Amini Arya, Jasem Jagar, Jones Bernard L, Robin Tyler P, McDermott Jessica D, Bhatia Shilpa, Raben David, Jimeno Antonio, Bowles Daniel W, Karam Sana D
Department of Radiation Oncology, University of Colorado School of Medicine, Aurora, CO, USA.
Department of Medicine, University of Colorado School of Medicine, Aurora, CO, USA.
Oral Oncol. 2016 May;56:1-7. doi: 10.1016/j.oraloncology.2016.02.011. Epub 2016 Mar 12.
This study identifies clinical characteristics associated with HPV-positive oropharynx squamous cell carcinoma (OPSCC) and evaluates predictors of overall survival (OS) in HPV-positive patients undergoing definitive treatment within the National Cancer Data Base (NCDB).
The NCDB was queried for patients ⩾18years old with OPSCC and known HPV status who underwent definitive treatment: surgery, radiation (RT), chemotherapy-RT (CRT), surgery+RT, surgery+CRT (S-CRT). Cox proportional hazards model was used for multivariate analysis (MVA) to evaluate predictors of OS by HPV status.
3952 patients were included: 2454 (62%) were HPV-positive. Median follow up was 23.7months (range, 1.0-54.5). Unadjusted 2-year OS rates for HPV-positive vs. negative were 93.1% vs. 77.8% (p<0.001) with an adjusted hazard ratio of 0.44 (95% CI, 0.36-0.53; p<0.001). MVA identified multimodality treatment including CRT (HR, 0.42; p=0.024) and S-RT (HR, 0.30; p=0.024), but not S-CRT (HR, 0.51; p=0.086), as predictors for improved OS in HPV-positive stage III-IVB disease. Multimodality treatment including S-CRT was associated with longer OS in HPV-negative OPSCC. Nodal stage was poorly associated with OS in HPV-positive cancers. The presence of positive margins and/or extracapsular extension was associated with worse OS in HPV-negative (HR, 2.11; p=0.008) but not HPV positive OPSCC (HR, 1.61; p=0.154).
The established demographic and clinical features of HPV-positive OPSCC were corroborated in the NCDB. Population analysis suggests that AJCC staging is poorly associated with OS in HPV-positive cancer, and traditional high-risk features may be less impactful. Bimodality therapy appears beneficial in HPV-positive HNSCC.
本研究确定与HPV阳性口咽鳞状细胞癌(OPSCC)相关的临床特征,并评估在国家癌症数据库(NCDB)中接受确定性治疗的HPV阳性患者的总生存期(OS)预测因素。
在NCDB中查询年龄≥18岁、患有OPSCC且已知HPV状态并接受确定性治疗(手术、放疗(RT)、化疗-放疗(CRT)、手术+RT、手术+CRT(S-CRT))的患者。采用Cox比例风险模型进行多变量分析(MVA),以按HPV状态评估OS的预测因素。
纳入3952例患者:2454例(62%)为HPV阳性。中位随访时间为23.7个月(范围1.0 - 54.5个月)。HPV阳性与阴性患者未经调整的2年总生存率分别为93.1%和77.8%(p<0.001),调整后的风险比为0.44(95%CI,0.36 - 0.53;p<0.001)。多变量分析确定,多模式治疗包括CRT(HR,0.42;p = 0.024)和S-RT(HR,0.30;p = 0.024),但不包括S-CRT(HR,0.51;p = 0.086),是HPV阳性III-IVB期疾病OS改善的预测因素。包括S-CRT的多模式治疗与HPV阴性OPSCC的较长OS相关。在HPV阳性癌症中,淋巴结分期与OS的相关性较差。切缘阳性和/或包膜外侵犯的存在与HPV阴性OPSCC的较差OS相关(HR,2.11;p = 0.008),但与HPV阳性OPSCC无关(HR,1.61;p = 0.154)。
NCDB证实了已确定的HPV阳性OPSCC的人口统计学和临床特征。人群分析表明,AJCC分期在HPV阳性癌症中与OS的相关性较差,传统的高危特征可能影响较小。双模式治疗似乎对HPV阳性头颈部鳞状细胞癌有益。