚期毒性相关且可能具有预测作用的临床因素。
对先前报道的三项放射治疗肿瘤学组(RTOG)关于局部晚期SCCHN的CCRT试验(RTOG 91-11、97-03和99-14)的一个亚组患者进行分析。在本次二次分析中,严重晚期毒性定义为慢性3至4级咽/喉毒性(RTOG/欧洲癌症研究与治疗组织晚期毒性评分系统)和/或登记后2年及以上需要饲管和/或3年内潜在的治疗相关死亡(如肺炎)。进行病例对照分析,采用多变量逻辑回归模型,纳入治疗前和治疗相关潜在因素。
共有230例患者可纳入本分析:99例有严重晚期毒性患者和131例对照;因此,43%的可评估患者有严重晚期毒性。多变量分析显示,与严重晚期毒性发生相关的显著变量为年龄较大(每年优势比1.05;P = 0.001);T分期较晚(优势比3.07;P = 0.0036);喉/下咽原发部位(优势比4.17;P = 0.0041);以及放化疗后行颈部清扫术(优势比2.39;P = 0.018)。
CCRT后严重晚期毒性很常见。年龄较大、T分期较晚和喉/下咽原发部位是强烈的独立危险因素。CCRT后行颈部清扫术与这些并发症风险增加相关。