Department of Otolaryngology-Head and Neck Surgery, UT Southwestern Medical Center, Dallas, TX, United States of America.
Department of Radiation Oncology, UT Southwestern Medical Center, Dallas, TX, United States of America.
Am J Otolaryngol. 2022 Sep-Oct;43(5):103555. doi: 10.1016/j.amjoto.2022.103555. Epub 2022 Aug 6.
To characterize the significance of patient-level influences, including smoking history, on oncologic outcomes in human papillomavirus (HPV)-mediated oropharyngeal cancer (OPC).
A bi-institutional retrospective cohort study of previously untreated, HPV+ OPC patients who underwent curative treatment from 1/1/2008 to 7/1/2018 was performed. The primary outcome was disease-free survival (DFS) and the primary exposure was ≤10 versus >10-pack-year (PY)-smoking history.
Among 953 OPC patients identified, 342 individuals with HPV+ OPC were included. The median patient age was 62 years, 33.0% had a > 10-PY-smoking history, 60.2% had AJCC8 stage I disease, and 35.0% underwent primary surgery. The median follow-up was 49 months (interquartile range [IQR] 32-75 months). Four-year DFS-estimates were similar among patients with ≤10-PY-smoking history (78.0%, 95% CI:71.7%-83.1%) compared to >10-PYs (74.8%; 95% CI:65.2%-82.0%; log-rank:p = 0.53). On univariate analysis, >10-PY-smoking history did not correlate with DFS (hazard ratio[HR]:1.15;95% CI:0.74-1.79) and remained nonsignificant when forced into the multivariable model. On adjusted analyses, stage, treatment paradigm, and age predicted DFS. Neither >10-PYs, nor any other definition of tobacco use (e.g., current smoker or > 20-PYs) was predictive of DFS, overall survival, or disease-specific survival. Conversely, age nonsignificantly and significantly predicted adjusted DFS (adjusted HR[aHR]:1.02,95% CI:0.997-1.05, p = 0.08), overall survival (aHR 1.05; 95% CI: 1.02-1.08; p = 0.002) and disease-specific survival (aHR 1.04;95% CI: 0.99-1.09;p = 0.09).
Other than age, patient-level influences may not be primary drivers of HPV+ OPC outcomes. Although limited by its modest sample size, our study suggests the significance of smoking has been overstated in this disease. These findings and the emerging literature collectively do not support risk-stratification employing the >10-PY threshold.
Level 4.
描述患者水平的影响因素的意义,包括吸烟史,对人乳头瘤病毒(HPV)介导的口咽癌(OPC)的肿瘤学结果的影响。
对 2008 年 1 月 1 日至 2018 年 7 月 1 日期间接受根治性治疗的未经治疗的、HPV+OPC 患者进行了一项双机构回顾性队列研究。主要结果是无病生存(DFS),主要暴露是吸烟史≤10 包年(PY)与>10 PY。
在确定的 953 例 OPC 患者中,纳入了 342 例 HPV+OPC 患者。患者的中位年龄为 62 岁,33.0%有>10 PY 的吸烟史,60.2%有 AJCC8 期疾病,35.0%接受了原发性手术。中位随访时间为 49 个月(四分位距[IQR]32-75 个月)。在吸烟史≤10 PY 的患者中,4 年 DFS 估计值与>10 PY 相似(78.0%,95%CI:71.7%-83.1%)(对数秩检验:p=0.53)。在单变量分析中,>10 PY 的吸烟史与 DFS 无相关性(风险比[HR]:1.15;95%CI:0.74-1.79),并且在多变量模型中仍然不显著。在调整后的分析中,分期、治疗方案和年龄预测了 DFS。>10 PY 吸烟史或任何其他吸烟定义(例如,当前吸烟者或>20 PY)均不能预测 DFS、总生存或疾病特异性生存。相反,年龄对调整后的 DFS 具有显著和非显著的预测作用(调整后的 HR[aHR]:1.02,95%CI:0.997-1.05,p=0.08)、总生存(aHR 1.05;95%CI:1.02-1.08;p=0.002)和疾病特异性生存(aHR 1.04;95%CI:0.99-1.09;p=0.09)。
除年龄外,患者水平的影响因素可能不是 HPV+OPC 结果的主要驱动因素。尽管由于样本量较小,存在一定局限性,但我们的研究表明,吸烟对这种疾病的影响被夸大了。这些发现和新兴文献都不支持采用>10 PY 阈值进行风险分层。
4 级。